58 results on '"T. Utterback"'
Search Results
2. Complete genome sequence of Neisseria meningitidis serogroup B strain MC58
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William C. Nelson, Debbie S. Parksey, Michelle L. Gwinn, Jonathan A. Eisen, John F. Heidelberg, J. Craig Venter, Karen A. Ketchum, Robert D. Fleischmann, Vincenzo Scarlato, John Gill, Robert J. Dodson, Haiying Qin, Hervé Tettelin, Robert T. DeBoy, Brian Dougherty, E. Richard Moxon, Jessica Vamathevan, Henry Cittone, Steven L. Salzberg, Nigel J. Saunders, Karen E. Nelson, Anne Ciecko, Li Sun, Hamilton O. Smith, Guido Grandi, Jeremy Peterson, Tanya Mason, Emily B. Clark, Owen White, Derek W. Hood, Claire M. Fraser, Erin Hickey, Eric Blair, T. Utterback, Vega Masignani, Alex C. Jeffries, John F. Peden, Daniel H. Haft, Matthew D. Cotton, Hoda Khouri, Mariagrazia Pizza, Rino Rappuoli, Tettelin H., Saunders N.J., Heidelberg J., Jeffries A.C., Nelson K.E., Eisen J.A., Ketchum K.A., Hood D.W., Peden J.F., Dodson R.J., Nelson W.C., Gwinn M.L., DeBoy R., Peterson J.D., Hickey E.K., Haft D.H., Salzberg S.L., White O., Fleischmann R.D., Dougherty B.A., Mason T., Ciecko A., Parksey D.S., Blair E., Cittone H., Clark E.B., Cotton M.D., Utterback T.R., Khouri H., Qin H., Vamathevan J., Gill J., Scarlato V., Masignani V., Pizza M., Grandi G., Sun L., Smith H.O., Fraser C.M., Moxon E.R., Rappuoli R., and Craig Venter J.
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Sequence analysis ,genome sequence ,genetic islands, phase variation ,Molecular Sequence Data ,Virulence ,Bacteremia ,Meningitis, Meningococcal ,Neisseria meningitidis ,medicine.disease_cause ,Genome ,Microbiology ,Evolution, Molecular ,Open Reading Frames ,Bacterial Proteins ,Operon ,medicine ,Antigenic variation ,Humans ,Serotyping ,Gene ,Bacterial Capsules ,Phylogeny ,Recombination, Genetic ,Genetics ,Phase variation ,Antigens, Bacterial ,Multidisciplinary ,biology ,Sequence Analysis, DNA ,biology.organism_classification ,Antigenic Variation ,Meningococcal Infections ,Fimbriae, Bacterial ,Mutation ,Neisseria lactamica ,DNA Transposable Elements ,Transformation, Bacterial ,Genome, Bacterial - Abstract
The 2,272,351–base pair genome ofNeisseria meningitidisstrain MC58 (serogroup B), a causative agent of meningitis and septicemia, contains 2158 predicted coding regions, 1158 (53.7%) of which were assigned a biological role. Three major islands of horizontal DNA transfer were identified; two of these contain genes encoding proteins involved in pathogenicity, and the third island contains coding sequences only for hypothetical proteins. Insights into the commensal and virulence behavior ofN. meningitidiscan be gleaned from the genome, in which sequences for structural proteins of the pilus are clustered and several coding regions unique to serogroup B capsular polysaccharide synthesis can be identified. Finally,N. meningitidiscontains more genes that undergo phase variation than any pathogen studied to date, a mechanism that controls their expression and contributes to the evasion of the host immune system.
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- 2016
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3. Genome sequences of the human body louse and its primary endosymbiont provide insights into the permanent parasitic lifestyle
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Daniel Gerlach, Reed M. Johnson, Granger G. Sutton, Si Hyeock Lee, Didier Raoult, Hongmei Li, Weilin Sun, Robert V. Bruggner, Greg Madey, NaiKuan Wang, Ryan C. Kennedy, Joseph P. Strycharz, David L. Reed, Hugh M. Robertson, Stephen C. Barker, Ewen F. Kirkness, Jeanne Romero-Severson, Montserrat Aguadé, Janice P. Vanzee, Scott Christley, Emily C. Kraus, Frank H. Collins, Brian J. Haas, Shelby L. Bidwell, Evgenia V. Kriventseva, Stephen L. Cameron, Omprakash Mittapalli, Justin Johnson, J. Craig Venter, Venu M. Margam, Julio Rozas, Aleksandar Popadić, Juan Manuel Anzola, Yoshinori Tomoyasu, Jan A. Veenstra, Catherine A. Hill, Evgeny M. Zdobnov, Jose M. C. Tubio, Allison A. Regier, Elisabet Caler, Christine G. Elsik, Claudio J. Struchiner, David Alvarez-Ponce, Dan Graur, Gregory A. Dasch, Manfredo J. Seufferheld, Brian P. Walenz, Barry R. Pittendrigh, Linda Hannick, Robert L. Strausberg, Henk R. Braig, Renfu Shao, Sara Guirao-Rico, Neil F. Lobo, Justin T. Reese, Robert M. Waterhouse, Jason M. Meyer, José M. C. Ribeiro, Marta Tojo, M. Alejandra Perotti, John M. Clark, Eran Elhaik, Lakshmi D. Viswanathan, Filipe G. Vieira, Kyong Sup Yoon, J. Spencer Johnston, May R. Berenbaum, Daniel Lawson, Maria F. Unger, T. Utterback, Vinita Joardar, Gerlach, Daniel, Kriventseva, Evgenia, Waterhouse, Robert, and Zdobnov, Evgeny
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0106 biological sciences ,Genome, Insect ,Molecular Sequence Data ,Genes, Insect ,Genomics ,Louse ,Pediculus humanus ,010603 evolutionary biology ,01 natural sciences ,Genome ,03 medical and health sciences ,Enterobacteriaceae ,Genome, Insect/*genetics ,biology.animal ,Lice Infestations/parasitology ,medicine ,Animals ,Genes, Insect/genetics ,Humans ,ddc:576.5 ,Pediculus/*genetics/*microbiology ,Symbiosis ,Genome, Bacterial/*genetics ,030304 developmental biology ,Comparative genomics ,Genetics ,0303 health sciences ,Multidisciplinary ,biology ,Enterobacteriaceae/genetics ,Pediculus ,Sequence Analysis, DNA ,Genome project ,Lice Infestations ,Biological Sciences ,Body louse ,biology.organism_classification ,medicine.disease ,Trench fever ,Genomics/methods ,Genes, Bacterial ,Genes, Bacterial/genetics ,Genome, Bacterial - Abstract
As an obligatory parasite of humans, the body louse ( Pediculus humanus humanus ) is an important vector for human diseases, including epidemic typhus, relapsing fever, and trench fever. Here, we present genome sequences of the body louse and its primary bacterial endosymbiont Candidatus Riesia pediculicola. The body louse has the smallest known insect genome, spanning 108 Mb. Despite its status as an obligate parasite, it retains a remarkably complete basal insect repertoire of 10,773 protein-coding genes and 57 microRNAs. Representing hemimetabolous insects, the genome of the body louse thus provides a reference for studies of holometabolous insects. Compared with other insect genomes, the body louse genome contains significantly fewer genes associated with environmental sensing and response, including odorant and gustatory receptors and detoxifying enzymes. The unique architecture of the 18 minicircular mitochondrial chromosomes of the body louse may be linked to the loss of the gene encoding the mitochondrial single-stranded DNA binding protein. The genome of the obligatory louse endosymbiont Candidatus Riesia pediculicola encodes less than 600 genes on a short, linear chromosome and a circular plasmid. The plasmid harbors a unique arrangement of genes required for the synthesis of pantothenate, an essential vitamin deficient in the louse diet. The human body louse, its primary endosymbiont, and the bacterial pathogens that it vectors all possess genomes reduced in size compared with their free-living close relatives. Thus, the body louse genome project offers unique information and tools to use in advancing understanding of coevolution among vectors, symbionts, and pathogens.
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- 2010
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4. The map-based sequence of the rice genome
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Shu Mei Liu, Hong-Hwa Chen, Kiran Kumar, Aki Iwabuchi, Luke J. Tallon, Yasuyuki Fujii, Yuichi Ito, Jennifer Currie, Douglas Fadrosh, Bruce Weaver, Hisakazu Iwama, Nahoko Fujitsuka, Arvind K. Bharti, Vivek Dalal, Eric Pelletier, Wataru Karasawa, Carol Soderlund, Masako Okamoto, Ajit K. Pal, Lei Zhang, Tomoko Maehara, Anupama Gaur, Tomotaro Nishikawa, Michiko Ikeda, Jingjie Zhu, Meizhong Luo, Yoshiharu Sato, Dibyendu Kumar, Mikiko Honda, Takuya Habara, Jianyu Song, Yuka Takazaki, Alok Singh, Ari Kikuta, Neilay Dedhia, Thomas E. Bureau, Eric Linton Victor Llaca, Nadia Demange, Yoshiaki Nagamura, Koh Ichi Kadowaki, Takanori Shimokawa, Kohei Arita, Patrick Wincker, Saori Hijishita, Kai Ying, Takahito Bito, Tae-Jin Yang, Mayu Yamamoto, Masahiro Yano, Paulo Dejalma Zimmer, Nagendra K. Singh, Atsuko Idonuma, Jia Liu, Anne Ciecko, Friedrich Engler, Shinji Naito, Pei Fang Lee, Hideki Nagasaki, Jianping Guan, Yoko Ichikawa, Sujit Dike, Shu Ouyang, Yuko Nakama, Masao Hamada, Saurabh Raghuvanshi, Ching San Chen, Teh Yuan Chow, Joseph Hsiao, Béatrice Segurens, Hiroaki Sakai, W. Richard McCombie, Nobukazu Namiki, Hiroyuki Kanamori, Mei-Chu Chung, Yiqi Lu, Claude Scarpelli, Kelly Moffat, Yoshino Chiden, Baltazar A. Antonio, Susan R. McCouch, Paramjit Khurana, Amy Bronzino Nelson, Tamara Feldblyum, Hiroshi Mizuno, Masatoshi Masukawa, Yoshihito Niimura, Tomoya Ohta, Joachim Messing, Yukiyo Ito, Lance E. Palmer, Antonio Costa de Oliveira, Nozomi Ono, Ai Ling Hour, Kumiko Tsuji, Qijun Weng, Michael W. Bevan, Guofan Hong, C. Robin Buell, Subodh K. Srivastava, Atul Bhargava, Galina Fuks, Masahiro Sugiura, Akio Miyao, Kristine Jones, John Yu Liou, Ayano Meguro, Aymeric R. De Vazeille, Mika Tsugane, Xiaohui Liu, Rie Fukunaka, Jean Weissenbach, Shu Jen Lin, Jayati Bera, Tomoya Baba, Yao-Cheng Lin, Lori Spiegel, Laurence Cattolico, Irfan Ahmad Ghazi, Shoko Saji, Jianzhong Wu, Danlin Fan, Takashi Gojobori, Rod A. Wing, Harumi Yamagata, Koji Arikawa, Shuliang Yu, Marcel Salanoubat, Yumi Nakamichi, Kristi Collura, Jetty S.S. Ammiraju, Vipin Gupta, Stephen I. Wright, Y. Huang, Qiang Zhao, Yuichi Katayose, Tingting Lu, Stacey E. Iobst, Akhilesh K. Tyagi, A. O'Shaughnessy, Tilak Raj Sharma, Hiroyoshi Aoki, Kazue Ito, Marina Nakashima, Vydianathan Ravi, J. F. Shaw, Takashi Matsumoto, Tamara Tsitrin, Yoshiyuki Mukai, Steve Reidmuller, Steve Young, Kozue Kamiya, Lidia Nascimento, Qi Feng, Shivani Johri, Kazuko Yukawa, Sylvie Samain, Hirohiko Hirochika, Kimiko Yamamoto, Matthew Reardon, Holly Cordum, Mu Kuei Chu, Kim Yul Ho, Victoria Zismann, Jessica Hill, Tomoko Ito, Gregory Wilson, Isamu Ohta, Bahattin Tanyolac, Amitabh Mohanty, Rie Yoshihara, Nikoleta Juretic, Bin Han, Jie Mu, Susan Van Aken, Satomi Hosokawa, Kayo Machita, Shaohua Jin, Odir Antônio Dellagostin, Satoshi Katagiri, Apichart Vanavichit, Takuji Sasaki, Douglas R. Hoen, Richard K. Wilson, Patrick Minx, Larry Overton, Rentao Song, Kimihiro Terasawa, Jang Ho Hahn, Steve Kavchok, Hiroko Yamane, Parul Khurana, Melissa De La Bastide, Gisela Orjeda, Francis Quetier, Katsumi Sakata, Anita Kapur, Hyeran Kim, Grace Pai, Ian Bancroft, Trilochan Mohapatra, Manami Negishi, Ya Ting Chao, Kanako Kurita, Mari Nakamura, Masaki Fujisawa, Maiko Ikeno, Yu Zhang, Miyuki Sakaguchi, Yuko Nagata, Harumi Kobayashi, Kamlesh Batra, Huisun Zhong, Mary Kim, T. Utterback, Shoji Yoshiki, A. Pandit, Chizuko Harada, Benjamin Burr, Jacqueline Jackson, Jitendra P. Khurana, Michie Shibata, Jiming Jiang, Hue Vuong, Chia Hsiung Cheng, Sachie Ito, Zhukuan Cheng, Qiaoping Yuan, Akiko Hayashi, Tatsumi Mizubayashi, Yeisoo Yu, Nathalie Choisne, Shubha Vij, Noriko Kobayashi, Vivekanand Balija, Hong Pang Wu, K. Sureshbabu, Ying Li, Theresa Zutavern, G. Sangsakoo, Kristen Gansberger, Yujun Zhang, Kazunori Waki, Weiwei Jin, R. Preston, Shigenori Ueda, Yilei Liu, Angélique D'Hont, Kwang-Jen Hsiao, Kumiko Sakai, Richard Bruskiewich, Luiz Anderson Teixeira de Mattos, Teri Rambo, Yue-Ie C. Hsing, Mahavir Yadav, Shinichi Yamamoto, Arnaud Couloux, Sally A. Leong, Kishor Gaikwad, Masumi Iijima, Takeshi Itoh, Gaspar Malone, Gladys Keizer, and Anupam Dixit
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Transposable element ,Identification ,RNA, Untranslated ,Euchromatin ,International Cooperation ,Centromere ,Molecular Sequence Data ,Arabidopsis ,Oryza sativa ,Biology ,Genes, Plant ,Zea mays ,Genome ,Chromosomes, Plant ,F30 - Génétique et amélioration des plantes ,Gene family ,Cloning, Molecular ,Gene ,Sorghum ,Synteny ,Cell Nucleus ,Organelles ,Genetics ,Polymorphism, Genetic ,Génome ,Multidisciplinary ,Computational Biology ,food and beverages ,Oryza ,Genomics ,Sequence Analysis, DNA ,Tandem Repeat Sequences ,Gène ,Multigene Family ,Proteome ,DNA Transposable Elements ,Carte génétique ,Genome, Plant ,Caractère agronomique - Abstract
Rice, one of the world's most important food plants, has important syntenic relationships with the other cereal species and is a model plant for the grasses. Here we present a map-based, finished quality sequence that covers 95% of the 389 Mb genome, including virtually all of the euchromatin and two complete centromeres. A total of 37,544 non-transposable-element-related protein-coding genes were identified, of which 71% had a putative homologue in Arabidopsis. In a reciprocal analysis, 90% of the Arabidopsis proteins had a putative homologue in the predicted rice proteome. Twenty-nine per cent of the 37,544 predicted genes appear in clustered gene families. The number and classes of transposable elements found in the rice genome are consistent with the expansion of syntenic regions in the maize and sorghum genomes. We find evidence for widespread and recurrent gene transfer from the organelles to the nuclear chromosomes. The map-based sequence has proven useful for the identification of genes underlying agronomic traits. The additional single-nucleotide polymorphisms and simple sequence repeats identified in our study should accelerate improvements in rice production.
