Mammalian X-chromosome inactivation and the XIST gene

Curr Opin Genet Dev. 1992 Jun;2(3):439-47. doi: 10.1016/s0959-437x(05)80155-8.

Abstract

X-chromosome inactivation is a unique developmental event that results in the cis-limited transcriptional inactivation of most genes on one of the two X chromosomes in female mammals. Studies in both human and mouse have demonstrated that X inactivation requires the presence in cis of a locus, the X-inactivation center, that is thought to be involved in the initiation and/or spreading of the inactivation signal in early development. Identification and characterization of a gene, XIST, which is located at or near the X-inactivation center and which is expressed specifically from the inactive X chromosome in both humans and mouse, suggests that it may be involved in X inactivation.

Publication types

  • Research Support, U.S. Gov't, P.H.S.
  • Review

MeSH terms

  • Animals
  • Chromatin / physiology
  • Chromosome Mapping
  • DNA / metabolism
  • Dosage Compensation, Genetic*
  • Humans
  • Methylation
  • Mice

Substances

  • Chromatin
  • DNA