Regulation of X-linked gene expression during early mouse development by

• Main Authors: Wang, Feng (Author), Shin, JongDae (Author), Shea, Jeremy M (Author), Yu, Jun (Author), Bošković, Ana (Author), Byron, Meg (Author), Zhu, Xiaochun (Author), Lawrence, Jeanne B (Author), Torres, Eduardo M (Author), Zhu, Lihua J (Author), Rando, Oliver J (Author), Bach, Ingolf (Author), Shalek, Alexander K (Contributor), Regev, Aviv (Contributor)
• Other Authors: Institute for Medical Engineering and Science (Contributor), Massachusetts Institute of Technology. Department of Biology (Contributor), Massachusetts Institute of Technology. Department of Chemistry (Contributor), Ragon Institute of MGH, MIT and Harvard (Contributor)
• Format: Article
• Language: English
• Published: eLife Sciences Publications, Ltd., 2017-05-02T13:33:16Z.
• Subjects: Article
• Online Access: Get fulltext

Mammalian X-linked gene expression is highly regulated as female cells contain two and male one X chromosome (X). To adjust the X gene dosage between genders, female mouse preimplantation embryos undergo an imprinted form of X chromosome inactivation (iXCI) that requires both Rlim (also known as Rnf12) and the long non-coding RNA Xist. Moreover, it is thought that gene expression from the single active X is upregulated to correct for bi-allelic autosomal (A) gene expression. We have combined mouse genetics with RNA-seq on single mouse embryos to investigate functions of Rlim on the temporal regulation of iXCI and Xist. Our results reveal crucial roles of Rlim for the maintenance of high Xist RNA levels, Xist clouds and X-silencing in female embryos at blastocyst stages, while initial Xist expression appears Rlim-independent. We find further that X/A upregulation is initiated in early male and female preimplantation embryos.