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- 2005
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5. The psychrophilic lifestyle as revealed by the genome sequence of Colwellia psychrerythraea 34H through genomic and proteomic analyses
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Eugene Melamud, Barbara A. Methé, Xijun Zhang, Tamara Feldblyum, Steven A. Sullivan, Robert J. Dodson, Ramana Madupu, Adrienne L. Huston, Tanja M. Davidsen, Bruce Weaver, Anthony S. Durkin, Martin Wu, Robert T. DeBoy, Janice Weidman, Liwei Zhou, John Moult, William C. Nelson, Claire M. Fraser, Karen E. Nelson, Lauren M. Brinkac, Sean C. Daugherty, Bahram Momen, James F. Kolonay, Jody W. Deming, Hoda Khouri, Matthew R. Lewis, and T. Utterback
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DNA, Bacterial ,Proteomics ,Membrane Fluidity ,Nitrogen ,Molecular Sequence Data ,Marine Biology ,Genomics ,Models, Biological ,Genome ,Bacterial Proteins ,Species Specificity ,Amino Acids ,Psychrophile ,Gene ,Whole genome sequencing ,Genetics ,Multidisciplinary ,biology ,Biological Sciences ,Cold Climate ,biology.organism_classification ,Carbon ,Proteome ,Energy Metabolism ,Gammaproteobacteria ,Genome, Bacterial ,Bacteria - Abstract
The completion of the 5,373,180-bp genome sequence of the marine psychrophilic bacterium Colwellia psychrerythraea 34H, a model for the study of life in permanently cold environments, reveals capabilities important to carbon and nutrient cycling, bioremediation, production of secondary metabolites, and cold-adapted enzymes. From a genomic perspective, cold adaptation is suggested in several broad categories involving changes to the cell membrane fluidity, uptake and synthesis of compounds conferring cryotolerance, and strategies to overcome temperature-dependent barriers to carbon uptake. Modeling of three-dimensional protein homology from bacteria representing a range of optimal growth temperatures suggests changes to proteome composition that may enhance enzyme effectiveness at low temperatures. Comparative genome analyses suggest that the psychrophilic lifestyle is most likely conferred not by a unique set of genes but by a collection of synergistic changes in overall genome content and amino acid composition.
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- 2005
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6. The genome sequence of the anaerobic, sulfate-reducing bacterium Desulfovibrio vulgaris Hildenborough
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Jonathan A. Eisen, George Dimitrov, Naomi L. Ward, A. Scott Durkin, Kevin Tran, Barbara A. Methé, Robert J. Dodson, Sean C. Daugherty, Tanja M. Davidsen, Robert T. DeBoy, Shelley A. Haveman, T. Utterback, Jeremy Peterson, James F. Kolonay, Derrick E. Fouts, Nikhat Zafar, Diana Radune, Claire M. Fraser, Rekha Seshadri, Mark Hance, Gerrit Voordouw, Daniel H. Haft, Ramana Madupu, Ian T. Paulsen, Christopher L. Hemme, Hoda Khouri, William C. Nelson, Steven A. Sullivan, Jeremy D. Selengut, John Gill, Lauren M. Brinkac, John F. Heidelberg, Liwei Zhou, Judy D. Wall, and Tamara Feldblyum
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Anaerobic respiration ,biology ,Molecular Sequence Data ,Biomedical Engineering ,Bioengineering ,Periplasmic space ,biology.organism_classification ,Applied Microbiology and Biotechnology ,Genome ,Bioremediation ,Biochemistry ,Molecular Medicine ,Desulfovibrio vulgaris ,Sulfate-reducing bacteria ,Energy Metabolism ,Gene ,Genome, Bacterial ,Bacteria ,Biotechnology - Abstract
Desulfovibrio vulgaris Hildenborough is a model organism for studying the energy metabolism of sulfate-reducing bacteria (SRB) and for understanding the economic impacts of SRB, including biocorrosion of metal infrastructure and bioremediation of toxic metal ions. The 3,570,858 base pair (bp) genome sequence reveals a network of novel c-type cytochromes, connecting multiple periplasmic hydrogenases and formate dehydrogenases, as a key feature of its energy metabolism. The relative arrangement of genes encoding enzymes for energy transduction, together with inferred cellular location of the enzymes, provides a basis for proposing an expansion to the 'hydrogen-cycling' model for increasing energy efficiency in this bacterium. Plasmid-encoded functions include modification of cell surface components, nitrogen fixation and a type-III protein secretion system. This genome sequence represents a substantial step toward the elucidation of pathways for reduction (and bioremediation) of pollutants such as uranium and chromium and offers a new starting point for defining this organism's complex anaerobic respiration.
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- 2004
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7. Jews in Medieval Christendom : Slay Them Not
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Kristine T. Utterback, Merrall L. Price, Kristine T. Utterback, and Merrall L. Price
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- Judaism (Christian theology)--History of doctrines--Middle Ages, 600-1500, Jews--History--70-1789, Christianity and other religions--Judaism, Judaism--Relations--Christianity, Christianity and antisemitism--History
- Abstract
In Jews in Medieval Christendom: Slay Them Not, an international group of scholars from numerous disciplines examines the manifold ways that medieval Christians coped with the presence of Jews in their midst. The collection's touchstone comes from St. Augustine's interpretation of Psalm 59:11: “Slay them not, lest my people forget: scatter them by thy power; and bring them down,” as it applied to Jews in Christendom, an interpretation that deeply affected medieval Christian strategies for dealing with Jews in Europe. This collection analyzes how medieval writers and artists, often explicitly invoking Augustine, employed his teachings on these strangers within Christian Europe. Contributors include: Nancy Bishop, Kate McGrath, Irven Resnick, Ephraim Shoham-Steiner, K.M. Kletter, Robert Stacey, Jennifer Hart Weed, Jay Ruud, Kristine T. Utterback, Merrall LLewelyn Price, Eveline Brugger, Birgit Wiedl, Carlee A. Bradbury, Judy Schaaf, Barbara Stevenson, Miriamne Ara Krummel, Albrecht Classen.
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- 2013
8. Genome sequence of the dissimilatory metal ion–reducing bacterium Shewanella oneidensis
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Jonathan A. Eisen, Jeremy Peterson, J. Craig Venter, Robert J. Dodson, Timothy D. Read, William C. Nelson, Lowell Umayam, John Gill, James Scott, Janice Weidman, K. Lee, T. Utterback, Kenneth H. Nealson, Robert T. DeBoy, Terry E. Meyer, Tamara Feldblyum, Lisa McDonald, Lauren M. Brinkac, Eric Gaidos, A. Scott Durkin, Claire M. Fraser, Kristy Berry, Sean C. Daugherty, Owen White, Karen E. Nelson, Hamilton O. Smith, Alex M. Wolf, Ian T. Paulsen, Hoda Khouri, Marjorie Impraim, Rekha Seshadri, John F. Heidelberg, A. I. Tsapin, Rebecca A. Clayton, Chris Lee, Daniel H. Haft, Jessica Vamathevan, Naomi L. Ward, Ramana Madupu, Barbara A. Methé, Maureen J. Beanan, James F. Kolonay, and Jacob L. Mueller
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Proteomics ,Shewanella ,Hydrogenase ,Cell Respiration ,Molecular Sequence Data ,Biomedical Engineering ,Gene Expression ,Bioengineering ,Computational biology ,Applied Microbiology and Biotechnology ,Genome ,Water Purification ,Genome engineering ,Electron Transport ,Open Reading Frames ,Plasmid ,Species Specificity ,Sequence Analysis, Protein ,Amino Acid Sequence ,Organic Chemicals ,Shewanella oneidensis ,Whole genome sequencing ,Genetics ,biology ,Gene Expression Regulation, Bacterial ,Sequence Analysis, DNA ,Periplasmic space ,biology.organism_classification ,Biodegradation, Environmental ,Metals ,Molecular Medicine ,Oxidation-Reduction ,Sequence Alignment ,Genome, Bacterial ,Water Pollutants, Chemical ,Plasmids ,Biotechnology - Abstract
Shewanella oneidensis is an important model organism for bioremediation studies because of its diverse respiratory capabilities, conferred in part by multicomponent, branched electron transport systems. Here we report the sequencing of the S. oneidensis genome, which consists of a 4,969,803-base pair circular chromosome with 4,758 predicted protein-encoding open reading frames (CDS) and a 161,613-base pair plasmid with 173 CDSs. We identified the first Shewanella lambda-like phage, providing a potential tool for further genome engineering. Genome analysis revealed 39 c-type cytochromes, including 32 previously unidentified in S. oneidensis, and a novel periplasmic [Fe] hydrogenase, which are integral members of the electron transport system. This genome sequence represents a critical step in the elucidation of the pathways for reduction (and bioremediation) of pollutants such as uranium (U) and chromium (Cr), and offers a starting point for defining this organism's complex electron transport systems and metal ion-reducing capabilities.
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- 2002
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9. A Novel Lipothrixvirus, SIFV, of the Extremely Thermophilic Crenarchaeon Sulfolobus
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Jakob K Kristjanson, Ingelore Holz, Ulrike Ziese, Karen E. Nelson, Hans Peter Arnold, T. Utterback, Jan F Weidmann, Marie Crosby, Hans-Peter Klenk, Wolfram Zillig, and Claire M. Fraser
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archaea ,genome sequence ,viruses ,Molecular Sequence Data ,Genome, Viral ,virion structure ,lipid envelope ,Genome ,Sulfolobus ,Open Reading Frames ,Viral Proteins ,chemistry.chemical_compound ,Viral envelope ,Virology ,Amino Acid Sequence ,ORFS ,Genetics ,Whole genome sequencing ,Base Sequence ,Sequence Homology, Amino Acid ,biology ,Crenarchaeota ,Helicase ,Sequence Analysis, DNA ,biology.organism_classification ,Open reading frame ,chemistry ,DNA, Viral ,Viruses ,biology.protein ,Electrophoresis, Polyacrylamide Gel ,Sequence Alignment ,DNA - Abstract
We describe a novel lipothrixvirus, SIFV, of the crenarchaeotal archaeon Sulfolobus islandicus. SIFV ( S . i slandicus f ilamentous v irus) has a linear virion with a linear double-stranded DNA genome. These two features coincide in several crenarchaeotal but not in any other viruses. The SIFV core is formed by a zipper-like array of DNA-associated protein subunits and is covered by a lipid envelope containing host lipids. We sequenced ∼96% of the virus genome excepting the DNA termini, which were modified in an unusual, yet uncharacterized, manner. Both, the 5′ and the 3′ DNA termini were insensitive to enzymatic degradation and labelling. Two open reading frames (ORFs) of the SIFV genome are likely to encode helicases and resemble uncharacterized ORFs from other archaea in sequence. Three ORFs showed sequence similarity with each other and each contained a glycosyl transferase motif. Another ORF of the SIFV genome showed significant sequence similarity to the ORF a291 from the well characterized, spindle-shaped Sulfolobus virus SSV1. Due to its structure, SIFV is classified as a lipothrixvirus.
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- 2000
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10. Jews in Medieval Christendom
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Merrall Llewelyn Price and Kristine T. Utterback
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History ,Judaism ,Interpretation (philosophy) ,Ancient history ,Classics - Abstract
In Jews in Medieval Christendom: Slay Them Not, a diverse group of international scholars from various disciplines considers Jewish/Christian relations in medieval Europe, based on St. Augustine’s interpretation of Psalm 51:11: “Slay them not, lest my people forget”.
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- 2013
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11. 'Conversi' Revert: Voluntary and Forced Return to Judaism in the Early Fourteenth Century
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Kristine T. Utterback
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Cultural Studies ,History ,Judaism ,Religious studies ,Coercion ,Christianity ,Politics ,Brute force ,Western europe ,Baptismal font ,Ethnology ,Christian culture - Abstract
Forced to choose between conversion and death, many medieval Jews chose to be baptized as Christians. While not all Jews in Western Europe faced such stark choices, during the fourteenth century pressure increased on the Jewish minority to join the Christian majority. Economic, social, and political barriers to Jews often made conversion a necessity or at least an advantage, exerting a degree of coercion even without brute force. Once baptized these new Christians, called conversi, were required to abandon their Jewish practices entirely. But what kind of life actually awaited these converts? In the abstract, the converts had clear options: they could either remain Christians or return to judaism. Reality would surely reveal a range of possibilities, however, as these conversi tried to live out their conversion or to reject it without running afoul of the authorities. While the dominant Christian culture undoubtedly exerted pressure to convert, Jews did not necessarily sit idly by while their people approached the baptismal font. Some conversi felt contrary pressure to take up Judaism again. In the most extreme cases, conversi who reverted to Judaism faced death as well. This paper examines forces exerted on Jewish converts to Christianity to return to Judaism, using examples from France and northern Spain in the first half of the fourteenth century.
