143 results on '"Polar mutation"'
Search Results
2. Transcription and Translation: Processes and Basic Regulation
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Birge, Edward A.
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- 2006
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3. Bacteria as Model Systems in Genetic Analysis
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Srivastava, Sheela, Srivastava, P. S., Srivastava, Sheela, and Srivastava, P. S.
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- 2003
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4. The hrp genes of Pantoea stewartii are Regulated by a Complex System that Senses Environmental Signals
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Merighi, M., Majerczak, D. R., Coplin, D. L., and De Boer, Solke H., editor
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- 2001
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5. Transcription and Translation: Processes and Basic Regulation
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Birge, Edward A. and Birge, Edward A.
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- 2000
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6. Insertion Sequences and Transposons
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Chandler, Mark S., de Bruijn, Frans J., editor, Lupski, James R., editor, and Weinstock, George M., editor
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- 1998
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7. A preliminary investigation into directed mutations in evolutionary algorithms
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Ghozeil, Adam, Fogel, David B., Goos, G., editor, Hartmanis, J., editor, van Leeuwen, J., editor, Voigt, Hans-Michael, editor, Ebeling, Werner, editor, Rechenberg, Ingo, editor, and Schwefel, Hans-Paul, editor
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- 1996
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8. Transcription and Translation: Processes and Basic Regulation
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Birge, Edward A. and Birge, Edward A.
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- 1994
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9. P
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Rieger, R., Michaelis, A., Green, M. M., Rieger, R., Michaelis, A., and Green, M. M.
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- 1991
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10. What the models do not tell us
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Lima-de-Faria, A. and Lima-de-Faria, A.
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- 2003
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11. Polar Mutation
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Rédei, George P.
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- 2008
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12. Two novel C-terminal frameshift mutations in the β-globin gene lead to rapid mRNA decay
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Pawel Szczesny, Anna Adamowicz-Salach, Andrzej Dziembowski, Katarzyna Rawa, Monika Gora, Urszula Demkow, Ewelina P. Owczarek, Roman J. Szczesny, Anna Klukowska, Beata Burzynska, and Danuta Plochocka
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Male ,0301 basic medicine ,Silent mutation ,lcsh:Internal medicine ,lcsh:QH426-470 ,RNA Stability ,DNA Mutational Analysis ,beta-Globins ,Biology ,medicine.disease_cause ,Cell Line ,Frameshift mutation ,Polar mutation ,03 medical and health sciences ,Exon ,hemic and lymphatic diseases ,Genetics ,medicine ,Humans ,Child ,Frameshift Mutation ,lcsh:RC31-1245 ,Genetics (clinical) ,Mutation ,Point mutation ,β- thalassemia ,beta-Thalassemia ,Exons ,Molecular biology ,Stop codon ,Open reading frame ,lcsh:Genetics ,030104 developmental biology ,Frameshift mutations ,mRNA degradation ,Poland ,Gene expression ,Research Article - Abstract
Background The thalassemia syndromes are classified according to the globin chain or chains whose production is affected. β-thalassemias are caused by point mutations or, more rarely, deletions or insertions of a few nucleotides in the β-globin gene or its immediate flanking sequences. These mutations interfere with the gene function either at the transcriptional, translational or posttranslational level. Methods Two cases of Polish patients with hereditary hemolytic anemia suspected of thalassemia were studied. DNA sequencing and mRNA quantification were performed. Stable human cell lines which express wild-type HBB and mutated versions were used to verify that detected mutation are responsible for mRNA degradation. Results We identified two different frameshift mutations positioned in the third exon of HBB. Both patients harboring these mutations present the clinical phenotype of thalassemia intermedia and showed dominant pattern of inheritance. In both cases the mutations do not generate premature stop codon. Instead, slightly longer protein with unnatural C-terminus could be produced. Interestingly, although detected mutations are not expected to induce NMD, the mutant version of mRNA is not detectable. Restoring of the open reading frame brought back the RNA to that of the wild-type level. Conclusion Our results show that a lack of natural stop codon due to the frameshift in exon 3 of β-globin gene causes rapid degradation of its mRNA and indicate existence of novel surveillance pathway. Electronic supplementary material The online version of this article (doi:10.1186/s12881-017-0428-1) contains supplementary material, which is available to authorized users.
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- 2017
13. A rapid and effective method for screening, sequencing and reporter verification of engineered frameshift mutations in zebrafish
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Shelby L. Steele, Sergey V. Prykhozhij, Jason N. Berman, and Babak Razaghi
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0301 basic medicine ,RNA Splicing ,Neuroscience (miscellaneous) ,SgRNA ,Medicine (miscellaneous) ,lcsh:Medicine ,Biology ,medicine.disease_cause ,Fluorescence ,General Biochemistry, Genetics and Molecular Biology ,Frameshift mutation ,Polar mutation ,03 medical and health sciences ,0302 clinical medicine ,Immunology and Microbiology (miscellaneous) ,Genome editing ,Genes, Reporter ,medicine ,lcsh:Pathology ,Animals ,CRISPR ,Resource Article ,Genetic Testing ,Cloning, Molecular ,Frameshift Mutation ,Cas9 ,Gene ,Reporter ,Zebrafish ,Genetics ,Mutation ,Base Sequence ,lcsh:R ,Reproducibility of Results ,Exons ,Sequence Analysis, DNA ,Zebrafish Proteins ,Zebra ,Exon skipping ,3. Good health ,Phenotype ,030104 developmental biology ,Genetic Engineering ,030217 neurology & neurosurgery ,lcsh:RB1-214 - Abstract
Clustered regularly interspaced palindromic repeats (CRISPR)/Cas-based adaptive immunity against pathogens in bacteria has been adapted for genome editing and applied in zebrafish (Danio rerio) to generate frameshift mutations in protein-coding genes. Although there are methods to detect, quantify and sequence CRISPR/Cas9-induced mutations, identifying mutations in F1 heterozygous fish remains challenging. Additionally, sequencing a mutation and assuming that it causes a frameshift does not prove causality because of possible alternative translation start sites and potential effects of mutations on splicing. This problem is compounded by the relatively few antibodies available for zebrafish proteins, limiting validation at the protein level. To address these issues, we developed a detailed protocol to screen F1 mutation carriers, and clone and sequence identified mutations. In order to verify that mutations actually cause frameshifts, we created a fluorescent reporter system that can detect frameshift efficiency based on the cloning of wild-type and mutant cDNA fragments and their expression levels. As proof of principle, we applied this strategy to three CRISPR/Cas9-induced mutations in pycr1a, chd7 and hace1 genes. An insertion of seven nucleotides in pycr1a resulted in the first reported observation of exon skipping by CRISPR/Cas9-induced mutations in zebrafish. However, of these three mutant genes, the fluorescent reporter revealed effective frameshifting exclusively in the case of a two-nucleotide deletion in chd7, suggesting activity of alternative translation sites in the other two mutants even though pycr1a exon-skipping deletion is likely to be deleterious. This article provides a protocol for characterizing frameshift mutations in zebrafish, and highlights the importance of checking mutations at the mRNA level and verifying their effects on translation by fluorescent reporters when antibody detection of protein loss is not possible., Summary: A new CRISPR/Cas9-based method of fluorescent reporter technology in zebrafish to confirm loss of gene function in this model.
