The murine Xe169 gene escapes X-inactivation like its human homologue

Nat Genet. 1994 Aug;7(4):491-6. doi: 10.1038/ng0894-491.

Abstract

Among a number of genes that escape X-chromosome inactivation in humans, three have been evaluated in mice and unexpectedly all three are subject to X-inactivation. We report here the cloning and expression studies of a novel mouse gene, Xe169, and show that it escapes X-inactivation like its human homologue. Xe169 was assigned to band F2/F3 on the mouse X chromosome by fluorescent in situ hybridization and Southern analysis indicates that the gene is located outside the pseudoautosomal region. Homologous, but divergent, sequences exist on the Y chromosome. In vitro and in vivo studies show that Xe169 is expressed from both the active and the inactive X chromosomes. Xe169 is the first cloned non-pseudoautosomal gene that escapes X-inactivation in mice.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Base Sequence
  • Chromosome Mapping
  • Cloning, Molecular
  • Cricetinae
  • DNA Primers / genetics
  • DNA, Complementary / genetics
  • Dosage Compensation, Genetic*
  • Female
  • Humans
  • In Situ Hybridization, Fluorescence
  • In Vitro Techniques
  • Mice
  • Mice, Inbred C57BL
  • Molecular Sequence Data
  • Muridae
  • Sequence Homology, Nucleic Acid
  • Species Specificity
  • X Chromosome

Substances

  • DNA Primers
  • DNA, Complementary

Associated data

  • GENBANK/L29563
  • GENBANK/L29564