Sister chromatid cohesion is mediated by individual cohesin complexes

Author:

Ochs Fena1ORCID,Green Charlotte1ORCID,Szczurek Aleksander Tomasz1,Pytowski Lior2ORCID,Kolesnikova Sofia34,Brown Jill5ORCID,Gerlich Daniel Wolfram3ORCID,Buckle Veronica5ORCID,Schermelleh Lothar1ORCID,Nasmyth Kim Ashley1ORCID

Affiliation:

1. Department of Biochemistry, University of Oxford, Oxford OX1 3QU, UK.

2. Sir William Dunn School of Pathology, University of Oxford, Oxford OX1 3RE, UK.

3. Institute of Molecular Biotechnology of the Austrian Academy of Sciences (IMBA), Vienna BioCenter (VBC), 1030 Vienna Austria.

4. Vienna BioCenter PhD Program, Doctoral School of the University of Vienna and Medical University of Vienna, 1030 Vienna Austria.

5. MRC Weatherall Institute of Molecular Medicine, University of Oxford, Oxford OX3 9DS, UK.

Abstract

Eukaryotic genomes are organized by loop extrusion and sister chromatid cohesion, both mediated by the multimeric cohesin protein complex. Understanding how cohesin holds sister DNAs together, and how loss of cohesion causes age-related infertility in females, requires knowledge as to cohesin’s stoichiometry in vivo. Using quantitative super-resolution imaging, we identified two discrete populations of chromatin-bound cohesin in postreplicative human cells. Whereas most complexes appear dimeric, cohesin that localized to sites of sister chromatid cohesion and associated with sororin was exclusively monomeric. The monomeric stoichiometry of sororin:cohesin complexes demonstrates that sister chromatid cohesion is conferred by individual cohesin rings, a key prediction of the proposal that cohesion arises from the co-entrapment of sister DNAs.

Publisher

American Association for the Advancement of Science (AAAS)

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