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Epigenetic pioneering by SWI/SNF family remodelers.
Ahmad, Kami; Brahma, Sandipan; Henikoff, Steven.
Afiliação
  • Ahmad K; Basic Sciences Division, Fred Hutchinson Cancer Center, Seattle, WA, USA.
  • Brahma S; University of Nebraska Medical Center, Department of Genetics, Cell Biology & Anatomy, Omaha, NE, USA.
  • Henikoff S; Basic Sciences Division, Fred Hutchinson Cancer Center, Seattle, WA, USA; Howard Hughes Medical Institute, Chevy Chase, MD, USA. Electronic address: steveh@fredhutch.org.
Mol Cell ; 84(2): 194-201, 2024 Jan 18.
Article em En | MEDLINE | ID: mdl-38016477
ABSTRACT
In eukaryotic genomes, transcriptional machinery and nucleosomes compete for binding to DNA sequences; thus, a crucial aspect of gene regulatory element function is to modulate chromatin accessibility for transcription factor (TF) and RNA polymerase binding. Recent structural studies have revealed multiple modes of TF engagement with nucleosomes, but how initial "pioneering" results in steady-state DNA accessibility for further TF binding and RNA polymerase II (RNAPII) engagement has been unclear. Even less well understood is how distant sites of open chromatin interact with one another, such as when developmental enhancers activate promoters to release RNAPII for productive elongation. Here, we review evidence for the centrality of the conserved SWI/SNF family of nucleosome remodeling complexes, both in pioneering and in mediating enhancer-promoter contacts. Consideration of the nucleosome unwrapping and ATP hydrolysis activities of SWI/SNF complexes, together with their architectural features, may reconcile steady-state TF occupancy with rapid TF dynamics observed by live imaging.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Fatores de Transcrição / Nucleossomos Idioma: En Revista: Mol Cell Assunto da revista: BIOLOGIA MOLECULAR Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Fatores de Transcrição / Nucleossomos Idioma: En Revista: Mol Cell Assunto da revista: BIOLOGIA MOLECULAR Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos