姜黄调节器官分化和休眠的转录景观和动态

IF 6.9 1区 生物学 Q1 PLANT SCIENCES
Xuezhu Liao, Mengmeng Hou, Yixuan Liu, Bing Xu, Xiaolong Huang, Christophe Bailly, Minlong Jia, Tengbo Huang, Zhiqiang Wu
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引用次数: 0

摘要

特殊器官的出现代表了关键的进化创新,使植物能够在不同的环境中茁壮成长。然而,这些性状的发育机制,特别是根茎等地下贮藏器官的发育机制,仍然知之甚少。暹罗郁金香(Curcuma alismatifolia Gagnep.)具有独特的修饰器官(如苞片、根茎和块根)和通过种子和根茎的双重繁殖策略,是探索器官分化和休眠调节的理想模型。通过全面的全器官转录组学分析,我们揭示了泽泻各器官的功能分化和保护。例如,外层苞片保留了与叶片相似的光合作用能力,而内部苞片失去了这种功能。根茎是一种重要的生殖器官,在不利条件下既是营养储存库,又是休眠驱动的生存机制。利用加权基因共表达网络分析(WGCNA),我们确定了与ABRE顺式作用元件相关的转录因子是根茎发育的关键调控因子。通过将转录组学数据与高温和植物激素处理、异源表达、双荧光素酶报告基因分析和酵母单杂交分析相结合,我们证明了细胞色素P450 (P450)基因,特别是ABA 8′-羟化酶1 (CYP707A1),在调节根茎休眠释放和高温反应中的核心作用。此外,我们发现CYP707A1受MYB转录因子96 (MYB96)、WRKY转录因子35 (WRKY35)、AP2/ERF和B3结构域转录因子RAV1 (RAV1)以及双组分反应调节因子ARR18 (ARR18)转录因子的调控,为全年生产提供了潜在的策略。本研究为研究姜科植物根茎和苞片等进化创新的形成和专门化建立了一个强有力的模型,揭示了它们的适应机制和对环境挑战的适应能力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The transcriptional landscape and dynamics regulating organ differentiation and dormancy in Curcuma alismatifolia
The emergence of specialized organs represents key evolutionary innovations that enable plants to thrive in diverse environments. However, the developmental mechanisms underlying these traits, particularly those of underground storage organs like rhizomes, remain poorly understood. Siam tulip (Curcuma alismatifolia Gagnep.), with its unique suite of modified organs (such as bracts, rhizomes, and tuberous roots) and dual reproductive strategies through seeds and rhizomes, serves as an ideal model for exploring organ differentiation and dormancy regulation. Through a comprehensive organ-wide transcriptomic analysis, we revealed functional differentiation and conservation across C. alismatifolia organs. For example, the outer bracts retain photosynthetic capacity similar to leaves, while the inner bracts have lost this function. The rhizome, a critical reproductive organ, acts as both a nutrient reservoir and a dormancy-driven survival mechanism in adverse conditions. Using Weighted Gene Co-expression Network Analysis (WGCNA), we identified transcription factors associated with ABRE cis-acting elements as key regulators of rhizome development. By integrating transcriptomic data with high-temperature and phytohormone treatments, heterologous expression, dual-luciferase reporter assays and yeast one-hybrid assays, we demonstrated the central role of cytochrome P450 (P450) genes, particularly ABA 8’-hydroxylase 1 (CYP707A1), in regulating rhizome dormancy release and high-temperature responses. Moreover, we showed that CYP707A1 is regulated by the MYB transcription factor 96 (MYB96), WRKY transcription factor 35 (WRKY35), AP2/ERF and B3 domain-containing transcription factor RAV1 (RAV1), and Two-component response regulator ARR18 (ARR18) transcription factors, offering potential strategies for year-round production. This study establishes C. alismatifolia as a powerful model for investigating the formation and specialization of evolutionary innovations like rhizomes and bracts, highlighting their adaptive mechanisms and resilience to environmental challenges in Zingiberaceae.
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来源期刊
Plant Physiology
Plant Physiology 生物-植物科学
CiteScore
12.20
自引率
5.40%
发文量
535
审稿时长
2.3 months
期刊介绍: Plant Physiology® is a distinguished and highly respected journal with a rich history dating back to its establishment in 1926. It stands as a leading international publication in the field of plant biology, covering a comprehensive range of topics from the molecular and structural aspects of plant life to systems biology and ecophysiology. Recognized as the most highly cited journal in plant sciences, Plant Physiology® is a testament to its commitment to excellence and the dissemination of groundbreaking research. As the official publication of the American Society of Plant Biologists, Plant Physiology® upholds rigorous peer-review standards, ensuring that the scientific community receives the highest quality research. The journal releases 12 issues annually, providing a steady stream of new findings and insights to its readership.
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