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.
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
Chemicals
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
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Courtier B
Unité de Génétique Moléculaire Murine, Institut Pasteur, Paris, France.
Heard E
Avner P
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