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编码假定的H3K4甲基转移酶,对植物发育至关重要。 (你提供的原文似乎不完整,句首有缺失内容。)

, , and Encode Putative H3K4 Methyltransferases and Are Critical for Plant Development.

作者信息

Chen Li-Qun, Luo Jin-Hong, Cui Zhen-Hai, Xue Ming, Wang Li, Zhang Xiao-Yu, Pawlowski Wojciech P, He Yan

机构信息

State Key Laboratory of Plant Physiology and Biochemistry, College of Biological Sciences, China Agricultural University, Beijing 100083, China.

National Maize Improvement Center of China, Beijing Key Laboratory of Crop Genetic Improvement, China Agricultural University, Beijing 100083, China.

出版信息

Plant Physiol. 2017 Jul;174(3):1795-1806. doi: 10.1104/pp.16.01944. Epub 2017 May 26.

Abstract

Methylation of Lys residues in the tail of the H3 histone is a key regulator of chromatin state and gene expression, conferred by a large family of enzymes containing an evolutionarily conserved SET domain. One of the main types of SET domain proteins are those controlling H3K4 di- and trimethylation. The genome of Arabidopsis () encodes 12 such proteins, including five ARABIDOPSIS TRITHORAX (ATX) proteins and seven ATX-Related proteins. Here, we examined three until-now-unexplored ATX proteins, ATX3, ATX4, and ATX5. We found that they exhibit similar domain structures and expression patterns and are redundantly required for vegetative and reproductive development. Concurrent disruption of the , , and genes caused marked reduction in H3K4me2 and H3K4me3 levels genome-wide and resulted in thousands of genes expressed ectopically. Furthermore, // triple mutants resulted in exaggerated phenotypes when combined with the mutant but not with Together, we conclude that , , and are redundantly required for H3K4 di- and trimethylation at thousands of sites located across the genome, and genomic features associated with targeted regions are different from the /-controlled sites in Arabidopsis.

摘要

H3组蛋白尾部赖氨酸残基的甲基化是染色质状态和基因表达的关键调节因子,由一大类含有进化上保守的SET结构域的酶赋予。SET结构域蛋白的主要类型之一是控制H3K4二甲基化和三甲基化的蛋白。拟南芥基因组编码12种此类蛋白,包括5种拟南芥三体同源蛋白(ATX)和7种ATX相关蛋白。在这里,我们研究了三种此前未被探索的ATX蛋白,即ATX3、ATX4和ATX5。我们发现它们具有相似的结构域结构和表达模式,并且在营养生长和生殖发育中是冗余必需的。同时破坏ATX3、ATX4和ATX5基因会导致全基因组范围内H3K4me2和H3K4me3水平显著降低,并导致数千个基因异位表达。此外,ATX3/ATX4/ATX5三重突变体与CLF突变体组合时会导致夸张的表型,但与SWN组合时则不会。我们共同得出结论,ATX3、ATX4和ATX5对于全基因组数千个位点的H3K4二甲基化和三甲基化是冗余必需的,并且与靶向区域相关的基因组特征与拟南芥中CLF/SWN控制的位点不同。

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