Arid1a-Plagl1-Hh signaling is indispensable for differentiation-associated cell cycle arrest of tooth root progenitors

Cell Rep. 2021 Apr 6;35(1):108964. doi: 10.1016/j.celrep.2021.108964.

Abstract

Chromatin remodelers often show broad expression patterns in multiple cell types yet can elicit cell-specific effects in development and diseases. Arid1a binds DNA and regulates gene expression during tissue development and homeostasis. However, it is unclear how Arid1a achieves its functional specificity in regulating progenitor cells. Using the tooth root as a model, we show that loss of Arid1a impairs the differentiation-associated cell cycle arrest of tooth root progenitors through Hedgehog (Hh) signaling regulation, leading to shortened roots. Our data suggest that Plagl1, as a co-factor, endows Arid1a with its cell-type/spatial functional specificity. Furthermore, we show that loss of Arid1a leads to increased expression of Arid1b, which is also indispensable for odontoblast differentiation but is not involved in regulation of Hh signaling. This study expands our knowledge of the intricate interactions among chromatin remodelers, transcription factors, and signaling molecules during progenitor cell fate determination and lineage commitment.

Keywords: Arid1a; Hh signaling; Plagl1; cell cycle; stem/progenitor cells.

Publication types

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

MeSH terms

  • Animals
  • Cell Cycle Checkpoints*
  • Cell Cycle Proteins / metabolism*
  • Cell Differentiation*
  • Cell Lineage
  • DNA-Binding Proteins / deficiency
  • DNA-Binding Proteins / metabolism*
  • Down-Regulation
  • Genes, Tumor Suppressor
  • Hedgehog Proteins / metabolism*
  • Mice
  • Mice, Inbred C57BL
  • Mice, Transgenic
  • Molar / metabolism
  • Odontoblasts / cytology
  • Odontoblasts / metabolism
  • Protein Binding
  • Signal Transduction*
  • Stem Cells / cytology
  • Stem Cells / metabolism*
  • Tooth Root / cytology*
  • Tooth Root / growth & development
  • Transcription Factors / deficiency
  • Transcription Factors / metabolism*
  • Transcription, Genetic
  • Up-Regulation
  • Zinc Finger Protein GLI1 / genetics
  • Zinc Finger Protein GLI1 / metabolism

Substances

  • Arid1a protein, mouse
  • Cell Cycle Proteins
  • DNA-Binding Proteins
  • Hedgehog Proteins
  • Plagl1 protein, mouse
  • Transcription Factors
  • Zinc Finger Protein GLI1