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dc.contributor.authorCorrette-Bennett, Stephanie E.
dc.contributor.authorMohlman, Natasha L.
dc.contributor.authorRosado, Zulma
dc.contributor.authorMiret, Juan J.
dc.contributor.authorHess, Patricia M.
dc.contributor.authorParker, Breck Olland
dc.contributor.authorLahue, Robert S.
dc.date2022-08-11T08:08:56.000
dc.date.accessioned2022-08-23T16:13:15Z
dc.date.available2022-08-23T16:13:15Z
dc.date.issued2001-10-16
dc.date.submitted2008-08-27
dc.identifier.citation<p>Nucleic Acids Res. 2001 Oct 15;29(20):4134-43.</p>
dc.identifier.issn1362-4962 (Electronic)
dc.identifier.doi10.1093/nar/29.20.4134
dc.identifier.pmid11600702
dc.identifier.urihttp://hdl.handle.net/20.500.14038/33578
dc.description.abstractSmall looped mispairs are efficiently corrected by mismatch repair. The situation with larger loops is less clear. Repair activity on large loops has been reported as anywhere from very low to quite efficient. There is also uncertainty about how many loop repair activities exist and whether any are conserved. To help address these issues, we studied large loop repair in Saccharomyces cerevisiae using in vivo and in vitro assays. Transformation of heteroduplexes containing 1, 16 or 38 nt loops led to >90% repair for all three substrates. Repair of the 38 base loop occurred independently of mutations in key genes for mismatch repair (MR) and nucleotide excision repair (NER), unlike other reported loop repair functions in yeast. Correction of the 16 base loop was mostly independent of MR, indicating that large loop repair predominates for this size heterology. Similarities between mammalian and yeast large loop repair were suggested by the inhibitory effects of loop secondary structure and by the role of defined nicks on the relative proportions of loop removal and loop retention products. These observations indicate a robust large loop repair pathway in yeast, distinct from MR and NER, and conserved in mammals.
dc.language.isoen_US
dc.relation<p><a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=11600702&dopt=Abstract">Link to article in PubMed</a></p>
dc.relation.urlhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC60213/
dc.subjectBase Pair Mismatch; Base Sequence; *DNA Repair; DNA, Fungal; Genes, Fungal; Mutation; Nucleic Acid Conformation; Nucleic Acid Heteroduplexes; Saccharomyces cerevisiae
dc.subjectLife Sciences
dc.subjectMedicine and Health Sciences
dc.titleEfficient repair of large DNA loops in Saccharomyces cerevisiae
dc.typeJournal Article
dc.source.journaltitleNucleic acids research
dc.source.volume29
dc.source.issue20
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/gsbs_sp/248
dc.identifier.contextkey606046
html.description.abstract<p>Small looped mispairs are efficiently corrected by mismatch repair. The situation with larger loops is less clear. Repair activity on large loops has been reported as anywhere from very low to quite efficient. There is also uncertainty about how many loop repair activities exist and whether any are conserved. To help address these issues, we studied large loop repair in Saccharomyces cerevisiae using in vivo and in vitro assays. Transformation of heteroduplexes containing 1, 16 or 38 nt loops led to >90% repair for all three substrates. Repair of the 38 base loop occurred independently of mutations in key genes for mismatch repair (MR) and nucleotide excision repair (NER), unlike other reported loop repair functions in yeast. Correction of the 16 base loop was mostly independent of MR, indicating that large loop repair predominates for this size heterology. Similarities between mammalian and yeast large loop repair were suggested by the inhibitory effects of loop secondary structure and by the role of defined nicks on the relative proportions of loop removal and loop retention products. These observations indicate a robust large loop repair pathway in yeast, distinct from MR and NER, and conserved in mammals.</p>
dc.identifier.submissionpathgsbs_sp/248
dc.contributor.departmentDepartment of Biochemistry and Molecular Pharmacology
dc.contributor.departmentGraduate School of Biomedical Sciences
dc.source.pages4134-43


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