Fiche publication


Date publication

août 2015

Journal

PLoS genetics

Auteurs

Membres identifiés du Cancéropôle Est :
Dr BARDET Anaïs


Tous les auteurs :
Stein C, Bardet AF, Roma G, Bergling S, Clay I, Ruchti A, Agarinis C, Schmelzle T, Bouwmeester T, Schübeler D, Bauer A

Résumé

YAP1 is a major effector of the Hippo pathway and a well-established oncogene. Elevated YAP1 activity due to mutations in Hippo pathway components or YAP1 amplification is observed in several types of human cancers. Here we investigated its genomic binding landscape in YAP1-activated cancer cells, as well as in non-transformed cells. We demonstrate that TEAD transcription factors mediate YAP1 chromatin-binding genome-wide, further explaining their dominant role as primary mediators of YAP1-transcriptional activity. Moreover, we show that YAP1 largely exerts its transcriptional control via distal enhancers that are marked by H3K27 acetylation and that YAP1 is necessary for this chromatin mark at bound enhancers and the activity of the associated genes. This work establishes YAP1-mediated transcriptional regulation at distal enhancers and provides an expanded set of target genes resulting in a fundamental source to study YAP1 function in a normal and cancer setting.

Mots clés

Acetylation, Adaptor Proteins, Signal Transducing, physiology, Base Sequence, Binding Sites, Cell Line, Tumor, Consensus Sequence, DNA-Binding Proteins, metabolism, Enhancer Elements, Genetic, Histones, metabolism, Humans, Nuclear Proteins, metabolism, Phosphoproteins, physiology, Protein Binding, Protein Processing, Post-Translational, TEA Domain Transcription Factors, Transcription Factors, metabolism, Transcriptional Activation, Transcriptome, YAP-Signaling Proteins

Référence

PLoS Genet. 2015 08;11(8):e1005465