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- 2017
14. Urea Utilization in Rhodobacter capsulatus is Regulated by NtrC
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Masepohl, B., Kaiser, B., Isakovic, N., Klipp, W., Pedrosa, Fabio O., editor, Hungria, Mariangela, editor, Yates, Geoffrey, editor, and Newton, William E., editor
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- 2000
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15. Molecular and functional analysis of the C-terminal region of human erythroid-specific 5-aminolevulinic synthase associated with X-linked dominant protoporphyria (XLDPP)
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Erica J. Fratz, Felix W. M. de Rooij, George Varigos, Jean-Charles Deybach, George Ostapowicz, Laurent Gouya, Elisabeth I. Minder, Jerome Clayton, Sarah Ducamp, Paul Wilson, Hervé Puy, Gloria C. Ferreira, Alice Rudd, Thibaud Lefebvre, Xiaoye Schneider-Yin, and Internal Medicine
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Protoporphyria, Erythropoietic ,DNA Mutational Analysis ,Molecular Sequence Data ,Mutant ,Gene mutation ,Biology ,medicine.disease_cause ,Frameshift mutation ,Polar mutation ,Young Adult ,Exon ,Genetics ,medicine ,Humans ,Amino Acid Sequence ,Frameshift Mutation ,Molecular Biology ,Gene ,Genetic Association Studies ,Genetics (clinical) ,Mutation ,Base Sequence ,Mosaicism ,Infant ,Genetic Diseases, X-Linked ,Exons ,Sequence Analysis, DNA ,General Medicine ,ALAS2 ,Molecular biology ,Pedigree ,Protein Structure, Tertiary ,Kinetics ,Codon, Nonsense ,Child, Preschool ,Mutagenesis, Site-Directed ,Female ,5-Aminolevulinate Synthetase - Abstract
Frameshift mutations in the last coding exon of the 5-aminolevulinate synthase (ALAS) 2 gene were described to activate the enzyme causing increased levels of zinc- and metal-free protoporphyrin in patients with X-linked dominant protoporphyria (XLDPP). Only two such so-called gain-of-function mutations have been reported since the description of XLDPP in 2008. In this study of four newly identified XLDPP families, we identified two novel ALAS2 gene mutations, a nonsense p.Q548X and a frameshift c.1651-1677del26bp, along with a known mutation (delAGTG) found in two unrelated families. Of relevance, a de novo somatic and germinal mosaicism was present in a delAGTG family. Such a phenomenon may explain the high proportion of this mutation in XLDPP worldwide. Enhancements of over 3- and 14-fold in the catalytic rate and specificity constant of purified recombinant XLDPP variants in relation to those of wild-type ALAS2 confirmed the gain of function ascribed to these enzymes. The fact that both p.Q548X and c.1651-1677del26bp are located in close proximity and upstream from the two previously described mutations led us to propose the presence of a large gain-of-function domain within the C-terminus of ALAS2. To test this hypothesis, we generated four additional nonsense mutants (p.A539X, p.G544X, p.G576X and p.V583X) surrounding the human XLDPP mutations and defined an ALAS2 gain-of-function domain with a minimal size of 33 amino acids. The identification of this gain-of-function domain provides important information on the enzymatic activity of ALAS2, which was proposed to be constitutively inhibited, either directly or indirectly, through its own C-terminus.
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- 2013
16. Termination and Antitermination in Transcription: Control of Gene Expression
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Adhya, Sankar, Gottesman, Max, de Crombrugghe, Benoit, Hollaender, Alexander, editor, Biswas, B. B., editor, Mandal, R. K., editor, Stevens, A., editor, and Cohn, W. E., editor
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- 1974
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17. Use of RP4 Plasmids Carrying Bacteriophase Mu Insertions in Nitrogen Fixing Bacteria Klebsiella Pneumoniae and Rhizobium Meliloti
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Rosenberg, C., Bergeron, B., Julliot, J. S., Dénarié, J., Hollaender, Alexander, editor, Burris, R. H., editor, Day, P. R., editor, Hardy, R. W. F., editor, Helinski, D. R., editor, Lamborg, M. R., editor, Owens, L., editor, and Valentine, R. C., editor
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- 1977
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18. Regulation
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Birge, Edward A. and Birge, Edward A.
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- 1988
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19. Regulation
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Birge, Edward A., Starr, Mortimer P., editor, and Birge, Edward A.
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- 1981
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20. Genetics of Dinitrogen Fixation
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Brill, W. J., Bothe, Hermann, editor, and Trebst, Achim, editor
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- 1981
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21. Properties of DNA Insertion Elements of E. coli
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Saedler, Heinz, Ghosal, Debabrota, Drews, Jürgen, editor, and Högenauer, Gregor, editor
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- 1977
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22. IS-Elements in Microorganisms
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Starlinger, Peter, Saedler, Heinz, Arber, W., editor, Henle, W., editor, Hofschneider, P. H., editor, Humphrey, J. H., editor, Jerne, N. K., editor, Koldovský, P., editor, Koprowski, H., editor, Maaløe, O., editor, Rott, R., editor, Schweiger, H. G., editor, Sela, M., editor, Syruček, L., editor, and Vogt, P. K., editor
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- 1976
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23. The Role of IS-Elements in E. coli
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Saedler, H., Ghosal, D., Hofschneider, Peter Hans, editor, and Starlinger, Peter, editor
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- 1978
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24. Spontaneous mutations
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Auerbach, Charlotte and Auerbach, Charlotte
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- 1976
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25. A Nonsense Mutation in Mycobacterium marinum That Is Suppressible by a Novel Mechanism
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Benjamin K. Johnson, Micah J. Ferrell, Rachel E. Bosserman, Cristal Reyna, Felix Mba Medie, Patricia A. DiGiuseppe Champion, Matthew M. Champion, Robert B. Abramovitch, and Emily A. Williams
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0301 basic medicine ,medicine.medical_specialty ,media_common.quotation_subject ,030106 microbiology ,Immunology ,Nonsense mutation ,Nonsense ,Virulence ,Mycobacterium Infections, Nontuberculous ,Biology ,Microbiology ,Polar mutation ,03 medical and health sciences ,Bacterial Proteins ,Molecular genetics ,medicine ,Amino Acid Sequence ,Gene ,Mycobacterium marinum ,media_common ,Genetics ,Base Sequence ,Gene Expression Regulation, Bacterial ,biology.organism_classification ,Molecular Pathogenesis ,Complementation ,Protein Transport ,Infectious Diseases ,Phenotype ,Codon, Nonsense ,Parasitology - Abstract
Mycobacterial pathogens use the ESAT-6 system 1 (Esx-1) exporter to promote virulence. Previously, we used gene disruption and complementation to conclude that the MMAR_0039 gene in Mycobacterium marinum is required to promote Esx-1 export. Here we applied molecular genetics, proteomics, and whole-genome sequencing to demonstrate that the MMAR_0039 gene is not required for Esx-1 secretion or virulence. These findings suggest that we initially observed an indirect mechanism of genetic complementation. We identified a spontaneous nonsense mutation in a known Esx-1-associated gene which causes a loss of Esx-1 activity. We show that the Esx-1 function was restored by nonsense suppression. Moreover, we identified a polar mutation in the ppsC gene which reduced cellular impermeability but did not impact cytotoxicity in macrophages. Our studies reveal insight into Esx-1 export, nonsense suppression, and cell envelope lipid biogenesis.
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- 2016
26. Regulatory interactions between the Hrp type III protein secretion system and coronatine biosynthesis in Pseudomonas syringae pv. tomato DC3000
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Alejandro Penaloza-Vazquez, Alan Collmer, Gail M. Preston, and Carol L. Bender
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Mutant ,Colony Count, Microbial ,Virulence ,Biology ,Microbiology ,Type three secretion system ,Polar mutation ,chemistry.chemical_compound ,Solanum lycopersicum ,Pseudomonas ,Pseudomonas syringae ,Secretion ,cardiovascular diseases ,Amino Acids ,Plant Diseases ,fungi ,food and beverages ,Coronatine ,Phytotoxin ,Gene Expression Regulation, Bacterial ,respiratory tract diseases ,Plant Leaves ,chemistry ,Indenes ,Bacterial Outer Membrane Proteins - Abstract
In P. syringae, the co-ordinated regulation of different systems required for pathogenicity and virulence seems logical but has not been established. This question was addressed in the present study by analysing production of the phytotoxin coronatine (COR) in defined hrp/hrc mutants of P. syringae pv. tomato DC3000. COR was produced in vitro by mutants of DC3000 defective in hrcC, which encodes an outer-membrane protein required for type III-mediated secretion. When inoculated in plants, hrcC mutants produced chlorotic regions indicative of COR production, but lacked the necrotic lesions produced by the wild-type DC3000. Furthermore, a DC3000 mutant containing a polar mutation in hrcC, which inactivates hrcC, hrpT and hrpV, produced significantly higher amounts of COR than the wild-type strain in vitro. This mutant was able to produce COR earlier and at lower cell densities than the wild-type. The results indicate that the hrp/hrc secretion system is not required for COR production, but mutations in this system may have regulatory effects on the production of virulence factors such as COR.
