Xce haplotypes show modified methylation in a region of the active X chromosome lying 3' to Xist

Proc Natl Acad Sci U S A. 1995 Apr 11;92(8):3531-5. doi: 10.1073/pnas.92.8.3531.

Abstract

During early mammalian embryogenesis, one of the two X chromosomes in somatic cells of the female becomes inactivated through a process that is thought to depend on a unique initiator region, the X-chromosome inactivation center (Xic). The recently characterized Xist sequence (X-inactive-specific transcript) is thought to be a possible candidate for Xic. In mice a further genetic element, the X chromosome-controlling element (Xce), is also known to influence the choice of which of the two X chromosomes is inactivated. We report that a region of the mouse X chromosome lying 15 kb distal to Xist contains several sites that show hypermethylation specifically associated with the active X chromosome. Analysis of this region in various Xce strains has revealed a correlation between the strength of the Xce allele carried and the methylation status of this region. We propose that such a region could be involved in the initial stages of the inactivation process and in particular in the choice of which of the two X chromosomes present in a female cell will be inactivated.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • DNA / metabolism
  • DNA Restriction-Modification Enzymes / metabolism*
  • Deoxyribonuclease HpaII
  • Deoxyribonucleases, Type II Site-Specific / metabolism
  • Dosage Compensation, Genetic*
  • Female
  • Genetic Variation
  • Haplotypes
  • Male
  • Methylation
  • Mice
  • Mice, Inbred Strains
  • Phosphoglycerate Kinase / genetics
  • RNA, Long Noncoding
  • RNA, Untranslated*
  • Regulatory Sequences, Nucleic Acid / genetics*
  • Restriction Mapping
  • Sex Differentiation / genetics
  • Species Specificity
  • Transcription Factors / genetics*
  • X Chromosome / genetics*

Substances

  • DNA Restriction-Modification Enzymes
  • RNA, Long Noncoding
  • RNA, Untranslated
  • Transcription Factors
  • XIST non-coding RNA
  • DNA
  • Phosphoglycerate Kinase
  • Deoxyribonuclease HpaII
  • Deoxyribonucleases, Type II Site-Specific
  • GTCGAC-specific type II deoxyribonucleases