PuSH - Publication Server of Helmholtz Zentrum München

Moretti, I.* ; Ciciliot, S.* ; Dyar, K.A. ; Abraham, R.* ; Murgia, M.* ; Agatea, L.* ; Akimoto, T.* ; Bicciato, S.* ; Forcato, M.* ; Pierre, P.* ; Uhlenhaut, N.H. ; Rigby, P.W.* ; Carvajal, J.J.* ; Blaauw, B.* ; Calabria, E.* ; Schiaffino, S.*

MRF4 negatively regulates adult skeletal muscle growth by repressing MEF2 activity.

Nat. Commun. 7:12397 (2016)
Publ. Version/Full Text Research data Research data DOI
Open Access Gold
Creative Commons Lizenzvertrag
The myogenic regulatory factor MRF4 is highly expressed in adult skeletal muscle but its function is unknown. Here we show that Mrf4 knockdown in adult muscle induces hypertrophy and prevents denervation-induced atrophy. This effect is accompanied by increased protein synthesis and widespread activation of muscle-specific genes, many of which are targets of MEF2 transcription factors. MEF2-dependent genes represent the top-ranking gene set enriched after Mrf4 RNAi and a MEF2 reporter is inhibited by co-transfected MRF4 and activated by Mrf4 RNAi. The Mrf4 RNAi-dependent increase in fibre size is prevented by dominant negative MEF2, while constitutively active MEF2 is able to induce myofibre hypertrophy. The nuclear localization of the MEF2 corepressor HDAC4 is impaired by Mrf4 knockdown, suggesting that MRF4 acts by stabilizing a repressor complex that controls MEF2 activity. These findings open new perspectives in the search for therapeutic targets to prevent muscle wasting, in particular sarcopenia and cachexia.
Additional Metrics?
Edit extra informations Login
Publication type Article: Journal article
Document type Scientific Article
Keywords Myosin Heavy-chain; Transcription Factors; Gene-expression; Heart-failure; Myogenin; Activation; Hdac4; Differentiation; Regeneration; Dysfunction
ISSN (print) / ISBN 2041-1723
e-ISSN 2041-1723
Quellenangaben Volume: 7, Issue: , Pages: , Article Number: 12397 Supplement: ,
Publisher Nature Publishing Group
Publishing Place London
Reviewing status Peer reviewed