4.8 Article

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

Journal

NUCLEIC ACIDS RESEARCH
Volume 47, Issue 22, Pages 11691-11708

Publisher

OXFORD UNIV PRESS
DOI: 10.1093/nar/gkz903

Keywords

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Funding

  1. National Research Foundation of Korea - Ministry of Science, ICT & Future Planning [NRF-2017R1A2B2005603, NRF-2018R1A5A1025077]
  2. Next-Generation BioGreen 21 Program [SSAC] [PJ01322801]
  3. Rural Development Administration, Republic of Korea [NIH-GM 044794]
  4. National Research Foundation of Korea (NRF) grant - Korea government (MSIT)

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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.

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