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A cohesin traffic pattern genetically linked to gene regulation.
Valton, Anne-Laure; Venev, Sergey V; Mair, Barbara; Khokhar, Eraj Shafiq; Tong, Amy H Y; Usaj, Matej; Chan, Katherine; Pai, Athma A; Moffat, Jason; Dekker, Job.
Afiliación
  • Valton AL; Department of Systems Biology, University of Massachusetts Chan Medical School, Worcester, MA, USA.
  • Venev SV; Howard Hughes Medical Institute, Chevy Chase, MD, USA.
  • Mair B; Department of Systems Biology, University of Massachusetts Chan Medical School, Worcester, MA, USA.
  • Khokhar ES; Donnelly Centre, University of Toronto, Toronto, Ontario, Canada.
  • Tong AHY; RNA Therapeutics Institute, University of Massachusetts Chan Medical School, Worcester, MA, USA.
  • Usaj M; Donnelly Centre, University of Toronto, Toronto, Ontario, Canada.
  • Chan K; Donnelly Centre, University of Toronto, Toronto, Ontario, Canada.
  • Pai AA; Donnelly Centre, University of Toronto, Toronto, Ontario, Canada.
  • Moffat J; RNA Therapeutics Institute, University of Massachusetts Chan Medical School, Worcester, MA, USA.
  • Dekker J; Donnelly Centre, University of Toronto, Toronto, Ontario, Canada.
Nat Struct Mol Biol ; 29(12): 1239-1251, 2022 12.
Article en En | MEDLINE | ID: mdl-36482254
Cohesin-mediated loop extrusion has been shown to be blocked at specific cis-elements, including CTCF sites, producing patterns of loops and domain boundaries along chromosomes. Here we explore such cis-elements, and their role in gene regulation. We find that transcription termination sites of active genes form cohesin- and RNA polymerase II-dependent domain boundaries that do not accumulate cohesin. At these sites, cohesin is first stalled and then rapidly unloaded. Start sites of transcriptionally active genes form cohesin-bound boundaries, as shown before, but are cohesin-independent. Together with cohesin loading, possibly at enhancers, these sites create a pattern of cohesin traffic that guides enhancer-promoter interactions. Disrupting this traffic pattern, by removing CTCF, renders cells sensitive to knockout of genes involved in transcription initiation, such as the SAGA complexes, and RNA processing such DEAD/H-Box RNA helicases. Without CTCF, these factors are less efficiently recruited to active promoters.
Asunto(s)

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Cromatina / Proteínas Cromosómicas no Histona Idioma: En Revista: Nat Struct Mol Biol Asunto de la revista: BIOLOGIA MOLECULAR Año: 2022 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Cromatina / Proteínas Cromosómicas no Histona Idioma: En Revista: Nat Struct Mol Biol Asunto de la revista: BIOLOGIA MOLECULAR Año: 2022 Tipo del documento: Article País de afiliación: Estados Unidos