Specific contributions of cohesin-SA1 and cohesin-SA2 to TADs and polycomb domains in embryonic stem cells

Cohesin exists in two variants carrying either STAG/SA1 or SA2. Here we have addressed their specific contributions to the unique spatial organization of the mouse embryonic stem cell genome, which ensures super-enhancer-dependent transcription of pluripotency factors and repression of lineage-speci...

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Detalhes bibliográficos
Autores: Cuadrado, Ana, Giménez-Llorente, Daniel, Kojic, Aleksandar, Rodríguez-Corsino, Miriam, Cuartero, Yasmina, Martín-Serrano, Guillermo, Gómez López, Gonzalo, Marti-Renom, Marc A., Losada, Ana
Tipo de documento: artigo
Estado:Versão publicada
Data de publicação:2019
País:España
Recursos:Universitat Pompeu Fabra
Repositório:Repositorio Digital de la UPF
OAI Identifier:oai:repositori.upf.edu:10230/42291
Acesso em linha:http://hdl.handle.net/10230/42291
http://dx.doi.org/10.1016/j.celrep.2019.05.078
Access Level:Acceso aberto
Palavra-chave:Cohesin
STAG1
STAG2
PRC1
Hox network
Pluripotency
Chromatin loop
CTCF
Compartment
Hi-C
Descrição
Resumo:Cohesin exists in two variants carrying either STAG/SA1 or SA2. Here we have addressed their specific contributions to the unique spatial organization of the mouse embryonic stem cell genome, which ensures super-enhancer-dependent transcription of pluripotency factors and repression of lineage-specification genes within Polycomb domains. We find that cohesin-SA2 facilitates Polycomb domain compaction through Polycomb repressing complex 1 (PRC1) recruitment and promotes the establishment of long-range interaction networks between distant Polycomb-bound promoters that are important for gene repression. Cohesin-SA1, in contrast, disrupts these networks, while preserving topologically associating domain (TAD) borders. The diverse effects of both complexes on genome topology may reflect two modes of action of cohesin. One, likely involving loop extrusion, establishes overall genome arrangement in TADs together with CTCF and prevents excessive segregation of same-class compartment regions. The other is required for organization of local transcriptional hubs such as Polycomb domains and super-enhancers, which define cell identity.