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The histone H2A deubiquitinase Usp16 regulates embryonic stem cell gene expression and lineage commitment

机译:组蛋白H2A去泛素酶Usp16调节胚胎干细胞基因表达和谱系承诺

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Polycomb Repressive Complex 1 and histone H2A ubiquitination (ubH2A) contribute to embryonic stem cell (ESC) pluripotency by repressing lineage-specific gene expression. However, whether active deubiquitination co-regulates ubH2A levels in ESCs and during differentiation is not known. Here we report that Usp16 , a histone H2A deubiquitinase, regulates H2A deubiquitination and gene expression in ESCs, and importantly, is required for ESC differentiation. Usp16 knockout is embryonic lethal in mice, but does not affect ESC viability or identity. Usp16 binds to the promoter regions of a large number of genes in ESCs, and Usp16 binding is inversely correlated with ubH2A levels, and positively correlates with gene expression levels. Intriguingly, Usp16 sup?/?/sup ESCs fail to differentiate due to ubH2A-mediated repression of lineage-specific genes. Finally, Usp16 , but not a catalytically inactive mutant, rescues the differentiation defects of Usp16 sup?/?/sup ESCs. Therefore, this study identifies Usp16 and H2A deubiquitination as critical regulators of ESC gene expression and differentiation.
机译:Polycomb Repressive Complex 1和组蛋白H2A泛素化(ubH2A)通过抑制谱系特异性基因表达来促进胚胎干细胞(ESC)的多能性。但是,尚不知道主动去泛素化是否会共同调节ESC和分化过程中的ubH2A水平。在这里我们报告说,Usp16,组蛋白H2A去泛素酶,调节ESC中的H2A去泛素化和基因表达,并且重要的是,ESC分化是必需的。 Usp16基因敲除对小鼠具有胚胎致死性,但不影响ESC的生存力或特性。 Usp16与ESC中大量基因的启动子区域结合,而Usp16结合与ubH2A水平成反比,与基因表达水平成正比。有趣的是,由于ubH2A介导的谱系特异性基因的阻遏,Usp16 ?/? ESC无法分化。最后,Usp16(不是催化失活的突变体)可以挽救Usp16 ?/? ESC的分化缺陷。因此,本研究确定Usp16和H2A去泛素化是ESC基因表达和分化的关键调控因子。

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