| Literature DB >> 28049731 |
Wukui Zhao1, Huan Tong1, Yikai Huang1, Yun Yan1, Huajian Teng1, Yin Xia2, Qing Jiang3, Jinzhong Qin4.
Abstract
The Polycomb group (PcG) proteins have an important role in controlling the expression of key genes implicated in embryonic development, differentiation, and decision of cell fates. Emerging evidence suggests that Polycomb repressive complexes 1 (PRC1) is defined by the six Polycomb group RING finger protein (Pcgf) paralogs, and Pcgf proteins can assemble into noncanonical PRC1 complexes. However, little is known about the precise mechanisms of differently composed noncanonical PRC1 in the maintenance of the pluripotent cell state. Here we disrupt the Pcgf genes in mouse embryonic stem cells by CRISPR-Cas9 and find Pcgf6 null embryonic stem cells display severe defects in self-renewal and differentiation. Furthermore, Pcgf6 regulates genes mostly involved in differentiation and spermatogenesis by assembling a noncanonical PRC1 complex PRC1.6. Notably, Pcgf6 deletion causes a dramatic decrease in PRC1.6 binding to target genes and no loss of H2AK119ub1. Thus, Pcgf6 is essential for recruitment of PRC1.6 to chromatin. Our results reveal a previously uncharacterized, H2AK119ub1-independent chromatin assembly associated with PRC1.6 complex.Entities:
Keywords: Polycomb; chromatin; embryonic stem cell; epigenetics; transcription regulation
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Year: 2017 PMID: 28049731 PMCID: PMC5314173 DOI: 10.1074/jbc.M116.763961
Source DB: PubMed Journal: J Biol Chem ISSN: 0021-9258 Impact factor: 5.157