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Functional crosstalk between the cohesin loader and chromatin remodelers.
Muñoz, Sofía; Jones, Andrew; Bouchoux, Céline; Gilmore, Tegan; Patel, Harshil; Uhlmann, Frank.
Afiliación
  • Muñoz S; Chromosome Segregation Laboratory, The Francis Crick Institute, London, UK. sofiamf@usal.es.
  • Jones A; Cell Cycle Control and the Maintenance of Genomic Stability Laboratory, Cancer Research Center (CIC), University of Salamanca, Salamanca, Spain. sofiamf@usal.es.
  • Bouchoux C; Proteomics Science Technology Platform, The Francis Crick Institute, London, UK.
  • Gilmore T; Chromosome Segregation Laboratory, The Francis Crick Institute, London, UK.
  • Patel H; Bioinformatics & Biostatistics Science Technology Platform, The Francis Crick Institute, London, UK.
  • Uhlmann F; Bioinformatics & Biostatistics Science Technology Platform, The Francis Crick Institute, London, UK.
Nat Commun ; 13(1): 7698, 2022 12 13.
Article en En | MEDLINE | ID: mdl-36509793
ABSTRACT
The cohesin complex participates in many structural and functional aspects of genome organization. Cohesin recruitment onto chromosomes requires nucleosome-free DNA and the Scc2-Scc4 cohesin loader complex that catalyzes topological cohesin loading. Additionally, the cohesin loader facilitates promoter nucleosome clearance in a yet unknown way, and it recognizes chromatin receptors such as the RSC chromatin remodeler. Here, we explore the cohesin loader-RSC interaction. Amongst multi-pronged contacts by Scc2 and Scc4, we find that Scc4 contacts a conserved patch on the RSC ATPase motor module. The cohesin loader directly stimulates in vitro nucleosome sliding by RSC, providing an explanation how it facilitates promoter nucleosome clearance. Furthermore, we observe cohesin loader interactions with a wide range of chromatin remodelers. Our results provide mechanistic insight into how the cohesin loader recognizes, as well as influences, the chromatin landscape, with implications for our understanding of human developmental disorders including Cornelia de Lange and Coffin-Siris syndromes.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Proteínas de Saccharomyces cerevisiae / Micrognatismo Límite: Humans Idioma: En Revista: Nat Commun Asunto de la revista: BIOLOGIA / CIENCIA Año: 2022 Tipo del documento: Article País de afiliación: Reino Unido

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Proteínas de Saccharomyces cerevisiae / Micrognatismo Límite: Humans Idioma: En Revista: Nat Commun Asunto de la revista: BIOLOGIA / CIENCIA Año: 2022 Tipo del documento: Article País de afiliación: Reino Unido