| Literature DB >> 33104214 |
Hao Du1, Chen Chen1, Yan Wang1, Yang Yang2, Zhuanzhuan Che1, Xiaoxu Liu1, Siyan Meng1, Chenghao Guo1, Manman Xu1, Haitong Fang1, Fengchao Wang3, Chengqi Lin1,4, Zhuojuan Luo1,4.
Abstract
Regulation of RNA stability plays a crucial role in gene expression control. Deadenylation is the initial rate-limiting step for the majority of RNA decay events. Here, we show that RING finger protein 219 (RNF219) interacts with the CCR4-NOT deadenylase complex. RNF219-CCR4-NOT exhibits deadenylation activity in vitro. RNA-seq analyses identify some of the 2-cell-specific genes and the neuronal genes significantly downregulated upon RNF219 knockdown, while upregulated after depletion of the CCR4-NOT subunit CNOT10 in mouse embryonic stem (ES) cells. RNF219 depletion leads to impaired neuronal lineage commitment during ES cell differentiation. Our study suggests that RNF219 is a novel interacting partner of CCR4-NOT and required for maintenance of ES cell pluripotency.Entities:
Keywords: CCR4–NOT; RNF219; deadenylation; protein complex; stem cell differentiation
Mesh:
Substances:
Year: 2020 PMID: 33104214 PMCID: PMC7883825 DOI: 10.1093/jmcb/mjaa061
Source DB: PubMed Journal: J Mol Cell Biol ISSN: 1759-4685 Impact factor: 6.216