Stabilization of Xist RNA mediates initiation of X chromosome inactivation

Cell. 1997 Oct 3;91(1):99-107. doi: 10.1016/s0092-8674(01)80012-x.

Abstract

The onset of X inactivation is preceded by a marked increase in the level of Xist RNA. Here we demonstrate that increased stability of Xist RNA is the primary determinant of developmental up-regulation. Unstable transcript is produced by both alleles in XX ES cells and in XX embryos prior to the onset of random X inactivation. Following differentiation, transcription of unstable RNA from the active X chromosome allele continues for a period following stabilization and accumulation of transcript on the inactive X allele. We discuss the implications of these findings in terms of models for the initiation of random and imprinted X inactivation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alleles
  • Animals
  • Blastocyst
  • Cell Differentiation
  • Cells, Cultured
  • Dactinomycin / pharmacology
  • Dosage Compensation, Genetic*
  • Female
  • Gene Expression Regulation / physiology
  • Male
  • Mice
  • Models, Genetic
  • Nucleic Acid Synthesis Inhibitors / pharmacology
  • RNA, Long Noncoding
  • RNA, Messenger / biosynthesis
  • RNA, Messenger / metabolism*
  • RNA, Untranslated*
  • Stem Cells
  • Transcription Factors / genetics*
  • Transcription, Genetic / physiology

Substances

  • Nucleic Acid Synthesis Inhibitors
  • RNA, Long Noncoding
  • RNA, Messenger
  • RNA, Untranslated
  • Transcription Factors
  • XIST non-coding RNA
  • Dactinomycin