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FHY3 和 FAR1 通过 miR156-SPL 模块介导的衰老途径整合光信号来调控拟南芥开花。

FHY3 and FAR1 Integrate Light Signals with the miR156-SPL Module-Mediated Aging Pathway to Regulate Arabidopsis Flowering.

机构信息

Biotechnology Research Institute, Chinese Academy of Agricultural Sciences, Beijing 100081, China.

Biotechnology Research Institute, Chinese Academy of Agricultural Sciences, Beijing 100081, China; Graduate School of Chinese Academy of Agricultural Sciences, Beijing 100081, China.

出版信息

Mol Plant. 2020 Mar 2;13(3):483-498. doi: 10.1016/j.molp.2020.01.013. Epub 2020 Feb 1.

DOI:10.1016/j.molp.2020.01.013
PMID:32017999
Abstract

In response to competition for light from their neighbors, shade-intolerant plants flower precociously to ensure reproductive success and survival. However, the molecular mechanisms underlying this key developmental switch are not well understood. Here, we show that a pair of Arabidopsis transcription factors essential for phytochrome A signaling, FAR-RED ELONGATED HYPOCOTYL3 (FHY3) and FAR-RED IMPAIRED RESPONSE1 (FAR1), regulate flowering time by integrating environmental light signals with the miR156-SPL module-mediated aging pathway. We found that FHY3 and FAR1 directly interact with three flowering-promoting SQUAMOSA-PROMOTER BINDING PROTEIN-LIKE (SPL) transcription factors, SPL3, SPL4, and SPL5, and inhibit their binding to the promoters of several key flowering regulatory genes, including FRUITFUL (FUL), LEAFY (LFY), APETALA1 (AP1), and MIR172C, thus downregulating their transcript levels and delaying flowering. Under simulated shade conditions, levels of SPL3/4/5 proteins increase, whereas levels of FHY3 and FAR1 proteins decline, thus releasing SPL3/4/5 from FHY3/FAR1 inhibition to allow activation of FUL, LFY, AP1, and MIR172C and, consequently, early flowering. Taken together, these results unravel a novel mechanism whereby plants regulate flowering time by integrating environmental cues (such as light conditions) and an internal developmental program (the miR156-SPL module-mediated aging pathway).

摘要

为了应对来自邻居的光竞争,耐荫植物会过早开花,以确保繁殖成功和生存。然而,这一关键发育开关的分子机制尚不清楚。在这里,我们表明,一对拟南芥转录因子 FAR-RED ELONGATED HYPOCOTYL3 (FHY3) 和 FAR-RED IMPAIRED RESPONSE1 (FAR1),对于光敏色素 A 信号至关重要,它们通过将环境光信号与 miR156-SPL 模块介导的衰老途径相整合,来调节开花时间。我们发现,FHY3 和 FAR1 直接与三个促进开花的 SQUAMOSA-PROMOTER BINDING PROTEIN-LIKE (SPL) 转录因子 SPL3、SPL4 和 SPL5 相互作用,并抑制它们与几个关键开花调节基因的启动子结合,包括 FRUITFUL (FUL)、LEAFY (LFY)、APETALA1 (AP1) 和 MIR172C,从而下调它们的转录水平并延迟开花。在模拟遮荫条件下,SPL3/4/5 蛋白水平增加,而 FHY3 和 FAR1 蛋白水平下降,从而使 SPL3/4/5 从 FHY3/FAR1 抑制中释放出来,允许 FUL、LFY、AP1 和 MIR172C 的激活,从而导致早期开花。总之,这些结果揭示了一种新的机制,植物通过整合环境线索(如光照条件)和内部发育程序(miR156-SPL 模块介导的衰老途径)来调节开花时间。

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