Distinct roles of cohesin-SA1 and cohesin-SA2 in 3D chromosome organization
Aleksandar Kojic, Ana CuadradoiD, Magali De KoninckiD, Daniel Giménez-LlorenteiD, Miriam Rodríguez-CorsinoiD, Gonzalo Goméz-LópeziD, François Le DilyiD, Marc A. Martı́-RenomiD, Ana LosadaiD
Abstract
In addition to mediating sister chromatid cohesion, cohesin plays a central role in DNA looping and segmentation of the genome into contact domains (TADs). Two variant cohesin complexes that contain either STAG/SA1 or SA2 are present in all cell types. Here we addressed their specific contribution to genome architecture in non-transformed human cells. We found that cohesin-SA1 drives stacking of cohesin rings at CTCF-bound sites and thereby contributes to the stabilization and preservation of TAD boundaries. In contrast, a more dynamic cohesin-SA2 promotes cell type-specific contacts between enhancers and promoters within TADs independently of CTCF. SA2 loss, a condition frequently observed in cancer cells, results in increased intra-TAD interactions, likely altering the expression of key cell identity genes.
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