| Literature DB >> 30428357 |
Natasha Jansz1, Tatyana Nesterova2, Andrew Keniry1, Megan Iminitoff3, Peter F Hickey1, Greta Pintacuda2, Osamu Masui4, Simon Kobelke5, Niall Geoghegan1, Kelsey A Breslin3, Tracy A Willson3, Kelly Rogers1, Graham F Kay6, Archa H Fox5, Haruhiko Koseki4, Neil Brockdorff2, James M Murphy1, Marnie E Blewitt7.
Abstract
We and others have recently reported that the SMC protein Smchd1 is a regulator of chromosome conformation. Smchd1 is critical for the structure of the inactive X chromosome and at autosomal targets such as the Hox genes. However, it is unknown how Smchd1 is recruited to these sites. Here, we report that Smchd1 localizes to the inactive X via the Xist-HnrnpK-PRC1 (polycomb repressive complex 1) pathway. Contrary to previous reports, Smchd1 does not bind Xist or other RNA molecules with any specificity. Rather, the localization of Smchd1 to the inactive X is H2AK119ub dependent. Following perturbation of this interaction, Smchd1 is destabilized, which has consequences for gene silencing genome-wide. Our work adds Smchd1 to the PRC1 silencing pathway for X chromosome inactivation.Entities:
Keywords: Hnrnpk; PRC1; Ring1B; Smchd1; X inactivation; Xist
Year: 2018 PMID: 30428357 DOI: 10.1016/j.celrep.2018.10.044
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423