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- 1995
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12. Worship at the church of your choice? Church attendance in mid- fourteenth-century Barcelona
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Kristine T. Utterback
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History ,Church attendance ,Law ,media_common.quotation_subject ,Legislation ,Altar ,Enforcement ,Worship ,media_common - Abstract
Despite various attempts to enforce church attendance at one's parish church, at least from the time of Lateran IV in 1215 and continued in synodal legislation, enforcement was not totally successful. This paper examines evidence which shows that some of the parishioners in the diocese of Barcelona in the mid-fourteenth century did in fact attend services away from their parish churches. The documents which illustrate these practices are drawn from the Communia registers of cases which came before the bishop's court in the diocese of Barcelona between 1344 and 1355. These registers show the diocesan attempts to regulate the practice of non-attendance by prohibition and threats to the clergy who were allowing it, as well as licenses which allowed just such worship outside the parish church, either at another church or at a private altar. The actual parish and diocesan practices illustrated in these registers help to balance the picture of an increasingly centralized church structure.
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- 1991
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13. The Sorcerer II Global Ocean Sampling expedition: northwest Atlantic through eastern tropical Pacific
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Jonathan A. Eisen, Luisa I. Falcón, Jeff Hoffman, Dongying Wu, Joseph E. Venter, Valeria Souza, Shannon J. Williamson, Karen Beeson, Kenneth H. Nealson, Yu-Hui Rogers, Aaron L. Halpern, Kelvin Li, Germán Bonilla-Rosso, Robert Friedman, Jason Freeman, Karin A. Remington, Clare Stewart, Michael Ferrari, Douglas B. Rusch, Holly Baden-Tillson, Shubha Sathyendranath, Marvin Frazier, Granger G. Sutton, T. Utterback, Eldredge Bermingham, Robert L. Strausberg, Karla B. Heidelberg, Luis E. Eguiarte, J. Craig Venter, Cynthia Andrews-Pfannkoch, Victor A. Gallardo, David M. Karl, Trevor Platt, Saul A. Kravitz, John F. Heidelberg, Giselle Tamayo-Castillo, Bao Duc Tran, Hamilton O. Smith, Joyce Thorpe, Shibu Yooseph, and Moran, Nancy A
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Pelagibacter ubique ,Genome evolution ,Food Chain ,QH301-705.5 ,Oceans and Seas ,Genomics ,Medical and Health Sciences ,General Biochemistry, Genetics and Molecular Biology ,Species Specificity ,Phylogenetics ,Genetics ,Biology (General) ,Clade ,Comparative genomics ,General Immunology and Microbiology ,biology ,Agricultural and Veterinary Sciences ,Ecology ,General Neuroscience ,Human Genome ,Computational Biology ,Biological Sciences ,biology.organism_classification ,Plankton ,Phylogenetic diversity ,Metagenomics ,General Agricultural and Biological Sciences ,Water Microbiology ,Biotechnology ,Developmental Biology - Abstract
The world's oceans contain a complex mixture of micro-organisms that are for the most part, uncharacterized both genetically and biochemically. We report here a metagenomic study of the marine planktonic microbiota in which surface (mostly marine) water samples were analyzed as part of the Sorcerer II Global Ocean Sampling expedition. These samples, collected across a several-thousand km transect from the North Atlantic through the Panama Canal and ending in the South Pacific yielded an extensive dataset consisting of 7.7 million sequencing reads (6.3 billion bp). Though a few major microbial clades dominate the planktonic marine niche, the dataset contains great diversity with 85% of the assembled sequence and 57% of the unassembled data being unique at a 98% sequence identity cutoff. Using the metadata associated with each sample and sequencing library, we developed new comparative genomic and assembly methods. One comparative genomic method, termed "fragment recruitment," addressed questions of genome structure, evolution, and taxonomic or phylogenetic diversity, as well as the biochemical diversity of genes and gene families. A second method, termed "extreme assembly," made possible the assembly and reconstruction of large segments of abundant but clearly nonclonal organisms. Within all abundant populations analyzed, we found extensive intra-ribotype diversity in several forms: (1) extensive sequence variation within orthologous regions throughout a given genome; despite coverage of individual ribotypes approaching 500-fold, most individual sequencing reads are unique; (2) numerous changes in gene content some with direct adaptive implications; and (3) hypervariable genomic islands that are too variable to assemble. The intra-ribotype diversity is organized into genetically isolated populations that have overlapping but independent distributions, implying distinct environmental preference. We present novel methods for measuring the genomic similarity between metagenomic samples and show how they may be grouped into several community types. Specific functional adaptations can be identified both within individual ribotypes and across the entire community, including proteorhodopsin spectral tuning and the presence or absence of the phosphate-binding gene PstS.
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- 2007
14. Draft Genome Sequence of the Sexually Transmitted Pathogen Trichomonas vaginalis
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Gareth D. Westrop, Cedric Simillion, Richard D. Hayes, Jan Tachezy, Pavel Dolezal, Owen White, Cheng-Hsun Chiu, Hanbang Zhang, Cheryl Y. M. Okumura, Felix D. Bastida-Corcuera, Ian T. Paulsen, Shehre-Banoo Malik, Sylke Müller, Joana C. Silva, Qi Zhao, T. Martin Embley, Robert P. Hirt, Steven L. Salzberg, Mark T. Brown, Mandira Mukherjee, Jeremy C. Mottram, Mihaela Pertea, Ying-Shiung Lee, Rachel E. Schneider, Michael C. Schatz, T. Utterback, Jennifer R. Wortman, Augusto Simoes-Barbosa, Chung-Li Shu, Alias J. Smith, Kazutoyo Osoegawa, Ivan Hrdy, Graham H. Coombs, Jacqueline A. Upcroft, Diego Miranda-Saavedra, Pieter J. de Jong, Peter G. Foster, Christophe Noël, Zuzana Zubáčová, Stepanka Vanacova, Katrin Henze, Brian J. Haas, Jane M. Carlton, U. Cecilia M. Alsmark, Peter Upcroft, Joel B. Dacks, Daniele Dessì, Thomas Sicheritz-Pontén, Yves Van de Peer, Arti Gupta, Claire M. Fraser-Liggett, Petrus Tang, Patricia J. Johnson, Tamara Feldblyum, Maria Villalvazo, Qinghu Ren, Shelby L. Bidwell, Arthur L. Delcher, R. L. Dunne, Ching C. Wang, John M. Logsdon, Pier Luigi Fiori, Sébastien Besteiro, Geoffrey J. Barton, and Lenka Horváthová
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Transposable element ,Gene Transfer, Horizontal ,Genes, Protozoan ,Molecular Sequence Data ,Protozoan Proteins ,Sexually Transmitted Diseases ,Trichomonas Infection ,Trichomonas Infections ,Biology ,medicine.disease_cause ,Genome ,Article ,medicine ,Trichomonas vaginalis ,Animals ,Humans ,RNA Processing, Post-Transcriptional ,Gene ,Genomic organization ,Repetitive Sequences, Nucleic Acid ,Whole genome sequencing ,Genetics ,Organelles ,Multidisciplinary ,Biological Transport ,Sequence Analysis, DNA ,DNA, Protozoan ,Oxidative Stress ,Multigene Family ,Horizontal gene transfer ,DNA Transposable Elements ,Genome, Protozoan ,Metabolic Networks and Pathways ,Hydrogen ,Peptide Hydrolases - Abstract
We describe the genome sequence of the protist Trichomonas vaginalis , a sexually transmitted human pathogen. Repeats and transposable elements comprise about two-thirds of the ∼160-megabase genome, reflecting a recent massive expansion of genetic material. This expansion, in conjunction with the shaping of metabolic pathways that likely transpired through lateral gene transfer from bacteria, and amplification of specific gene families implicated in pathogenesis and phagocytosis of host proteins may exemplify adaptations of the parasite during its transition to a urogenital environment. The genome sequence predicts previously unknown functions for the hydrogenosome, which support a common evolutionary origin of this unusual organelle with mitochondria.
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- 2007
15. Authorized Limit Evaluation of Spent Granular Activated Carbon Used for Vapor-Phase Remediation at the Lawrence Livermore National Laboratory Livermore, California
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T Utterback and R Devany
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education.field_of_study ,Engineering ,Waste management ,business.industry ,Environmental remediation ,Population ,Environmental engineering ,Radioactive waste ,Remedial action ,Hazardous waste ,Mixed waste ,Radiation protection ,Resource Conservation and Recovery Act ,business ,education - Abstract
This report provides a technical basis for establishing radiological release limits for granular activated carbon (GAC) containing very low quantities of tritium and radon daughter products generated during environmental remediation activities at Lawrence Livermore National Laboratory (LLNL). This evaluation was conducted according to the Authorized Limit procedures specified in United States Department of Energy (DOE) Order 5400.5, Radiation Protection of the Public and the Environment (DOE, 1993) and related DOE guidance documents. The GAC waste is currently being managed by LLNL as a Resource Conservation and Recovery Act (RCRA) mixed waste. Significant cost savings can be achieved by developing an Authorized Limit under DOE Order 5400.5 since it would allow the waste to be safely disposed as a hazardous waste at a permitted off-site RCRA treatment and disposal facility. LLNL generates GAC waste during vapor-phase soil remediation in the Trailer 5475 area. While trichloroethylene and other volatile organic compounds (VOCs) are the primary targets of the remedial action, a limited amount of tritium and radon daughter products are contained in the GAC at the time of disposal. As defined in DOE Order 5400.5, an Authorized Limit is a level of residual radioactive material that will result in an annual publicmore » dose of 100 milliroentgen-equivalent man per year (mrem/year) or less. In 1995, DOE issued additional release requirements for material sent to a landfill that is not an authorized low-level radioactive waste disposal facility. Per guidance, the disposal site will be selected based on a risk/benefit assessment under the As-Low-As-Reasonably-Achievable (ALARA) process while ensuring that individual doses to the public are less than 25 mrem in a year, ground water is protected, the release would not necessitate further remedial action for the disposal site, and the release is coordinated with all appropriate authorities. The 1995 release requirements also state that Authorized Limits may be approved by DOE field office managers without DOE headquarters (EH-1) approval if a reasonably conservative dose assessment demonstrates that: (1) Public doses will not exceed one mrem per year individually or 10 person-rem/year collectively; (2) Appropriate record keeping and data collection procedures are in place; (3) Copies of the release evaluation and procedures are properly maintained; and (4) Coordination with all applicable state and federal agencies is documented. Based on the above guidelines, this report uses one mrem/year for individual members of the public and 10 person-rem/year for the collective population as upper-bound doses for the determination of Authorized Limits.« less
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- 2007
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16. EXPLORING THE OCEAN'S MICROBES: SEQUENCING THE SEVEN SEAS
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Bao Tran, Jeff Hoffman, Valeria Souza, Brooke A. Dill, David M. Karl, Joyce Thorpe, Robert Friedman, Shubha Sathyendranath, German Bonilla, Vineet Bafna, Shaojie Zhang, Douglas B. Rusch, Shibu Yooseph, Joseph E. Venter, Kenneth H. Nealson, J. Craig Venter, Cyrus Foote, Jason Freemen, Holly Baden-Tillson, Eldredge Bermingham, Cindy Pfannkoch, Giselle Tamayo, Victor A. Gallardo, Shannon J. Williamson, Karen Beeson, Trevor Platt, Hamilton O. Smith, Yu-Hui Rogers, John F. Heidelberg, Karin A. Remington, Robert L. Strausberg, Clare Stewart, Jonathan A. Eisen, Luis E. Eguiarte, Aaron L. Halpern, Marvin Frazier, Luisa I. Falcón, Charles H. Howard, T. Utterback, Granger G. Sutton, Dongying Wu, and Karla B. Heidelberg
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German ,Fishery ,Nova scotia ,Genomic research ,Mexico city ,language ,Biology ,Falcon ,Archaeology ,computer ,language.human_language ,computer.programming_language - Abstract
Marvin E. Frazier,Douglas B. Rusch, Aaron L. Halpern, Karla B. Heidelberg, Granger Sutton, Shannon Williamson, Shibu Yooseph, Dongying Wu, Jonathan A. Eisen, Jeff Hoffman, Charles H. Howard, Cyrus Foote, Brooke A. Dill, Karin Remington, Karen Beeson, Bao Tran, Hamilton Smith, Holly Baden-Tillson, Clare Stewart, Joyce Thorpe, Jason Freemen, Cindy Pfannkoch, Joseph E. Venter, John Heidelberg, Terry Utterback, Yu-Hui Rogers, Shaojie Zhang, Vineet Bafna, Luisa Falcon, Valeria Souza,German Bonilla, Luis E. Eguiarte , David M. Karl, Ken Nealson, Shubha Sathyendranath, Trevor Platt, Eldredge Bermingham, Victor Gallardo, Giselle Tamayo, Robert Friedman, Robert Strausberg, J. Craig Venter 1 J. Craig Venter Institute, Rockville, Maryland, United States Of America 2 The Institute For Genomic Research, Rockville, Maryland, United States Of America 3 Department of Computer Science, University of California San Diego 4 Instituto de Ecologia Dept. Ecologia Evolutiva, National Autonomous University of Mexico Mexico City, 04510 Distrito Federal, Mexico 5 University of Hawaii, Honolulu, United States of America 6 Dept. of Earth Sciences, University of Southern California, Los Angeles, California, United States of America 7 Dalhousie University, Halifax, Nova Scotia, Canada 8 Smithsonian Tropical Research Institute, Balboa, Ancon, Republic of Panama 9 University of Concepcion, Concepcion, Chile 10 University of Costa Rica, San Pedro, San Jose, Republic of Costa Rica
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- 2006
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17. Insights on evolution of virulence and resistance from the complete genome analysis of an early methicillin-resistant Staphylococcus aureus strain and a biofilm-producing methicillin-resistant Staphylococcus epidermidis strain
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Robert J. Dodson, Lingxia Jiang, Chris Lee, Claire M. Fraser, Derrick E. Fouts, Daniel H. Haft, Sean C. Daugherty, Jacques Ravel, Haiying Qin, Steven R. Gill, Ioana R. Hance, Mauren Beanan, George Dimitrov, A. Scott Durkin, Ian T. Paulsen, Jessica Vamathevan, James F. Kolonay, Karen E. Nelson, Emmanuel F. Mongodin, Kevin Tran, Kathy Kang, T. Utterback, Samuel V. Angiuoli, Gordon L. Archer, Robert T. DeBoy, Lauren M. Brinkac, Jan Weidman, R. Madupu, and H. Khouri
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Staphylococcus aureus ,Gene Transfer, Horizontal ,Genomic Islands ,Genomics and Proteomics ,Molecular Sequence Data ,Virulence ,Biology ,medicine.disease_cause ,Microbiology ,Genome ,Virulence factor ,Evolution, Molecular ,Open Reading Frames ,Staphylococcus epidermidis ,medicine ,Molecular Biology ,Phylogeny ,Polyglutamate ,Methicillin-resistant Staphylococcus epidermidis ,Chromosome Mapping ,biology.organism_classification ,Methicillin-resistant Staphylococcus aureus ,Biofilms ,Methicillin Resistance ,Genome, Bacterial - Abstract
Staphylococcus aureus is an opportunistic pathogen and the major causative agent of numerous hospital- and community-acquired infections. Staphylococcus epidermidis has emerged as a causative agent of infections often associated with implanted medical devices. We have sequenced the ∼2.8-Mb genome of S. aureus COL, an early methicillin-resistant isolate, and the ∼2.6-Mb genome of S. epidermidis RP62a, a methicillin-resistant biofilm isolate. Comparative analysis of these and other staphylococcal genomes was used to explore the evolution of virulence and resistance between these two species. The S. aureus and S. epidermidis genomes are syntenic throughout their lengths and share a core set of 1,681 open reading frames. Genome islands in nonsyntenic regions are the primary source of variations in pathogenicity and resistance. Gene transfer between staphylococci and low-GC-content gram-positive bacteria appears to have shaped their virulence and resistance profiles. Integrated plasmids in S. epidermidis carry genes encoding resistance to cadmium and species-specific LPXTG surface proteins. A novel genome island encodes multiple phenol-soluble modulins, a potential S. epidermidis virulence factor. S. epidermidis contains the cap operon, encoding the polyglutamate capsule, a major virulence factor in Bacillus anthracis . Additional phenotypic differences are likely the result of single nucleotide polymorphisms, which are most numerous in cell envelope proteins. Overall differences in pathogenicity can be attributed to genome islands in S. aureus which encode enterotoxins, exotoxins, leukocidins, and leukotoxins not found in S. epidermidis .
