956 results on '"Nucleic Acids"'
Search Results
2. Yeast: An Experimental Organism for Modern Biology.
- Author
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Botstein, David and Fink, Gerald R.
- Abstract
Discusses the applicability and advantages of using yeasts as popular and ideal model systems for studying and understanding eukaryotic biology at the cellular and molecular levels. Cites experimental tractability and the cooperative tradition of the research community of yeast biologists as reasons for this success. (RT)
- Published
- 1988
3. Sex and Violence in Neuroscience.
- Author
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Barnes, Deborah M.
- Abstract
Describes advances made in the understanding of how sex hormones may modify various cognitive skills, how normal brain signaling mechanisms may cause nerve cell death, and how many cells appear to hold genetic agents which determine their own destruction. (RT)
- Published
- 1988
4. Making Sense of Antisense.
- Author
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Moffat, Anne Simon
- Abstract
Discussed are novel ways of blocking gene expression by using antisense RNA. The use of antisense technology in plant development and its possible use in human disease therapy are described. (KR)
- Published
- 1991
5. Innate virus-sensing pathways in B cell systemic autoimmunity.
- Author
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Vinuesa, Carola G., Grenov, Amalie, and Kassiotis, George
- Subjects
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B cells , *ANTIGEN receptors , *AUTOIMMUNITY , *NATURAL immunity , *T cell receptors , *NUCLEIC acids , *B cell receptors , *AUTOANTIGENS - Abstract
Although all multicellular organisms have germ line–encoded innate receptors to sense pathogen-associated molecular patterns, vertebrates also evolved adaptive immunity based on somatically generated antigen receptors on B and T cells. Because randomly generated antigen receptors may also react with self-antigens, tolerance checkpoints operate to limit but not completely prevent autoimmunity. These two systems are intricately linked, with innate immunity playing an instrumental role in the induction of adaptive antiviral immunity. In this work, we review how inborn errors of innate immunity can instigate B cell autoimmunity. Increased nucleic acid sensing, often resulting from defects in metabolizing pathways or retroelement control, can break B cell tolerance and converge into TLR7-, cGAS-STING–, or MAVS-dominant signaling pathways. The resulting syndromes span a spectrum that ranges from chilblain and systemic lupus to severe interferonopathies. [ABSTRACT FROM AUTHOR]
- Published
- 2023
- Full Text
- View/download PDF
6. Mutant IDH1 inhibition induces dsDNA sensing to activate tumor immunity.
- Author
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Meng-Ju Wu, Hiroshi Kondo, Kammula, Ashwin V., Yi Xiao, Dhiab, Sofiene, Qin Xu, Slater, Chloe J., and Lei Shi
- Subjects
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CYTOTOXIC T cells , *DNA demethylation , *IMMUNITY , *NUCLEIC acids , *TYPE I interferons , *REVERSE transcriptase - Abstract
The article discusses a study published in Science Advances by Meng-Ju Wu, Hiroshi Kondo, Ashwin V. Kammula, and colleagues that centers on the impact of mutant IDH1 (mIDH1) inhibition on tumor immunity. It is reported that mutations in IDH1 generate (R)-2-hydroxyglutarate (R-2HG), an "oncometabolite" that disrupts cellular metabolism and epigenetic regulation, contributing to immune evasion in mIDH1 solid tumors by excluding cytotoxic CD8+ T cells.
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- 2024
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7. Structural basis for RNA-guided DNA cleavage by IscB-ωRNA and mechanistic comparison with Cas9.
- Author
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Schuler, Gabriel, Chunyi Hu, and Ke, Ailong
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CRISPRS , *NUCLEOTIDE sequence , *NUCLEOPROTEINS , *NUCLEASES , *NUCLEIC acids - Abstract
Class 2 CRISPR effectors Cas9 and Cas12 may have evolved from nucleases in IS200/IS605 transposons. IscB is about two-fifths the size of Cas9 but shares a similar domain organization. The associated wRNA plays the combined role of CRISPR RNA (crRNA) and trans-activating CRISPR RNA (tracrRNA) to guide double-stranded DNA (dsDNA) cleavage. Here we report a 2.78-angstrom cryo- electron microscopy structure of IscB-wRNA bound to a dsDNA target, revealing the architectural and mechanistic similarities between IscB and Cas9 ribonucleoproteins. Target-adjacent motif recognition, R-loop formation, and DNA cleavage mechanisms are explained at high resolution. wRNA plays the equivalent function of REC domains in Cas9 and contacts the RNA-DNA heteroduplex. The IscB-specific PLMP domain is dispensable for RNA-guided DNA cleavage. The transition from ancestral IscB to Cas9 involved dwarfing the wRNA and introducing protein domain replacements. [ABSTRACT FROM AUTHOR]
- Published
- 2022
- Full Text
- View/download PDF
8. Small-molecule activation of OGG1 increases oxidative DNA damage repair by gaining a new function.
- Author
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Michel, Maurice, Benítez-Buelga, Carlos, Calvo, Patricia A., Hanna, Bishoy M. F., Mortusewicz, Oliver, Masuyer, Geoffrey, Davies, Jonathan, Wallner, Olov, Sanjiv, Kumar, Albers, Julian J., Castañeda-Zegarra, Sergio, Jemth, Ann-Sofie, Visnes, Torkild, Sastre-Perona, Ana, Danda, Akhilesh N., Homan, Evert J., Marimuthu, Karthick, Zhenjun, Zhao, Chi, Celestine N., and Sarno, Antonio
- Subjects
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APURINIC endodeoxyribonuclease , *PHENYLALANINE , *NUCLEIC acids , *DNA damage , *SMALL molecules - Abstract
Oxidative DNA damage is recognized by 8-oxoguanine (8-oxoG) DNA glycosylase 1 (OGG1), which excises 8-oxoG, leaving a substrate for apurinic endonuclease 1 (APE1) and initiating repair. Here, we describe a small molecule (TH10785) that interacts with the phenylalanine-319 and glycine-42 amino acids of OGG1, increases the enzyme activity 10-fold, and generates a previously undescribed b, d-lyase enzymatic function. TH10785 controls the catalytic activity mediated by a nitrogen base within its molecular structure. In cells, TH10785 increases OGG1 recruitment to and repair of oxidative DNA damage. This alters the repair process, which no longer requires APE1 but instead is dependent on polynucleotide kinase phosphatase (PNKP1) activity. The increased repair of oxidative DNA lesions with a small molecule may have therapeutic applications in various diseases and aging. [ABSTRACT FROM AUTHOR]
- Published
- 2022
- Full Text
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9. CRISPR-CasF from huge phages is a hypercompact genome editor.
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Pausch, Patrick, Al-Shayeb, Basem, Bisom-Rapp, Ezra, Tsuchida, Connor A., Li, Zheng, Cress, Brady F., Knott, Gavin J., Jacobsen, Steven E., Banfield, Jillian F., and Doudna, Jennifer A.
