Cohesin mediates DNA loop extrusion and sister chromatid cohesion by distinct mechanisms

• Published in: Molecular cell Vol. 83; no. 17; pp. 3049 - 3063.e6
• Main Authors: Nagasaka, Kota, Davidson, Iain F., Stocsits, Roman R., Tang, Wen, Wutz, Gordana, Batty, Paul, Panarotto, Melanie, Litos, Gabriele, Schleiffer, Alexander, Gerlich, Daniel W., Peters, Jan-Michael
• Format: Journal Article
• Language: English
• Published: United States 07.09.2023
• Subjects: Binding Sites; Cell Cycle Proteins - genetics; Chromatids - genetics; Chromosomal Proteins, Non-Histone - genetics; Cohesins; Humans; chromatin architectures; cohesin; CTCF; TADs; cohesion; DNA loop extrusion
• ISSN: 1097-2765; 1097-4164; 1097-4164
• DOI: 10.1016/j.molcel.2023.07.024

Cohesin connects CTCF-binding sites and other genomic loci in cis to form chromatin loops and replicated DNA molecules in trans to mediate sister chromatid cohesion. Whether cohesin uses distinct or related mechanisms to perform these functions is unknown. Here, we describe a cohesin hinge mutant that can extrude DNA into loops but is unable to mediate cohesion in human cells. Our results suggest that the latter defect arises during cohesion establishment. The observation that cohesin's cohesion and loop extrusion activities can be partially separated indicates that cohesin uses distinct mechanisms to perform these two functions. Unexpectedly, the same hinge mutant can also not be stopped by CTCF boundaries as well as wild-type cohesin. This suggests that cohesion establishment and cohesin's interaction with CTCF boundaries depend on related mechanisms and raises the possibility that both require transient hinge opening to entrap DNA inside the cohesin ring.