Myogenic microRNA expression requires ATP-dependent chromatin remodeling enzyme function

Mol Cell Biol. 2010 Jul;30(13):3176-86. doi: 10.1128/MCB.00214-10. Epub 2010 Apr 26.

Abstract

Knockdown of the Brg1 ATPase subunit of SWI/SNF chromatin remodeling enzymes in developing zebrafish caused stunted tail formation and altered sarcomeric actin organization, which phenocopies the loss of the microRNA processing enzyme Dicer, or the knockdown of myogenic microRNAs. Furthermore, myogenic microRNA expression and differentiation was blocked in Brg1 conditional myoblasts differentiated ex vivo. The binding of Brg1 upstream of myogenic microRNA sequences correlated with MyoD binding and accessible chromatin structure in satellite cells and myofibers, and it was required for chromatin accessibility and microRNA expression in a tissue culture model for myogenesis. The results implicate ATP-dependent chromatin remodelers in myogenic microRNA gene regulation.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adaptor Proteins, Signal Transducing
  • Adenosine Triphosphate / metabolism*
  • Animals
  • Cells, Cultured
  • Chromatin / metabolism*
  • Chromatin Assembly and Disassembly*
  • DNA Helicases / genetics
  • DNA Helicases / metabolism*
  • Gene Expression Regulation
  • Mice
  • Mice, Inbred C57BL
  • MicroRNAs / genetics
  • MicroRNAs / metabolism*
  • Muscle Development / genetics*
  • Myoblasts / cytology
  • Myoblasts / physiology
  • Nuclear Proteins / genetics
  • Nuclear Proteins / metabolism*
  • Oligonucleotides, Antisense / genetics
  • Oligonucleotides, Antisense / metabolism
  • Ribonuclease III / genetics
  • Ribonuclease III / metabolism
  • Transcription Factors / genetics
  • Transcription Factors / metabolism*
  • Zebrafish / anatomy & histology
  • Zebrafish / embryology
  • Zebrafish / genetics
  • Zebrafish Proteins / genetics
  • Zebrafish Proteins / metabolism*

Substances

  • Adaptor Proteins, Signal Transducing
  • Chromatin
  • MicroRNAs
  • Nuclear Proteins
  • Oligonucleotides, Antisense
  • Transcription Factors
  • Zebrafish Proteins
  • smarca4a protein, zebrafish
  • Adenosine Triphosphate
  • Ribonuclease III
  • Smarca4 protein, mouse
  • DNA Helicases