- Subjects
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GENOME editing , *CRISPRS , *NUCLEIC acids , *PROKARYOTES , *BACTERIOPHAGES - Abstract
CRISPR-Cas systems are found widely in prokaryotes, where they provide adaptive immunity against virus infection and plasmid transformation. We describe a minimal functional CRISPR-Cas system, comprising a single ~70-kilodalton protein, CasF, and a CRISPR array, encoded exclusively in the genomes of huge bacteriophages. CasF uses a single active site for both CRISPR RNA (crRNA) processing and crRNA-guided DNA cutting to target foreign nucleic acids. This hypercompact system is active in vitro and in human and plant cells with expanded target recognition capabilities relative to other CRISPR-Cas proteins. Useful for genome editing and DNA detection but with a molecular weight half that of Cas9 and Cas12a genome-editing enzymes, CasF offers advantages for cellular delivery that expand the genome editing toolbox. [ABSTRACT FROM AUTHOR]
- Published
- 2020
- Full Text
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10. Barcoded microbial system for high-resolution object provenance.
- Author
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Qian, Jason, Lu, Zhi-xiang, Mancuso, Christopher P., Jhuang, Han-Ying, del Carmen Barajas-Ornelas, Rocío, Boswell, Sarah A., Ramírez-Guadiana, Fernando H., Jones, Victoria, Sonti, Akhila, Sedlack, Kole, Artzi, Lior, Jung, Giyoung, Arammash, Mohammad, Pettit, Mary E., Melfi, Michael, Lyon, Lorena, Owen, Siân V., Baym, Michael, Khalil, Ahmad S., and Silver, Pamela A.
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HEALTH , *FOOD safety , *NUCLEIC acids , *COMMERCE , *SPORES - Abstract
Determining where an object has been is a fundamental challenge for human health, commerce, and food safety. Location-specific microbes in principle offer a cheap and sensitive way to determine object provenance. We created a synthetic, scalable microbial spore system that identifies object provenance in under 1 hour at meter-scale resolution and near single-spore sensitivity and can be safely introduced into and recovered from the environment. This system solves the key challenges in object provenance: persistence in the environment, scalability, rapid and facile decoding, and biocontainment. Our system is compatible with SHERLOCK, a Cas13a RNA-guided nucleic acid detection assay, facilitating its implementation in a wide range of applications. [ABSTRACT FROM AUTHOR]
- Published
- 2020
- Full Text
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11. Uncovering the functional diversity of rare CRISPR-Cas systems with deep terascale clustering.
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Altae-Tran, Han, Kannan, Soumya, Suberski, Anthony J., Mears, Kepler S., Demircioglu, F. Esra, Moeller, Lukas, Kocalar, Selin, Oshiro, Rachel, Makarova, Kira S., Macrae, Rhiannon K., Koonin, Eugene V., and Feng Zhang
- Subjects
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BASE pairs , *NUCLEIC acids , *GENOME editing , *GENE regulatory networks , *SINGLE-stranded DNA - Abstract
The article focuses on the development of FLSHclust, a fast locality-sensitive hashing–based clustering algorithm for mining large sequence databases. Topics discussed include the identification of 188 previously unreported CRISPR-associated systems, diverse enzymatic activities linked to CRISPR systems, and the potential for developing these findings into biotechnologies.
- Published
- 2023
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12. Tighter biosecurity rules unveiled.
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BIOSECURITY , *NUCLEIC acids , *NONPROFIT organizations - Abstract
The article focuses on tighter biosecurity rules, aiming to prevent misuse of nucleic acids and genetic material including stricter guidelines for selling these products, extending regulations to shorter nucleotide sequences and the potential for international guidelines on biosecurity.
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- 2023
13. A cryptic clue to neurodegeneration?
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O’Brien, Niamh and Mizielinska, Sarah
- Subjects
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RNA , *NUCLEIC acids , *MESSENGER RNA , *NEURODEGENERATION , *PROTEINS - Abstract
The article discusses the role of alternative RNA splicing in neurons and how dysregulation of this process lead to the production of truncated mRNAs and proteins contributed to neurodegenerative diseases. Topics include examines the mechanism of cryptic exon missplicing of STMN2 RNA and the role of the protein TDP-43 in this process.
- Published
- 2023
- Full Text
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14. DNA methylation networks underlying mammalian traits.
- Author
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Haghani, Amin
- Subjects
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DNA methylation , *LIFE spans , *NUCLEIC acids - Abstract
For this study, we generated cytosine DNA methylation (DNAm) profiles (n = 15,456) from 348 mammalian species using a methylation array platform that targets highly conserved cytosines. INTRODUCTION: Comparative epigenomics is an emerging field that combines epigenetic signatures with phylogenetic relationships to elucidate species characteristics such as maximum life span. This suggests that long-living species evolved mechanisms that maintain low methylation levels in these chromatin states that would favor higher expression levels of genes essential for an organism's survival. [Extracted from the article]
- Published
- 2023
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15. Principles of human pre-60S biogenesis.
- Author
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Broeck, Arnaud Vanden and Klinge, Sebastian
- Subjects
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RIBOSOMAL proteins , *HUMAN beings , *RIBOSOMAL RNA , *NUCLEIC acids , *MESSENGER RNA - Abstract
Assembly of both ribosomal subunits in human cells is initiated in the nucleolus, followed by nuclear and cytoplasmic maturation, and requires more than 200 ribosome assembly factors catalyzing modification, processing, and folding of ribosomal RNA (rRNA). To functionally study rRNA processing, we developed an in vivo recombinant ribosome assembly assay using an engineered human rDNA locus to investigate whether rRNA elements within ITS2 and the 28S rRNA are required for large ribosomal subunit biogenesis. INTRODUCTION: Ribosomes, two-subunit RNA-protein nanomachines, translate messenger RNA (mRNA) into proteins in all living organisms. [Extracted from the article]
- Published
- 2023
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16. Multiplexed and portable nucleic acid detection platform with Cas13, Cas12a, and Csm6.
