HTL/KAI2 信号可替代光来控制植物萌芽。

IF 4 2区 生物学 Q1 GENETICS & HEREDITY PLoS Genetics Pub Date : 2024-10-21 eCollection Date: 2024-10-01 DOI:10.1371/journal.pgen.1011447
Jenna E Hountalas, Michael Bunsick, Zhenhua Xu, Andrea A Taylor, Gianni Pescetto, George Ly, François-Didier Boyer, Christopher S P McErlean, Shelley Lumba
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引用次数: 0

摘要

植物监测光照和温度等多种环境线索,以确保它们在正确的时间和地点发芽。一些专门植物,如昙花一现的随火杂草和根寄生植物,主要根据特定环境中的小分子来发芽。虽然这些物种来自不同的支系,但它们使用相同的光敏感性/卡里克蛋白过敏性 2(HTL/KAI2)信号通路来感知不同的小分子,这表明该通路存在趋同进化。在这里,我们发现拟南芥的 HTL/KAI2 信号绕过了萌芽的光照要求。HTL/KAI2 的下游成分 MAX2 1 抑制剂(SMAX1)会在黑暗中积累,并且是 PHYTOCHROME INTERACTING FACTOR 1/PHYTOCHROME INTERACTING FACTOR 3-LIKE 5(PIF1/PIL5)调节有利于萌芽的激素反应途径所必需的。HTL/KAI2 与光信号的相互作用可能有助于解释昙花一现的寄生杂草等专性植物是如何进化其萌芽行为以适应特定环境的。
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HTL/KAI2 signaling substitutes for light to control plant germination.

Plants monitor multiple environmental cues, such as light and temperature, to ensure they germinate at the right time and place. Some specialist plants, like ephemeral fire-following weeds and root parasitic plants, germinate primarily in response to small molecules found in specific environments. Although these species come from distinct clades, they use the same HYPOSENSITIVE TO LIGHT/KARRIKIN INSENSITIVE 2 (HTL/KAI2) signaling pathway, to perceive different small molecules suggesting convergent evolution on this pathway. Here, we show that HTL/KAI2 signaling in Arabidopsis thaliana bypasses the light requirement for germination. The HTL/KAI2 downstream component, SUPPRESSOR OF MAX2 1 (SMAX1) accumulates in the dark and is necessary for PHYTOCHROME INTERACTING FACTOR 1/PHYTOCHROME INTERACTING FACTOR 3-LIKE 5 (PIF1/PIL5) to regulate hormone response pathways conducive to germination. The interaction of HTL/KAI2 and light signaling may help to explain how specialist plants like ephemeral and parasitic weeds evolved their germination behaviour in response to specific environments.

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PLoS Genetics
PLoS Genetics GENETICS & HEREDITY-
自引率
2.20%
发文量
438
期刊介绍: PLOS Genetics is run by an international Editorial Board, headed by the Editors-in-Chief, Greg Barsh (HudsonAlpha Institute of Biotechnology, and Stanford University School of Medicine) and Greg Copenhaver (The University of North Carolina at Chapel Hill). Articles published in PLOS Genetics are archived in PubMed Central and cited in PubMed.
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