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- 2016
27. Strong-Polar Mutations in the Galactose Operon of E. coli
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Starlinger, Peter, Jordan, Elke, Saedler, Heinz, Wittmann, H. G., editor, and Schuster, H., editor
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- 1968
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28. OtpR regulated the growth, cell morphology of B. melitensis and tolerance to β-lactam agents
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Qingmin Wu, Chunyan Zhang, Xiaolei Gao, Wenjuan Liu, Hao Dong, and Wenxiao Liu
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Penicillin binding proteins ,General Veterinary ,Cell division ,Operon ,Mutant ,Drug Tolerance ,General Medicine ,Biology ,beta-Lactams ,biology.organism_classification ,Cell morphology ,Microbiology ,Tryptic soy broth ,Anti-Bacterial Agents ,Polar mutation ,chemistry.chemical_compound ,Bacterial Proteins ,chemistry ,Brucella melitensis ,Polymyxin B ,Sequence Deletion - Abstract
The intracellular pathogen, Brucella melitensis, possesses an operon with two components: otpR (BMEI0066), which encodes a response regulator, and BMEI0067, which encodes a putative cAMP-dependent protein kinase regulatory subunit. Previous studies have shown that a polar mutation in the BMEI0066 gene significantly decreased virulence and stress tolerance in Brucella. In this study, we constructed non-polar mutant with deletion of otpR, as well as its complementary strain to further investigate the function of otpR. The ΔotpR mutant produced smaller colonies on TSA plates, and grew slower in tryptic soy broth compared to 16M or the otpR-complemented strain CotpR. Electron microscopy revealed that ΔotpR displayed an unusual, irregular deformation of the cell surface in contrast to the native coccobacillus shape of 16M. These results showed that OtpR played a key role in the maintenance of cell shape. To determine the effect of the otpR mutant on antibiotic susceptibility, compared the parent strain, the mutant was two- to eight-fold more susceptible to all the β-lactam antibiotics tested. Furthermore, comparative real-time qPCR of genes that related to penicillin binding proteins of cell wall synthesis and cell division showed that the otpR mutation resulted in reduced expression of pbp1C, pbp6B, pbp6C and ftsQ. Taken together, these data revealed that the OtpR activity is necessary for growth, and cell morphology and tolerance to β-lactam agents of B. melitensis.
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- 2012
29. Identification of frequently mutated genes with relevance to nonsense mediated mRNA decay in the high microsatellite instability cancers
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Nara Shin, Hee Jung Choi, Won Kyu Kim, Meiying Song, Hwanseok Rhee, Kwon Tae You, Hanna Lee, Suk Woo Nam, and Hoguen Kim
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Genetics ,Cancer Research ,Candidate gene ,Mutation ,Blotting, Western ,Nonsense-mediated decay ,Down-Regulation ,Biology ,medicine.disease_cause ,Polymerase Chain Reaction ,digestive system diseases ,Frameshift mutation ,Polar mutation ,Oncology ,Cell Line, Tumor ,Neoplasms ,medicine ,Humans ,RNA, Messenger ,Mutation frequency ,Frameshift Mutation ,Carcinogenesis ,Gene ,Microsatellite Repeats ,Oligonucleotide Array Sequence Analysis - Abstract
Frameshift mutations at coding mononucleotide repeats (cMNR) are frequent in high-microsatellite instability (MSI-H) cancers. Frameshift mutations in cMNR result in the formation of a premature termination codon (PTC) in the transcribed mRNA, and these abnormal mRNAs are generally degraded by nonsense mediated mRNA decay (NMD). We have identified novel genes that are frequently mutated at their cMNR by blocking NMD in two MSI-H cancer cell lines. After blocking NMD, we screened for differentially expressed genes using DNA microarrays, and then used database analysis to select 28 candidate genes containing cMNR with more than 9 nucleotide repeats. cMNR mutations have not been previously reported in MSI-H cancers for 15 of the 28 genes. We analyzed the cMNR mutation of each of the 15 genes in 10 MSI-H cell lines and 21 MSI-H cancers, and found frequent mutations of 12 genes in MSI-H cell lines and cancers, but not in microsatellite stable (MSS) cancers. Among these genes, the most frequently mutated in MSI-H cell lines were MLL3 (70%), PHACTR4 (70%), RUFY2 (50%) and TBC1D23 (50%). MLL3, which has already been implicated in cancer, had the highest mutation frequency in MSI-H cancers (48%). Our combined approach of NMD block, database search, and mutation analysis has identified a large number of genes mutated in their cMNR in MSI-H cancers. The identified mutations are expected to contribute to MSI-H tumorigenesis by causing an absence of gene expression or low gene dosage effects.
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- 2010
30. Implication of C-terminal mutation of PopA ofRalstonia solanacearumstrain OE1-1 in suppression of bacterial wilt
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Akinori Kiba, Yusufumi Hikichi, Kouhei Ohnishi, and Ayami Kanda
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Ralstonia solanacearum ,biology ,Operon ,Bacterial wilt ,Mutant ,food and beverages ,Virulence ,Plant Science ,Horticulture ,biology.organism_classification ,Microbiology ,Polar mutation ,Genetics ,Arabidopsis thaliana ,Agronomy and Crop Science ,Bacteria - Abstract
Ralstonia solanacearum strain OE1-1 causes bacterial wilt on tobacco plants. The popA-mutant 31b, derived from OE1-1 by insertion of transposon Tn4431, did not cause wilt on tobacco plants inoculated through the roots. However, when 31b was directly inoculated into xylem vessels, the tobacco plants wilted, similarly to those inoculated with OE1-1. 31b retained its exopolysaccharide productivity and its type-III secretion function. Furthermore, 31b grew in intercellular spaces and systemically infected tobacco plants, similarly to OE1-1. popA consists of an operon with popB and popC, and suppression of popB and popC expression resulting from polar mutation by transposon insertion did not affect the virulence of 31b. The mutated popA (popA31b) was composed of 960 nucleotides, including 39 derived from Tn4431. A recombinant mutant from OE1-1, where popA31b was introduced by marker exchange, showed the same phenotype as 31b. PopA31b protein was extracellularly secreted by 31b co-cultured with Arabidopsis thaliana. These results suggest that PopA31b extracellularly secreted by 31b in intercellular spaces may be implicated in suppression of disease development, leading to inability of the bacteria to induce wilt on plants. Taken together, interactions between host plants and R. solanacearum existing in intercellular spaces immediately after invasion may be involved in disease development.
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- 2009
31. Nature and mRNA effect of 282 differentNF1point mutations: focus on splicing alterations
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Eva Pros, Pere Fábregas, Thamar Martín, Eduard Serra, Conxi Lázaro, and Carolina Gómez
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Silent mutation ,Mutation rate ,DNA Mutational Analysis ,Biology ,medicine.disease_cause ,Frameshift mutation ,Polar mutation ,Genetics ,medicine ,Humans ,Point Mutation ,RNA, Messenger ,Frameshift Mutation ,Gene ,Germ-Line Mutation ,Genetics (clinical) ,Mutation ,Neurofibromin 1 ,Models, Genetic ,Point mutation ,DNA ,Molecular biology ,Complementation ,Alternative Splicing ,Mutagenesis, Insertional ,Phenotype ,Genetic Techniques ,RNA - Abstract
Neurofibromatosis type 1 (NF1) is a common autosomal dominant genetic disorder caused by mutations in the NF1 gene. In this paper we report our experience using the cDNA-SSCP/HD analysis as a mutational screening approach and the double characterization of all mutations at the DNA and RNA levels. Two hundred and eighty-two different mutations (in 374 independent patients) were identified, 140 of which were novel in our population. Most of these mutations are unique and distributed along the gene. However, we also detected 37 recurrent mutations. Our approach is limited with respect to the detection of single base substitutions, but it is highly effective in the detection of frameshift mutations and mutations that affect the correct splicing. Due to this bias we focus here in the characterization of these two types of mutations. Forty-seven percent of mutations found were frameshift mutations, with small deletions being 2.3 times more common than small insertions. At the mRNA level, 44% of mutations affected the correct splicing, 80% of them located in the consensus sequences, with the donor site being much more frequently involved. The remaining 20% consisted of mutations located in deep intronic sites and mutations located in the coding region. In general the latter group produces different types of mutated transcripts with specific proportions for each mutation. The double characterization of mutations at the DNA and RNA levels enables to detect a broader spectrum of mutations than any single level approach, and provides a greater understanding of their molecular pathogenesis. © 2008 Wiley-Liss, Inc.