- Author
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Gootenberg, Jonathan S., Abudayyeh, Omar O., Kellner, Max J., Joung, Julia, Collins, James J., and Zhang, Feng
- Subjects
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NUCLEIC acid amplification techniques , *MOLECULAR diagnosis , *CRISPRS , *ENZYMOLOGY , *NUCLEIC acid analysis , *NUCLEIC acids - Abstract
Rapid detection of nucleic acids is integral for clinical diagnostics and biotechnological applications. We recently developed a platform termed SHERLOCK (specific high-sensitivity enzymatic reporter unlocking) that combines isothermal preamplification with Cas13 to detect single molecules of RNA or DNA. Through characterization of CRISPR enzymology and application development, we report here four advances integrated into SHERLOCK version 2 (SHERLOCKv2) (i) four-channel single-reaction multiplexing with orthogonal CRISPR enzymes; (ii) quantitative measurement of input as low as 2 attomolar; (iii) 3.5-fold increase in signal sensitivity by combining Cas13 with Csm6, an auxiliary CRISPR-associated enzyme; and (iv) lateral-flow readout. SHERLOCKv2 can detect Dengue or Zika virus single-stranded RNA as well as mutations in patient liquid biopsy samples via lateral flow, highlighting its potential as a multiplexable, portable, rapid, and quantitative detection platform of nucleic acids. [ABSTRACT FROM AUTHOR]
- Published
- 2018
- Full Text
- View/download PDF
17. The piRNA targeting rules and the resistance to piRNA silencing in endogenous genes.
- Author
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Donglei Zhang, Shikui Tu, Stubna, Michael, Wei-Sheng Wu, Wei-Che Huang, Zhiping Weng, and Heng-Chi Lee
- Subjects
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RNA , *GENOMES , *TRANSGENES , *CAENORHABDITIS elegans , *NUCLEIC acids - Abstract
Piwi-interacting RNAs (piRNAs) silence transposons to safeguard genome integrity in animals. However, the functions of the many piRNAs that do not map to transposons remain unknown. Here, we show that piRNA targeting in Caenorhabditis elegans can tolerate a few mismatches but prefer perfect pairing at the seed region. The broad targeting capacity of piRNAs underlies the germline silencing of transgenes in C. elegans. Transgenes engineered to avoid piRNA recognition are stably expressed. Many endogenous germline-expressed genes also contain predicted piRNA targeting sites, and periodic An/Tn clusters (PATCs) are an intrinsic signal that provides resistance to piRNA silencing. Together, our study revealed the piRNA targeting rules and highlights a distinct strategy that C. elegans uses to distinguish endogenous from foreign nucleic acids. [ABSTRACT FROM AUTHOR]
- Published
- 2018
- Full Text
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18. Kinetics of dCas9 target search in Escherichia coli.
- Author
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Lawson Jones, Daniel, Leroy, Prune, Unoson, Cecilia, Fange, David, Ćurić, Vladimir, Lawson, Michael J., and Elf, Johan
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ESCHERICHIA coli , *RNA , *NUCLEOTIDE sequence , *FLUORESCENCE microscopy , *NUCLEIC acids - Abstract
How fast can a cell locate a specific chromosomal DNA sequence specified by a single-stranded oligonucleotide? To address this question, we investigate the intracellular search processes of the Cas9 protein, which can be programmed by a guide RNA to bind essentially any DNA sequence. This targeting flexibility requires Cas9 to unwind the DNA double helix to test for correct base pairing to the guide RNA. Here we study the search mechanisms of the catalytically inactive Cas9 (dCas9) in living Escherichia coli by combining single-molecule fluorescence microscopy and bulk restriction-protection assays. We find that it takes a single fluorescently labeled dCas9 6 hours to find the correct target sequence, which implies that each potential target is bound for less than 30 milliseconds. Once bound, dCas9 remains associated until replication. To achieve fast targeting, both Cas9 and its guide RNA have to be present at high concentrations. [ABSTRACT FROM AUTHOR]
- Published
- 2017
- Full Text
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19. Nucleic acid detection with CRISPR-Cas13a/C2c2.
- Author
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Gootenberg, Jonathan S., Abudayyeh, Omar O., Jeong Wook Lee, Essletzbichler, Patrick, Dy, Aaron J., Julia Joung, Verdine, Vanessa, Donghia, Nina, Daringer, Nichole M., Freije, Catherine A., Myhrvold, Cameron, Bhattacharyya, Roby P., Livny, Jonathan, Regev, Aviv, Koonin, Eugene V., Hung, Deborah T., Sabeti, Pardis C., Collins, James J., and Feng Zhang
- Subjects
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NUCLEIC acids , *BIOMOLECULES , *NUCLEOTIDE sequence , *PATHOGENIC microorganisms , *DNA - Abstract
Rapid, inexpensive, and sensitive nucleic acid detection may aid point-of-care pathogen detection, genotyping, and disease monitoring.The RNA-guided, RNA-targeting clustered regularly interspaced short palindromic repeats (CRISPR) effector Cas13a (previously known as C2c2) exhibits a “collateral effect” of promiscuous ribonuclease activity upon target recognition.We combine the collateral effect of Cas13a with isothermal amplification to establish a CRISPR-based diagnostic (CRISPR-Dx), providing rapid DNA or RNA detection with attomolar sensitivity and single-base mismatch specificity.We use this Cas13a-based molecular detection platform, termed Specific High-Sensitivity Enzymatic Reporter UnLOCKing (SHERLOCK), to detect specific strains of Zika and Dengue virus, distinguish pathogenic bacteria, genotype human DNA, and identify mutations in cell-free tumor DNA. Furthermore, SHERLOCK reaction reagents can be lyophilized for cold-chain independence and long-term storage and be readily reconstituted on paper for field applications. [ABSTRACT FROM AUTHOR]
- Published
- 2017
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20. Experimental measurement of binding energy, selectivity, and allostery using fluctuation theorems.
- Author
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Camunas-Soler, Joan, Alemany, Anna, and Ritort, Felix
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BINDING energy , *FLUCTUATIONS (Physics) , *THERMODYNAMICS , *RECEPTOR-ligand complexes , *CHEMICAL equilibrium , *ALLOSTERIC regulation , *NUCLEIC acids , *PEPTIDES - Abstract
Thermodynamic bulk measurements of binding reactions rely on the validity of the law of mass action and the assumption of a dilute solution. Yet, important biological systems such as allosteric ligand-receptor binding, macromolecular crowding, or misfolded molecules may not follow these assumptions and may require a particular reaction model. Here we introduce a fluctuation theorem for ligand binding and an experimental approach using single-molecule force spectroscopy to determine binding energies, selectivity, and allostery of nucleic acids and peptides in a model-independent fashion. A similar approach could be used for proteins. This work extends the use of fluctuation theorems beyond unimolecular folding reactions, bridging the thermodynamics of small systems and the basic laws of chemical equilibrium. [ABSTRACT FROM AUTHOR]
- Published
- 2017
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21. RESEARCH.
- Author
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S. N. V., V. V., J. S., A. B., L. P., P. R. S., L. B. R., S. Y. M., S. T. S., B. A. P., C. A., Y. S., T. S. R., B. G., and A. M. S.
- Subjects
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SEMIMETALS , *NUCLEIC acids , *T cells , *PATHOGENIC microorganisms , *RENEWABLE energy sources - Abstract
The article focuses on several research articles that were published in the periodical on topics including magnetic Weyl semimetals, tracking nucleic acids in living cells; and Memory T cells (MTCs). It mentions that (MTCs) help the host to respond quickly and effectively to subsequent challenges by the same pathogen. It also mentions about importance of electrochemical conversion involving water and oxygen molecules in future clean and renewable energy production and storage.
- Published
- 2019
22. new products: dna/rna analysis.
