Negative elongation factor regulates muscle progenitor expansion for efficient myofiber repair and stem cell pool repopulation

Dev Cell. 2021 Apr 5;56(7):1014-1029.e7. doi: 10.1016/j.devcel.2021.02.025. Epub 2021 Mar 17.

Abstract

Negative elongation factor (NELF) is a critical transcriptional regulator that stabilizes paused RNA polymerase to permit rapid gene expression changes in response to environmental cues. Although NELF is essential for embryonic development, its role in adult stem cells remains unclear. In this study, through a muscle-stem-cell-specific deletion, we showed that NELF is required for efficient muscle regeneration and stem cell pool replenishment. In mechanistic studies using PRO-seq, single-cell trajectory analyses and myofiber cultures revealed that NELF works at a specific stage of regeneration whereby it modulates p53 signaling to permit massive expansion of muscle progenitors. Strikingly, transplantation experiments indicated that these progenitors are also necessary for stem cell pool repopulation, implying that they are able to return to quiescence. Thus, we identified a critical role for NELF in the expansion of muscle progenitors in response to injury and revealed that progenitors returning to quiescence are major contributors to the stem cell pool repopulation.

Keywords: NELF; PEDF signaling; muscle regeneration; muscle stem cells; nascent transcript stability; p53 signaling; promoter proximal pausing; stem cell niche; stem cell self-renewal; transcriptional regulation.

Publication types

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

MeSH terms

  • Animals
  • Cell Differentiation
  • Cells, Cultured
  • Eye Proteins / metabolism
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Muscle Development
  • Muscle, Skeletal / physiology*
  • Nerve Growth Factors / metabolism
  • Regeneration / genetics
  • Satellite Cells, Skeletal Muscle / cytology
  • Satellite Cells, Skeletal Muscle / metabolism
  • Satellite Cells, Skeletal Muscle / physiology*
  • Satellite Cells, Skeletal Muscle / transplantation
  • Serpins / metabolism
  • Signal Transduction
  • Transcription Factors / genetics
  • Transcription Factors / physiology*
  • Transcriptome
  • Tumor Suppressor Protein p53 / metabolism

Substances

  • Eye Proteins
  • Nerve Growth Factors
  • Serpins
  • Transcription Factors
  • Trp53 protein, mouse
  • Tumor Suppressor Protein p53
  • negative elongation factor
  • pigment epithelium-derived factor