果蝇多梳蛋白家族抑制复合物的组蛋白甲基转移酶活性

Histone methyltransferase activity of a Drosophila Polycomb group repressor complex.

作者信息

Müller Jürg, Hart Craig M, Francis Nicole J, Vargas Marcus L, Sengupta Aditya, Wild Brigitte, Miller Ellen L, O'Connor Michael B, Kingston Robert E, Simon Jeffrey A

机构信息

EMBL, Gene Expression Programme, Meyerhofstr. 1, 69117 Heidelberg, Germany.

出版信息

Cell. 2002 Oct 18;111(2):197-208. doi: 10.1016/s0092-8674(02)00976-5.

Abstract

Polycomb group (PcG) proteins maintain transcriptional repression during development, likely by creating repressive chromatin states. The Extra Sex Combs (ESC) and Enhancer of Zeste [E(Z)] proteins are partners in an essential PcG complex, but its full composition and biochemical activities are not known. A SET domain in E(Z) suggests this complex might methylate histones. We purified an ESC-E(Z) complex from Drosophila embryos and found four major subunits: ESC, E(Z), NURF-55, and the PcG repressor, SU(Z)12. A recombinant complex reconstituted from these four subunits methylates lysine-27 of histone H3. Mutations in the E(Z) SET domain disrupt methyltransferase activity in vitro and HOX gene repression in vivo. These results identify E(Z) as a PcG protein with enzymatic activity and implicate histone methylation in PcG-mediated silencing.

摘要

多梳蛋白家族(PcG)蛋白可能通过形成抑制性染色质状态,在发育过程中维持转录抑制。额外性梳(ESC)蛋白和增强子结合蛋白 [E(Z)] 是一种重要的PcG复合物中的伙伴,但该复合物的完整组成和生化活性尚不清楚。E(Z) 中的一个SET结构域表明该复合物可能使组蛋白甲基化。我们从果蝇胚胎中纯化了一种ESC-E(Z) 复合物,发现了四个主要亚基:ESC、E(Z)、NURF-55和PcG阻遏物SU(Z)12。由这四个亚基重构的重组复合物使组蛋白H3的赖氨酸-27甲基化。E(Z) SET结构域中的突变在体外破坏甲基转移酶活性,在体内破坏HOX基因抑制。这些结果确定E(Z) 是一种具有酶活性的PcG蛋白,并表明组蛋白甲基化参与PcG介导的沉默作用。

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