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MafB, WDR77, and ß-catenin interact with each other and have similar genome association profiles.
He, Lizhi; Gao, Mingshi; Pratt, Henry; Weng, Zhiping; Struhl, Kevin.
Afiliação
  • He L; Dept. Biological Chemistry and Molecular Pharmacology, Harvard Medical School, Boston, MA, United states of America.
  • Gao M; Program in Bioinformatics and Integrative Biology, University of Massachusetts Medical School, Worcester, MA, United states of America.
  • Pratt H; Program in Bioinformatics and Integrative Biology, University of Massachusetts Medical School, Worcester, MA, United states of America.
  • Weng Z; Program in Bioinformatics and Integrative Biology, University of Massachusetts Medical School, Worcester, MA, United states of America.
  • Struhl K; Dept. Biological Chemistry and Molecular Pharmacology, Harvard Medical School, Boston, MA, United states of America.
PLoS One ; 17(4): e0264799, 2022.
Article em En | MEDLINE | ID: mdl-35482762
ABSTRACT
MafB (a bZIP transcription factor), ß-catenin (the ultimate target of the Wnt signal transduction pathway that acts as a transcriptional co-activator of LEF/TCF proteins), and WDR77 (a transcriptional co-activator of multiple hormone receptors) are important for breast cellular transformation. Unexpectedly, these proteins interact directly with each other, and they have similar genomic binding profiles. Furthermore, while some of these common target sites coincide with those bound by LEF/TCF, the majority are located just downstream of transcription initiation sites at a position near paused RNA polymerase (Pol II) and the +1 nucleosome. Occupancy levels of these factors at these promoter-proximal sites are strongly correlated with the level of paused Pol II and transcriptional activity.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Beta Catenina / Cateninas Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Beta Catenina / Cateninas Idioma: En Ano de publicação: 2022 Tipo de documento: Article