SPT6 promotes epidermal differentiation and blockade of an intestinal-like phenotype through control of transcriptional elongation

Nat Commun. 2021 Feb 4;12(1):784. doi: 10.1038/s41467-021-21067-w.

Abstract

In adult tissue, stem and progenitor cells must tightly regulate the balance between proliferation and differentiation to sustain homeostasis. How this exquisite balance is achieved is an area of active investigation. Here, we show that epidermal genes, including ~30% of induced differentiation genes already contain stalled Pol II at the promoters in epidermal stem and progenitor cells which is then released into productive transcription elongation upon differentiation. Central to this process are SPT6 and PAF1 which are necessary for the elongation of these differentiation genes. Upon SPT6 or PAF1 depletion there is a loss of human skin differentiation and stratification. Unexpectedly, loss of SPT6 also causes the spontaneous transdifferentiation of epidermal cells into an intestinal-like phenotype due to the stalled transcription of the master regulator of epidermal fate P63. Our findings suggest that control of transcription elongation through SPT6 plays a prominent role in adult somatic tissue differentiation and the inhibition of alternative cell fate choices.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Adult Stem Cells / physiology
  • Cell Differentiation / genetics*
  • Cell Transdifferentiation / genetics
  • Cells, Cultured
  • Chromatin Immunoprecipitation Sequencing
  • Epidermis / physiology*
  • Gene Knockdown Techniques
  • Humans
  • Infant, Newborn
  • Keratinocytes
  • Male
  • Primary Cell Culture
  • Promoter Regions, Genetic
  • RNA Polymerase II / metabolism
  • RNA, Small Interfering / metabolism
  • RNA-Seq
  • Tissue Culture Techniques
  • Transcription Elongation, Genetic*
  • Transcription Factors / genetics
  • Transcription Factors / metabolism*
  • Tumor Suppressor Proteins / metabolism

Substances

  • PAF1 protein, human
  • RNA, Small Interfering
  • SUPT6H protein, human
  • TP63 protein, human
  • Transcription Factors
  • Tumor Suppressor Proteins
  • RNA Polymerase II