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- 2005
18. The genome of the basidiomycetous yeast and human pathogen Cryptococcus neoformans
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Martin Krzywinski, Heesun Shin, Paola Roncaglia, Joseph Heitman, Readman Chiu, Natasja Wye, Dan Bruno, James A. Fraser, Ian Bosdet, Thomas G. Mitchell, Paolo Amedeo, Charles A. Specht, James W. Kronstad, Brian L. Wickes, Marilyn Fukushima, Jacqueline E. Schein, Richard W. Hyman, Carrie Mathewson, Alla Shvartsbeyn, Klaus B. Lengeler, Robert E. Marra, Brian J. Haas, Aaron Tenney, Hean L. Koo, Deborah S. Fox, June Kwon-Chung, Jennifer R. Wortman, Claire M. Fraser, Maureen J. Donlin, Brendan J. Loftus, Cletus D'Souza, Ronald W. Davis, Jonathan E. Allen, Jennifer K. Lodge, Martin Shumway, Marco A. Marra, Iain J. Anderson, Eula Fung, Viktoriya Grinberg, Steven J.M. Jones, Bernard B. Suh, Rama Maiti, Jianmin Fu, Molly Miranda, Michael R. Brent, T. Utterback, Tamara L. Doering, Guilhem Janbon, Florenta R. Riggs, Jessica Vamathevan, Steven L. Salzberg, Don Rowley, James Huang, Mihaela Pertea, and University of Groningen
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Transposable element ,Transcription, Genetic ,Virulence Factors ,Genes, Fungal ,Molecular Sequence Data ,Polymorphism, Single Nucleotide ,Genome ,SEQUENCE ,Article ,Fungal Proteins ,SACCHAROMYCES-CEREVISIAE ,Cell Wall ,Polysaccharides ,Humans ,RNA, Antisense ,Genomic library ,Gene ,Gene Library ,Genomic organization ,Cryptococcus neoformans ,Genetics ,Fungal protein ,Polymorphism, Genetic ,Multidisciplinary ,Virulence ,biology ,Alternative splicing ,Computational Biology ,Sequence Analysis, DNA ,biology.organism_classification ,Introns ,EVOLUTION ,Alternative Splicing ,Phenotype ,DNA Transposable Elements ,Chromosomes, Fungal ,Genome, Fungal - Abstract
Cryptococcus neoformans is a basidiomycetous yeast ubiquitous in the environment, a model for fungal pathogenesis, and an opportunistic human pathogen of global importance. We have sequenced its â¼20-megabase genome, which contains â¼6500 intron-rich gene structures and encodes a transcriptome abundant in alternatively spliced and antisense messages. The genome is rich in transposons, many of which cluster at candidate centromeric regions. The presence of these transposons may drive karyotype instability and phenotypic variation. C. neoformans encodes unique genes that may contribute to its unusual virulence properties, and comparison of two phenotypically distinct strains reveals variation in gene content in addition to sequence polymorphisms between the genomes.
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- 2005
19. Enrichment of gene-coding sequences in maize by genome filtration
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M. A. Budiman, Catherine A. Whitelaw, T. Feldblyum, S. van Heeringen, M. Williams, Yuandan Lee, Li Zheng, John Quackenbush, K. Schubert, Jeffrey L. Bennetzen, N. Lakey, Yinan Yuan, Phillip SanMiguel, Agnes P. Chan, Claire M. Fraser, Roger N. Beachy, Svetlana Karamycheva, Foo Cheung, J.A. Bedell, Geo Pertea, A. Resnick, Steven B. Riedmuller, S. van Aken, W. B. Barbazuk, and T. Utterback
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DNA, Plant ,Retroelements ,Transcription, Genetic ,Molecular Sequence Data ,Gene Dosage ,Hybrid genome assembly ,Biology ,Genes, Plant ,Genome ,Zea mays ,DNA sequencing ,Chromosomes, Plant ,Contig Mapping ,Cloning, Molecular ,Gene ,Genome size ,Gene Library ,Repetitive Sequences, Nucleic Acid ,Genetics ,Expressed Sequence Tags ,Multidisciplinary ,Contig ,Computational Biology ,Genome project ,Sequence Analysis, DNA ,DNA Methylation ,Databases, Nucleic Acid ,Sequence Alignment ,Genome, Plant ,Reference genome - Abstract
Approximately 80% of the maize genome comprises highly repetitive sequences interspersed with single-copy, gene-rich sequences, and standard genome sequencing strategies are not readily adaptable to this type of genome. Methodologies that enrich for genic sequences might more rapidly generate useful results from complex genomes. Equivalent numbers of clones from maize selected by techniques called methylation filtering and High C 0 t selection were sequenced to generate â¼200,000 reads (approximately 132 megabases), which were assembled into contigs. Combination of the two techniques resulted in a sixfold reduction in the effective genome size and a fourfold increase in the gene identification rate in comparison to a nonenriched library.
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- 2003
20. Genome of Geobacter sulfurreducens: metal reduction in subsurface environments
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Bao Tran, Jeremy D. Selengut, H. Khouri, R. Madupu, S. van Aken, Nikhat Zafar, Sean C. Daugherty, Lauren M. Brinkac, Ian T. Paulsen, James F. Kolonay, T. Utterback, John F. Heidelberg, Michelle L. Gwinn, Dongying Wu, Robert T. DeBoy, Tanja M. Davidsen, Tamara Feldblyum, Daniel H. Haft, Claudia M. Romero, J. Weidman, Karen E. Nelson, Naomi L. Ward, Derek R. Lovley, William C. Nelson, Claire M. Fraser, Jonathan A. Eisen, Robert J. Dodson, Martin Wu, Barbara A. Methé, Maureen J. Beanan, Owen White, Heather Forberger, Steven A. Sullivan, and Anthony S. Durkin
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Movement ,chemistry.chemical_element ,Computational biology ,Acetates ,Genome ,Metal ,Electron Transport ,Open Reading Frames ,Bioremediation ,Bacterial Proteins ,Acetyl Coenzyme A ,Genes, Regulator ,Anaerobiosis ,Geobacter sulfurreducens ,Organism ,Phylogeny ,Multidisciplinary ,biology ,Ecology ,Chemotaxis ,Cytochromes c ,Chromosomes, Bacterial ,biology.organism_classification ,Electron transport chain ,Aerobiosis ,Carbon ,chemistry ,Genes, Bacterial ,Metals ,visual_art ,visual_art.visual_art_medium ,Energy Metabolism ,Geobacter ,Oxidation-Reduction ,Genome, Bacterial ,Hydrogen - Abstract
The complete genome sequence of Geobacter sulfurreducens , a δ-proteobacterium, reveals unsuspected capabilities, including evidence of aerobic metabolism, one-carbon and complex carbon metabolism, motility, and chemotactic behavior. These characteristics, coupled with the possession of many two-component sensors and many c-type cytochromes, reveal an ability to create alternative, redundant, electron transport networks and offer insights into the process of metal ion reduction in subsurface environments. As well as playing roles in the global cycling of metals and carbon, this organism clearly has the potential for use in bioremediation of radioactive metals and in the generation of electricity.
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- 2003
21. Role of mobile DNA in the evolution of vancomycin-resistant Enterococcus faecalis
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R. Madupu, Sean C. Daugherty, William C. Nelson, J. Upton, Scott Durkin, James F. Kolonay, L. Banerjei, Robert J. Dodson, John F. Heidelberg, Steven R. Gill, Ian T. Paulsen, Derrick E. Fouts, Lowell Umayam, Garry S. A. Myers, Brian Dougherty, Robert T. DeBoy, Jessica Vamathevan, Rekha Seshadri, T. Utterback, Karen E. Nelson, K. A. Ketchum, T. Hansen, Jonathan A. Eisen, Lauren M. Brinkac, Bao Tran, H Tettelin, H. Khouri, Jyoti Shetty, Claire M. Fraser, Timothy D. Read, Maureen J. Beanan, and Diana Radune
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Transposable element ,Gene Transfer, Horizontal ,General Science & Technology ,Virulence Factors ,Biology ,Genome ,Synteny ,Enterococcus faecalis ,Bacterial Adhesion ,Microbiology ,Open Reading Frames ,Plasmid ,Bacterial Proteins ,Lysogenic cycle ,Drug Resistance, Multiple, Bacterial ,Humans ,Adhesins, Bacterial ,Lysogeny ,Gram-Positive Bacterial Infections ,Conserved Sequence ,Genetics ,Whole genome sequencing ,Multidisciplinary ,Virulence ,Nucleic acid sequence ,Vancomycin Resistance ,Sequence Analysis, DNA ,biochemical phenomena, metabolism, and nutrition ,Chromosomes, Bacterial ,biology.organism_classification ,Biological Evolution ,Interspersed Repetitive Sequences ,Oxidative Stress ,Conjugation, Genetic ,DNA Transposable Elements ,Mobile genetic elements ,Carrier Proteins ,Digestive System ,Genome, Bacterial ,Plasmids - Abstract
The complete genome sequence of Enterococcus faecalis V583, a vancomycin-resistant clinical isolate, revealed that more than a quarter of the genome consists of probable mobile or foreign DNA. One of the predicted mobile elements is a previously unknown vanB vancomycin-resistance conjugative transposon. Three plasmids were identified, including two pheromone-sensing conjugative plasmids, one encoding a previously undescribed pheromone inhibitor. The apparent propensity for the incorporation of mobile elements probably contributed to the rapid acquisition and dissemination of drug resistance in the enterococci.
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- 2003
22. Complete genome sequence and comparative analysis of the metabolically versatile Pseudomonas putida KT2440
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A. Düsterhöft, Jonathan A. Eisen, Daniel S. Kosack, Robert J. Dodson, A. Moazzez, V. A. P. Martins Dos Santos, Claire M. Fraser, H. Hilbert, Jeremy Peterson, J. Lauber, Kevin Tran, H. Wedler, Maureen J. Beanan, Owen White, D. Moestl, Jörg D. Hoheisel, Ramana Madupu, Sean C. Daugherty, C. Kiewitz, Mark A. Holmes, Robert T. DeBoy, P. Chris Lee, Erik Holtzapple, Hoda Khouri, Burkhard Tümmler, Diana Stjepandic, David J. Scanlan, Lauren M. Brinkac, Derrick E. Fouts, K. Lee, Ioana R. Hance, Mihai Pop, Christian Weinel, William C. Nelson, M. Rizzo, Steven R. Gill, Ian T. Paulsen, James F. Kolonay, Kenneth N. Timmis, T. Utterback, Sabina Heim, Karen E. Nelson, and M. Straetz
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Sequence analysis ,Molecular Sequence Data ,Virulence ,Computational biology ,medicine.disease_cause ,Microbiology ,Genome ,Open Reading Frames ,Microbial ecology ,Bacterial Proteins ,medicine ,Life Science ,Pseudomonas exotoxin ,Gene ,Ecology, Evolution, Behavior and Systematics ,Phylogeny ,Genetics ,Whole genome sequencing ,biology ,Base Sequence ,Pseudomonas aeruginosa ,Pseudomonas putida ,biology.organism_classification ,Genes, Bacterial ,Energy Metabolism ,Genome, Bacterial - Abstract
Pseudomonas putida is a metabolically versatile saprophytic soil bacterium that has been certified as a biosafety host for the cloning of foreign genes. The bacterium also has considerable potential for biotechnological applications. Sequence analysis of the 6.18 Mb genome of strain KT2440 reveals diverse transport and metabolic systems. Although there is a high level of genome conservation with the pathogenic Pseudomonad Pseudomonas aeruginosa (85% of the predicted coding regions are shared), key virulence factors including exotoxin A and type III secretion systems are absent. Analysis of the genome gives insight into the non-pathogenic nature of P. putida and points to potential new applications in agriculture, biocatalysis, bioremediation and bioplastic production.
