Santos-Rosa Helena, Kirmizis Antonis, Nelson Christopher, Bartke Till, Saksouk Nehme, Cote Jacques, Kouzarides Tony
Gurdon Institute and Department of Pathology, Tennis Court Road, Cambridge CB2 1QN, UK.
Nat Struct Mol Biol. 2009 Jan;16(1):17-22. doi: 10.1038/nsmb.1534. Epub 2008 Dec 14.
Induction of gene expression in yeast and human cells involves changes in the histone modifications associated with promoters. Here we identify a histone H3 endopeptidase activity in Saccharomyces cerevisiae that may regulate these events. The endopeptidase cleaves H3 after Ala21, generating a histone that lacks the first 21 residues and shows a preference for H3 tails carrying repressive modifications. In vivo, the H3 N terminus is clipped, specifically within the promoters of genes following the induction of transcription. H3 clipping precedes the process of histone eviction seen when genes become fully active. A truncated H3 product is not generated in yeast carrying a mutation of the endopeptidase recognition site (H3 Q19A L20A) and gene induction is defective in these cells. These findings identify clipping of H3 tails as a previously uncharacterized modification of promoter-bound nucleosomes, which may result in the localized clearing of repressive signals during the induction of gene expression.
酵母和人类细胞中基因表达的诱导涉及与启动子相关的组蛋白修饰的变化。在这里,我们在酿酒酵母中鉴定出一种组蛋白H3内肽酶活性,它可能调节这些事件。该内肽酶在Ala21之后切割H3,产生一种缺少前21个残基的组蛋白,并且对携带抑制性修饰的H3尾巴表现出偏好。在体内,H3的N末端被剪切,特别是在转录诱导后基因的启动子内。H3剪切先于基因完全激活时观察到的组蛋白驱逐过程。在携带内肽酶识别位点突变(H3 Q19A L20A)的酵母中不会产生截短的H3产物,并且这些细胞中的基因诱导存在缺陷。这些发现将H3尾巴的剪切确定为启动子结合核小体的一种以前未被表征的修饰,这可能导致基因表达诱导过程中抑制信号的局部清除。