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由“氪石”组蛋白H3甲基转移酶调控CpNpG DNA甲基化

Control of CpNpG DNA methylation by the KRYPTONITE histone H3 methyltransferase.

作者信息

Jackson James P, Lindroth Anders M, Cao Xiaofeng, Jacobsen Steven E

机构信息

Department of Molecular, Cell and Developmental Biology, University of California, Los Angeles 90095, USA.

出版信息

Nature. 2002 Apr 4;416(6880):556-60. doi: 10.1038/nature731. Epub 2002 Mar 17.

Abstract

Gene silencing in eukaryotes is associated with the formation of heterochromatin, a complex of proteins and DNA that block transcription. Heterochromatin is characterized by the methylation of cytosine nucleotides of the DNA, the methylation of histone H3 at lysine 9 (H3 Lys 9), and the specific binding of heterochromatin protein 1 (HP1) to methylated H3 Lys 9 (refs 1-7). Although the relationship between these chromatin modifications is generally unknown, in the fungus Neurospora crassa, DNA methylation acts genetically downstream of H3 Lys 9 methylation. Here we report the isolation of KRYPTONITE, a methyltransferase gene specific to H3 Lys 9, identified in a mutant screen for suppressors of gene silencing at the Arabidopsis thaliana SUPERMAN (SUP) locus. Loss-of-function kryptonite alleles resemble mutants in the DNA methyltransferase gene CHROMOMETHYLASE3 (CMT3), showing loss of cytosine methylation at sites of CpNpG trinucleotides (where N is A, C, G or T) and reactivation of endogenous retrotransposon sequences. We show that CMT3 interacts with an Arabidopsis homologue of HP1, which in turn interacts with methylated histones. These data suggest that CpNpG DNA methylation is controlled by histone H3 Lys 9 methylation, through interaction of CMT3 with methylated chromatin.

摘要

真核生物中的基因沉默与异染色质的形成有关,异染色质是一种由蛋白质和DNA组成的复合体,可阻断转录。异染色质的特征在于DNA胞嘧啶核苷酸的甲基化、组蛋白H3赖氨酸9(H3 Lys 9)的甲基化以及异染色质蛋白1(HP1)与甲基化的H3 Lys 9的特异性结合(参考文献1 - 7)。虽然这些染色质修饰之间的关系通常尚不清楚,但在真菌粗糙脉孢菌中,DNA甲基化在H3 Lys 9甲基化的遗传下游起作用。在这里,我们报告了KRYPTONITE的分离,它是一种H3 Lys 9特异性甲基转移酶基因,在拟南芥SUPERMAN(SUP)基因座的基因沉默抑制子突变体筛选中被鉴定出来。功能缺失的kryptonite等位基因类似于DNA甲基转移酶基因CHROMOMETHYLASE3(CMT3)中的突变体,在CpNpG三核苷酸位点(其中N为A、C、G或T)显示胞嘧啶甲基化缺失以及内源性逆转座子序列的重新激活。我们表明CMT3与HP1的拟南芥同源物相互作用,而该同源物又与甲基化组蛋白相互作用。这些数据表明,通过CMT3与甲基化染色质的相互作用,CpNpG DNA甲基化受组蛋白H3 Lys 9甲基化的控制。

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