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ZNF143 binds DNA and stimulates transcripstion initiation to activate and repress direct target genes.
Dong, Jinhong; Scott, Thomas G; Mukherjee, Rudradeep; Guertin, Michael J.
Afiliación
  • Dong J; Center for Cell Analysis and Modeling, University of Connecticut, Farmington, Connecticut, United States of America.
  • Scott TG; Department of Biochemistry and Molecular Genetics, University of Virginia, Charlottesville, Virginia, United States of America.
  • Mukherjee R; Center for Cell Analysis and Modeling, University of Connecticut, Farmington, Connecticut, United States of America.
  • Guertin MJ; Center for Cell Analysis and Modeling, University of Connecticut, Farmington, Connecticut, United States of America.
bioRxiv ; 2024 May 15.
Article en En | MEDLINE | ID: mdl-38798607
ABSTRACT
Transcription factors bind to sequence motifs and act as activators or repressors. Transcription factors interface with a constellation of accessory cofactors to regulate distinct mechanistic steps to regulate transcription. We rapidly degraded the essential and ubiquitously expressed transcription factor ZNF143 to determine its function in the transcription cycle. ZNF143 facilitates RNA Polymerase initiation and activates gene expression. ZNF143 binds the promoter of nearly all its activated target genes. ZNF143 also binds near the site of genic transcription initiation to directly repress a subset of genes. Although ZNF143 stimulates initiation at ZNF143-repressed genes (i.e. those that increase expression upon ZNF143 depletion), the molecular context of binding leads to cis repression. ZNF143 competes with other more efficient activators for promoter access, physically occludes transcription initiation sites and promoter-proximal sequence elements, and acts as a molecular roadblock to RNA Polymerases during early elongation. The term context specific is often invoked to describe transcription factors that have both activation and repression functions. We define the context and molecular mechanisms of ZNF143-mediated cis activation and repression.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: BioRxiv Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: BioRxiv Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Estados Unidos