- Published
- 2008
32. Competency for Nonsense-Mediated Reduction in Collagen X mRNA Is Specified by the 3′ UTR and Corresponds to the Position of Mutations in Schmid Metaphyseal Chondrodysplasia
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Shireen R. Lamandé, Jacqueline T. Tan, Friederike Kremer, Katrina M. Bell, Susanna Freddi, John F. Bateman, and Naomi L. Baker
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Untranslated region ,RNA Stability ,Nonsense mutation ,Biology ,Osteochondrodysplasias ,medicine.disease_cause ,Polar mutation ,Mice ,Exon ,Report ,Genetics ,medicine ,Animals ,Humans ,Coding region ,Genetics(clinical) ,RNA, Messenger ,3' Untranslated Regions ,Genetics (clinical) ,Mutation ,Base Sequence ,Exons ,medicine.disease ,Molecular biology ,Mice, Mutant Strains ,Schmid metaphyseal chondrodysplasia ,Stop codon ,Codon, Nonsense ,Collagen Type X - Abstract
Nonsense-mediated decay (NMD) is a eukaryotic cellular RNA surveillance and quality-control mechanism that degrades mRNA containing premature stop codons (nonsense mutations) that otherwise may exert a deleterious effect by the production of dysfunctional truncated proteins. Collagen X (COL10A1) nonsense mutations in Schmid-type metaphyseal chondrodysplasia are localized in a region toward the 3′ end of the last exon (exon 3) and result in mRNA decay, in contrast to most other genes in which terminal-exon nonsense mutations are resistant to NMD. We introduce nonsense mutations into the mouse Col10a1 gene and express these in a hypertrophic-chondrocyte cell line to explore the mechanism of last-exon mRNA decay of Col10a1 and demonstrate that mRNA decay is spatially restricted to mutations occurring in a 3′ region of the exon 3 coding sequence; this region corresponds to where human mutations have been described. This localization of mRNA-decay competency suggested that a downstream region, such as the 3′ UTR, may play a role in specifying decay of mutant Col10a1 mRNA containing nonsense mutations. We found that deleting any of the three conserved sequence regions within the 3′ UTR (region I, 23 bp; region II, 170 bp; and region III, 76 bp) prevented mutant mRNA decay, but a smaller 13 bp deletion within region III was permissive for decay. These data suggest that the 3′ UTR participates in collagen X last-exon mRNA decay and that overall 3′ UTR configuration, rather than specific linear-sequence motifs, may be important in specifying decay of Col10a1 mRNA containing nonsense mutations.
- Published
- 2008
33. Nonsense Mutations in hERG Cause a Decrease in Mutant mRNA Transcripts by Nonsense-Mediated mRNA Decay in Human Long-QT Syndrome
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Benjamin D. Horne, Li Zhang, Qiuming Gong, G. Michael Vincent, and Zhengfeng Zhou
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Adult ,Male ,ERG1 Potassium Channel ,congenital, hereditary, and neonatal diseases and abnormalities ,Nonsense-mediated decay ,Nonsense mutation ,hERG ,Biology ,Kidney ,Transfection ,medicine.disease_cause ,Article ,Adenoviridae ,Frameshift mutation ,Rats, Sprague-Dawley ,Polar mutation ,Physiology (medical) ,Genes, Synthetic ,medicine ,Animals ,Humans ,Point Mutation ,Myocytes, Cardiac ,Lymphocytes ,RNA, Messenger ,Cycloheximide ,Frameshift Mutation ,Cells, Cultured ,Aged ,Protein Synthesis Inhibitors ,Messenger RNA ,Mutation ,Point mutation ,Middle Aged ,Molecular biology ,Ether-A-Go-Go Potassium Channels ,Pedigree ,Rats ,Long QT Syndrome ,Animals, Newborn ,Codon, Nonsense ,Trans-Activators ,biology.protein ,Female ,RNA Interference ,Cardiology and Cardiovascular Medicine ,RNA Helicases - Abstract
Background— Long-QT syndrome type 2 (LQT2) is caused by mutations in the human ether-a-go-go-related gene ( hERG ). More than 30% of the LQT2 mutations result in premature termination codons. Degradation of premature termination codon–containing mRNA transcripts by nonsense-mediated mRNA decay is increasingly recognized as a mechanism for reducing mRNA levels in a variety of human diseases. However, the role of nonsense-mediated mRNA decay in LQT2 mutations has not been explored. Methods and Results— We examined the expression of hERG mRNA in lymphocytes from patients carrying the R1014X mutation using a technique of allele-specific transcript quantification. The R1014X mutation led to a reduced level of mutant mRNA compared with that of the wild-type allele. The decrease in mutant mRNA also was observed in the LQT2 nonsense mutations W1001X and R1014X using hERG minigenes expressed in HEK293 cells or neonatal rat ventricular myocytes. Treatment with the protein synthesis inhibitor cycloheximide or RNA interference–mediated knockdown of the Upf1 protein resulted in the restoration of mutant mRNA to levels comparable to that of the wild-type minigene, suggesting that hERG nonsense mutations are subject to nonsense-mediated mRNA decay. Conclusions— These results indicate that LQT2 nonsense mutations cause a decrease in mutant mRNA levels by nonsense-mediated mRNA decay rather than production of truncated proteins. Our findings suggest that the degradation of hERG mutant mRNA by nonsense-mediated mRNA decay is an important mechanism in LQT2 patients with nonsense or frameshift mutations.
- Published
- 2007
34. Exploitation of a β-lactamase reporter gene fusion in the carbapenem antibiotic production operon to study adaptive evolution in Erwinia carotovora
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George P. C. Salmond and Steven D. Bowden
- Subjects
DNA, Bacterial ,Transcription, Genetic ,Operon ,Molecular Sequence Data ,Mutant ,Adaptation, Biological ,Colony Count, Microbial ,Erwinia ,Microbiology ,beta-Lactamases ,Evolution, Molecular ,Polar mutation ,Genes, Reporter ,Transcription (biology) ,Selection, Genetic ,Promoter Regions, Genetic ,Gene ,Recombination, Genetic ,Genetics ,Reporter gene ,Base Sequence ,biology ,Promoter ,biology.organism_classification ,Anti-Bacterial Agents ,Artificial Gene Fusion ,Blotting, Southern ,Pectobacterium carotovorum ,Carbapenems ,Mutation ,DNA Transposable Elements ,Ampicillin Resistance - Abstract
Erwinia carotovorasubsp.carotovorastrain ATTn10 produces theβ-lactam antibiotic 1-carbapen-2-em-3-carboxylic acid (carbapenem) by expressing thecarABCDEFGHoperon. Mutants exhibiting increased carbapenem gene transcription were positively selected using an engineered strain with a functionalβ-lactamase translational fusion incarH, the last gene of the operon. However, spontaneous ampicillin-resistant mutants were isolated even when transcription ofcarH : : blaMwas blocked by a strongly polar mutation incarE. The mechanism of resistance was shown to be due to cryptic IS10elements transposing upstream ofcarH : : blaM, thereby providing new promoters enablingcarH : : blaMtranscription. Southern blots showed that IS10was present in multicopy in ATTn10. In addition, a Tn10genetic remnant was discovered. The results offer insights into the genetic archaeology of strain ATTn10 and highlight the powerful impacts of cryptic IS elements in bacterial adaptive evolution.
