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Functional interdependence at the chromatin level between the MKK6/p38 and IGF1/PI3K/AKT pathways during muscle differentiation.

Molecular cell | Oct 26, 2007

During muscle regeneration, the mechanism integrating environmental cues at the chromatin of muscle progenitors is unknown. We show that inflammation-activated MKK6-p38 and insulin growth factor 1 (IGF1)-induced PI3K/AKT pathways converge on the chromatin of muscle genes to target distinct components of the muscle transcriptosome. p38 alpha/beta kinases recruit the SWI/SNF chromatin-remodeling complex; AKT1 and 2 promote the association of MyoD with p300 and PCAF acetyltransferases, via direct phosphorylation of p300. Pharmacological or genetic interference with either pathway led to partial assembly of discrete chromatin-bound complexes, which reflected two reversible and distinct cellular phenotypes. Remarkably, PI3K/AKT blockade was permissive for chromatin recruitment of MEF2-SWI/SNF complex, whose remodeling activity was compromised in the absence of MyoD and acetyltransferases. The functional interdependence between p38 and IGF1/PI3K/AKT pathways was further established by the evidence that blockade of AKT chromatin targets was sufficient to prevent the activation of the myogenic program triggered by deliberate activation of p38 signaling.

Pubmed ID: 17964260 RIS Download

Mesh terms: Acetylation | Animals | Cell Line | Cell Shape | Chromatin | Chromones | E1A-Associated p300 Protein | Gene Expression Regulation, Developmental | Imidazoles | Insulin-Like Growth Factor I | MAP Kinase Kinase 6 | Mice | Morpholines | Muscle Development | MyoD Protein | Myoblasts | Myogenic Regulatory Factors | Phenotype | Phosphatidylinositol 3-Kinases | Phosphorylation | Promoter Regions, Genetic | Protein Kinase Inhibitors | Proto-Oncogene Proteins c-akt | Pyridines | RNA Interference | RNA, Small Interfering | Signal Transduction | Transcription, Genetic | Transfection | p300-CBP Transcription Factors | p38 Mitogen-Activated Protein Kinases

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Associated grants

  • Agency: NIAMS NIH HHS, Id: R01 AR052779
  • Agency: NIAMS NIH HHS, Id: R01 AR052779-02
  • Agency: Telethon, Id: TCR05004

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