DNA double‐strand breaks regulate the cleavage‐independent release of Rec8‐cohesin during yeast meiosis

Author:

Fajish Ghanim1,Challa Kiran1,Salim Sagar2,VP Ajith2,Mwaniki Stephen1,Zhang Ruihao1,Fujita Yurika1,Ito Masaru1,Nishant Koodali T.2,Shinohara Akira1ORCID

Affiliation:

1. Institute for Protein Research, Osaka University Suita Osaka Japan

2. School of Biology Indian Institute of Science, Education and Research Thiruvananthapuram India

Abstract

AbstractThe mitotic cohesin complex necessary for sister chromatid cohesion and chromatin loop formation shows local and global association to chromosomes in response to DNA double‐strand breaks (DSBs). Here, by genome‐wide binding analysis of the meiotic cohesin with Rec8, we found that the Rec8‐localization profile along chromosomes is altered from middle to late meiotic prophase I with cleavage‐independent dissociation. Each Rec8‐binding site on the chromosome axis follows a unique alternation pattern with dissociation and probably association. Centromeres showed altered Rec8 binding in late prophase I relative to mid‐prophase I, implying chromosome remodeling of the regions. Rec8 dissociation ratio per chromosome is correlated well with meiotic DSB density. Indeed, the spo11 mutant deficient in meiotic DSB formation did not change the distribution of Rec8 along chromosomes in late meiotic prophase I. These suggest the presence of a meiosis‐specific regulatory pathway for the global binding of Rec8‐cohesin in response to DSBs.

Funder

Department of Science and Technology

Japan Society for the Promotion of Science

Council for Scientific and Industrial Research, South Africa

Publisher

Wiley

Subject

Cell Biology,Genetics

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