The Francis Crick Institute
Browse

Biochemical reconstitution of sister chromatid cohesion establishment during DNA replication

Download (5.38 MB)
journal contribution
posted on 2025-10-10, 10:42 authored by Masashi Minamino, John FX Diffley, Frank Uhlmann
Concomitant with DNA replication, the ring-shaped cohesin complex encircles both newly synthesized sister chromatids, enabling their faithful segregation during cell divisions. Our molecular understanding of how cohesin co-entraps both replication products remains incomplete. Here, we reconstitute sister chromatid cohesion establishment using purified budding yeast proteins. Cohesin rings, initially loaded onto template DNA, remain DNA bound during complete DNA synthesis. Some of these cohesin rings encircle both sister chromatids, consistent with the idea that replisomes traverse through cohesin rings. Often, however, cohesin ends up embracing only one of the two replication products, suggesting that a two-step capture mechanism operates during cohesion establishment. Additionally, DNA replication initiates new cohesin recruitment as a further means to generate sister chromatid cohesion. Our results illustrate that more than one pathway leads to sister chromatid cohesion, and they make cohesion establishment amenable to direct biochemical exploration.

Funding

Wellcome Trust (Grant ID: 219527/Z/19/Z) Wellcome Trust (Grant ID: 220244/Z/20/Z) Medical Research Council (Grant ID: cc2002) Medical Research Council (Grant ID: cc2137) Crick (Grant ID: CC2002, Grant title: Diffley CC2002) Crick (Grant ID: CC2137, Grant title: Uhlmann CC2137) Wellcome Trust (Grant ID: 219527/Z/19/Z, Grant title: WT 219527/Z/19/Z) Wellcome Trust (Grant ID: 220244/Z/20/Z, Grant title: WT 220244/Z/20/Z)

History