- Subjects
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MOLECULAR probes , *NUCLEIC acids - Abstract
The article evaluates several products including the Nucleic Acid Extraction Kits for Pathogen Detection from AMS Biotechnology, In Situ Hybridization Probes from BioGenex, and the Chromatrap Homogenizer Spin Column from Porvair Sciences.
- Published
- 2022
23. Direct observation of transition paths during the folding of proteins and nucleic acids.
- Author
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Neupane, Krishna, Foster, Daniel A. N., Dee, Derek R., Hao Yu, Feng Wang, and Woodside, Michael T.
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PROTEIN folding , *NUCLEIC acids , *ACTIVATION energy , *MOLECULAR structure , *SINGLE molecules - Abstract
Transition paths, the fleeting trajectories through the transition states that dominate the dynamics of biomolecular folding reactions, encapsulate the critical information about how structure forms.Owing to their brief duration, however, they have not previously been observed directly.We measured transition paths for both nucleic acid and protein folding, using optical tweezers to observe the microscopic diffusive motion of single molecules traversing energy barriers.The average transit times and the shapes of the transit-time distributions agreed well with theoretical expectations for motion over the one-dimensional energy landscapes reconstructed for the samemolecules, validating the physical theory of folding reactions.These measurements provide a first look at the critical microscopic events that occur during folding, opening exciting new avenues for investigating folding phenomena. [ABSTRACT FROM AUTHOR]
- Published
- 2016
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24. Toward single-molecule proteomics.
- Author
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Bošković, Filip and Keyser, Ulrich F.
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NANOPORES , *NUCLEIC acids , *POLYMERASE chain reaction , *GENOMICS , *NUCLEOTIDES - Abstract
The article discusses nanopore re-reading of single proteins. Topics including copying of nucleic acids, through polymerase chain reaction (PCR), enabled next-generation sequencing technology; proteins are more important for functioning of genomics and transcriptomics approaches; and Nanopore DNA sequencing involves ionic current sensing for the identification of single nucleotides in nanopores.
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- 2021
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25. Biomarkers on the brain: Putting biomarkers together for a better understanding of the nervous system.
- Author
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Smith, Caitlin
- Subjects
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BIOLOGICAL tags , *NEUROPHYSIOLOGY , *DRUG development , *PLURIPOTENT stem cells , *NUCLEIC acids - Abstract
The article discusses biomarkers' use in understanding the nervous system aiding in testing, diagnosis and drug development. Topics include detection of biomarkers within blood, use of pluripotent stem cells for detecting biomarkers, and using biomarker signatures in understanding dysfunctions in the nervous system. Also included are details on the use of nucleic acid equipment for detecting biomarkers.
- Published
- 2017
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26. Getting droplets into shape.
- Author
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Snead, Wilton T. and Gladfelter, Amy S.
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NUCLEIC acids , *LIQUID-liquid interfaces , *SURFACE tension - Abstract
The article presents the discussion on condensed droplets of protein and nucleic acid regulating a variety of cellular functions from signaling to RNA processing including liquid-liquid emulsions being stabilized by materials reducing the surface tension.
- Published
- 2021
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27. Engineering of a superhelicase through conformational control.
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Arslan, Sinan, Khafizov, Rustem, Thomas, Christopher D., Chemla, Yann R., and Taekjip Ha
- Subjects
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DNA helicases regulation , *PROTEIN conformation , *DNA denaturation , *PROTEIN engineering , *NUCLEIC acids , *CROSSLINKING of nucleic acids , *CROSSLINKING (Polymerization) , *BASE pairs - Abstract
Conformational control of biomolecular activities can reveal functional insights and enable the engineering of novel activities. Here we show that conformational control through intramolecular cross-linking of a helicase monomer with undetectable unwinding activity converts it into a superhelicase that can unwind thousands of base pairs processively, even against a large opposing force. A natural partner that enhances the helicase activity is shown to achieve its stimulating role also by selectively stabilizing the active conformation. Our work provides insight into the regulation of nucleic acid unwinding activity and introduces a monomeric superhelicase without nuclease activities, which may be useful for biotechnological applications. [ABSTRACT FROM AUTHOR]
- Published
- 2015
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28. Determination of in vivo target search kinetics of regulatory noncoding RNA.
- Author
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Jingyi Fei, Digvijay Singh, Qiucen Zhang, Seongjin Park, Balasubramanian, Divya, Golding, Ido, Vanderpool, Carin K., and Taekjip Ha
- Subjects
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NON-coding RNA , *BASE pairs , *NUCLEIC acids , *BACTERIAL RNA , *MESSENGER RNA , *MATHEMATICAL models , *GLUCOSE transporters - Abstract
Base-pairing interactions between nucleic acids mediate target recognition in many biological processes. We developed a super-resolution imaging and modeling platform that enabled the in vivo determination of base pairing-mediated target recognition kinetics. We examined a stress-induced bacterial small RNA, SgrS, which induces the degradation of target messenger RNAs (mRNAs). SgrS binds to a primary target mRNA in a reversible and dynamic fashion, and formation of SgrS-mRNA complexes is rate-limiting, dictating the overall regulation efficiency in vivo. Examination of a secondary target indicated that differences in the target search kinetics contribute to setting the regulation priority among different target mRNAs. This super-resolution imaging and analysis approach provides a conceptual framework that can be generalized to other small RNA systems and other target search processes. [ABSTRACT FROM AUTHOR]
- Published
- 2015
- Full Text
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29. Programmable materials and the nature of the DNA bond.
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Jones, Matthew R., Seeman, Nadrian C., and Mirkin, Chad A.
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DNA , *CHEMICAL bonds , *NUCLEIC acids , *VALENCE (Chemistry) , *DNA machinery , *NANOSTRUCTURES , *CELLULAR automata , *METHODOLOGY - Abstract
For over half a century, the biological roles of nucleic acids as catalytic enzymes, intracellular regulatory molecules, and the carriers of genetic information have been studied extensively. More recently, the sequence-specific binding properties of DNA have been exploited to direct the assembly of materials at the nanoscale. Integral to any methodology focused on assembling matter from smaller pieces is the idea that final structures have well-defined spacings, orientations, and stereo-relationships. This requirement can be met by using DNA-based constructs that present oriented nanoscale bonding elements from rigid core units. Here, we draw analogy between such building blocks and the familiar chemical concepts of "bonds" and "valency" and review two distinct but related strategies that have used this design principle in constructing new configurations of matter. [ABSTRACT FROM AUTHOR]
- Published
- 2015
- Full Text
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30. Architecture of the cytoplasmic face of the nuclear pore.
