X-Chromosome Kiss and Tell: How the Xs Go Their Separate Ways

  1. M.C. ANGUERA,
  2. B.K. SUN,
  3. N. XU, and
  4. J.T. LEE
  1. Howard Hughes Medical Institute, Department of Molecular Biology, Massachusetts General Hospital, Department of Genetics, Harvard Medical School, Boston, Massachusetts 02114

Abstract

Loci associated with noncoding RNAs have important roles in X-chromosome inactivation (XCI), the dosage compensationmechanism by which one of two X chromosomes in female cells becomes transcriptionally silenced. The Xs start out asepigenetically equivalent chromosomes, but XCI requires a cell to treat two identical X chromosomes in completely differentways: One X chromosome must remain transcriptionally active while the other becomes repressed. In the embryo of eutherianmammals, the choice to inactivate the maternal or paternal X chromosome is random. The fact that the Xs always adoptopposite fates hints at the existence of a trans-sensing mechanism to ensure the mutually exclusive silencing of one of thetwo Xs. This paper highlights recent evidence supporting a model for mutually exclusive choice that involves homologouschromosome pairing and the placement of asymmetric chromatin marks on the two Xs.

Footnotes

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