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Recruitment of Rec8, Pds5 and Rad61/Wapl to meiotic homolog pairing, recombination, axis formation and S-phaseopen access

Authors
Hong, SoogilJoo, Jeong H.Yun, HyeseonKleckner, NancyKim, Keun Pil
Issue Date
Dec-2019
Publisher
NLM (Medline)
Citation
Nucleic acids research, v.47, no.22, pp 11691 - 11708
Pages
18
Journal Title
Nucleic acids research
Volume
47
Number
22
Start Page
11691
End Page
11708
URI
https://scholarworks.bwise.kr/cau/handle/2019.sw.cau/37563
DOI
10.1093/nar/gkz903
ISSN
1362-4962
1362-4962
Abstract
We have explored the meiotic roles of cohesin modulators Pds5 and Rad61/Wapl, in relation to one another, and to meiotic kleisin Rec8, for homolog pairing, all physically definable steps of recombination, prophase axis length and S-phase progression, in budding yeast. We show that Pds5 promotes early steps of recombination and thus homolog pairing, and also modulates axis length, with both effects independent of a sister chromatid. [Pds5+Rec8] promotes double-strand break formation, maintains homolog bias for crossover formation and promotes S-phase progression. Oppositely, the unique role of Rad61/Wapl is to promote non-crossover recombination by releasing [Pds5+Rec8]. For this effect, Rad61/Wapl probably acts to maintain homolog bias by preventing channeling into sister interactions. Mysteriously, each analyzed molecule has one role that involves neither of the other two. Overall, the presented findings suggest that Pds5's role in maintenance of sister chromatid cohesion during the mitotic prophase-analogous stage of G2/M is repurposed during meiosis prophase to promote interactions between homologs. © The Author(s) 2019. Published by Oxford University Press on behalf of Nucleic Acids Research.
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자연과학대학 (생명과학과)
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