METTL5-mediated 18S rRNA m6A modification enhances ribosome assembly and ABA response in Arabidopsis

IF 23.7 Q1 MICROBIOLOGY
iMeta Pub Date : 2025-06-13 DOI:10.1002/imt2.70055
Ping Li, Yu Zhang, Songyao Zhang, Jinqi Ma, Sheng Fan, Lisha Shen
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引用次数: 0

Abstract

METTL5 catalyzes the N6-methyladenosine (m6A) methylation at A1771 in 18S rRNA, a modification essential for its association with the ribosomal protein RPL24A, facilitating the assembly of 80S ribosome. This facilitates the translation of mRNAs encoding the detoxifying glutathione S-transferase (GST) enzymes, thereby maintaining normal reactive oxygen species (ROS) levels and ensuring proper abscisic acid (ABA) responses. In mettl5 mutants, the absence of m6A1771 compromises RPL24A incorporation and ribosome assembly, impairing the translation of GSTs. This results in ROS excessive accumulation and hypersensitivity to ABA.

Abstract Image

mettl5介导的18S rRNA m6A修饰增强拟南芥核糖体组装和ABA反应
METTL5在18S rRNA A1771位点催化n6 -甲基腺苷(m6A)甲基化,这是其与核糖体蛋白RPL24A结合所必需的修饰,促进了80S核糖体的组装。这有助于编码解毒谷胱甘肽s -转移酶(GST)酶的mrna的翻译,从而维持正常的活性氧(ROS)水平并确保适当的脱落酸(ABA)反应。在mettl5突变体中,m6A1771的缺失损害了RPL24A的结合和核糖体的组装,损害了gst的翻译。这导致ROS过度积累和对ABA过敏。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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CiteScore
10.80
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