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Cohesin's DNA exit gate is distinct from its entrance gate and is regulated by acetylation.

Cell | Aug 31, 2012

http://www.ncbi.nlm.nih.gov/pubmed/22901742

Sister chromatid cohesion is mediated by entrapment of sister DNAs by a tripartite ring composed of cohesin's Smc1, Smc3, and α-kleisin subunits. Cohesion requires acetylation of Smc3 by Eco1, whose role is to counteract an inhibitory (antiestablishment) activity associated with cohesin's Wapl subunit. We show that mutations abrogating antiestablishment activity also reduce turnover of cohesin on pericentric chromatin. Our results reveal a "releasing" activity inherent to cohesin complexes transiently associated with Wapl that catalyzes their dissociation from chromosomes. Fusion of Smc3's nucleotide binding domain to α-kleisin's N-terminal domain also reduces cohesin turnover within pericentric chromatin and permits establishment of Wapl-resistant cohesion in the absence of Eco1. We suggest that releasing activity opens the Smc3/α-kleisin interface, creating a DNA exit gate distinct from its proposed entry gate at the Smc1/3 interface. According to this notion, the function of Smc3 acetylation is to block its dissociation from α-kleisin. The functional implications of regulated ring opening are discussed.

Pubmed ID: 22901742 RIS Download

Mesh terms: Acetylation | Acetyltransferases | Cell Cycle Proteins | Chromosomal Proteins, Non-Histone | Chromosomes, Fungal | DNA Replication | Nuclear Proteins | Saccharomyces cerevisiae | Saccharomyces cerevisiae Proteins

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Associated grants

  • Agency: Wellcome Trust, Id: 091911
  • Agency: Cancer Research UK, Id: 12386
  • Agency: Cancer Research UK, Id:
  • Agency: Wellcome Trust, Id:

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