Spatio-temporal coordination of cell cycle exit, fusion and differentiation of adult muscle precursors by Drosophila Erect wing (Ewg)

Mech Dev. 2016 Aug:141:109-118. doi: 10.1016/j.mod.2016.03.004. Epub 2016 Mar 31.

Abstract

The mechanisms of cell cycle exit by myoblasts during skeletal muscle development are poorly understood. Cell cycle arrest is known to be a prerequisite for myoblast fusion and subsequent differentiation. Despite tremendous knowledge on myoblast fusion and differentiation, tissue-specific factors that spatio-temporally regulate the cell cycle exit are not well known. In this paper, we show that the transcriptional factor/co-activator "Erect wing" (Ewg) synchronises myoblast cell cycle exit with that of the fusion process. Ewg-null myoblasts show delayed temporal development of dorsal longitudinal muscles (DLMs), a group of indirect flight muscles (IFMs), which culminates to abnormal and asymmetric muscle pattern. A role for Ewg in cell cycle exit at G1/S stage is also shown. Reducing Cyclin E dose in Ewg-null mutant rescues the lack of IFMs and flight ability. Thus, we show that Ewg repression of Cyclin E expression is required for the arrest of myoblast proliferation and initiate myoblast fusion and terminal differentiation.

Keywords: Cyclin E; Drosophila; Erect wing; Muscle development; NRF-1.

MeSH terms

  • Animals
  • Cell Cycle Checkpoints / genetics
  • Cell Differentiation / genetics
  • Cyclin E / genetics*
  • Drosophila Proteins / genetics*
  • Drosophila melanogaster / genetics
  • Drosophila melanogaster / growth & development*
  • Muscle Development / genetics
  • Myoblasts / metabolism
  • Neuropeptides / genetics*
  • Transcription Factors / genetics*
  • Wings, Animal / growth & development*
  • Wings, Animal / metabolism

Substances

  • Cyclin E
  • Drosophila Proteins
  • EWG protein, Drosophila
  • Neuropeptides
  • Transcription Factors