MYC bHLH转录因子不平等遗传冗余是拟南芥幼苗光形态发生的基础。

IF 2.3 3区 生物学 Q2 PLANT SCIENCES
Plant Direct Pub Date : 2025-02-13 eCollection Date: 2025-02-01 DOI:10.1002/pld3.70042
Vikas Garhwal, Sreya Das, Sreeramaiah N Gangappa
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引用次数: 0

摘要

光是控制植物生长发育最重要的生态信号之一。植物已经进化出复杂的机制来应对波动的光信号。在拟南芥中,bHLH转录因子MYC2, MYC3和MYC4已被证明在保护植物免受草食性和坏死性病原体的侵害中发挥重要作用。虽然MYC2在光介导的幼苗发育中的作用已经有了一些详细的研究,但MYC3和MYC4的作用仍有待发现。在这里,我们发现MYC4负调控幼苗光形态发生,而MYC3的功能似乎是多余的。然而,遗传分析表明,MYC3/MYC4共同对幼苗光形态发育起积极调节作用,因为myc3myc4双突变体比MYC3和MYC4单突变体和Col-0表现出更大的下胚轴生长。有趣的是,MYC2在myc3myc4双突变背景(myc2myc3myc4)中的功能缺失导致下胚轴生长比在WL、BL和FRL中的myc3myc4双突变体进一步增强,这表明MYC2/3/4共同在优化幼苗光形态发生中发挥了重要的积极作用。此外,MYC3/MYC4在遗传和物理上与HY5相互作用,部分抑制其控制下胚轴和光色素积累的功能。此外,我们的研究结果表明,COP1通过26S蛋白酶体途径与MYC3和MYC4进行物理相互作用和降解,并控制它们对黑暗和光线的反应,从而微调HY5功能和幼苗光形态发生。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Unequal Genetic Redundancies Among MYC bHLH Transcription Factors Underlie Seedling Photomorphogenesis in Arabidopsis.

Light is one of the most critical ecological cues controlling plant growth and development. Plants have evolved complex mechanisms to cope with fluctuating light signals. In Arabidopsis, bHLH transcription factors MYC2, MYC3, and MYC4 have been shown to play a vital role in protecting plants against herbivory and necrotrophic pathogens. While the role of MYC2 in light-mediated seedling development has been studied in some detail, the role of MYC3 and MYC4 still needs to be discovered. Here, we show that MYC4 negatively regulates seedling photomorphogenesis, while the MYC3 function seems redundant. However, the genetic analysis reveals that MYC3/MYC4 together act as positive regulators of seedling photomorphogenic growth as the myc3myc4 double mutants showed exaggerated hypocotyl growth compared to the myc3 and myc4 single mutants and Col-0. Intriguingly, the loss of MYC2 function in the myc3myc4 double mutant background (myc2myc3myc4) resulted in further enhancement in the hypocotyl growth than myc3myc4 double mutants in WL, BL and FRL, suggesting that MYC2/3/4 together play an essential and positive role in meditating optimal seedling photomorphogenesis. Besides, MYC3/MYC4 genetically and physically interact with HY5 to partially inhibit its function in controlling hypocotyl and photo-pigment accumulation. Moreover, our results suggest that COP1 physically interacts and degrades MYC3 and MYC4 through the 26S proteasomal pathway and controls their response to dark and light for fine-tuning HY5 function and seedling photomorphogenesis.

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来源期刊
Plant Direct
Plant Direct Environmental Science-Ecology
CiteScore
5.00
自引率
3.30%
发文量
101
审稿时长
14 weeks
期刊介绍: Plant Direct is a monthly, sound science journal for the plant sciences that gives prompt and equal consideration to papers reporting work dealing with a variety of subjects. Topics include but are not limited to genetics, biochemistry, development, cell biology, biotic stress, abiotic stress, genomics, phenomics, bioinformatics, physiology, molecular biology, and evolution. A collaborative journal launched by the American Society of Plant Biologists, the Society for Experimental Biology and Wiley, Plant Direct publishes papers submitted directly to the journal as well as those referred from a select group of the societies’ journals.
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