| Yeast Pch2 promotes domainal axis organization, timely recombination progression, and arrest of defective recombinosomes during meiosis. | |
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MedLine Citation:
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PMID: 18305165 Owner: NLM Status: MEDLINE |
Abstract/OtherAbstract:
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We show that, during budding yeast meiosis, axis ensemble Hop1/Red1 and synaptonemal complex (SC) component Zip1 tend to occur in alternating strongly staining domains. The widely conserved AAA+-ATPase Pch2 mediates this pattern, likely by means of direct intervention along axes. Pch2 also coordinately promotes timely progression of cross-over (CO) and noncross-over (NCO) recombination. Oppositely, in a checkpoint-triggering aberrant situation (zip1Delta), Pch2 mediates robust arrest of stalled recombination complexes, likely via nucleolar localization. We suggest that, during WT meiosis, Pch2 promotes progression of SC-associated CO and NCO recombination complexes at a regulated early-midpachytene transition that is rate-limiting for later events; in contrast, during defective meiosis, Pch2 ensures that aberrant recombination complexes fail to progress so that intermediates can be harmlessly repaired during eventual return to growth. Positive vs. negative roles of Pch2 in the two situations are analogous to positive vs. negative roles of Mec1/ATR, suggesting that Pch2 might mediate Mec1/ATR activity. We further propose that regulatory surveillance of normal and abnormal interchromosomal interactions in mitotic and meiotic cells may involve "structure-dependent interchromosomal interaction" (SDIX) checkpoints. |
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Authors:
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G Valentin Börner; Aekam Barot; Nancy Kleckner |
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Publication Detail:
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Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't Date: 2008-02-27 |
Journal Detail:
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Title: Proceedings of the National Academy of Sciences of the United States of America Volume: 105 ISSN: 1091-6490 ISO Abbreviation: Proc. Natl. Acad. Sci. U.S.A. Publication Date: 2008 Mar |
Date Detail:
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Created Date: 2008-03-05 Completed Date: 2008-04-18 Revised Date: 2009-11-18 |
Medline Journal Info:
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Nlm Unique ID: 7505876 Medline TA: Proc Natl Acad Sci U S A Country: United States |
Other Details:
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Languages: eng Pagination: 3327-32 Citation Subset: IM |
Affiliation:
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Department of Molecular and Cellular Biology, Harvard University, Cambridge, MA 02138, USA. |
Export Citation:
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| MeSH Terms | |
Descriptor/Qualifier:
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Adenosine Triphosphatases
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physiology* Cell Cycle Proteins / physiology* Chromosomes, Fungal Crossing Over, Genetic DNA-Binding Proteins / metabolism* Meiosis* Nuclear Proteins / physiology* Pachytene Stage* Recombination, Genetic Saccharomyces cerevisiae / cytology Saccharomyces cerevisiae Proteins / metabolism*, physiology* Saccharomycetales |
| Grant Support | |
ID/Acronym/Agency:
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R01 GM044794/GM/NIGMS NIH HHS |
| Chemical | |
Reg. No./Substance:
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0/Cell Cycle Proteins; 0/DNA-Binding Proteins; 0/HOP1 protein, S cerevisiae; 0/Nuclear Proteins; 0/Pch2 protein, S cerevisiae; 0/RED1 protein, S cerevisiae; 0/Saccharomyces cerevisiae Proteins; 0/Zip1 protein, S cerevisiae; EC 3.6.1.-/Adenosine Triphosphatases |
| Comments/Corrections | |
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