- Published
- 2006
35. IS-Elements in Bacteria
- Author
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Starlinger, P., Stich, W., editor, Ruhenstroth-Bauer, G., editor, Heimpel, H., editor, Neth, Rolf, editor, Gallo, Robert C., editor, Mannweiler, Klaus, editor, and Moloney, William C., editor
- Published
- 1976
- Full Text
- View/download PDF
36. Nonsense mutations in the essential gene SUP35 of Saccharomyces cerevisiae are non-lethal
- Author
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Michel Philippe, Galina A. Zhouravleva, Denis Kiktev, Svetlana Chabelskaya, and Sergey G. Inge-Vechtomov
- Subjects
Silent mutation ,Saccharomyces cerevisiae Proteins ,Prions ,media_common.quotation_subject ,Genes, Fungal ,Mutant ,Nonsense ,Nonsense mutation ,macromolecular substances ,Biology ,Polar mutation ,Genetics ,Missense mutation ,Molecular Biology ,DNA Primers ,Suppressor mutation ,media_common ,Genes, Essential ,Base Sequence ,Point mutation ,General Medicine ,Blotting, Northern ,Molecular biology ,Codon, Nonsense ,Genes, Lethal ,Peptide Termination Factors - Abstract
In the present work we have characterized for the first time non-lethal nonsense mutations in the essential gene SUP35, which codes for the translation termination factor eRF3 in Saccharomyces cerevisiae. The screen used was based on selection for simultaneous suppression of two auxotrophic nonsense mutations. Among 48 mutants obtained, sixteen were distinguished by the production of a reduced amount of eRF3, suggesting the appearance of nonsense mutations. Fifteen of the total mutants were sequenced, and the presence of nonsense mutations was confirmed for nine of them. Thus a substantial fraction of the sup35 mutations recovered are nonsense mutations located in different regions of SUP35, and such mutants are easily identified by the fact that they express reduced amounts of eRF3. Nonsense mutations in the SUP35 gene do not lead to a decrease in levels of SUP35 mRNA and do not influence the steady-state level of eRF1. The ability of these mutations to complement SUP35 gene disruption mutations in different genetic backgrounds and in the absence of any tRNA suppressor mutation was demonstrated. The missense mutations studied, unlike nonsense mutations, do not decrease steady-state amounts of eRF3.
- Published
- 2004
37. A reassessment of the response of the bacterial ribosome to the frameshift stimulatory signal of the human immunodeficiency virus type 1
- Author
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Mélissa Léger, Léa Brakier-Gingras, and Sacha Sidani
- Subjects
Biology ,Slippery sequence ,Molecular biology ,Ribosome ,Article ,Ribosomal frameshift ,Stop codon ,Frameshift mutation ,Polar mutation ,A-site ,Eukaryotic translation ,Genes, Reporter ,RNA, Ribosomal, 16S ,Mutation ,Codon, Terminator ,Escherichia coli ,HIV-1 ,Nucleic Acid Conformation ,RNA, Viral ,Ribosomes ,Molecular Biology - Abstract
HIV-1 uses a programmed -1 ribosomal frameshift to produce the precursor of its enzymes. This frameshift occurs at a specific slippery sequence followed by a stimulatory signal, which was recently shown to be a two-stem helix, for which a three-purine bulge separates the upper and lower stems. In the present study, we investigated the response of the bacterial ribosome to this signal, using a translation system specialized for the expression of a firefly luciferase reporter. The HIV-1 frameshift region was inserted at the beginning of the coding sequence of the luciferase gene, such that its expression requires a −1 frameshift. Mutations that disrupt the upper or the lower stem of the frameshift stimulatory signal or replace the purine bulge with pyrimidines decreased the frameshift efficiency, whereas compensatory mutations that re-form both stems restored the frame-shift efficiency to near wild-type level. These mutations had the same effect in a eukaryotic translation system, which shows that the bacterial ribosome responds like the eukaryote ribosome to the HIV-1 frameshift stimulatory signal. Also, we observed, in contrast to a previous report, that a stop codon immediately 3′ to the slippery sequence does not decrease the frameshift efficiency, ruling out a proposal that the frameshift involves the deacylated-tRNA and the peptidyl-tRNA in the E and P sites of the ribosome, rather than the peptidyl-tRNA and the aminoacyl-tRNA in the P and A sites, as commonly assumed. Finally, mutations in 16S ribosomal RNA that facilitate the accommodation of the incoming aminoacyl-tRNA in the A site decreased the frameshift efficiency, which supports a previous suggestion that the frameshift occurs when the aminoacyl-tRNA occupies the A/T entry site.
- Published
- 2004
38. Operons in eukaryotes
- Author
-
Thomas Blumenthal
- Subjects
Cytoplasm ,Transcription, Genetic ,Operon ,Biology ,Biochemistry ,Polar mutation ,Eukaryotic translation ,Bacterial transcription ,Genetics ,Protein biosynthesis ,Animals ,RNA, Messenger ,Caenorhabditis elegans ,Promoter Regions, Genetic ,Molecular Biology ,Gene ,Messenger RNA ,Binding Sites ,Genome ,Alternative Splicing ,Internal ribosome entry site ,Drosophila melanogaster ,Multigene Family ,Protein Biosynthesis ,Ribosomes - Abstract
It was thought that polycistronic transcription is a characteristic of bacteria and archaea, where many of the genes are clustered in operons composed of two to more than ten genes. By contrast, the genes of eukaryotes are generally considered to be monocistronic, each with its own promoter at the 5' end and a transcription terminator at the 3' end; however, it has recently become clear that not all eukaryotic genes are transcribed monocistronically. Numerous instances of polycistronic transcription in eukaryotes, from protists to chordates, have been reported. These can be divided into two broad types. Dicistronic transcription units specify a messenger RNA (mRNA) encoding two separate genes that is transported to the cytoplasm and translated in that form. Presumably, internal ribosome entry sites (IRES), or some form of translational re-initiation following the stop codon, are responsible for allowing translation of the downstream gene. In the other type, the initial transcript is processed by 3' end cleavage and trans-splicing to create monocistronic mRNAs that are transported to the cytoplasm and translated. Like bacterial operons, eukaryotic operons often result in co-expression of functionally related proteins.
- Published
- 2004
39. smFRET Reveals Structural Basis for Conformational Misfolding of a Cystic Fibrosis Mutation in CFTR
- Author
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Georg Krainer, Tracy A. Stone, Charles M. Deber, Antoine Treff, Ariana Rath, Henry Chang, Andreas Hartmann, and Michael Schlierf
- Subjects
education.field_of_study ,Membrane insertion ,Population ,Biophysics ,Biology ,medicine.disease ,Cystic fibrosis ,Cystic fibrosis transmembrane conductance regulator ,Polar mutation ,Membrane ,Förster resonance energy transfer ,Biochemistry ,Membrane protein ,medicine ,biology.protein ,education - Abstract
Cystic fibrosis (CF) is the most common lethal genetic disease among the Western population caused by mutations in the Cystic Fibrosis Transmembrane Conductance Regulator (CFTR). The development of effective therapeutic agents against CF requires a molecular understanding of how mutation-related structural alterations lead to impaired functioning of CFTR. The main cause for CF are processing mutations frequently found within CFTR-transmembrane (TM) segments which affect co-translational folding and insertion. However, the underlying molecular mechanisms for misfolding remain obscure, mainly because of the unavailability of high-resolution structures and a lack of methods suitable for studying membrane protein structure-function relationships.Devising a divide-and-conquer approach in combination with single-molecule FRET (smFRET), we present here a strategy to gain novel insights into the structural basis for conformational misfolding in CFTR. Using this approach, we study the CF-phenotypic polar mutation V232D located within the fourth TM helix (TM4) of CFTR. In vivo folding and insertion of TM4 is functionally coupled with TM3 where both TM segments are co-translationally inserted into the membrane as a TM helix-loop-helix hairpin motif (TM3/4). Utilizing this minimal folding unit, we employ smFRET as a molecular ruler to readout structural alterations imposed on the helical packing of the TM3/4 hairpin upon mutation. In contrast to earlier findings that suggested a TM lock between TM3 and TM4 by a non-native H-bond, our results reveal that V232D TM3/4 associates with membranes in an open conformation. This implies that the charged residue imposes an energy penalty on membrane insertion of the hairpin. We propose a model for CF pathogenesis where partitioning of V232D TM3/4 into the interfacial region leads to misfolding of CFTR during co-translational membrane insertion and inhibits maturation by trapping the protein as a partially folded intermediate.
