NCAPG Dynamically Coordinates the Myogenesis of Fetal Bovine Tissue by Adjusting Chromatin Accessibility

Int J Mol Sci. 2020 Feb 13;21(4):1248. doi: 10.3390/ijms21041248.

Abstract

NCAPG is a subunit of condensin I that plays a crucial role in chromatin condensation during mitosis. NCAPG has been demonstrated to be associated with farm animal growth traits. However, its role in regulating myoblast differentiation is still unclear. We used myoblasts derived from fetal bovine tissue as an in vitro model and found that NCAPG was expressed during myogenic differentiation in the cytoplasm and nucleus. Silencing NCAPG prolonged the mitosis and impaired the differentiation due to increased myoblast apoptosis. After 1.5 days of differentiation, silencing NCAPG enhanced muscle-specific gene expression. An assay for transposase-accessible chromatin- high throughput sequencing (ATAC-seq) revealed that silencing NCAPG altered chromatin accessibility to activating protein 1 (AP-1) and its subunits. Knocking down the expression of the AP-1 subunits fos-related antigen 2 (FOSL2) or junB proto-oncogene (JUNB) enhanced part of the muscle-specific gene expression. In conclusion, our data provide valuable evidence about NCAPG's function in myogenesis, as well as its potential role in gene expression.

Keywords: AP-1; NCAPG; bovine myoblasts; chromatin accessibility; myogenesis.

MeSH terms

  • Animals
  • Cattle
  • Cell Cycle Proteins / genetics*
  • Cell Differentiation / genetics
  • Chromatin / genetics
  • Fetal Development / genetics*
  • Fetus / metabolism
  • Fos-Related Antigen-2 / genetics*
  • High-Throughput Nucleotide Sequencing
  • Humans
  • Mitosis / genetics
  • Muscle Development / genetics*
  • Myoblasts / metabolism
  • Proto-Oncogene Mas
  • Transcription Factor AP-1 / genetics*
  • Transcription Factors / genetics*
  • Transposases / genetics

Substances

  • Cell Cycle Proteins
  • Chromatin
  • FOSL2 protein, human
  • Fos-Related Antigen-2
  • JunB protein, human
  • MAS1 protein, human
  • NCAPG protein, human
  • Proto-Oncogene Mas
  • Transcription Factor AP-1
  • Transcription Factors
  • Transposases