- Author
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Bley, Christopher J., Nie, Si, Mobbs, George W., Petrovic, Stefan, Gres, Anna T., Liu, Xiaoyu, Mukherjee, Somnath, Harvey, Sho, Huber, Ferdinand M., Lin, Daniel H., Brown, Bonnie, Tang, Aaron W., Rundlet, Emily J., Correia, Ana R., Chen, Shane, Regmi, Saroj G., Stevens, Taylor A., Jette, Claudia A., Dasso, Mary, and Patke, Alina
- Subjects
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EUKARYOTIC cells , *NUCLEAR pore complex , *NUCLEAR membranes , *NUCLEOCYTOPLASMIC interactions , *RIBOSOMES , *NUCLEIC acids - Abstract
The article informs about subcellular compartmentalization of eukaryotic cells requires selective transport of folded proteins and protein– nucleic acid complexes. Topics include eukaryotic cells embedded in nuclear envelope pores, which are generated by the circumscribed fusion of the inner and outer nuclear membranes; and nuclear pore complexes (NPCs) are the sole bidirectional gateways for nucleocytoplasmic transport remodeling of messenger ribonucleoprotein particles (mRNPs).
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- 2022
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31. Anomalous COVID-19 tests hinder researchers.
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Robinson-McCarthy, Lindsey R., Mijalis, Alexander J., Filsinger, Gabriel T., de Puig, Helena, Donghia, Nina M., Schaus, Thomas E., Rasmussen, Robert A., Ferreira, Raphael, Lunshof, Jeantine E., Chao, George, Ter-Ovanesyan, Dmitry, Dodd, Oliver, Kuru, Erkin, Sesay, Adama M., Rainbow, Joshua, Pawlowski, Andrew C., Wannier, Timothy M., Yin, Peng, Collins, James J., and Ingber, Donald E.
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SARS-CoV-2 , *COVID-19 testing , *COVID-19 pandemic , *SURVEILLANCE detection , *NUCLEIC acids , *POLYMERASE chain reaction - Abstract
The article focuses on universities conduct a large proportion of the community surveillance testing for severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). It mentions shifted focus to SARS-CoV-2 research to address critical needs during this pandemic and non-infectious SARSCoV-2 nucleic acids and subsequently tested positive during SARS-CoV-2 surveillance screening. It also mentions polymerase chain reaction tests, other DNA amplification tests and approved nucleic acid tests.
- Published
- 2021
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32. An Epidermal MicroRNA Regulates Neuronal Migration Through Control of the Cellular Glycosylation State.
- Author
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Pedersen, Mikael Egebjerg, Snieckute, Goda, Kagias, Konstantinos, Nehammer, Camilla, Multhaupt, Hinke A. B., Couchman, John R., and Pocock, Roger
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MICRORNA , *GLYCOSYLATION , *PROTEOGLYCANS , *GLYCOPROTEINS , *CAENORHABDITIS elegans , *NUCLEIC acids - Abstract
An appropriate balance in glycosylation of proteoglycans is crucial for their ability to regulate animal development. Here, we report that the Caenorhabditis elegans microRNA mir-79, an ortholog of mammalian miR-9, controls sugar-chain homeostasis by targeting two proteins in the proteoglycan biosynthetic pathway: a chondroitin synthase (SQV-5; squashed vulva-5) and a uridine 5'-diphosphate- sugar transporter (SQV-7). Loss of mir-79 causes neurodevelopmental defects through SQV-5 and SQV-7 dysregulation in the epidermis. This results in a partial shutdown of heparan sulfate biosynthesis that impinges on a LON-2/glypican pathway and disrupts neuronal migration. Our results identify a regulatory axis controlled by a conserved microRNA that maintains proteoglycan homeostasis in cells. [ABSTRACT FROM AUTHOR]
- Published
- 2013
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33. DNA Gridiron Nanostructures Based on Four-Arm Junctions.
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Dongran Han, Pal, Suchetan, Yang Yang, Shuoxing Jiang, Nangreave, Jeanette, Yan Liu, and Hao Yan
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NANOTECHNOLOGY , *DNA synthesis , *MOLECULAR self-assembly , *NUCLEIC acids , *NANOSTRUCTURED materials synthesis , *DOUBLE helix structure - Abstract
Engineering wireframe architectures and scaffolds of increasing complexity is one of the important challenges in nanotechnology. We present a design strategy to create gridiron-like DNA structures. A series of four-arm junctions are used as vertices within a network of double-helical DNA fragments. Deliberate distortion of the junctions from their most relaxed conformations ensures that a scaffold strand can traverse through individual vertices in multiple directions. DNA gridirons were assembled, ranging from two-dimensional arrays with reconfigurability to multilayer and three-dimensional structures and curved objects. [ABSTRACT FROM AUTHOR]
- Published
- 2013
- Full Text
- View/download PDF
34. RNA-Guided Human Genome Engineering via Cas9.
- Author
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Mali, Prashant, Yang, Luhan, Esvelt, Kevin M., Aach, John, Guell, Marc, DiCarlo, James E., Norville, Julie E., and Church, George M.
- Subjects
- *
HUMAN genome , *RNA , *ARCHAEBACTERIA , *BACTERIA , *NUCLEIC acids , *BIOTRANSFORMATION (Metabolism) , *PLURIPOTENT stem cells , *EXONS (Genetics) , *GENETIC engineering - Abstract
Bacteria and archaea have evolved adaptive immune defenses, termed clustered regularly interspaced short palindromic repeats (CRISPRVCRISPR-associated (Cas) systems, that use short RNA to direct degradation of foreign nucleic acids. Here, we engineer the type II bacterial CRISPR system to function with custom guide RNA (gRNA) in human cells. For the endogenous AAVS1 locus, we obtained targeting rates of 10 to 25% in 293T cells, 13 to 8% in K562 cells, and 2 to 4% in induced pluripotent stem cells. We show that this process relies on CRISPR components; is sequence-specific; and, upon simultaneous introduction of multiple gRNAs, can effect multiplex editing of target loci. We also compute a genome-wide resource of ~190 K unique gRNAs targeting ~40.5% of human exons. Our results establish an RNA-guided editing tool for facile, robust, and multiplexable human genome engineering. [ABSTRACT FROM AUTHOR]
- Published
- 2013
- Full Text
- View/download PDF
35. Structural Basis of Transcription Initiation.
- Author
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Yu Zhang, Yu Feng, Chatterjee, Sujoy, Tuske, Steve, Ho, Mary X., Arnold, Eddy, and Ebright, Richard H.
- Subjects
- *
GENETIC transcription , *RNA polymerases , *PROMOTERS (Genetics) , *THERMUS thermophilus , *BACTERIAL genetics , *NUCLEIC acids , *DNA - Abstract
The article discusses research investigating the structural basis of transcription initiation in which RNA polymerase (RNAP) binds and unwinds promoter DNA to form an RNAP-promoter open complex (RPo). The authors report crystal structures of the bacteria Thermus thermophilus' RPo and a RPo in complex with a ribodinucleotide primer at 2.9 and 3.0 angstrom (Å) resolution, respectively. A discussion on how researchers obtained a structure of RPo via the use of a synthetic nucleic-acid scaffold corresponding to the transcription bubble and downstream double-stranded DNA (dsDNA) is presented.
- Published
- 2012
- Full Text
- View/download PDF
36. RNA Mimics of Green Fluorescent Protein.
- Author
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Paige, Jeremy S., Wu, Karen Y., and Jaffrey, Samie R.
