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
EMBL, Gene Expression Programme, Meyerhofstr. 1, 69117 Heidelberg, Germany.
Cell. 2002 Oct 18;111(2):197-208. doi: 10.1016/s0092-8674(02)00976-5.
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.
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。