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dc.contributor.authorGianno Pannafino
dc.contributor.authorEric Alani
dc.contributor.otherDepartment of Molecular Biology and Genetics, Cornell University, Ithaca, NY 14853-2703, USA
dc.contributor.otherDepartment of Molecular Biology and Genetics, Cornell University, Ithaca, NY 14853-2703, USA
dc.date.accessioned2025-10-09T05:27:40Z
dc.date.available2025-10-09T05:27:40Z
dc.date.issued01-04-2021
dc.identifier.urihttps://www.mdpi.com/2073-4409/10/4/948
dc.identifier.urihttp://digilib.fisipol.ugm.ac.id/repo/handle/15717717/41041
dc.description.abstractThe MutL family of DNA mismatch repair proteins (MMR) acts to maintain genomic integrity in somatic and meiotic cells. In baker’s yeast, the MutL homolog (MLH) MMR proteins form three heterodimeric complexes, MLH1-PMS1, MLH1-MLH2, and MLH1-MLH3. The recent discovery of human PMS2 (homolog of baker’s yeast PMS1) and MLH3 acting independently of human MLH1 in the repair of somatic double-strand breaks questions the assumption that MLH1 is an obligate subunit for MLH function. Here we provide a summary of the canonical roles for MLH factors in DNA genomic maintenance and in meiotic crossover. We then present the phenotypes of cells lacking specific MLH subunits, particularly in meiotic recombination, and based on this analysis, propose a model for an independent early role for MLH3 in meiosis to promote the accurate segregation of homologous chromosomes in the meiosis I division.
dc.language.isoEN
dc.publisherMDPI AG
dc.subject.lccCytology
dc.titleCoordinated and Independent Roles for MLH Subunits in DNA Repair
dc.typeArticle
dc.description.keywordsMutL homologs
dc.description.keywordsMLH
dc.description.keywordsDNA mismatch repair
dc.description.keywordsmeiosis
dc.description.keywordsHolliday junction resolution
dc.description.keywordshomologous recombination
dc.description.doi10.3390/cells10040948
dc.title.journalCells
dc.identifier.e-issn2073-4409
dc.identifier.oaioai:doaj.org/journal:b7fcd1e83f814b738c9624513ddfa93b
dc.journal.infoVolume 10, Issue 4


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