- Subjects
- *
GREEN fluorescent protein , *PROTEIN folding , *NUCLEOTIDE sequence , *FLUORESCENCE , *NUCLEIC acids - Abstract
Green fluorescent protein (GFP) and its derivatives have transformed the use and analysis of proteins for diverse applications. Like proteins, RNA has complex roles in cellular function and is increasingly used for various applications, but a comparable approach for fluorescently tagging RNA is lacking. Here, we describe the generation of RNA aptamers that bind fluorophores resembling the fluorophore in GFP. These RNA-fluorophore complexes create a palette that span the visible spectrum. An RNA-fluorophore complex, termed Spinach, resembles enhanced GFP and emits a green fluorescence comparable in brightness with fluorescent proteins. Spinach is markedly resistant to photobleaching, and Spinach fusion RNAs can be imaged in living cells. These RNA mimics of GFP provide an approach for genetic encoding of fluorescent RNAs. [ABSTRACT FROM AUTHOR]
- Published
- 2011
- Full Text
- View/download PDF
37. No Evidence of Murine-Like Gammaretroviruses in CFS Patients Previously Identified as XMRV-Infected.
- Author
-
Knox, Konstance, Carrigan, Donald, Simmons, Graham, Teque, Fernando, Yanchen Zhou, Hackett Jr., John, Xiaoxing Qiu, Ka-Cheung Luk, Schochetman, Gerald, Knox, Allyn, Kogelnik, Andreas M., and Levy, Jay A.
- Subjects
- *
CHRONIC fatigue syndrome , *ETIOLOGY of diseases , *RETROVIRUS diseases , *MOUSE leukemia viruses , *DIAGNOSTIC use of polymerase chain reaction , *REVERSE transcriptase polymerase chain reaction , *VIRAL antibodies , *NUCLEIC acids - Abstract
Members of the gammaretroviruses--such as murine leukemia viruses (MLVs), most notably XMRV [xenotropic murine leukemia virus (X-MLV)-related virus--have been reported to be present in the blood of patients with chronic fatigue syndrome (CFS). We evaluated blood samples from 61 patients with CFS from a single clinical practice, 43 of whom had previously been identified as XMRV-positive. Our analysis included polymerase chain reaction and reverse transcription polymerase chain reaction procedures for detection of viral nucleic acids and assays for detection of infectious virus and virus-specific antibodies. We found no evidence of XMRV or other MLVs in these blood samples. In addition, we found that these gammaretroviruses were strongly (X-MLV) or partially (XMRV) susceptible to inactivation by sera from CFS patients and healthy controls, which suggested that establishment of a successful MLV infection in humans would be unlikely. Consistent with previous reports, we detected MLV sequences in commercial laboratory reagents. Our results indicate that previous evidence (inking XMRV and MLVs to CFS is likely attributable to laboratory contamination. [ABSTRACT FROM AUTHOR]
- Published
- 2011
- Full Text
- View/download PDF
38. Mutagenic Processing of Ribonucleotides in DNA by Yeast Topoisomerase I.
- Author
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Kim, Nayun, Huang, Shar-yin N., Williams, Jessica S., C. Li, Yue, Clark, Alan B., Jang-Eun Cho, Kunkel, Thomas A., Pommier, Yves, and Jinks-Robertson, Sue
- Subjects
- *
DNA topoisomerase I , *RIBONUCLEASES , *ENZYMES , *RNA , *NUCLEIC acids , *METABOLISM , *DNA , *DNA polymerases , *ARGININE , *MOLECULAR structure , *TUMORS - Abstract
The ribonuclease (RNase) H class of enzymes degrades the RNA component of RNA:DNA hybrids and is important in nucleic acid metabolism. RNase H2 is specialized to remove single ribonucleotides [ribonucleoside monophosphates (rNMPs)] from duplex DNA, and its absence in budding yeast has been associated with the accumulation of deletions within short tandem repeats. Here, we demonstrate that rNMP-associated deletion formation requires the activity of Top1, a topoisomerase that relaxes supercoils by reversibly nicking duplex DNA. The reported studies extend the role of Top1 to include the processing of rNMPs in genomic DNA into irreversible single-strand breaks, an activity that can have distinct mutagenic consequences and may be relevant to human disease. [ABSTRACT FROM AUTHOR]
- Published
- 2011
- Full Text
- View/download PDF
39. A Packing Mechanism for Nucleosome Organization Reconstituted Across a Eukaryotic Genome.
- Author
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Zhenhai Zhang, Wippo, Christian J., Wal, Megha, Ward, Elissa, Korber, Philipp, and Pugh, B. Franklin
- Subjects
- *
GENES , *NUCLEOTIDE sequence , *EUKARYOTIC cells , *GENETIC transcription , *DNA , *ADENOSINE triphosphate , *NUCLEIC acids , *CHROMATIN - Abstract
Near the 5' end of most eukaryotic genes, nucleosomes form highly regular arrays that begin at canonical distances from the transcriptional start site. Determinants of this and other aspects of genomic nucleosome organization have been ascribed to statistical positioning, intrinsically DNA-encoded positioning, or some aspect of transcription initiation. Here, we provide evidence for a different explanation. Biochemical reconstitution of proper nucleosome positioning, spacing, and occupancy levels was achieved across the 5' ends of most yeast genes by adenosine triphosphate-dependent trans-acting factors. These transcription-independent activities override DNA-intrinsic positioning and maintain uniform spacing at the 5' ends of genes even at low nucleosome densities. Thus, an active, nonstatistical nucleosome packing mechanism creates chromatin organizing centers at the 5' ends of genes where important regulatory elements reside. [ABSTRACT FROM AUTHOR]
- Published
- 2011
- Full Text
- View/download PDF
40. The C-Ala Domain Brings Together Editing and Aminoacylation Functions on One tRNA.
- Author
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Min Gun, Chong, Yeeting E., Beebe, Kirk, Shapiro, Ryan, Xiang-Lei Yang, and Schimmel, Paul
- Subjects
- *
ACYLATION , *PROTEIN synthesis , *TRANSFER RNA , *AMINO acids , *LIGASES , *NUCLEIC acids - Abstract
Protein synthesis involves the accurate attachment of amino acids to their matching transfer RNA (tRNA) molecules. Mistranslating the amino acids serine or glycine for alanine is prevented by the function of independent but collaborative aminoacylation and editing domains of alanyl-tRN synthetases (AlaRSs). We show that the C-Ala domain plays a key role in AlaRS function. The C-Ala domain is universally tethered to the editing domain both in AlaRS and in many homologous free-standing editing proteins. Crystal structure and functional analyses showed that C-Ala forms an ancient single-stranded nucleic acid binding motif that promotes cooperative binding of both aminoacylation and editing domains to tRNAALA. In addition, C-Ala may have played an essential role in the evolution of AlaRSs by coupling aminoacylation to editing to prevent mistranslation [ABSTRACT FROM AUTHOR]
