决定大豆光周期敏感性的关键抑制反馈回路

IF 10.7 1区 生物学 Q1 CELL BIOLOGY Developmental cell Pub Date : 2024-04-29 DOI:10.1016/j.devcel.2024.04.004
Xiaohui Zhao, Haiyang Li, Lingshuang Wang, Jianhao Wang, Zerong Huang, Haiping Du, Yaru Li, Jiahui Yang, Milan He, Qun Cheng, Xiaoya Lin, Baohui Liu, Fanjiang Kong
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引用次数: 0

摘要

光周期敏感性对大豆开花、适应性和产量至关重要。在大豆中,光周期敏感性以黄昏复合体(EC)为中心,该复合体调节核心转录因子 E1 的转录水平,从而调节开花。然而,人们对 EC 的活性调控知之甚少。我们的研究确定了 E2/GIGANTEA(GI)及其同源物如何通过与 EC 的相互作用来调节光周期敏感性。在长日照期间,E2与蓝光受体黄素结合、凯尔奇重复、F盒1(FKF1)相互作用,导致EC成分J/ELF3降解。EC 还通过与其启动子结合来抑制 E2 的表达。这种相互作用形成了一个光周期调控环,维持对光周期的敏感性。这一环路的破坏会导致敏感性下降,影响大豆的适应性和产量。了解这一环路的动态对分子育种至关重要,可降低大豆的光周期敏感性,培育出适应性更强、产量更高的品种,从而有可能培育出对光周期不敏感的品种,用于更广泛的农业应用。
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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A critical suppression feedback loop determines soybean photoperiod sensitivity

Photoperiod sensitivity is crucial for soybean flowering, adaptation, and yield. In soybean, photoperiod sensitivity centers around the evening complex (EC) that regulates the transcriptional level of the core transcription factor E1, thereby regulating flowering. However, little is known about the regulation of the activity of EC. Our study identifies how E2/GIGANTEA (GI) and its homologs modulate photoperiod sensitivity through interactions with the EC. During long days, E2 interacts with the blue-light receptor flavin-binding, kelch repeat, F box 1 (FKF1), leading to the degradation of J/ELF3, an EC component. EC also suppresses E2 expression by binding to its promoter. This interplay forms a photoperiod regulatory loop, maintaining sensitivity to photoperiod. Disruption of this loop leads to losing sensitivity, affecting soybean’s adaptability and yield. Understanding this loop’s dynamics is vital for molecular breeding to reduce soybean’s photoperiod sensitivity and develop cultivars with better adaptability and higher yields, potentially leading to the creation of photoperiod-insensitive varieties for broader agricultural applications.

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来源期刊
Developmental cell
Developmental cell 生物-发育生物学
CiteScore
18.90
自引率
1.70%
发文量
203
审稿时长
3-6 weeks
期刊介绍: Developmental Cell, established in 2001, is a comprehensive journal that explores a wide range of topics in cell and developmental biology. Our publication encompasses work across various disciplines within biology, with a particular emphasis on investigating the intersections between cell biology, developmental biology, and other related fields. Our primary objective is to present research conducted through a cell biological perspective, addressing the essential mechanisms governing cell function, cellular interactions, and responses to the environment. Moreover, we focus on understanding the collective behavior of cells, culminating in the formation of tissues, organs, and whole organisms, while also investigating the consequences of any malfunctions in these intricate processes.
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