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ATXR5和ATXR6是染色质结构和基因沉默所需的H3K27单甲基转移酶。

ATXR5 and ATXR6 are H3K27 monomethyltransferases required for chromatin structure and gene silencing.

作者信息

Jacob Yannick, Feng Suhua, LeBlanc Chantal A, Bernatavichute Yana V, Stroud Hume, Cokus Shawn, Johnson Lianna M, Pellegrini Matteo, Jacobsen Steven E, Michaels Scott D

机构信息

Department of Biology, Indiana University, Bloomington, Indiana, USA.

出版信息

Nat Struct Mol Biol. 2009 Jul;16(7):763-8. doi: 10.1038/nsmb.1611. Epub 2009 Jun 7.

Abstract

Constitutive heterochromatin in Arabidopsis thaliana is marked by repressive chromatin modifications, including DNA methylation, histone H3 dimethylation at Lys9 (H3K9me2) and monomethylation at Lys27 (H3K27me1). The enzymes catalyzing DNA methylation and H3K9me2 have been identified; alterations in these proteins lead to reactivation of silenced heterochromatic elements. The enzymes responsible for heterochromatic H3K27me1, in contrast, remain unknown. Here we show that the divergent SET-domain proteins ARABIDOPSIS TRITHORAX-RELATED PROTEIN 5 (ATXR5) and ATXR6 have H3K27 monomethyltransferase activity, and atxr5 atxr6 double mutants have reduced H3K27me1 in vivo and show partial heterochromatin decondensation. Mutations in atxr5 and atxr6 also lead to transcriptional activation of repressed heterochromatic elements. Notably, H3K9me2 and DNA methylation are unaffected in double mutants. These results indicate that ATXR5 and ATXR6 form a new class of H3K27 methyltransferases and that H3K27me1 represents a previously uncharacterized pathway required for transcriptional repression in Arabidopsis.

摘要

拟南芥中的组成型异染色质以抑制性染色质修饰为特征,包括DNA甲基化、组蛋白H3赖氨酸9位二甲基化(H3K9me2)和赖氨酸27位一甲基化(H3K27me1)。催化DNA甲基化和H3K9me2的酶已被鉴定出来;这些蛋白质的改变会导致沉默的异染色质元件重新激活。相比之下,负责异染色质H3K27me1的酶仍然未知。在此,我们表明,具有不同功能的SET结构域蛋白拟南芥三胸相关蛋白5(ATXR5)和ATXR6具有H3K27单甲基转移酶活性,并且atxr5 atxr6双突变体在体内H3K27me1减少,并表现出部分异染色质解聚。atxr5和atxr6中的突变还导致被抑制的异染色质元件转录激活。值得注意的是,双突变体中的H3K9me2和DNA甲基化不受影响。这些结果表明,ATXR5和ATXR6形成了一类新的H3K27甲基转移酶,并且H3K27me1代表了拟南芥转录抑制所需的一条以前未被表征的途径。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e9e7/2754316/53c71cf1f5e4/nihms113168f1.jpg

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