- Published
- 2017
40. Stop that nonsense!
- Author
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Catherine L. Jopling
- Subjects
QH301-705.5 ,media_common.quotation_subject ,Science ,Nonsense-mediated decay ,Nonsense mutation ,Nonsense ,nonsense mutation ,macromolecular substances ,nonsense-mediated mRNA decay ,Biology ,medicine.disease_cause ,Biochemistry ,intron retention ,General Biochemistry, Genetics and Molecular Biology ,Polar mutation ,medicine ,Humans ,RNA, Messenger ,human ,Biology (General) ,media_common ,Genetics ,Mutation ,General Immunology and Microbiology ,microRNA ,General Neuroscience ,fungi ,food and beverages ,Cell Biology ,General Medicine ,premature termination codon ,Stop codon ,Nonsense Mediated mRNA Decay ,APC ,MicroRNAs ,Gene Expression Regulation ,Medicine ,nonsense mutant ,Premature Termination Codon ,mutation ,Research Article - Abstract
Numerous studies have established important roles for microRNAs (miRNAs) in regulating gene expression. Here, we report that miRNAs also serve as a surveillance system to repress the expression of nonsense mRNAs that may produce harmful truncated proteins. Upon recognition of the premature termination codon by the translating ribosome, the downstream portion of the coding region of an mRNA is redefined as part of the 3′ untranslated region; as a result, the miRNA-responsive elements embedded in this region can be detected by miRNAs, triggering accelerated mRNA deadenylation and translational inhibition. We demonstrate that naturally occurring cancer-causing APC (adenomatous polyposis coli) nonsense mutants which escape nonsense-mediated mRNA decay (NMD) are repressed by miRNA-mediated surveillance. In addition, we show that miRNA-mediated surveillance and exon–exon junction complex-mediated NMD are not mutually exclusive and act additively to enhance the repressive activity. Therefore, we have uncovered a new role for miRNAs in repressing nonsense mutant mRNAs. DOI: http://dx.doi.org/10.7554/eLife.03032.001, eLife digest To produce a protein from a gene, the sequence of the gene must be transcribed to produce a molecule of messenger RNA (mRNA). The sequence of the mRNA is then read in groups of three letters at a time (called codons), and each codon instructs for a particular amino acid to be added into the protein. Some codons, however, do not code for an amino acid and instead these ‘stop codons’ mark the end of a protein. If a DNA letter is added, lost, or changed, this mutation can sometimes produce a stop codon too early in the mRNA sequence. This is called a nonsense mutation, and produces truncated proteins that either work incorrectly or do not work at all, which can harm the organism. For example, people with a nonsense mutation in the human tumor suppressor gene called APC—which normally stops uncontrolled cell growth and division—are more likely to develop colon cancer than people without this mutation. Cells in the body employ several different surveillance mechanisms to detect nonsense mutations. The best-known mechanism involves a large protein group called the exon–exon junction complex (EJC), which binds to sites within the mRNA. The cellular translation machinery removes all the EJCs bound to a normal mRNA during the production of proteins. If the translation machinery reaches a stop codon too early, so that EJCs located downstream of it are not removed, the mRNA molecule is destroyed. However, this mechanism does not work for all genes—including APC. Very short sections of RNA called microRNAs regulate protein production by causing mRNAs to degrade and by inhibiting their translation, and Zhao et al. have now found that microRNAs also act as a defense against nonsense mutations in the APC gene. A premature stop codon exposes sites further along the mRNA molecule that microRNA molecules bind to, which triggers the breaking down of the mRNA and inhibits its translation. The microRNA surveillance system works independently of the system involving the EJC. However, both mechanisms can work in parallel alongside each other, which provides extra protection against nonsense mutations. Zhao et al. also found that microRNAs can protect against nonsense mutations in several other types of gene found in human cells. Therefore, microRNA surveillance is likely to be a common method employed by cells to restrict the production of potentially harmful truncated proteins. DOI: http://dx.doi.org/10.7554/eLife.03032.002
- Published
- 2014
41. Directionality of DNA replication fork movement strongly affects the generation of spontaneous mutations in Escherichia coli
- Author
-
Hironobu Matsumura, Kaoru Yoshiyama, Hisaji Maki, and Kumiko Higuchi
- Subjects
DNA Replication ,Base Pair Mismatch ,DNA Mutational Analysis ,Molecular Sequence Data ,Biology ,medicine.disease_cause ,Polymerase Chain Reaction ,Frameshift mutation ,Polar mutation ,Bacterial Proteins ,Structural Biology ,Escherichia coli ,medicine ,Point Mutation ,Directionality ,Frameshift Mutation ,Molecular Biology ,Gene ,DNA Polymerase III ,Adenosine Triphosphatases ,Genetics ,Mutation ,Base Sequence ,Models, Genetic ,Ribosomal Protein S9 ,Escherichia coli Proteins ,Mutagenesis ,DNA Replication Fork ,Molecular biology ,MutS DNA Mismatch-Binding Protein ,DNA-Binding Proteins ,Genes, Bacterial ,DNA mismatch repair ,Plasmids - Abstract
Using a pair of plasmids carrying the rpsL target sequence in different orientations to the replication origin, we analyzed a large number of forward mutations generated in wild-type and mismatch-repair deficient (MMR(-)) Escherichia coli cells to assess the effects of directionality of replication-fork movement on spontaneous mutagenesis and the generation of replication error. All classes of the mutations found in wild-type cells but not MMR(-) cells were strongly affected by the directionality of replication fork movement. It also appeared that the directionality of replication-fork movement governs the directionality of sequence substitution mutagenesis, which occurred in wild-type cells at a frequency comparable to base substitutions and single-base frameshift mutations. A very strong orientation-dependent hot-spot site for single-base frameshift mutations was discovered and demonstrated to be caused by the same process involved in sequence substitution mutagenesis. It is surprising that dnaE173, a potent mutator mutation specific for sequence substitution as well as single-base frameshift, did not enhance the frequency of the hot-spot frameshift mutation. Furthermore, the frequency of the hot-spot frameshift mutation was unchanged in the MMR(-) strain, whereas the mutHLS-dependent mismatch repair system efficiently suppressed the generation of single-base frameshift mutations. These results suggested that the hot-spot frameshift mutagenesis might be initiated at a particular location containing a DNA lesion, and thereby produce a premutagenic replication intermediate resistant to MMR. Significant numbers of spontaneous single-base frameshift mutations are probably caused by similar mechanisms.
- Published
- 2001
42. Yeast Frameshift Suppressor Mutations in the Genes Coding for Transcription Factor Mbf1p and Ribosomal Protein S3: Evidence for Autoregulation of S3 Synthesis
- Author
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Irving I. Edelman, Patricia G. Wilson, Doris Ursic, James L. Hendrick, Mark G. Sandbaken, and Michael R. Culbertson
- Subjects
Ribosomal Proteins ,Untranslated region ,Saccharomyces cerevisiae Proteins ,Time Factors ,Databases, Factual ,Transcription, Genetic ,Genes, Fungal ,Gene Dosage ,Biology ,Frameshift mutation ,Polar mutation ,Suppression, Genetic ,Transformation, Genetic ,Genetics ,Coding region ,RNA, Messenger ,Frameshift Mutation ,Promoter Regions, Genetic ,Gene ,Transcription factor ,Alleles ,Translational frameshift ,Dose-Response Relationship, Drug ,Models, Genetic ,Phenotype ,Mutation ,Trans-Activators ,5' Untranslated Regions ,Synonymous substitution ,Copper ,Research Article ,Plasmids ,Transcription Factors - Abstract
The SUF13 and SUF14 genes were identified among extragenic suppressors of +1 frameshift mutations. SUF13 is synonymous with MBF1, a single-copy nonessential gene coding for a POLII transcription factor. The suf13-1 mutation is a two-nucleotide deletion in the SUF13/MBF1 coding region. A suf13::TRP1 null mutant suppresses +1 frameshift mutations, indicating that suppression is caused by loss of SUF13 function. The suf13-1 suppressor alters sensitivity to aminoglycoside antibiotics and reduces the accumulation of his4-713 mRNA, suggesting that suppression is mediated at the translational level. The SUF14 gene is synonymous with RPS3, a single-copy essential gene that codes for the ribosomal protein S3. The suf14-1 mutation is a missense substitution in the coding region. Increased expression of S3 limits the accumulation of SUF14 mRNA, suggesting that expression is autoregulated. A frameshift mutation in SUF14 that prevents full-length translation eliminated regulation, indicating that S3 is required for regulation. Using CUP1-SUF14 and SUF14-lacZ fusions, run-on transcription assays, and estimates of mRNA half-life, our results show that transcription plays a minor role if any in regulation and that the 5′-UTR is necessary but not sufficient for regulation. A change in mRNA decay rate may be the primary mechanism for regulation.