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- 2003
23. Whole-genome comparison of Mycobacterium tuberculosis clinical and laboratory strains
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Steven L. Salzberg, Robert T. DeBoy, Hoda Khouri, William R. Jacobs, L. Carpenter, T. Utterback, Maria D. Ermolaeva, Owen White, Jonathan A. Eisen, J. C. Venter, Lowell Umayam, Robert J. Dodson, Erin Hickey, William R. Bishai, Arthur L. Delcher, Daniel H. Haft, Janice Weidman, Robert D. Fleischmann, A. Mikula, John Gill, Jeremy Peterson, William C. Nelson, David Alland, Michelle L. Gwinn, James F. Kolonay, and Claire M. Fraser
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Nonsynonymous substitution ,Molecular Sequence Data ,Virulence ,Biology ,Microbiology ,Genome ,Polymorphism, Single Nucleotide ,Mycobacterium tuberculosis ,Evolution, Molecular ,Bacterial Proteins ,Genetic variation ,Gene family ,Humans ,Tuberculosis ,Genetic variability ,Molecular Biology ,Gene ,Phylogeny ,Genetics ,Polymorphism, Genetic ,Genetic Variation ,Sequence Analysis, DNA ,biology.organism_classification ,Sequence Alignment ,Genome, Bacterial ,Population Genetics and Evolution - Abstract
Virulence and immunity are poorly understood inMycobacterium tuberculosis.We sequenced the complete genome of theM. tuberculosisclinical strain CDC1551 and performed a whole-genome comparison with the laboratory strain H37Rv in order to identify polymorphic sequences with potential relevance to disease pathogenesis, immunity, and evolution. We found large-sequence and single-nucleotide polymorphisms in numerous genes. Polymorphic loci included a phospholipase C, a membrane lipoprotein, members of an adenylate cyclase gene family, and members of the PE/PPE gene family, some of which have been implicated in virulence or the host immune response. Several gene families, including the PE/PPE gene family, also had significantly higher synonymous and nonsynonymous substitution frequencies compared to the genome as a whole. We tested a large sample ofM. tuberculosisclinical isolates for a subset of the large-sequence and single-nucleotide polymorphisms and found widespread genetic variability at many of these loci. We performed phylogenetic and epidemiological analysis to investigate the evolutionary relationships among isolates and the origins of specific polymorphic loci. A number of these polymorphisms appear to have occurred multiple times as independent events, suggesting that these changes may be under selective pressure. Together, these results demonstrate that polymorphisms amongM. tuberculosisstrains are more extensive than initially anticipated, and genetic variation may have an important role in disease pathogenesis and immunity.
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- 2002
24. Complete genome sequence of a virulent isolate of Streptococcus pneumoniae
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Jeremy Peterson, Jonathan A. Eisen, Ingeborg Holt, Robert T. DeBoy, Anthony S. Durkin, Daniel H. Haft, Robert J. Dodson, Lowell Umayam, Michelle L. Gwinn, Fan Yang, James F. Kolonay, Brian Dougherty, Matthew R. Lewis, Tamara Feldblyum, Brendan J. Loftus, Cheryl L. Hansen, Diana Radune, J. C. Venter, Hervé Tettelin, John F. Heidelberg, Timothy D. Read, Donald A. Morrison, Owen White, Ian T. Paulsen, S. K. Hollingshead, T. Dickinson, Alex M. Wolf, Steven L. Salzberg, Erik Holtzapple, Karen E. Nelson, Lisa McDonald, Hamilton O. Smith, Scott N. Peterson, William C. Nelson, Claire M. Fraser, Samuel V. Angiuoli, Erin Hickey, T. Utterback, and Hoda Khouri
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DNA, Bacterial ,Sequence analysis ,Virulence ,Biology ,medicine.disease_cause ,Genome ,Microbiology ,Bacterial Proteins ,Species Specificity ,Gene Duplication ,Streptococcus pneumoniae ,medicine ,Insertion sequence ,rRNA Operon ,Gene ,Genomic organization ,Oligonucleotide Array Sequence Analysis ,Repetitive Sequences, Nucleic Acid ,Whole genome sequencing ,Genetics ,Recombination, Genetic ,Antigens, Bacterial ,Base Composition ,Multidisciplinary ,Computational Biology ,Hexosamines ,Sequence Analysis, DNA ,Chromosomes, Bacterial ,Genes, Bacterial ,Bacterial Vaccines ,DNA Transposable Elements ,Carbohydrate Metabolism ,Carrier Proteins ,Genome, Bacterial - Abstract
The 2,160,837–base pair genome sequence of an isolate of Streptococcus pneumoniae , a Gram-positive pathogen that causes pneumonia, bacteremia, meningitis, and otitis media, contains 2236 predicted coding regions; of these, 1440 (64%) were assigned a biological role. Approximately 5% of the genome is composed of insertion sequences that may contribute to genome rearrangements through uptake of foreign DNA. Extracellular enzyme systems for the metabolism of polysaccharides and hexosamines provide a substantial source of carbon and nitrogen for S. pneumoniae and also damage host tissues and facilitate colonization. A motif identified within the signal peptide of proteins is potentially involved in targeting these proteins to the cell surface of low–guanine/cytosine (GC) Gram-positive species. Several surface-exposed proteins that may serve as potential vaccine candidates were identified. Comparative genome hybridization with DNA arrays revealed strain differences in S. pneumoniae that could contribute to differences in virulence and antigenicity.
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- 2001
25. Sequence and analysis of chromosome 3 of the plant Arabidopsis thaliana
- Author
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Jean Weissenbach, William C. Nierman, Christopher D. Town, A Perez-Perez, R. Cooke, Brian J. Haas, Samir Kaul, T Kato, Claire Fujii, J Militscher, Mitsuyo Kohara, Steven L. Salzberg, A Conrad, Hans-Werner Mewes, D. Haase, M. Scharfe, S Bangert, Hean L. Koo, W. Ansorge, Laurence Cattolico, Patrick Wincker, Rama Maiti, Marcel Salanoubat, Erika Asamizu, Bénédicte Purnelle, Luke J. Tallon, M flores, Grace Pai, P Brottier, Kumi Idesawa, Richard Holland, P Sellers, J C Venter, S Nakayama, Michela D'Angelo, Holger Erfle, Berthold Fartmann, Ai Matsuno, Elena Casacuberta, Barbara Simionati, T Wada, R Wiedelmann, Amparo Monfort, Chiaki Kiyokawa, M. Rizzo, Jeremy Peterson, D. Vitale, Joan Climent, M. Schäfer, C Takeuchi, Gertrud Mannhaupt, Terrance Shea, P Navarro, Gerald Nyakatura, Pere Puigdomènech, R Mache, Leslie A. Grivell, S. van Aken, Paolo Zaccaria, Stephen Rudd, H. Voss, B Ottenwälder, Todd Creasy, J Reichelt, C Berger-Llauro, M Laudie, K Hornischer, H Drzonek, J P Alcaraz, Kai Lemcke, M Unseld, N Jordan, C Robert, Shusei Sato, T Kimura, S Müller-Auer, Naomi Nakazaki, W Saurin, Daphne Preuss, M. de Haan, J Jenkins, Francis Quetier, D Duchemin, Xiaoying Lin, Alberto Pallavicini, A Watanabe, Petra Brandt, Klaus F. X. Mayer, Heiko Schoof, M Yamada, Javier Terol, Satoshi Tabata, Benes, John Gill, François Artiguenave, Yoshie Kishida, Nathalie Choisne, O Schön, C. Gabel, E Wurmbach, Michael A. Rieger, Alessandro Vezzi, T Kaneko, T. H. Löhnert, Owen White, G Kauer, M Matsumoto, M. Fuchs, A Walts, G Nordsiek, Michel Delseny, Shigemi Sasamoto, H Kranz, Rosario Liguori, Yasukazu Nakamura, David Masuy, H. Blöcker, De Simone, Miho Yasuda, Tamara Feldblyum, B. Obermaier, Giorgio Valle, Manuel Pérez-Alonso, Sayaka Shinpo, Kumiko Kawashima, A Cottet, Anagnostis Argiriou, T Rooney, A.C. Maarse, Dongying Wu, C Collado, T. Utterback, Claire M. Fraser, M. D. Bargues, Stefano Toppo, Marc Boutry, Akiko Muraki, Salanoubat, M., Lemcke, K., Rieger, M., Ansorge, W., Unseld, M., Fartmann, B., Valle, G., Blocker, H., Perezalonso, M., Obermaier, B., Delseny, M., Boutry, M., Grivell, L. A., Mache, R., Puigdomenech, P., DE SIMONE, V., Choisne, N., Artiguenave, F., Robert, C., Brottier, P., Wincker, P., Cattolico, L., Weissenbach, J., Saurin, W., Quetier, F., Schafer, M., Mullerauer, S., Gabel, C., Fuchs, M., Benes, V., Wurmbach, E., Drzonek, H., Erfle, H., Jordan, N., Bangert, S., Wiedelmann, R., Kranz, H., Voss, H., Holland, R., Brandt, P., Nyakatura, G., Vezzi, A., D'Angelo, M., Pallavicini, Alberto, Toppo, S., Simionati, B., Conrad, A., Hornischer, K., Kauer, G., Lohnert, T. H., Nordsiek, G., Reichelt, J., Scharfe, M., Schon, O., Bargues, M., Terol, J., Climent, J., Navarro, P., Collado, C., Perezperez, A., Ottenwalder, B., Duchemin, D., Cooke, R., Laudie, M., Bergerllauro, C., Purnelle, B., Masuy, D., DE HAAN, M., Maarse, A. C., Alcaraz, J. P., Cottet, A., Casacuberta, E., Monfort, A., Argiriou, A., Flores, M., Liguori, R., Vitale, D., Mannhaupt, G., Haase, D., and Schoof, H.
- Subjects
DNA, Plant ,Sequence analysis ,Arabidopsis ,plant ,Genome ,Complete sequence ,Gene Duplication ,Centromere ,Plant genomics ,model organism ,Humans ,genomic structure ,Gene ,Plant Proteins ,Genetics ,Multidisciplinary ,biology ,Chromosome ,Chromosome Mapping ,Sequence Analysis, DNA ,biology.organism_classification ,genome sequencing ,Chromosome 3 ,Genome, Plant - Abstract
Arabidopsis thaliana is an important model system for plant biologists. In 1996 an international collaboration (the Arabidopsis Genome Initiative) was formed to sequence the whole genome of Arabidopsis and in 1999 the sequence of the first two chromosomes was reported. The sequence of the last three chromosomes and an analysis of the whole genome are reported in this issue. Here we present the sequence of chromosome 3, organized into four sequence segments (contigs). The two largest (13.5 and 9.2 Mb) correspond to the top (long) and the bottom (short) arms of chromosome 3, and the two small contigs are located in the genetically defined centromere. This chromosome encodes 5,220 of the roughly 25,500 predicted protein-coding genes in the genome. About 20% of the predicted proteins have significant homology to proteins in eukaryotic genomes for which the complete sequence is available, pointing to important conserved cellular functions among eukaryotes.
- Published
- 2000
26. Genome sequence of the radioresistant bacterium Deinococcus radiodurans R1
- Author
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Robert J. Dodson, Kelly Moffat, T. Utterback, M. Crosby, Haiying Qin, L. Aravind, Jessica Vamathevan, Karen E. Nelson, Hamilton O. Smith, K. A. Ketchum, Jonathan A. Eisen, J C Venter, Steven L. Salzberg, Michael J. Daly, Jeremy Peterson, Lingxia Jiang, Michelle L. Gwinn, Erin Hickey, John F. Heidelberg, Claire M. Fraser, Lisa McDonald, Kenneth W. Minton, Robert D. Fleischmann, Kira S. Makarova, William C. Nelson, Mian Shen, C. Zalewski, Delwood Richardson, P. Lam, W. Pamphile, Owen White, and Daniel H. Haft
- Subjects
DNA, Bacterial ,DNA Repair ,Base pair ,DNA repair ,Ultraviolet Rays ,Molecular Sequence Data ,medicine.disease_cause ,Genome ,Radiation Tolerance ,Article ,Open Reading Frames ,Plasmid ,Bacterial Proteins ,medicine ,Deinococcus ,Thermus ,Repetitive Sequences, Nucleic Acid ,Genetics ,Multidisciplinary ,biology ,Superoxide Dismutase ,Deinococcus radiodurans ,Sequence Analysis, DNA ,Chromosomes, Bacterial ,biology.organism_classification ,Deinococcus deserti ,Catalase ,Physical Chromosome Mapping ,Gram-Positive Cocci ,Oxidative Stress ,Genes, Bacterial ,Deinococcus geothermalis ,Energy Metabolism ,Genome, Bacterial ,DNA Damage ,Plasmids - Abstract
The complete genome sequence of the radiation-resistant bacterium Deinococcus radiodurans R1 is composed of two chromosomes (2,648,638 and 412,348 base pairs), a megaplasmid (177,466 base pairs), and a small plasmid (45,704 base pairs), yielding a total genome of 3,284,156 base pairs. Multiple components distributed on the chromosomes and megaplasmid that contribute to the ability of D. radiodurans to survive under conditions of starvation, oxidative stress, and high amounts of DNA damage were identified. Deinococcus radiodurans represents an organism in which all systems for DNA repair, DNA damage export, desiccation and starvation recovery, and genetic redundancy are present in one cell.