- Published
- 2009
41. Self-Assembling Sequence-Adaptive Peptide Nucleic Acids.
- Author
-
Ura, Yasuyuki, Beierle, John M., Leman, Luke J., Orgel, Leslie E., and Ghadiri, M. Reza
- Subjects
- *
MOLECULAR self-assembly , *NUCLEIC acids , *PEPTIDES , *POLYMER research , *OLIGOMERS , *SOLUTION (Chemistry) , *BIOMEDICAL materials - Abstract
Several classes of nucleic add analogs have been reported, but no synthetic informational polymer has yet proven responsive to selection pressures under enzyme-free conditions. Here, we introduce an oligomer family that efficiently self-assembles by means of reversible covalent anchoring of nucleobase recognition units onto simple oligo-dipeptide backbones [thioester peptide nucleic adds (tPNAs)] and undergoes dynamic sequence modification in response to changing templates in solution. The oligomers specifically self-pair with complementary tPNA strands and cross-pair with RNA and DNA in Watson-Crick fashion. Thus, tPNA combines base-pairing interactions with the side-chain functionalities of typical peptides and proteins. These characteristics might prove advantageous for the design or selection of catalytic constructs or biomaterials that are capable of dynamic sequence repair and adaptation. [ABSTRACT FROM AUTHOR]
- Published
- 2009
- Full Text
- View/download PDF
42. HIN-200 Proteins Regulate Caspase Activation in Response to Foreign Cytoplasmic DNA.
- Author
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Roberts, Tara L., Idris, Adi, Dunn, Jasmyn A., Kelly, Greg M., Burnton, Carol M., Hodgson, Samatha, Hardy, Lani L., Garceau, Valerie, Sweet, Matthew J., Ross, Ian L., Hume, David A., and Stacey, Katryn J.
- Subjects
- *
PROTEIN research , *IMMUNE system , *NUCLEIC acids , *CYTOPLASM , *CELL death , *MACROPHAGES , *GENE transfection , *GENETICS - Abstract
The mammalian innate immune system is activated by foreign nucleic acids. Detection of double-stranded DNA (dsDNA) in the cytoplasm triggers characteristic antiviral responses and macrophage cell death. Cytoplasmic dsDNA rapidly activated caspase 3 and caspase 1 in bone marrow-derived macrophages. We identified the HIN-200 family member and candidate lupus susceptibility factor, p202, as a dsDNA binding protein that bound stably and rapidly to transfected DNA. Knockdown studies showed p202 to be an inhibitor of DNA-induced caspase activation. Conversely, the related pyrin domain--containing HIN-200 factor, AIM2 (p210), was required for caspase activation by cytoplasmic dsDNA. This work indicates that HIN-200 proteins can act as pattern recognition receptors mediating responses to cytoplasmic dsDNA. [ABSTRACT FROM AUTHOR]
- Published
- 2009
- Full Text
- View/download PDF
43. Small CRISPR RNAs Guide Antiviral Defense in Prokaryotes.
- Author
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Brouns, Stan J. J., Jore, Matthijs M., Lundgren, Magnus, Westra, Edze R., Stijkhuis, Rik J. H., Snijders, Ambrosius P. L., Dickman, Mark J., Makarova, Kira S., Koonin, Eugene V., and van der Oost, John
- Subjects
- *
PROKARYOTES , *BACTERIA , *VIRUSES , *NUCLEIC acids , *GENETIC transformation , *RNA , *PROTEINS , *ENDONUCLEASES , *RIBOSE , *NON-coding RNA - Abstract
Prokaryotes acquire virus resistance by integrating short fragments of viral nucleic acid into clusters of regularly interspaced short palindromic repeats (CRISPRs). Here we show how virus-derived sequences contained in CRISPRs are used by CRISPR-associated (Cas) proteins from the host to mediate an antiviral response that counteracts infection. After transcription of the CRISPR, a complex of Cas proteins termed Cascade cleaves a CRISPR RNA precursor in each repeat and retains the cleavage products containing the virus-derived sequence. Assisted by the helicase Cas3, these mature CRISPR RNAs then serve as small guide RNAs that enable Cascade to interfere with virus proliferation. Our results demonstrate that the formation of mature guide RNAs by the CRISPR RNA endonuclease subunit of Cascade is a mechanistic requirement for antiviral defense. [ABSTRACT FROM AUTHOR]
- Published
- 2008
- Full Text
- View/download PDF
44. Regulation of CD45 Alternative Splicing by Heterogeneous Ribonucleoprotein, hnRNPLL.
- Author
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Oberdoerffer, Shalini, Moita, Luis Ferreira, Neems, Daniel, Freitas, Rui P., Hacohen, Nir, and Rao, Anjana
- Subjects
- *
T cells , *LYMPHOCYTES , *PHOSPHATASES , *ESTERASES , *RNA , *RIBOSE , *NUCLEIC acids , *ERYTHROPOIETIN , *CELLS - Abstract
The transition from naïve to activated T cells is marked by alternative splicing of pre-mRNA encoding the transmembrane phosphatase CD45. Using a short hairpin RNA interference screen, we identified heterogeneous ribonucleoprotein L-like (hnRNPLL) as a critical inducible regulator of CD45 alternative splicing. HnRNPLL was up-regulated in stimulated T cells, bound CD45 transcripts, and was both necessary and sufficient for CD45 alternative splicing. Depletion or overexpression of hnRNPLL in B and T cell lines and primary T cells resulted in reciprocal alteration of CD45RA and RO expression. Exon array analysis suggested that hnRNPLL acts as a global regulator of alternative splicing in activated T cells. Induction of hnRNPLL during hematopoietic cell activation and differentiation may allow cells to rapidly shift their transcriptomes to favor proliferation and inhibit cell death. [ABSTRACT FROM AUTHOR]
- Published
- 2008
- Full Text
- View/download PDF
45. Virus Attenuation by Genome-Scale Changes in Codon Pair Bias.
- Author
-
Coleman, J. Robert, Papamichai, Dimitris, Skiena, Steven, Futcher, Bruce, Wimmer, Eckard, and Mueller, Steffen
- Subjects
- *
AMINO acids , *LABORATORY mice , *ORGANIC acids , *DNA , *NUCLEIC acids , *GENES , *DEOXYRIBOSE , *POLIOVIRUS , *ENTEROVIRUSES - Abstract
As a result of the redundancy of the genetic code, adjacent pairs of amino acids can be encoded by as many as 36 different pairs of synonymous codons. A species-specific "codon pair bias" provides that some synonymous codon pairs are used more or Less frequently than statistically predicted. We synthesized de novo large DNA molecules using hundreds of over- or underrepresented synonymous codon pairs to encode the poliovirus capsid protein. Underrepresented codon pairs caused decreased rates of protein translation, and polioviruses containing such amino acid-independent changes were attenuated in mice. Polioviruses thus customized were used to immunize mice and provided protective immunity after challenge. This "death by a thousand cuts" strategy could be generally applicable to attenuating many kinds of viruses. [ABSTRACT FROM AUTHOR]
- Published
- 2008
- Full Text
- View/download PDF
46. β-Arrestin--Mediated Localization of Smoothened to the Primary Cilium.
