Npac Is A Co-factor of Histone H3K36me3 and Regulates Transcriptional Elongation in Mouse Embryonic Stem Cells
- Author:
Yu SUE
1
;
Li JIA
;
Ji GUANXU
;
Ng Long ZHEN
;
Siew JIAMIN
;
Lo Ning WAN
;
Ye YING
;
Chew Yuan YUAN
;
Long Chau YUN
;
Zhang WENSHENG
;
Guccione ERNESTO
;
Loh Han YUIN
;
Jiang ZHI-HONG
;
Yang HENRY
;
Wu QIANG
Author Information
1. Department of Biochemistry,Yong Loo Lin School of Medicine,National University of Singapore,Singapore 117597,Singapore
- Keywords:
Npac;
Pluripotency;
Reprogramming;
Histone H3K36me3;
Transcriptional elongation
- From:
Genomics, Proteomics & Bioinformatics
2022;20(1):110-128
- CountryChina
- Language:Chinese
-
Abstract:
Chromatin modification contributes to pluripotency maintenance in embryonic stem cells(ESCs).However,the related mechanisms remain obscure.Here,we show that Npac,a"reader"of histone H3 lysine 36 trimethylation(H3K36me3),is required to maintain mouse ESC(mESC)pluripotency since knockdown of Npac causes mESC differentiation.Depletion of Npac in mouse embryonic fibroblasts(MEFs)inhibits reprogramming efficiency.Furthermore,our chromatin immunoprecipitation followed by sequencing(ChIP-seq)results of Npac reveal that Npac co-localizes with histone H3K36me3 in gene bodies of actively transcribed genes in mESCs.Interestingly,we find that Npac interacts with positive transcription elongation factor b(p-TEFb),Ser2-phosphorylated RNA Pol Ⅱ(RNA Pol Ⅱ Ser2P),and Ser5-phosphorylated RNA Pol Ⅱ(RNA Pol Ⅱ Ser5P).Furthermore,depletion of Npac disrupts transcriptional elongation of the pluripotency genes Nanog and Rifl.Taken together,we propose that Npac is essential for the transcriptional elongation of pluripotency genes by recruiting p-TEFb and interact-ing with RNA Pol Ⅱ Ser2P and Ser5P.