- Published
- 1999
27. Inquisition and Medieval Society: Power, Discipline, and Resistance in Languedoc. By James B. Given (Ithaca, Cornell University Press, 1997) 255 pp. $39.95
- Author
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Kristine T. Utterback
- Subjects
Power (social and political) ,History ,History and Philosophy of Science ,Ethnology ,Electrical and Electronic Engineering ,Ancient history ,Resistance (creativity) ,Atomic and Molecular Physics, and Optics - Published
- 1999
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28. Inquisitorial Inquiries: Brief Lives of Secret Jews and Other Heretics
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Kristine T. Utterback, Richard L. Kagan, and Abigail Dyer
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Cultural Studies ,History - Published
- 2006
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29. The Diocese of Barcelona during the Black Death: The Register 'Notule Communium' 15 (1348-1349) by Richard Francis Gyug
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Kristine T. Utterback
- Subjects
History ,Register (music) ,General Arts and Humanities ,Genealogy ,Demography - Published
- 1996
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30. Parentesco, poder y mentalidad: La nobleza castellana, siglos XII-XV.Isabel Beceiro Pita , Ricardo Córdoba de la Llave
- Author
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Kristine T. Utterback
- Subjects
Cultural Studies ,Philosophy ,History ,Literature and Literary Theory ,Visual Arts and Performing Arts ,Religious studies - Published
- 1993
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31. Erratum: The complete genome sequence of the hyperthermophilic, sulphate-reducing archaeon Archaeoglobus fulgidus
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Lixin Zhou, C. Fujli, Norman H. Lee, A. Glodek, Anthony R. Kerlavage, Gary J. Olsen, P. W. Sadow, Matthew D. Cotton, Cheryl Bowman, Nikos C. Kyrpides, Jeannine D. Gocayne, Tanya Mason, Jeremy Peterson, Keith McKenney, Rebecca A. Clayton, Brendan J. Loftus, Mark Raymond Adams, Lisa McDonald, J F Tomb, Ross Overbeek, C. R. Woese, Erin Hickey, Karen E. Nelson, Claudia I. Reich, David E. Graham, Hamilton O. Smith, T. Spriggs, Hans-Peter Klenk, Sean M. Sykes, Stacey Garland, Ewen F. Kirkness, Leslie Klis McNeil, Jonathan H. Badger, Claire M. Fraser, Steven R. Gill, Patricia Artiach, Scott N. Peterson, Delwood Richardson, J C Venter, Brian Dougherty, J. F. Weldman, John Quackenbush, Michelle L. Gwinn, Robert D. Fleischmann, K. A. Ketchum, Owen White, Brian P. Kaine, R. J. Dodaon, T. Utterback, K. P. D'Andrea, and Granger G. Sutton
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Whole genome sequencing ,Multidisciplinary ,Archaeoglobus fulgidus ,Computational biology ,Biology ,Erratum - Published
- 1998
32. The Date of Composition of Bishops' Registers from the Plague Years in the Diocese of Barcelona
- Author
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K. T. Utterback
- Subjects
History ,biology ,Religious studies ,Ancient history ,Bishops ,Plague (disease) ,biology.organism_classification ,Archaeology ,Administration (government) - Abstract
The material presented below grew out of a study of episcopal administration in the diocese of Barcelona in the mid-fourteenth century. Among the bishops' registers which were analysed for the study, three proved especially important: two from the communia, or general, series, Notule communium 15 and 16 (NC 15 and NC 16); and one from the collations series, Registrum collationum 9 (CO 9), covering the years 1345–51. The registers record both a period – 1345–8 – of presumably normal diocesan administration, and the plague period – the so-called Black Death struck Barcelona in spring 1348. The communia and collations series were selected both because they provided information about general diocesan administration and because the two series were conflated beginning with NC 15 in 1348, and remained separate until 1361.
- Published
- 1988
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33. 'Cum Multimodi Curiositatis': A Musical Treatise from Eleventh-Century Catalonia
- Author
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Kristine T. Utterback
- Subjects
Cultural Studies ,History ,Literature and Literary Theory ,Visual Arts and Performing Arts ,Poetry ,media_common.quotation_subject ,Religious studies ,Musical ,Art ,Music education ,Eleventh ,Folio ,Philosophy ,State (polity) ,Petitioner ,Classics ,Scriptorium ,media_common - Abstract
THE Breviarium de musica by a monk named Oliva is the initial treatise found in MS Ripoll 42, and it indicates the state of musica speculativa at the monastery of Santa Maria de Ripoll in the mid-eleventh century. Ripoll, located near the Spanish-French border north of Barcelona, was a major intellectual center in medieval Catalonia. Its scriptorium began ca. 935, during the abbacy of Arnulfus, and by the mid-eleventh century its library contained nearly two hundred books.' Musical manuscripts from the eleventh century indicate that Ripoll was actively concerned with musica practica; Angles suggested that Ripoll was among the earliest monasteries to employ the singleline staff.2 The unique treatise to be considered here indicates that members of the community were also interested in theoretical music, musica speculativa. Much can be ascertained about the level of this interest from Oliva's introduction to his treatise. In it he explained that he was writing for someone who wanted to learn about the theory of the monochord. Since he was writing to fill a void, it is obvious that Ripoll had no copy of Boethius's De institutione musicae, the sixth-century treatise which played such an enormous role in medieval musical study. However, Oliva had been sufficiently trained in Boethian theory to give a summary of portions of De musica from memory. Further, there was someone else at the monastery who was anxious to learn that theory, anxious enough to send messengers to neighboring monasteries to beg for books, after the petitioner's friend had refused to lend them to him. Unfortunately, Oliva did not mention the monasteries to which the ardent student had sent messengers, nor is the friend from whom he had hoped to borrow books named. If Oliva were known as a music teacher, the petitioner would presumably have applied to him first for instruction. The mention of the promise of favors and kindnesses to be bestowed on the author indicates that the student was his superior. Oliva did not mention the name of the student for whom he was writing, although Angles referred to a monk named Peter as the dedicatee.3 Presumably Angles assumed this from the poem on folio 5r, also by Oliva, which is usually called Versus de monocordo. It is written in a different but contemporary hand. In it Peter is mentioned twice, once as "fratre Petre." This may be the same Peter who became abbot of Ripoll in 1046 and died in 1056.4 Discussions of MS Ripoll 42 have centered on the
- Published
- 1979
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34. Teobaldo II de Navarra (1253-1270): Gobierno de la monarquía y recursos financieros. M. Raquel García Arancón , Angel J. Martín Duque
- Author
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Kristine T. Utterback
- Subjects
Cultural Studies ,Philosophy ,History ,Literature and Literary Theory ,Visual Arts and Performing Arts ,Religious studies - Published
- 1988
- Full Text
- View/download PDF
35. The Medieval Crown of Aragon: A Short History. T. N. Bisson
- Author
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Kristine T. Utterback
- Subjects
Cultural Studies ,Philosophy ,History ,Literature and Literary Theory ,Visual Arts and Performing Arts ,Crown (botany) ,Religious studies ,Theology - Published
- 1989
- Full Text
- View/download PDF
36. Islet primary cilia motility controls insulin secretion.
- Author
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Cho JH, Li ZA, Zhu L, Muegge BD, Roseman HF, Lee EY, Utterback T, Woodhams LG, Bayly PV, and Hughes JW
- Subjects
- Adenosine metabolism, Animals, Calcium metabolism, Dyneins metabolism, Glucose metabolism, Humans, Insulin Secretion, Mice, Cilia chemistry, Diabetes Mellitus, Type 2
- Abstract
Primary cilia are specialized cell-surface organelles that mediate sensory perception and, in contrast to motile cilia and flagella, are thought to lack motility function. Here, we show that primary cilia in human and mouse pancreatic islets exhibit movement that is required for glucose-dependent insulin secretion. Islet primary cilia contain motor proteins conserved from those found in classic motile cilia, and their three-dimensional motion is dynein-driven and dependent on adenosine 5'-triphosphate and glucose metabolism. Inhibition of cilia motion blocks beta cell calcium influx and insulin secretion. Human beta cells have enriched ciliary gene expression, and motile cilia genes are altered in type 2 diabetes. Our findings redefine primary cilia as dynamic structures having both sensory and motile function and establish that pancreatic islet cilia movement plays a regulatory role in insulin secretion.
- Published
- 2022
- Full Text
- View/download PDF
37. The Sorcerer II Global Ocean Sampling expedition: northwest Atlantic through eastern tropical Pacific.
- Author
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Rusch DB, Halpern AL, Sutton G, Heidelberg KB, Williamson S, Yooseph S, Wu D, Eisen JA, Hoffman JM, Remington K, Beeson K, Tran B, Smith H, Baden-Tillson H, Stewart C, Thorpe J, Freeman J, Andrews-Pfannkoch C, Venter JE, Li K, Kravitz S, Heidelberg JF, Utterback T, Rogers YH, Falcón LI, Souza V, Bonilla-Rosso G, Eguiarte LE, Karl DM, Sathyendranath S, Platt T, Bermingham E, Gallardo V, Tamayo-Castillo G, Ferrari MR, Strausberg RL, Nealson K, Friedman R, Frazier M, and Venter JC
- Subjects
- Computational Biology, Food Chain, Oceans and Seas, Plankton, Species Specificity, Water Microbiology
- Abstract
The world's oceans contain a complex mixture of micro-organisms that are for the most part, uncharacterized both genetically and biochemically. We report here a metagenomic study of the marine planktonic microbiota in which surface (mostly marine) water samples were analyzed as part of the Sorcerer II Global Ocean Sampling expedition. These samples, collected across a several-thousand km transect from the North Atlantic through the Panama Canal and ending in the South Pacific yielded an extensive dataset consisting of 7.7 million sequencing reads (6.3 billion bp). Though a few major microbial clades dominate the planktonic marine niche, the dataset contains great diversity with 85% of the assembled sequence and 57% of the unassembled data being unique at a 98% sequence identity cutoff. Using the metadata associated with each sample and sequencing library, we developed new comparative genomic and assembly methods. One comparative genomic method, termed "fragment recruitment," addressed questions of genome structure, evolution, and taxonomic or phylogenetic diversity, as well as the biochemical diversity of genes and gene families. A second method, termed "extreme assembly," made possible the assembly and reconstruction of large segments of abundant but clearly nonclonal organisms. Within all abundant populations analyzed, we found extensive intra-ribotype diversity in several forms: (1) extensive sequence variation within orthologous regions throughout a given genome; despite coverage of individual ribotypes approaching 500-fold, most individual sequencing reads are unique; (2) numerous changes in gene content some with direct adaptive implications; and (3) hypervariable genomic islands that are too variable to assemble. The intra-ribotype diversity is organized into genetically isolated populations that have overlapping but independent distributions, implying distinct environmental preference. We present novel methods for measuring the genomic similarity between metagenomic samples and show how they may be grouped into several community types. Specific functional adaptations can be identified both within individual ribotypes and across the entire community, including proteorhodopsin spectral tuning and the presence or absence of the phosphate-binding gene PstS.
- Published
- 2007
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38. Comparative analysis of 87,000 expressed sequence tags from the fumonisin-producing fungus Fusarium verticillioides.
- Author
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Brown DW, Cheung F, Proctor RH, Butchko RA, Zheng L, Lee Y, Utterback T, Smith S, Feldblyum T, Glenn AE, Plattner RD, Kendra DF, Town CD, and Whitelaw CA
- Subjects
- Amino Acid Sequence, Base Sequence, DNA, Fungal chemistry, DNA, Fungal genetics, Fusarium metabolism, Gene Expression Regulation, Fungal, Genes, Regulator, Introns, Molecular Sequence Data, RNA Processing, Post-Transcriptional, RNA, Fungal genetics, RNA, Messenger genetics, Sequence Analysis, DNA, Expressed Sequence Tags, Fumonisins metabolism, Fusarium genetics, Gene Expression Profiling, Gene Library, Genes, Fungal
- Abstract
Fusarium verticillioides (teleomorph Gibberella moniliformis) is a pathogen of maize worldwide and produces fumonisins, a family of mycotoxins that have been associated with several animal diseases as well as cancer in humans. In this study, we sought to identify fungal genes that affect fumonisin production and/or the plant-fungal interaction. We generated over 87,000 expressed sequence tags from nine different cDNA libraries that correspond to 11,119 unique sequences and are estimated to represent 80% of the genomic complement of genes. A comparative analysis of the libraries showed that all 15 genes in the fumonisin gene cluster were differentially expressed. In addition, nine candidate fumonisin regulatory genes and a number of genes that may play a role in plant-fungal interaction were identified. Analysis of over 700 FUM gene transcripts from five different libraries provided evidence for transcripts with unspliced introns and spliced introns with alternative 3' splice sites. The abundance of the alternative splice forms and the frequency with which they were found for genes involved in the biosynthesis of a single family of metabolites as well as their differential expression suggest they may have a biological function. Finally, analysis of an EST that aligns to genomic sequence between FUM12 and FUM13 provided evidence for a previously unidentified gene (FUM20) in the FUM gene cluster.
