Epigenetic regulation of male fate commitment from an initially bipotential system

Mol Cell Endocrinol. 2018 Jun 15:468:19-30. doi: 10.1016/j.mce.2018.01.009. Epub 2018 Feb 2.

Abstract

A fundamental goal in biology is to understand how distinct cell types containing the same genetic information arise from a single stem cell throughout development. Sex determination is a key developmental process that requires a unidirectional commitment of an initially bipotential gonad towards either the male or female fate. This makes sex determination a unique model to study cell fate commitment and differentiation in vivo. We have focused this review on the accumulating evidence that epigenetic mechanisms contribute to the bipotential state of the fetal gonad and to the regulation of chromatin accessibility during and immediately downstream of the primary sex-determining switch that establishes the male fate.

Keywords: Cell fate commitment; Development; Epigenetics; Gonad; Plasticity; Sex determination.

Publication types

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

MeSH terms

  • Animals
  • Chromatin / metabolism
  • DNA Methylation / genetics
  • Epigenesis, Genetic*
  • Genes, sry
  • Histones / metabolism
  • Male
  • SOX Transcription Factors / genetics
  • SOX Transcription Factors / metabolism

Substances

  • Chromatin
  • Histones
  • SOX Transcription Factors