The RING-type E3 ligase RIE1 sustains leaf longevity by specifically targeting AtACS7 to fine-tune ethylene production in Arabidopsis

乙烯 拟南芥 衰老 泛素连接酶 拟南芥 突变体 生物合成 细胞生物学 生物化学 生物 化学 泛素 基因 催化作用
作者
Xianglin Tang,Yuanyuan Mei,Kaixuan He,Ran Liu,Xiaoyan Lv,Yujia Zhao,Wenjing Li,Qian Wang,Qianhong Gong,Shengnan Li,Chang Xu,Zheng Xu,Qingyu Cao,Dan Wang,Ning Ning Wang
出处
期刊:Proceedings of the National Academy of Sciences of the United States of America [National Academy of Sciences]
卷期号:121 (48)
标识
DOI:10.1073/pnas.2411271121
摘要

Ethylene is widely recognized as a positive regulator of leaf senescence. However, how plants coordinate the biosynthesis of ethylene to meet the requirements of senescence progression has not been determined. The rate-limiting enzyme in the ethylene biosynthesis pathway is ACC synthase. AtACS7 was previously considered one of the major contributors to the synthesis of “senescence ethylene” in Arabidopsis . However, the “brake signal” that fine-tunes the expression of AtACS7 to ensure optimal ethylene production during leaf development has yet to be identified. In the present study, the RING-H2 zinc-finger protein RIE1 was found to specifically interact with and ubiquitinate AtACS7, among all functional ACSs in Arabidopsis , to promote its degradation. Overexpression of RIE1 markedly decreased ethylene biosynthesis and delayed leaf senescence, whereas loss of function of RIE1 significantly increased ethylene emission and accelerated leaf senescence. The ethylene-related phenotypes of RIE1 overexpressing or knockout mutants were effectively rescued by the ethylene precursor ACC or the competitive inhibitor of ACS, respectively. In particular, AtACS7-induced precocious leaf senescence was strongly enhanced by the loss of RIE1 but was significantly attenuated by the overexpression of RIE1 . The specific regions of interaction between AtACS7 and RIE1, as well as the major ubiquitination sites of AtACS7, were further investigated. All results demonstrated that RIE1 functions as an important modulator of ethylene biosynthesis during leaf development by specifically targeting AtACS7 for degradation, thereby enabling plants to produce the optimal levels of ethylene needed.
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