- Published
- 2001
43. [Untitled]
- Author
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A. S. Borkhsenius, O. N. Tikhodeev, Kulikov Vn, Sergey G. Inge-Vechtomov, F. S. Forafonov, and V. V. Alenin
- Subjects
Genetics ,Mutation ,Translational frameshift ,biology ,Mutagenesis ,Saccharomyces cerevisiae ,biology.organism_classification ,medicine.disease_cause ,Saccharomyces ,Frameshift mutation ,Polar mutation ,medicine ,Release factor - Abstract
Special search for frameshift mutations, which are suppressed by the cytoplasmic [PSI] factor and by omnipotent nonsense suppressors (recessive mutations in theSUP35and SUP45genes), partially inactivating a translation termination complex, was initiated in theLYS2gene in the yeast Saccharomyces cerevisiae.Mutations were obtained after exposure to UV light and treatment with a mixture of 1,6- and 1,8-dinitropyrene (DNP). This mixture was shown to induce mutations of the frameshift type with a high frequency. The majority of these mutations were insertions of one A or T, which is in good agreement with the data obtained in studies of DNP-induced mutagenesis in other eukaryotes. Frameshift suppression was shown on the example of the mutation obtained in this work (lys2-90), which carried the insertion of an extra T in the sequence of five T. This frameshift suppression was first shown to occur in the presence of the [PSI] factor (i.e., due to the prionization of the translation release factor eRF3) and as a result of mutations in genes SUP35orSUP45, which partially inactivate translation termination factors eRF3 and eRF1, respectively. Alternative mechanisms of programmed translational frameshifting in the course of translation and the possibility of enhancing the effectiveness of such frameshifting in the presence of the [PSI] factor are considered.
- Published
- 2001
44. A frameshift mitochondrial complex I gene mutation in a patient with dystonia and cataracts: is the mutation pathogenic?
- Author
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J T Greenamyre, Mark A. Tarnopolsky, David Simon, and Donald R. Johns
- Subjects
Male ,Mutation rate ,Blotting, Western ,DNA Mutational Analysis ,Gene mutation ,Biology ,medicine.disease_cause ,DNA, Mitochondrial ,Cataract ,Frameshift mutation ,Polar mutation ,Genetics ,medicine ,Humans ,Missense mutation ,NADH, NADPH Oxidoreductases ,Frameshift Mutation ,Letters to the Editor ,Genetics (clinical) ,Family Health ,Mutation ,Base Sequence ,Point mutation ,NADH Dehydrogenase ,Heteroplasmy ,Pedigree ,Dystonia ,Female - Abstract
Editor—Mitochondrial DNA (MtDNA) is highly polymorphic. Each person is estimated to differ from another on average at about 25 base pairs among the 16 569 that comprise the mitochondrial genome.1 Thus, only a small fraction of mtDNA variants are likely to be of pathogenic significance. Criteria currently used for determining the likelihood that a missense mutation is pathogenic include heteroplasmy (the percentage of mtDNA molecules within a cell or tissue harbouring a mutation), evolutionary conservation of the altered amino acid, a maternal inheritance pattern, absence of the mutation in controls, clinical features commonly linked to known pathogenic mtDNA mutations, and defects in mitochondrial morphologies and enzyme activities.1 However, these criteria are inadequate for several reasons. Many mitochondrial missense mutations are homoplasmic. Pathogenic mtDNA mutations are typically characterised by incomplete penetrance, even when homoplasmic, presumably reflecting interactions with environmental and genetic factors.2 As a result, inherited mtDNA mutations may manifest as “sporadic” disorders rather than with the classical maternal inheritance pattern. Biochemical assays may also be inconclusive, as the expression of a defect in mitochondrial function depends on the nuclear background and tissue type in which the mutation is studied.3 ,4 As a result, mtDNA mutations identified in rare families or subjects with a putative mitochondrial genetic disorder are often of uncertain pathogenic significance. Over 100 point mutations have been identified in mitochondrial genes in association with human disease, at least 45 of which are missense mutations in protein encoding genes.5 However, frameshift mtDNA mutations are exceedingly rare. An acquired frameshift 4 bp deletion mutation was identified in the cytochrome b gene at nucleotide position (np) 14 787-14 790 in a patient with parkinsonism-MELAS overlap syndrome6 and somatic mutations including frameshift mutations have been found in human cancers.7 ,8In contrast, inherited frameshift …
- Published
- 2001
45. Nonsense mutations in the human β-globin gene lead to unexpected levels of cytoplasmic mRNA accumulation
- Author
-
Paula Pacheco, Madalena Ávila, Paula Faustino, João Lavinha, Angela Inacio, Susana Brito Dos Santos, and Luísa Romão
- Subjects
Silent mutation ,Messenger RNA ,Splice site mutation ,Nonsense mutation ,Immunology ,Cell Biology ,Hematology ,Biology ,Molecular biology ,Biochemistry ,Polar mutation ,Exon ,Synonymous substitution ,Gene - Abstract
Generally, nonsense codons 50 bp or more upstream of the 3′-most intron of the human β-globin gene reduce mRNA abundance. In contrast, dominantly inherited β-thalassemia is frequently associated with nonsense mutations in the last exon. In this work, murine erythroleukemia (MEL) cells were stably transfected with human β-globin genes mutated within each of the 3 exons, namely at codons 15 (TGG→TGA), 39 (C→T), or 127 (C→T). Primer extension analysis after erythroid differentiation induction showed codon 127 (C→T) mRNA accumulated in the cytoplasm at approximately 20% of the normal mRNA level. Codon 39 (C→T) mutation did not result in significant mRNA accumulation. Unexpectedly, codon 15 (TGG→TGA) mRNA accumulated at approximately 90%. Concordant results were obtained when reticulocyte mRNA from 2 carriers for this mutation was studied. High mRNA accumulation of codon 15 nonsense-mutated gene was revealed to be independent of the type of nonsense mutation and the genomic background in which this mutation occurs. To investigate the effects of other nonsense mutations located in the first exon on the mRNA level, nonsense mutations at codons 5, 17, and 26 were also cloned and stably transfected into MEL cells. After erythroid differentiation induction, mRNAs with a mutation at codon 5 or 17 were detected at high levels, whereas the mutation at codon 26 led to low mRNA levels. These findings suggest that nonsense-mediated mRNA decay is not exclusively dependent on the localization of mutations relative to the 3′-most intron. Other factors may also contribute to determine the cytoplasmic nonsense-mutated mRNA level in erythroid cells.
- Published
- 2000
46. Genetic Complementation and Kinetic Analyses of Rhodobacter capsulatus ORF1696 Mutants Indicate that the ORF1696 Protein Enhances Assembly of the Light-Harvesting I Complex
- Author
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J T Beatty, C. S. Young, and R. C. Reyes
- Subjects
Genetics ,Rhodobacter ,Strain (chemistry) ,biology ,Genetic Complementation Test ,Photosynthetic Reaction Center Complex Proteins ,Mutant ,Light-Harvesting Protein Complexes ,Genetics and Molecular Biology ,biology.organism_classification ,Microbiology ,Molecular biology ,Rhodobacter capsulatus ,Polar mutation ,Complementation ,Kinetics ,Open Reading Frames ,Structure-Activity Relationship ,Open reading frame ,Plasmid ,Bacterial Proteins ,Molecular Biology ,Gene - Abstract
Rhodobacter capsulatus ORF1696 mutant strains were created by insertion of antibiotic resistance cartridges at different sites within the ORF1696 gene in a strain that lacks the light-harvesting II (LHII) complex. Steady-state absorption spectroscopy profiles and the kinetics of the light-harvesting I (LHI) complex assembly and decay were used to evaluate the function of the ORF1696 protein in various strains. All of the mutant strains were found to be deficient in the LHI complex, including one (ΔNae) with a disruption located 13 codons before the 3′ end of the gene. A 5′-proximal disruption after the 31st codon of ORF1696 resulted in a mutant strain (ΔMun) with a novel absorption spectrum. The two strains with more 3′ disruptions (ΔStu and ΔNae) were restored nearly to the parental strain phenotype when trans complemented with a plasmid expressing the ORF1696 gene, but ΔMun was not. The absorption spectrum of ΔMun resembled that of a strain which had a polar mutation in ORF1696 . We suggest that a rho -dependent transcription termination site exists between the Mun I and proximal Stu I sites of ORF1696 . A comparison of LHI complex assembly kinetics showed that assembly occurred 2.6-fold faster in the parental strain than in strain ΔStu. In contrast, LHI complex decay occurred 1.7-fold faster in the ORF1696 parental strain than in ΔStu. These results indicate that the ORF1696 protein has a major effect on LHI complex assembly, and models of ORF1696 function are proposed.
