A Branched SNF1 ‐Related Protein Kinase 2 Signalling Cascade Controls ABA ‐Induced Ethylene Production and Regulates Both Fruit Ripening and Reproductive Growth

成熟 生物 更年期 乙烯 细胞生物学 激酶 生物化学 蛋白激酶A 信号转导 磷酸化 极光A激酶 转录因子 生长素 抄写(语言学) 蛋白质生物合成 针脚1 蛋白质磷酸化 蛋白质降解 信号 基因 植物 刺猬信号通路 转录调控 翻译(生物学) 基因表达调控 细胞信号 生物合成 拟南芥 生长素极性运输
作者
Zhengrong Dai,Yating Li,Changsheng Zhai,Jie Li,Zeng Ya-juan,Jinyao Ouyang,Bihua He,Wei Wang,Pingyin Guan,Don Grierson,Kai Chen,Wensuo Jia
出处
期刊:Plant Biotechnology Journal [Wiley]
标识
DOI:10.1111/pbi.70501
摘要

ABSTRACT Control of fruit ripening, quality and yield is of major scientific, nutritional and commercial importance. The burst of ethylene (ET) production at the initiation of ripening is the most critical event controlling climacteric (CL) fruit ripening, yet little is known about how it is initiated. ABA is known to be capable of inducing ET production in many biological processes. However, the mechanism for this ABA induced ET production (AEP) and its potential importance in the burst of ET production that initiates ripening are unclear. Here, we report a branched signalling network involving ABA‐activation of multiple SlSnRK2 (SNF1‐related protein kinase 2) kinases, which, when overexpressed in tomato, stimulated ABA‐induced ET production. Two key components, SlSnRK2.1 and SlSnRK2.4, phosphorylate an HD‐Zip homeobox transcription factor, SlHB1, which transcriptionally activates ACC oxidase ( SlACO1 ), required for ethylene synthesis. Concurrently, SlSnRK2.1 and SlSnRK2.4 phosphorylate two mitogen‐activated protein kinases, SlMPK1/2, resulting in the post‐translational stabilisation of ACC synthase (SlACS2), which generates the precursor 1‐aminocyclopropane‐1‐carboxylic acid (ACC) that is converted to ET by ACO1. Removal of SlSnRK2.1 by CRISPR/Cas9 mutation was sufficient to alter the progress of fruit ripening. These results indicate that ABA is a primary hormonal signal modulating CL fruit ripening that stimulates ethylene production by targeting different steps in the ethylene biosynthesis pathway by both transcriptional and post‐translational mechanisms. Further analysis revealed that removal of SlSnRK2.1 signalling also affected other aspects of the life cycle by prolonging the flowering period and suppressing seed development, indicating the potential for modifying fruit cropping and seedlessness.

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