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E3 泛素连接酶 SINA4 和 SINA11 通过靶向苹果中的 IAA29-ARF5-1-ERF3 模块调节花色苷生物合成。

E3 ubiquitin ligases SINA4 and SINA11 regulate anthocyanin biosynthesis by targeting the IAA29-ARF5-1-ERF3 module in apple.

机构信息

Apple Technology Innovation Center of Shandong Province, College of Horticulture Science and Engineering, Shandong Agricultural University, Tai-An, Shandong, China.

CAS Key Laboratory of Plant Germplasm Enhancement and Specialty Agriculture, Wuhan Botanical Garden, Hubei Hongshan Laboratory, The Innovative Academy of Seed Design of Chinese Academy of Sciences, Wuhan, China.

出版信息

Plant Cell Environ. 2023 Dec;46(12):3902-3918. doi: 10.1111/pce.14709. Epub 2023 Sep 1.

Abstract

Auxin/indole-3-acetic acid (AUX/IAA) and auxin response factor (ARF) proteins are important components of the auxin signalling pathway, but their ubiquitination modification and the mechanism of auxin-mediated anthocyanin biosynthesis remain elusive. Here, the ARF MdARF5-1 was identified as a negative regulator of anthocyanin biosynthesis in apple, and it integrates auxin and ethylene signals by inhibiting the expression of the ethylene response factor MdERF3. The auxin repressor MdIAA29 decreased the inhibitory effect of MdARF5-1 on anthocyanin biosynthesis by attenuating the transcriptional inhibition of MdERF3 by MdARF5-1. In addition, the E3 ubiquitin ligases MdSINA4 and MdSINA11 played negative and positive regulatory roles in anthocyanin biosynthesis by targeting MdIAA29 and MdARF5-1 for ubiquitination degradation, respectively. MdSINA4 destabilized MdSINA11 to regulate anthocyanin accumulation in response to auxin signalling. In sum, our data revealed the crosstalk between auxin and ethylene signals mediated by the IAA29-ARF5-1-ERF3 module and provide new insights into the ubiquitination modification of the auxin signalling pathway.

摘要

生长素/吲哚-3-乙酸(Auxin/IAA)和生长素响应因子(ARF)蛋白是生长素信号通路的重要组成部分,但生长素介导的花色素苷生物合成的泛素化修饰及其机制仍不清楚。本研究鉴定了苹果中的 ARF MdARF5-1 是花色素苷生物合成的负调控因子,它通过抑制乙烯响应因子 MdERF3 的表达来整合生长素和乙烯信号。生长素抑制剂 MdIAA29 通过减弱 MdARF5-1 对 MdERF3 的转录抑制作用,降低了 MdARF5-1 对花色素苷生物合成的抑制作用。此外,E3 泛素连接酶 MdSINA4 和 MdSINA11 通过分别靶向 MdIAA29 和 MdARF5-1 进行泛素化降解,在花色素苷生物合成中发挥负调控和正调控作用。MdSINA4 使 MdSINA11 失稳,以响应生长素信号调节花色素苷的积累。总之,我们的数据揭示了 IAA29-ARF5-1-ERF3 模块介导的生长素和乙烯信号之间的串扰,并为生长素信号通路的泛素化修饰提供了新的见解。

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