1. Tsix-deficient X chromosome does not undergo inactivation in the embryonic lineage in males: implications for Tsix-independent silencing of Xist
- Author
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Tatsuya Ohhata, Hiroyuki Sasaki, Yuko Hoki, and Takashi Sado
- Subjects
Regulation of gene expression ,Genetics ,Lineage (genetic) ,Somatic cell ,XIST ,Tsix ,Biology ,Molecular Biology ,Skewed X-inactivation ,Genetics (clinical) ,X-inactivation ,X chromosome - Abstract
Differential induction of the X-linked non-coding Xist gene is a key event in the process of X inactivation occurring in female mammalian embryos. Xist is negatively regulated in cis by its antisense gene Tsix through modification of the chromatin structure. The maternal Xist allele, which is normally silent in the extraembryonic lineages, is ectopically activated when Tsix is disrupted on the same chromosome, and subsequently the maternal X chromosome undergoes inactivation in the extraembryonic lineages even in males. However, it is still unknown whether the single Tsix-deficient X chromosome (XΔTsix) in males is also inactivated in the embryonic lineage. Here, we show that both male and female embryos carrying a maternally derived XΔTsix could survive if the extraembryonic tissues were complemented by wild-type tetraploid cells. In addition, Xist on the XΔTsix was properly silenced and methylated at CpG sites in adult male somatic cells. These results indicate that the embryonic lethality caused by the maternal XΔTsix is solely attributable to the defects in the extraembryonic lineages. XΔTsix does not seem to undergo inactivation in the embryonic lineage in males, suggesting the presence of a Tsix-independent silencing mechanism for Xist in the embryonic lineage.
- Published
- 2006
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