Species differences in TSIX/Tsix reveal the roles of these genes in X-chromosome inactivation.
Ontology highlight
ABSTRACT: Transcriptional silencing of the human inactive X chromosome is induced by the XIST gene within the human X-inactivation center. The XIST allele must be turned off on one X chromosome to maintain its activity in cells of both sexes. In the mouse placenta, where X inactivation is imprinted (the paternal X chromosome is always inactive), the maternal Xist allele is repressed by a cis-acting antisense transcript, encoded by the Tsix gene. However, it remains to be seen whether this antisense transcript protects the future active X chromosome during random inactivation in the embryo proper. We recently identified the human TSIX gene and showed that it lacks key regulatory elements needed for the imprinting function of murine Tsix. Now, using RNA FISH for cellular localization of transcripts in
SUBMITTER: Migeon BR
PROVIDER: S-EPMC379161 | biostudies-literature | 2002 Aug
REPOSITORIES: biostudies-literature
ACCESS DATA