- Published
- 2005
- Full Text
- View/download PDF
39. Sequence, annotation, and analysis of synteny between rice chromosome 3 and diverged grass species.
- Author
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Buell CR, Yuan Q, Ouyang S, Liu J, Zhu W, Wang A, Maiti R, Haas B, Wortman J, Pertea M, Jones KM, Kim M, Overton L, Tsitrin T, Fadrosh D, Bera J, Weaver B, Jin S, Johri S, Reardon M, Webb K, Hill J, Moffat K, Tallon L, Van Aken S, Lewis M, Utterback T, Feldblyum T, Zismann V, Iobst S, Hsiao J, de Vazeille AR, Salzberg SL, White O, Fraser C, Yu Y, Kim H, Rambo T, Currie J, Collura K, Kernodle-Thompson S, Wei F, Kudrna K, Ammiraju JS, Luo M, Goicoechea JL, Wing RA, Henry D, Oates R, Palmer M, Pries G, Saski C, Simmons J, Soderlund C, Nelson W, de la Bastide M, Spiegel L, Nascimento L, Huang E, Preston R, Zutavern T, Palmer L, O'Shaughnessy A, Dike S, McCombie WR, Minx P, Cordum H, Wilson R, Jin W, Lee HR, Jiang J, and Jackson S
- Subjects
- Arabidopsis genetics, Chromosome Mapping, Chromosomes, Artificial, Bacterial genetics, Genes, Plant, Minisatellite Repeats, Molecular Sequence Data, Oryza classification, Physical Chromosome Mapping, Poaceae classification, Proteome, Species Specificity, Zea mays classification, Zea mays genetics, Chromosomes, Plant genetics, Oryza genetics, Poaceae genetics
- Abstract
Rice (Oryza sativa L.) chromosome 3 is evolutionarily conserved across the cultivated cereals and shares large blocks of synteny with maize and sorghum, which diverged from rice more than 50 million years ago. To begin to completely understand this chromosome, we sequenced, finished, and annotated 36.1 Mb ( approximately 97%) from O. sativa subsp. japonica cv Nipponbare. Annotation features of the chromosome include 5915 genes, of which 913 are related to transposable elements. A putative function could be assigned to 3064 genes, with another 757 genes annotated as expressed, leaving 2094 that encode hypothetical proteins. Similarity searches against the proteome of Arabidopsis thaliana revealed putative homologs for 67% of the chromosome 3 proteins. Further searches of a nonredundant amino acid database, the Pfam domain database, plant Expressed Sequence Tags, and genomic assemblies from sorghum and maize revealed only 853 nontransposable element related proteins from chromosome 3 that lacked similarity to other known sequences. Interestingly, 426 of these have a paralog within the rice genome. A comparative physical map of the wild progenitor species, Oryza nivara, with japonica chromosome 3 revealed a high degree of sequence identity and synteny between these two species, which diverged approximately 10,000 years ago. Although no major rearrangements were detected, the deduced size of the O. nivara chromosome 3 was 21% smaller than that of japonica. Synteny between rice and other cereals using an integrated maize physical map and wheat genetic map was strikingly high, further supporting the use of rice and, in particular, chromosome 3, as a model for comparative studies among the cereals.
- Published
- 2005
- Full Text
- View/download PDF
40. Insights on evolution of virulence and resistance from the complete genome analysis of an early methicillin-resistant Staphylococcus aureus strain and a biofilm-producing methicillin-resistant Staphylococcus epidermidis strain.
- Author
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Gill SR, Fouts DE, Archer GL, Mongodin EF, Deboy RT, Ravel J, Paulsen IT, Kolonay JF, Brinkac L, Beanan M, Dodson RJ, Daugherty SC, Madupu R, Angiuoli SV, Durkin AS, Haft DH, Vamathevan J, Khouri H, Utterback T, Lee C, Dimitrov G, Jiang L, Qin H, Weidman J, Tran K, Kang K, Hance IR, Nelson KE, and Fraser CM
- Subjects
- Biofilms, Chromosome Mapping, Gene Transfer, Horizontal, Genomic Islands, Molecular Sequence Data, Open Reading Frames, Phylogeny, Staphylococcus aureus metabolism, Staphylococcus aureus pathogenicity, Staphylococcus epidermidis metabolism, Staphylococcus epidermidis pathogenicity, Virulence genetics, Evolution, Molecular, Genome, Bacterial, Methicillin Resistance genetics, Staphylococcus aureus genetics, Staphylococcus epidermidis genetics
- Abstract
Staphylococcus aureus is an opportunistic pathogen and the major causative agent of numerous hospital- and community-acquired infections. Staphylococcus epidermidis has emerged as a causative agent of infections often associated with implanted medical devices. We have sequenced the approximately 2.8-Mb genome of S. aureus COL, an early methicillin-resistant isolate, and the approximately 2.6-Mb genome of S. epidermidis RP62a, a methicillin-resistant biofilm isolate. Comparative analysis of these and other staphylococcal genomes was used to explore the evolution of virulence and resistance between these two species. The S. aureus and S. epidermidis genomes are syntenic throughout their lengths and share a core set of 1,681 open reading frames. Genome islands in nonsyntenic regions are the primary source of variations in pathogenicity and resistance. Gene transfer between staphylococci and low-GC-content gram-positive bacteria appears to have shaped their virulence and resistance profiles. Integrated plasmids in S. epidermidis carry genes encoding resistance to cadmium and species-specific LPXTG surface proteins. A novel genome island encodes multiple phenol-soluble modulins, a potential S. epidermidis virulence factor. S. epidermidis contains the cap operon, encoding the polyglutamate capsule, a major virulence factor in Bacillus anthracis. Additional phenotypic differences are likely the result of single nucleotide polymorphisms, which are most numerous in cell envelope proteins. Overall differences in pathogenicity can be attributed to genome islands in S. aureus which encode enterotoxins, exotoxins, leukocidins, and leukotoxins not found in S. epidermidis.
- Published
- 2005
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41. Genomic insights into methanotrophy: the complete genome sequence of Methylococcus capsulatus (Bath).
- Author
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Ward N, Larsen Ø, Sakwa J, Bruseth L, Khouri H, Durkin AS, Dimitrov G, Jiang L, Scanlan D, Kang KH, Lewis M, Nelson KE, Methé B, Wu M, Heidelberg JF, Paulsen IT, Fouts D, Ravel J, Tettelin H, Ren Q, Read T, DeBoy RT, Seshadri R, Salzberg SL, Jensen HB, Birkeland NK, Nelson WC, Dodson RJ, Grindhaug SH, Holt I, Eidhammer I, Jonasen I, Vanaken S, Utterback T, Feldblyum TV, Fraser CM, Lillehaug JR, and Eisen JA
- Subjects
- Bacterial Proteins chemistry, Carbon chemistry, Electron Transport, Fatty Acids chemistry, Genome, Bacterial, Genomics methods, Methane chemistry, Models, Biological, Molecular Sequence Data, Nitrogen chemistry, Oxygen chemistry, Oxygen metabolism, Peptides chemistry, Phylogeny, Sequence Analysis, DNA, Gene Expression Regulation, Bacterial, Genome, Methane metabolism, Methylococcus capsulatus genetics
- Abstract
Methanotrophs are ubiquitous bacteria that can use the greenhouse gas methane as a sole carbon and energy source for growth, thus playing major roles in global carbon cycles, and in particular, substantially reducing emissions of biologically generated methane to the atmosphere. Despite their importance, and in contrast to organisms that play roles in other major parts of the carbon cycle such as photosynthesis, no genome-level studies have been published on the biology of methanotrophs. We report the first complete genome sequence to our knowledge from an obligate methanotroph, Methylococcus capsulatus (Bath), obtained by the shotgun sequencing approach. Analysis revealed a 3.3-Mb genome highly specialized for a methanotrophic lifestyle, including redundant pathways predicted to be involved in methanotrophy and duplicated genes for essential enzymes such as the methane monooxygenases. We used phylogenomic analysis, gene order information, and comparative analysis with the partially sequenced methylotroph Methylobacterium extorquens to detect genes of unknown function likely to be involved in methanotrophy and methylotrophy. Genome analysis suggests the ability of M. capsulatus to scavenge copper (including a previously unreported nonribosomal peptide synthetase) and to use copper in regulation of methanotrophy, but the exact regulatory mechanisms remain unclear. One of the most surprising outcomes of the project is evidence suggesting the existence of previously unsuspected metabolic flexibility in M. capsulatus, including an ability to grow on sugars, oxidize chemolithotrophic hydrogen and sulfur, and live under reduced oxygen tension, all of which have implications for methanotroph ecology. The availability of the complete genome of M. capsulatus (Bath) deepens our understanding of methanotroph biology and its relationship to global carbon cycles. We have gained evidence for greater metabolic flexibility than was previously known, and for genetic components that may have biotechnological potential., Competing Interests: The authors have declared that no conflicts of interest exist.
- Published
- 2004
- Full Text
- View/download PDF
42. Phylogenomics of the reproductive parasite Wolbachia pipientis wMel: a streamlined genome overrun by mobile genetic elements.
- Author
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Wu M, Sun LV, Vamathevan J, Riegler M, Deboy R, Brownlie JC, McGraw EA, Martin W, Esser C, Ahmadinejad N, Wiegand C, Madupu R, Beanan MJ, Brinkac LM, Daugherty SC, Durkin AS, Kolonay JF, Nelson WC, Mohamoud Y, Lee P, Berry K, Young MB, Utterback T, Weidman J, Nierman WC, Paulsen IT, Nelson KE, Tettelin H, O'Neill SL, and Eisen JA
- Subjects
- Adenosine Triphosphate chemistry, Animals, Cell Lineage, DNA chemistry, DNA genetics, DNA Primers chemistry, Drosophila melanogaster microbiology, Evolution, Molecular, Gene Deletion, Gene Duplication, Gene Library, Genes, Bacterial, Genome, Genome, Bacterial, Glycolysis, Interspersed Repetitive Sequences, Models, Genetic, Molecular Sequence Data, Open Reading Frames, Parasites, Phylogeny, Polymerase Chain Reaction, Protein Structure, Tertiary, Purines chemistry, Genomics methods, Wolbachia genetics
- Abstract
The complete sequence of the 1,267,782 bp genome of Wolbachia pipientis wMel, an obligate intracellular bacteria of Drosophila melanogaster, has been determined. Wolbachia, which are found in a variety of invertebrate species, are of great interest due to their diverse interactions with different hosts, which range from many forms of reproductive parasitism to mutualistic symbioses. Analysis of the wMel genome, in particular phylogenomic comparisons with other intracellular bacteria, has revealed many insights into the biology and evolution of wMel and Wolbachia in general. For example, the wMel genome is unique among sequenced obligate intracellular species in both being highly streamlined and containing very high levels of repetitive DNA and mobile DNA elements. This observation, coupled with multiple evolutionary reconstructions, suggests that natural selection is somewhat inefficient in wMel, most likely owing to the occurrence of repeated population bottlenecks. Genome analysis predicts many metabolic differences with the closely related Rickettsia species, including the presence of intact glycolysis and purine synthesis, which may compensate for an inability to obtain ATP directly from its host, as Rickettsia can. Other discoveries include the apparent inability of wMel to synthesize lipopolysaccharide and the presence of the most genes encoding proteins with ankyrin repeat domains of any prokaryotic genome yet sequenced. Despite the ability of wMel to infect the germline of its host, we find no evidence for either recent lateral gene transfer between wMel and D. melanogaster or older transfers between Wolbachia and any host. Evolutionary analysis further supports the hypothesis that mitochondria share a common ancestor with the alpha-Proteobacteria, but shows little support for the grouping of mitochondria with species in the order Rickettsiales. With the availability of the complete genomes of both species and excellent genetic tools for the host, the wMel-D. melanogaster symbiosis is now an ideal system for studying the biology and evolution of Wolbachia infections., Competing Interests: The authors have declared that no conflicts of interest exist.
- Published
- 2004
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43. Enrichment of gene-coding sequences in maize by genome filtration.
- Author
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Whitelaw CA, Barbazuk WB, Pertea G, Chan AP, Cheung F, Lee Y, Zheng L, van Heeringen S, Karamycheva S, Bennetzen JL, SanMiguel P, Lakey N, Bedell J, Yuan Y, Budiman MA, Resnick A, Van Aken S, Utterback T, Riedmuller S, Williams M, Feldblyum T, Schubert K, Beachy R, Fraser CM, and Quackenbush J
- Subjects
- Chromosomes, Plant genetics, Cloning, Molecular, Computational Biology, Contig Mapping, DNA Methylation, DNA, Plant genetics, Databases, Nucleic Acid, Expressed Sequence Tags, Gene Dosage, Gene Library, Molecular Sequence Data, Repetitive Sequences, Nucleic Acid, Retroelements, Sequence Alignment, Transcription, Genetic, Genes, Plant, Genome, Plant, Sequence Analysis, DNA methods, Zea mays genetics
- Abstract
Approximately 80% of the maize genome comprises highly repetitive sequences interspersed with single-copy, gene-rich sequences, and standard genome sequencing strategies are not readily adaptable to this type of genome. Methodologies that enrich for genic sequences might more rapidly generate useful results from complex genomes. Equivalent numbers of clones from maize selected by techniques called methylation filtering and High C0t selection were sequenced to generate approximately 200,000 reads (approximately 132 megabases), which were assembled into contigs. Combination of the two techniques resulted in a sixfold reduction in the effective genome size and a fourfold increase in the gene identification rate in comparison to a nonenriched library.
- Published
- 2003
- Full Text
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44. The complete genome sequence of the Arabidopsis and tomato pathogen Pseudomonas syringae pv. tomato DC3000.
- Author
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Buell CR, Joardar V, Lindeberg M, Selengut J, Paulsen IT, Gwinn ML, Dodson RJ, Deboy RT, Durkin AS, Kolonay JF, Madupu R, Daugherty S, Brinkac L, Beanan MJ, Haft DH, Nelson WC, Davidsen T, Zafar N, Zhou L, Liu J, Yuan Q, Khouri H, Fedorova N, Tran B, Russell D, Berry K, Utterback T, Van Aken SE, Feldblyum TV, D'Ascenzo M, Deng WL, Ramos AR, Alfano JR, Cartinhour S, Chatterjee AK, Delaney TP, Lazarowitz SG, Martin GB, Schneider DJ, Tang X, Bender CL, White O, Fraser CM, and Collmer A
- Subjects
- Base Sequence, Biological Transport, Molecular Sequence Data, Plant Growth Regulators biosynthesis, Plasmids, Pseudomonas metabolism, Pseudomonas pathogenicity, Reactive Oxygen Species, Siderophores biosynthesis, Virulence, Arabidopsis microbiology, Genome, Bacterial, Solanum lycopersicum microbiology, Pseudomonas genetics
- Abstract
We report the complete genome sequence of the model bacterial pathogen Pseudomonas syringae pathovar tomato DC3000 (DC3000), which is pathogenic on tomato and Arabidopsis thaliana. The DC3000 genome (6.5 megabases) contains a circular chromosome and two plasmids, which collectively encode 5,763 ORFs. We identified 298 established and putative virulence genes, including several clusters of genes encoding 31 confirmed and 19 predicted type III secretion system effector proteins. Many of the virulence genes were members of paralogous families and also were proximal to mobile elements, which collectively comprise 7% of the DC3000 genome. The bacterium possesses a large repertoire of transporters for the acquisition of nutrients, particularly sugars, as well as genes implicated in attachment to plant surfaces. Over 12% of the genes are dedicated to regulation, which may reflect the need for rapid adaptation to the diverse environments encountered during epiphytic growth and pathogenesis. Comparative analyses confirmed a high degree of similarity with two sequenced pseudomonads, Pseudomonas putida and Pseudomonas aeruginosa, yet revealed 1,159 genes unique to DC3000, of which 811 lack a known function.