- Author
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Kovacs, Jeffrey J., Whalen, Erin J., Renshui Liu, Kunhong Xiao, Jihee Kim, Minyong Chen, Jiangbo Wang, Wei Chen, and Lefkowitz, Robert J.
- Subjects
- *
KINESIN , *RNA , *CARCINOGENESIS , *CELLS , *ENDOCYTOSIS , *CELL physiology , *NUCLEIC acids , *ABSORPTION (Physiology) , *EPITHELIUM - Abstract
β-Arrestins have important roles in the regulation of seven-transmembrane receptors (7TMRs). Smoothened (Smo) is a 7TMR that mediates effects of Hedgehog on developmental processes and whose dysregulation may cause tumorigenesis. β-Arrestins are required for endocytosis of Smo and signaling to Gli transcription factors. In mammalian cells, Smo-dependent signaling requires translocation to primary cilia. We demonstrated that β-arrestins mediate the activity-dependent interaction of Smo and the kinesin motor protein Kif3A. This multimeric complex localized to primary cilia and was disrupted in cells transfected with β-arrestin small interfering RNA. β-Arrestin 1 or β-arrestin 2 depletion prevented the localization of Smo to primary cilia and the Smo-dependent activation of Gli. These results suggest roles for β-arrestins in mediating the intracellular transport of a 7TMR to its obligate subcellular location for signaling. [ABSTRACT FROM AUTHOR]
- Published
- 2008
- Full Text
- View/download PDF
47. A Phylogenomic Study of Birds Reveals Their Evolutionary History.
- Author
-
Hackett, Shannon J., Kimball, Rebecca T., Reddy, Sushma, Bowie, Rauri C. K., Braun, Edward L., Braun, Michael J., Chojnowski, Jena L., Cox, W. Andrew, Kin-Lan Han, Harshman, John, Huddleston, Christopher J., Marks, Ben D., Miglia, Kathleen J., Moore, William S., Sheldon, Frederick H., Steadman, David W., Witt, Christopher C., and Yuri, Tamaki
- Subjects
- *
NUCLEIC acids , *NUCLEOTIDE sequence , *BIRD evolution , *PHYLOGENY , *BIOLOGICAL evolution , *IMMUNOTAXONOMY , *CLADISTIC analysis , *DNA , *BIRD watching - Abstract
Deep avian evolutionary relationships have been difficult to resolve as a result of a putative explosive radiation. Our study examined ∼32 kilobases of aligned nuclear DNA sequences from 19 independent loci for 169 species, representing all major extant groups, and recovered a robust phylogeny from a genome-wide signal supported by multiple analytical methods. We documented well-supported, previously unrecognized interordinal relationships (such as a sister relationship between passerines and parrots) and corroborated previously contentious groupings (such as flamingos and grebes). Our conclusions challenge current classifications and alter our understanding of trait evolution; for example, some diurnal birds evolved from nocturnal ancestors. Our results provide a valuable resource for phylogenetic and comparative studies in birds. [ABSTRACT FROM AUTHOR]
- Published
- 2008
- Full Text
- View/download PDF
48. Activation of the Cellular DNA Damage Response in the Absence of DNA Lesions.
- Author
-
Soutoglou, Evi and Misteli, Tom
- Subjects
- *
GENES , *DNA , *NUCLEOPROTEINS , *CHROMOSOMES , *NUCLEIC acids , *DEOXYRIBOSE , *CHROMATIN , *PROTEIN kinases , *MOLECULAR genetics - Abstract
The cellular DNA damage response (DDR) is initiated by the rapid recruitment of repair factors to the site of DNA damage to form a multiprotein repair complex. How the repair complex senses damaged DNA and then activates the DDR is not welt understood. We show that prolonged binding of DNA repair factors to chromatin can elicit the DDR in an ATM (ataxia telangiectasia mutated)- and DNAPK (DNA-dependent protein kinase)-dependent manner in the absence of DNA damage. Targeting of single repair factors to chromatin revealed a hierarchy of protein interactions within the repair complex and suggests amplification of the damage signal. We conclude that activation of the DDR does not require DNA damage and stable association of repair factors with chromatin is likely a critical step in triggering, amplifying, and maintaining the DDR signal. [ABSTRACT FROM AUTHOR]
- Published
- 2008
- Full Text
- View/download PDF
49. Widespread Translational Inhibition by Plant miRNAs and siRNAs.
- Author
-
Brodersen, Peter, Sakvarelidze-Achard, Lali, Bruun-Rasmussen, Marianne, Dunoyer, Patrice, Yamamoto, Yoshiharu V., Sieburth, Leslie, and Voinnet, Olivier
- Subjects
- *
RNA , *NUCLEIC acids , *BIOMOLECULES , *NUCLEOTIDES , *ARABIDOPSIS , *GENETIC transformation , *ENZYMES , *CYTOSKELETON , *PROTEINS - Abstract
High complementarity between plant microRNAs (miRNAs) and their messenger RNA targets is thought to cause silencing, prevalently by endonucleolytic cleavage. We have isolated Arabidopsis mutants defective in miRNA action. Their analysis provides evidence that plant miRNA-guided silencing has a widespread translational inhibitory component that is genetically separable from endonucleolytic cleavage. We further show that the same is true of silencing mediated by small interfering RNA (siRNA) populations. Translational repression is effected in part by the ARGONAUTE proteins AG01 and AG010. It also requires the activity of the microtubule-severing enzyme katanin, implicating cytoskeleton dynamics in miRNA action, as recently suggested from animal studies. Also as in animals, the decapping component VARICOSE (V(S)/Ge-1 is required for translational repression by miRNAs, which suggests that the underlying mechanisms in the two kingdoms are related. [ABSTRACT FROM AUTHOR]
- Published
- 2008
- Full Text
- View/download PDF
50. The Epigenetic Landscape of Plants.
- Author
-
Xiaoyu Zhang
- Subjects
- *
DNA , *RNA , *BASIC proteins , *METHYLATION , *HISTONES , *CHROMATIN , *NUCLEIC acids , *TRANSCRIPTION factors , *MOLECULAR structure - Abstract
In plants, DNA methylation, histone modifications, and RNA interference play critically important roles in regulating chromatin structure, thereby profoundly affecting transcription and other molecular events. Recent advances in microarray and high-throughput sequencing technologies have enabled genome-wide studies of these pathways in great detail. The vast amounts of ‘epigenomic’ data generated so far have provided new insights into the mechanisms and functions of these pathways and have broadened our understanding of the structure and organization of plant chromatin as a whole. [ABSTRACT FROM AUTHOR]
- Published
- 2008
- Full Text
- View/download PDF
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