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

Genes Cells. 2024 Jan;29(1):86-98. doi: 10.1111/gtc.13081. Epub 2023 Nov 15.

Abstract

The 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.

Keywords: DNA double-strand breaks; Rec8; chromosomes; cohesin; meiosis; meiotic recombination.

MeSH terms

  • Cell Cycle Proteins / genetics
  • Cell Cycle Proteins / metabolism
  • Cohesins
  • DNA / metabolism
  • DNA Breaks, Double-Stranded
  • Meiosis*
  • Saccharomyces cerevisiae* / genetics
  • Saccharomyces cerevisiae* / metabolism

Substances

  • Cell Cycle Proteins
  • Cohesins
  • DNA
  • REC8 protein, S cerevisiae