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- 2003
- Full Text
- View/download PDF
45. The sequence and analysis of Trypanosoma brucei chromosome II.
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El-Sayed NM, Ghedin E, Song J, MacLeod A, Bringaud F, Larkin C, Wanless D, Peterson J, Hou L, Taylor S, Tweedie A, Biteau N, Khalak HG, Lin X, Mason T, Hannick L, Caler E, Blandin G, Bartholomeu D, Simpson AJ, Kaul S, Zhao H, Pai G, Van Aken S, Utterback T, Haas B, Koo HL, Umayam L, Suh B, Gerrard C, Leech V, Qi R, Zhou S, Schwartz D, Feldblyum T, Salzberg S, Tait A, Turner CM, Ullu E, White O, Melville S, Adams MD, Fraser CM, and Donelson JE
- Subjects
- Animals, Antigens, Protozoan genetics, Chromosome Mapping, DNA, Protozoan chemistry, Gene Duplication, Genes, Protozoan genetics, Molecular Sequence Data, Pseudogenes genetics, Recombination, Genetic, Sequence Analysis, DNA, Chromosomes genetics, DNA, Protozoan genetics, Trypanosoma brucei brucei genetics
- Abstract
We report here the sequence of chromosome II from Trypanosoma brucei, the causative agent of African sleeping sickness. The 1.2-Mb pairs encode about 470 predicted genes organised in 17 directional clusters on either strand, the largest cluster of which has 92 genes lined up over a 284-kb region. An analysis of the GC skew reveals strand compositional asymmetries that coincide with the distribution of protein-coding genes, suggesting these asymmetries may be the result of transcription-coupled repair on coding versus non-coding strand. A 5-cM genetic map of the chromosome reveals recombinational 'hot' and 'cold' regions, the latter of which is predicted to include the putative centromere. One end of the chromosome consists of a 250-kb region almost exclusively composed of RHS (pseudo)genes that belong to a newly characterised multigene family containing a hot spot of insertion for retroelements. Interspersed with the RHS genes are a few copies of truncated RNA polymerase pseudogenes as well as expression site associated (pseudo)genes (ESAGs) 3 and 4, and 76 bp repeats. These features are reminiscent of a vestigial variant surface glycoprotein (VSG) gene expression site. The other end of the chromosome contains a 30-kb array of VSG genes, the majority of which are pseudogenes, suggesting that this region may be a site for modular de novo construction of VSG gene diversity during transposition/gene conversion events.
- Published
- 2003
- Full Text
- View/download PDF
46. Role of mobile DNA in the evolution of vancomycin-resistant Enterococcus faecalis.
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Paulsen IT, Banerjei L, Myers GS, Nelson KE, Seshadri R, Read TD, Fouts DE, Eisen JA, Gill SR, Heidelberg JF, Tettelin H, Dodson RJ, Umayam L, Brinkac L, Beanan M, Daugherty S, DeBoy RT, Durkin S, Kolonay J, Madupu R, Nelson W, Vamathevan J, Tran B, Upton J, Hansen T, Shetty J, Khouri H, Utterback T, Radune D, Ketchum KA, Dougherty BA, and Fraser CM
- Subjects
- Adhesins, Bacterial genetics, Bacterial Adhesion, Bacterial Proteins genetics, Carrier Proteins genetics, Carrier Proteins metabolism, Chromosomes, Bacterial genetics, Conjugation, Genetic, Conserved Sequence, DNA Transposable Elements, Digestive System microbiology, Drug Resistance, Multiple, Bacterial, Enterococcus faecalis drug effects, Enterococcus faecalis pathogenicity, Enterococcus faecalis physiology, Gene Transfer, Horizontal, Gram-Positive Bacterial Infections microbiology, Humans, Lysogeny, Open Reading Frames, Oxidative Stress, Plasmids, Synteny, Virulence genetics, Virulence Factors genetics, Biological Evolution, Enterococcus faecalis genetics, Genome, Bacterial, Interspersed Repetitive Sequences, Sequence Analysis, DNA, Vancomycin Resistance genetics
- Abstract
The complete genome sequence of Enterococcus faecalis V583, a vancomycin-resistant clinical isolate, revealed that more than a quarter of the genome consists of probable mobile or foreign DNA. One of the predicted mobile elements is a previously unknown vanB vancomycin-resistance conjugative transposon. Three plasmids were identified, including two pheromone-sensing conjugative plasmids, one encoding a previously undescribed pheromone inhibitor. The apparent propensity for the incorporation of mobile elements probably contributed to the rapid acquisition and dissemination of drug resistance in the enterococci.
- Published
- 2003
- Full Text
- View/download PDF
47. Complete genome sequence and comparative analysis of the metabolically versatile Pseudomonas putida KT2440.
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Nelson KE, Weinel C, Paulsen IT, Dodson RJ, Hilbert H, Martins dos Santos VA, Fouts DE, Gill SR, Pop M, Holmes M, Brinkac L, Beanan M, DeBoy RT, Daugherty S, Kolonay J, Madupu R, Nelson W, White O, Peterson J, Khouri H, Hance I, Chris Lee P, Holtzapple E, Scanlan D, Tran K, Moazzez A, Utterback T, Rizzo M, Lee K, Kosack D, Moestl D, Wedler H, Lauber J, Stjepandic D, Hoheisel J, Straetz M, Heim S, Kiewitz C, Eisen JA, Timmis KN, Düsterhöft A, Tümmler B, and Fraser CM
- Subjects
- Bacterial Proteins genetics, Base Sequence, Genes, Bacterial genetics, Molecular Sequence Data, Phylogeny, Pseudomonas aeruginosa genetics, Pseudomonas aeruginosa metabolism, Pseudomonas putida metabolism, Energy Metabolism, Genome, Bacterial, Open Reading Frames genetics, Pseudomonas putida genetics
- Abstract
Pseudomonas putida is a metabolically versatile saprophytic soil bacterium that has been certified as a biosafety host for the cloning of foreign genes. The bacterium also has considerable potential for biotechnological applications. Sequence analysis of the 6.18 Mb genome of strain KT2440 reveals diverse transport and metabolic systems. Although there is a high level of genome conservation with the pathogenic Pseudomonad Pseudomonas aeruginosa (85% of the predicted coding regions are shared), key virulence factors including exotoxin A and type III secretion systems are absent. Analysis of the genome gives insight into the non-pathogenic nature of P. putida and points to potential new applications in agriculture, biocatalysis, bioremediation and bioplastic production.
- Published
- 2002
- Full Text
- View/download PDF
48. Whole-genome comparison of Mycobacterium tuberculosis clinical and laboratory strains.
- Author
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Fleischmann RD, Alland D, Eisen JA, Carpenter L, White O, Peterson J, DeBoy R, Dodson R, Gwinn M, Haft D, Hickey E, Kolonay JF, Nelson WC, Umayam LA, Ermolaeva M, Salzberg SL, Delcher A, Utterback T, Weidman J, Khouri H, Gill J, Mikula A, Bishai W, Jacobs WR Jr, Venter JC, and Fraser CM
- Subjects
- Bacterial Proteins genetics, Bacterial Proteins metabolism, Genetic Variation, Humans, Molecular Sequence Data, Mycobacterium tuberculosis genetics, Mycobacterium tuberculosis immunology, Phylogeny, Polymorphism, Genetic, Polymorphism, Single Nucleotide, Sequence Alignment, Tuberculosis immunology, Evolution, Molecular, Genome, Bacterial, Mycobacterium tuberculosis pathogenicity, Sequence Analysis, DNA, Tuberculosis microbiology
- Abstract
Virulence and immunity are poorly understood in Mycobacterium tuberculosis. We sequenced the complete genome of the M. tuberculosis clinical strain CDC1551 and performed a whole-genome comparison with the laboratory strain H37Rv in order to identify polymorphic sequences with potential relevance to disease pathogenesis, immunity, and evolution. We found large-sequence and single-nucleotide polymorphisms in numerous genes. Polymorphic loci included a phospholipase C, a membrane lipoprotein, members of an adenylate cyclase gene family, and members of the PE/PPE gene family, some of which have been implicated in virulence or the host immune response. Several gene families, including the PE/PPE gene family, also had significantly higher synonymous and nonsynonymous substitution frequencies compared to the genome as a whole. We tested a large sample of M. tuberculosis clinical isolates for a subset of the large-sequence and single-nucleotide polymorphisms and found widespread genetic variability at many of these loci. We performed phylogenetic and epidemiological analysis to investigate the evolutionary relationships among isolates and the origins of specific polymorphic loci. A number of these polymorphisms appear to have occurred multiple times as independent events, suggesting that these changes may be under selective pressure. Together, these results demonstrate that polymorphisms among M. tuberculosis strains are more extensive than initially anticipated, and genetic variation may have an important role in disease pathogenesis and immunity.
- Published
- 2002
- Full Text
- View/download PDF
49. Complete genome sequence of Caulobacter crescentus.
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Nierman WC, Feldblyum TV, Laub MT, Paulsen IT, Nelson KE, Eisen JA, Heidelberg JF, Alley MR, Ohta N, Maddock JR, Potocka I, Nelson WC, Newton A, Stephens C, Phadke ND, Ely B, DeBoy RT, Dodson RJ, Durkin AS, Gwinn ML, Haft DH, Kolonay JF, Smit J, Craven MB, Khouri H, Shetty J, Berry K, Utterback T, Tran K, Wolf A, Vamathevan J, Ermolaeva M, White O, Salzberg SL, Venter JC, Shapiro L, and Fraser CM
- Subjects
- Adaptation, Biological genetics, Cell Cycle genetics, DNA Methylation, Dinucleotide Repeats, Molecular Sequence Data, Peptide Hydrolases genetics, Phylogeny, Signal Transduction, Transcription, Genetic, Caulobacter crescentus genetics, Genome, Bacterial
- Abstract
The complete genome sequence of Caulobacter crescentus was determined to be 4,016,942 base pairs in a single circular chromosome encoding 3,767 genes. This organism, which grows in a dilute aquatic environment, coordinates the cell division cycle and multiple cell differentiation events. With the annotated genome sequence, a full description of the genetic network that controls bacterial differentiation, cell growth, and cell cycle progression is within reach. Two-component signal transduction proteins are known to play a significant role in cell cycle progression. Genome analysis revealed that the C. crescentus genome encodes a significantly higher number of these signaling proteins (105) than any bacterial genome sequenced thus far. Another regulatory mechanism involved in cell cycle progression is DNA methylation. The occurrence of the recognition sequence for an essential DNA methylating enzyme that is required for cell cycle regulation is severely limited and shows a bias to intergenic regions. The genome contains multiple clusters of genes encoding proteins essential for survival in a nutrient poor habitat. Included are those involved in chemotaxis, outer membrane channel function, degradation of aromatic ring compounds, and the breakdown of plant-derived carbon sources, in addition to many extracytoplasmic function sigma factors, providing the organism with the ability to respond to a wide range of environmental fluctuations. C. crescentus is, to our knowledge, the first free-living alpha-class proteobacterium to be sequenced and will serve as a foundation for exploring the biology of this group of bacteria, which includes the obligate endosymbiont and human pathogen Rickettsia prowazekii, the plant pathogen Agrobacterium tumefaciens, and the bovine and human pathogen Brucella abortus.
- Published
- 2001
- Full Text
- View/download PDF
50. Sequence and analysis of chromosome 1 of the plant Arabidopsis thaliana.
- Author
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Theologis A, Ecker JR, Palm CJ, Federspiel NA, Kaul S, White O, Alonso J, Altafi H, Araujo R, Bowman CL, Brooks SY, Buehler E, Chan A, Chao Q, Chen H, Cheuk RF, Chin CW, Chung MK, Conn L, Conway AB, Conway AR, Creasy TH, Dewar K, Dunn P, Etgu P, Feldblyum TV, Feng J, Fong B, Fujii CY, Gill JE, Goldsmith AD, Haas B, Hansen NF, Hughes B, Huizar L, Hunter JL, Jenkins J, Johnson-Hopson C, Khan S, Khaykin E, Kim CJ, Koo HL, Kremenetskaia I, Kurtz DB, Kwan A, Lam B, Langin-Hooper S, Lee A, Lee JM, Lenz CA, Li JH, Li Y, Lin X, Liu SX, Liu ZA, Luros JS, Maiti R, Marziali A, Militscher J, Miranda M, Nguyen M, Nierman WC, Osborne BI, Pai G, Peterson J, Pham PK, Rizzo M, Rooney T, Rowley D, Sakano H, Salzberg SL, Schwartz JR, Shinn P, Southwick AM, Sun H, Tallon LJ, Tambunga G, Toriumi MJ, Town CD, Utterback T, Van Aken S, Vaysberg M, Vysotskaia VS, Walker M, Wu D, Yu G, Fraser CM, Venter JC, and Davis RW
- Subjects
- Chromosome Mapping, DNA, Plant, Gene Duplication, Molecular Sequence Data, Multigene Family, Plant Proteins genetics, RNA, Transfer genetics, Arabidopsis genetics, Genome, Plant
- Abstract
The genome of the flowering plant Arabidopsis thaliana has five chromosomes. Here we report the sequence of the largest, chromosome 1, in two contigs of around 14.2 and 14.6 megabases. The contigs extend from the telomeres to the centromeric borders, regions rich in transposons, retrotransposons and repetitive elements such as the 180-base-pair repeat. The chromosome represents 25% of the genome and contains about 6,850 open reading frames, 236 transfer RNAs (tRNAs) and 12 small nuclear RNAs. There are two clusters of tRNA genes at different places on the chromosome. One consists of 27 tRNA(Pro) genes and the other contains 27 tandem repeats of tRNA(Tyr)-tRNA(Tyr)-tRNA(Ser) genes. Chromosome 1 contains about 300 gene families with clustered duplications. There are also many repeat elements, representing 8% of the sequence.
- Published
- 2000
- Full Text
- View/download PDF
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