异染色质感应组蛋白去甲基化酶 IBM1 的动态进化。

IF 4 2区 生物学 Q1 GENETICS & HEREDITY
PLoS Genetics Pub Date : 2024-07-11 eCollection Date: 2024-07-01 DOI:10.1371/journal.pgen.1011358
Yinwen Zhang, Hosung Jang, Ziliang Luo, Yinxin Dong, Yangyang Xu, Yamini Kantamneni, Robert J Schmitz
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引用次数: 0

摘要

异染色质对于维持基因组的稳定性至关重要,尤其是在开花植物中,它依赖于 H3K9 甲基转移酶 KRYPTONITE (KYP) 和 DNA 甲基转移酶 CHROMOMETHYLASE3 (CMT3) 的反馈回路。H3K9 去甲基化酶 INCREASED IN BONSAI METHYLATION 1(IBM1)可以抵消转录基因中 KYP-CMT3 活性的有害影响。IBM1 在拟南芥中的表达受到第 7 个内含子甲基化的独特调控,使其能够监测全球 H3K9me2 水平。我们发现甲基化内含子在有花植物中普遍存在,其基本序列呈现动态进化。我们还发现 KYP、CMT3 和 IBM1 在有花植物中存在广泛的遗传和表达变异。我们发现拟南芥品种类似于弱ibm1突变体,而十字花科植物则存在IBM1表达减少或缺失的情况。拟南芥中的 cmt3 突变体减轻了 IBM1 的有害影响,而某些开花植物中 IBM1 活性降低的进化过程可以解释为什么经常出现 CMT3 活性降低或丧失以及基因体 DNA 甲基化丧失的自然现象。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Dynamic evolution of the heterochromatin sensing histone demethylase IBM1.

Heterochromatin is critical for maintaining genome stability, especially in flowering plants, where it relies on a feedback loop involving the H3K9 methyltransferase, KRYPTONITE (KYP), and the DNA methyltransferase CHROMOMETHYLASE3 (CMT3). The H3K9 demethylase INCREASED IN BONSAI METHYLATION 1 (IBM1) counteracts the detrimental consequences of KYP-CMT3 activity in transcribed genes. IBM1 expression in Arabidopsis is uniquely regulated by methylation of the 7th intron, allowing it to monitor global H3K9me2 levels. We show the methylated intron is prevalent across flowering plants and its underlying sequence exhibits dynamic evolution. We also find extensive genetic and expression variations in KYP, CMT3, and IBM1 across flowering plants. We identify Arabidopsis accessions resembling weak ibm1 mutants and Brassicaceae species with reduced IBM1 expression or deletions. Evolution towards reduced IBM1 activity in some flowering plants could explain the frequent natural occurrence of diminished or lost CMT3 activity and loss of gene body DNA methylation, as cmt3 mutants in A. thaliana mitigate the deleterious effects of IBM1.

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来源期刊
PLoS Genetics
PLoS Genetics GENETICS & HEREDITY-
自引率
2.20%
发文量
438
期刊介绍: PLOS Genetics is run by an international Editorial Board, headed by the Editors-in-Chief, Greg Barsh (HudsonAlpha Institute of Biotechnology, and Stanford University School of Medicine) and Greg Copenhaver (The University of North Carolina at Chapel Hill). Articles published in PLOS Genetics are archived in PubMed Central and cited in PubMed.
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