P53 suppresses muscle differentiation at the myogenin step in response to genotoxic stress.
Ontology highlight
ABSTRACT: Acute muscle injury and physiological stress from chronic muscle diseases and aging lead to impairment of skeletal muscle function. This raises the question of whether p53, a cellular stress sensor, regulates muscle tissue repair under stress conditions. By investigating muscle differentiation in the presence of genotoxic stress, we discovered that p53 binds directly to the myogenin promoter and represses transcription of myogenin, a member of the MyoD family of transcription factors that plays a critical role in driving terminal muscle differentiation. This reduction of myogenin protein is observed in G1-arrested cells and leads to decreased expression of late but not early differentiation markers. In response to acute genotoxic stress, p53-mediated repression of myogenin reduces post-mit
SUBMITTER: Yang ZJ
PROVIDER: S-EPMC4356341 | biostudies-literature | 2015 Apr
REPOSITORIES: biostudies-literature
ACCESS DATA