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MEM1 在保护拟南芥基因组免受 DNA 损伤、抑制 ATM/SOG1 介导的 DNA 损伤反应以及拮抗全基因组 DNA 过度甲基化中的作用。

Roles of MEM1 in safeguarding Arabidopsis genome against DNA damage, inhibiting ATM/SOG1-mediated DNA damage response, and antagonizing global DNA hypermethylation.

机构信息

College of Life Sciences, Nanjing Agricultural University, Nanjing, 210095, China.

College of Plant Protection, Nanjing Agricultural University, Nanjing, 210095, China.

出版信息

J Integr Plant Biol. 2022 Jan;64(1):87-104. doi: 10.1111/jipb.13200.

DOI:10.1111/jipb.13200
PMID:34859586
Abstract

Arabidopsis methylation elevated mutant 1 (mem1) mutants have elevated levels of global DNA methylation. In this study, such mutant alleles showed increased sensitivity to methyl methanesulfonate (MMS). In mem1 mutants, an assortment of genes engaged in DNA damage response (DDR), especially DNA-repair-associated genes, were largely upregulated without MMS treatment, suggestive of activation of the DDR pathway in them. Following MMS treatment, expression levels of multiple DNA-repair-associated genes in mem1 mutants were generally lower than in Col-0 plants, which accounted for the MMS-sensitive phenotype of the mem1 mutants. A group of DNA methylation pathway genes were upregulated in mem1 mutants under non-MMS-treated conditions, causing elevated global DNA methylation, especially in RNA-directed DNA methylation (RdDM)-targeted regions. Moreover, MEM1 seemed to help ATAXIA-TELANGIECTASIA MUTATED (ATM) and/or SUPPRESSOR OF GAMMA RESPONSE 1 (SOG1) to fully activate/suppress transcription of a subset of genes regulated simultaneously by MEM1 and ATM and/or SOG1, because expression of such genes decreased/increased consistently in mem1 and atm and/or sog1 mutants, but the decreases/increases in the mem1 mutants were not as dramatic as in the atm and/or sog1 mutants. Thus, our studies reveals roles of MEM1 in safeguarding genome, and interrelationships among DNA damage, activation of DDR, DNA methylation/demethylation, and DNA repair.

摘要

拟南芥甲基化升高突变体 1(mem1)突变体具有升高的全基因组 DNA 甲基化水平。在这项研究中,此类突变等位基因对甲基甲磺酸酯(MMS)表现出更高的敏感性。在 mem1 突变体中,参与 DNA 损伤反应(DDR)的一系列基因,特别是与 DNA 修复相关的基因,在没有 MMS 处理的情况下被大量上调,提示它们的 DDR 途径被激活。在 MMS 处理后,mem1 突变体中多个与 DNA 修复相关的基因的表达水平普遍低于 Col-0 植物,这解释了 mem1 突变体对 MMS 的敏感性表型。一组 DNA 甲基化途径基因在非 MMS 处理条件下在 mem1 突变体中上调,导致全基因组 DNA 甲基化升高,特别是在 RNA 指导的 DNA 甲基化(RdDM)靶向区域。此外,MEM1 似乎有助于 ATAXIA-TELANGIECTASIA MUTATED(ATM)和/或 SUPPRESSOR OF GAMMA RESPONSE 1(SOG1)充分激活/抑制由 MEM1 和 ATM 和/或 SOG1 同时调控的一组基因的转录,因为这些基因在 mem1 和 atm 和/或 sog1 突变体中的表达一致下降/增加,但 mem1 突变体中的下降/增加并不如 atm 和/或 sog1 突变体中那样显著。因此,我们的研究揭示了 MEM1 在保护基因组、DNA 损伤、DDR 激活、DNA 甲基化/去甲基化和 DNA 修复之间的相互关系中的作用。

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