- Published
- 1998
47. Characterization of mutations affecting the Escherichia coli essential GTPase era that suppress two temperature-sensitive dnaG alleles
- Author
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Bradford S. Powell, Robert A. Britton, Donald L. Court, and James R. Lupski
- Subjects
Operon ,Molecular Sequence Data ,Mutant ,DNA Primase ,GTPase ,Biology ,medicine.disease_cause ,Microbiology ,GTP Phosphohydrolases ,Polar mutation ,DnaG ,Suppression, Genetic ,Bacterial Proteins ,GTP-Binding Proteins ,Mutant protein ,Escherichia coli ,medicine ,Amino Acid Sequence ,Genes, Suppressor ,Molecular Biology ,Alleles ,Mutation ,Escherichia coli Proteins ,Temperature ,RNA-Binding Proteins ,RNA Nucleotidyltransferases ,Molecular biology ,Phenotype ,Genes, Bacterial ,Guanosine Triphosphate ,Primase ,Research Article - Abstract
Two suppressor mutations of the temperature-sensitive DNA primase mutant dnaG2903 have been characterized. The gene responsible for suppression, era, encodes an essential GTPase of Escherichia coli. One mutation, rnc-15, is an insertion of an IS1 element within the leader region of the rnc operon and causes a polar defect on the downstream genes of the operon. A previously described polar mutation, rnc-40, was also able to suppress dnaG2903. The other mutation, era-1, causes a single amino acid substitution (P17R) in the G1 region of the GTP-binding domain of Era. Analysis of the GTPase activity of the Era-1 mutant protein showed a four- to five-fold decrease in the ability to convert GTP to GDP. Thus, lowered expression of wild-type Era caused by the polar mutations and reduced GTPase activity caused by the era-1 mutation suppresses dnaG2903 as well as a second dnaG allele, parB. Phenotypic analysis of the era-1 mutant at 25 degrees C showed that 10% of the cells contain four segregated nucleoids, indicative of a delay in cell division. Possible mechanisms of suppression of dnaG and roles for Era are discussed.
- Published
- 1997
48. A Translation Frameshift Mutation Induced by a Cytosine Insertion in the Polycystic Kidney Disease 2 Gene (PKD2)
- Author
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Xenophontos, Stavroulla L., Constantinides, Rolandos, Hayashi, Tomohito, Mochizuki, Toshio, Somlo, Stefan, Pierides, Alkis M., Constantinou-Deltas, Constantinos D., and Constantinou-Deltas, Constantinos D. [0000-0001-5549-9169]
- Subjects
onset age ,Male ,Silent mutation ,Mutation rate ,family ,TRPP Cation Channels ,single strand conformation polymorphism ,frameshift mutation ,Nonsense mutation ,nonsense mutation ,arginine ,Biology ,Frameshift mutation ,Polar mutation ,Cytosine ,male ,genetic linkage ,Genetics ,stop codon ,Humans ,Missense mutation ,human ,exon ,cytosine ,Molecular Biology ,Genetics (clinical) ,clinical article ,article ,Membrane Proteins ,General Medicine ,Polycystic Kidney, Autosomal Dominant ,Stop codon ,Pedigree ,kidney polycystic disease ,Mutagenesis, Insertional ,female ,priority journal ,chromosome 4q ,Protein Biosynthesis ,glutamine ,amino terminal sequence ,Female ,cyprus ,Synonymous substitution - Abstract
Mutations in the PKD2 gene on the long arm of chromosome 4 are responsible for ~ 15% of cases of polycystic kidney disease. Perhaps the only difference from the more common ADPKD1 cases is the rate of progression of cystic changes, and the age of onset, which is 10-15 years later for the ADPKD2 form. In Cyprus there are at least three large families, documented by molecular linkage analysis, that map to the PKD2 locus. For two of them the defects were recently shown to be nonsense mutations at positions arginine 742 and glutamine 405. In this report, we describe the mutation in the third family, CY1602. For this, the entire coding sequence was systematically screened by single strand conformation analysis and heteroduplex formation. A novel mutation was identified in exon 2 where a new cytosine residue was inserted immediately after codon 231 (231insC). It causes a translation frameshift and is expected to lead to the introduction of 37 novel amino acids before the translation reaches a new STOP codon. It is the most amino terminal mutation reported to date, and based on the protein's modeled structure, is predicted to be within the first transmembrane domain. It is the fourth PKD2 mutation reported thus far, and the first which is not a nonsense mutation. 6 949 952 Cited By :22
- Published
- 1997
49. New developments in post-transcriptional regulation of operons by small RNAs
- Author
-
Carin K. Vanderpool and Divya Balasubramanian
- Subjects
Genetics ,Operon ,RNA Stability ,Translation (biology) ,Cell Biology ,Gene Expression Regulation, Bacterial ,Biology ,RyhB ,Polar mutation ,RNA, Bacterial ,Genes ,Genes, Bacterial ,Transfer RNA ,Gene expression ,RNA, Small Untranslated ,RNA, Messenger ,Molecular Biology ,Gene ,Post-transcriptional regulation ,Base Pairing ,Point of View - Abstract
Small regulatory RNAs (sRNAs) are influential post-transcriptional modulators of gene expression in bacteria. They regulate gene expression by base pairing to target mRNAs, leading to inhibition of translation and/or alteration of mRNA stability. Recently, several sRNAs have been discovered to regulate genes encoded in operons. In some cases, these sRNAs regulate all the genes encoded by the polycistronic mRNA (coordinate regulation) while in other cases, only a select subset of cistrons is controlled by the sRNA (discoordinate regulation). In this point of view, mechanisms of regulation and characteristics of sRNA-mRNA interactions involving polycistronic mRNAs are described. The diversity in mechanisms represented by these few characterized examples suggests that we still have much to learn about sRNA regulation of long polycistronic messages.
- Published
- 2013
50. Identification of mutations in seven Chinese patients with X-linked chronic granulomatous disease
- Author
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Siu Yuen Chan, Yu-Lung Lau, and Y F Hui
- Subjects
Silent mutation ,Genetics ,Mutation rate ,Mutation ,Splice site mutation ,Point mutation ,Immunology ,Nonsense mutation ,Cell Biology ,Hematology ,Biology ,medicine.disease_cause ,Biochemistry ,Molecular biology ,Frameshift mutation ,Polar mutation ,medicine - Abstract
X-linked chronic granulomatous disease (CGD) is due to mutations in the gp91phox gene on Xp21.1. Studies in white and Japanese X-linked CGD patients have shown mutations in nearly every exon. We studied the molecular defect of seven Chinese patients with X-linked CGD from six unrelated families. Mutations were located by single-strand conformation polymorphism and then defined by sequence analysis. The mutations were two different amino acid substitutions, a nonsense mutation, an in-frame trinucleotide deletion, a single A insertion causing a frameshift, and a premature stop. Lastly, a rare splice site mutation caused by G to A transition at the terminal nucleotide of exon 3, resulting in the skipping of exon 3, was found. The possible effects of these mutations on protein structure-function or splicing were discussed. Together with previous reports, the A insertion in the run of six As from nucleotide 749 to 754 and the G to A transition at the terminal position of exon 3 may be mutation hotspots of the gp91phox gene. The extreme heterogeneous mutations found in our patients suggest the absence of ethnic group-specific mutation.
- Published
- 1996
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