PLX163147

GSE112095: Role of SmcHD1 in the establishment of the epigenetic states required for the maintenance of X chromosome inactivation [RNA-seq]

Organsim mouse
Type RNASEQ
Target gene
Project ARCHS4

It has been shown that functional deficiency of SmcHD1, a noncanonical member of SMC family proteins, results in derepression of X-inactivated genes in postimplantation female mouse embryos. In this study, we found that derepression of X-inactivated genes accompanied a local reduction in the enrichment of H3K27me3 in mouse embryonic fibroblasts (MEFs) prepared from female fetuses deficient for SmcHD1. SOURCE: Koji Nagao (nagao@bio.sci.osaka-u.ac.jp) - Obuse Lab. Osaka University

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