دورية أكاديمية

RecQ helicase, Sgs1, and XPF family endonuclease, Mus81-Mms4, resolve aberrant joint molecules during meiotic recombination.

التفاصيل البيبلوغرافية
العنوان: RecQ helicase, Sgs1, and XPF family endonuclease, Mus81-Mms4, resolve aberrant joint molecules during meiotic recombination.
المؤلفون: Oh SD; Department of Microbiology, University of California, Davis, One Shields Avenue, Davis, CA 95616, USA., Lao JP, Taylor AF, Smith GR, Hunter N
المصدر: Molecular cell [Mol Cell] 2008 Aug 08; Vol. 31 (3), pp. 324-36.
نوع المنشور: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
اللغة: English
بيانات الدورية: Publisher: Cell Press Country of Publication: United States NLM ID: 9802571 Publication Model: Print Cited Medium: Internet ISSN: 1097-4164 (Electronic) Linking ISSN: 10972765 NLM ISO Abbreviation: Mol Cell Subsets: MEDLINE
أسماء مطبوعة: Publication: Cambridge Ma : Cell Press
Original Publication: Cambridge, Mass. : Cell Press, c1997-
مواضيع طبية MeSH: Meiosis*, DNA-Binding Proteins/*metabolism , Endonucleases/*metabolism , RecQ Helicases/*metabolism , Recombination, Genetic/*genetics , Saccharomyces cerevisiae/*cytology , Saccharomyces cerevisiae/*enzymology , Saccharomyces cerevisiae Proteins/*metabolism , Trans-Activators/*metabolism, Chromosome Segregation ; Crossing Over, Genetic/genetics ; Cyclin B/metabolism ; DNA Breaks, Double-Stranded ; DNA, Cruciform/ultrastructure ; Flap Endonucleases ; Mutation/genetics ; Time Factors
مستخلص: Saccharomyces cerevisiae RecQ helicase, Sgs1, and XPF family endonuclease, Mus81-Mms4, are implicated in processing joint molecule (JM) recombination intermediates. We show that cells lacking either enzyme frequently experience chromosome segregation problems during meiosis and that when both enzymes are absent attempted segregation fails catastrophically. In all cases, segregation appears to be impeded by unresolved JMs. Analysis of the DNA events of recombination indicates that Sgs1 limits aberrant JM structures that result from secondary strand-invasion events and often require Mus81-Mms4 for their normal resolution. Aberrant JMs contain high levels of single Holliday junctions and include intersister JMs, multichromatid JMs comprising three and four chromatids, and newly identified recombinant JMs containing two chromatids, one of which has undergone crossing over. Despite persistent JMs in sgs1 mms4 double mutants, crossover and noncrossover products still form at high levels. We conclude that Sgs1 and Mus81-Mms4 collaborate to eliminate aberrant JMs, whereas as-yet-unidentified enzymes process normal JMs.
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معلومات مُعتمدة: R01 GM031693-25 United States GM NIGMS NIH HHS; GM031693 United States GM NIGMS NIH HHS; R01 GM074223-04 United States GM NIGMS NIH HHS; GM74223 United States GM NIGMS NIH HHS; R01 GM031693 United States GM NIGMS NIH HHS; R56 GM031693 United States GM NIGMS NIH HHS; R01 GM074223 United States GM NIGMS NIH HHS
المشرفين على المادة: 0 (CLB2 protein, S cerevisiae)
0 (Cyclin B)
0 (DNA, Cruciform)
0 (DNA-Binding Proteins)
0 (Saccharomyces cerevisiae Proteins)
0 (Trans-Activators)
EC 3.1.- (Endonucleases)
EC 3.1.- (Flap Endonucleases)
EC 3.1.- (MUS81 protein, S cerevisiae)
EC 3.1.22.- (MMS4 protein, S cerevisiae)
EC 3.6.1.- (SGS1 protein, S cerevisiae)
EC 3.6.4.12 (RecQ Helicases)
تواريخ الأحداث: Date Created: 20080812 Date Completed: 20080905 Latest Revision: 20240312
رمز التحديث: 20240312
مُعرف محوري في PubMed: PMC2587322
DOI: 10.1016/j.molcel.2008.07.006
PMID: 18691965
قاعدة البيانات: MEDLINE
الوصف
تدمد:1097-4164
DOI:10.1016/j.molcel.2008.07.006