Acetylation is important for MyoD function in adult mice

  • Arnaud Duquet
  • , Anna Polesskaya
  • , Sylvain Cuvellier
  • , Slimane Ait-Si-Ali
  • , Patrick Héry
  • , Linda L. Pritchard
  • , Matthieu Gerard
  • , Annick Harel-Bellan

Research output: Contribution to journalArticlepeer-review

Abstract

Acetylation is a post-translational modification that influences the activity of numerous proteins in vitro. Among them, the myogenic transcription factor MyoD shows an increased transcriptional activity in vitro when acetylated on two lysines (K): lysines 99 and 102. Here, we have investigated the biological relevance of this acetylation in vivo. Using specific antibodies, we show that endogenous MyoD is acetylated on lysines 99 and 102 in myoblasts. Moreover, we show the functional importance of acetylation in live animals by using a mutant of MyoD in which lysines 99 and 102 were replaced by arginines (R). Knock-in embryos homozygous for the MyoDR99,102 allele expressed slightly reduced levels of MyoD but developed normally. However, the knock-in homozygous adult mice showed a phenotype that was almost identical to that of MyoD-knockout animals, including delayed muscle regeneration in vivo and an increased number of myoblasts but with reduced differentiation potential in vitro. Together, these results show the importance of MyoD acetylation for adult myogenesis.

Original languageEnglish
Pages (from-to)1140-1146
Number of pages7
JournalEMBO Reports
Volume7
Issue number11
DOIs
Publication statusPublished - 1 Nov 2006
Externally publishedYes

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