基于多组学的番茄适应多因子胁迫组合研究

IF 6.9 1区 生物学 Q1 PLANT SCIENCES
Lidia S Pascual, Enrique Serna, Abdul Ghani, Zhen Lyu, Manish Sridhar Immadi, Trupti Joshi, Mohit Verma, José L Rambla, Aurelio Gómez-Cadenas, Ron Mittler, Sara I Zandalinas
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引用次数: 0

摘要

在不同的气候变化情景下,多因子胁迫组合(MFSC)正成为作物生产力的主要制约因素。虽然MFSC的生理影响已经在不同的植物物种中被表征,但MFSC的分子和代谢作用仍然不明确。在这里,我们使用综合多组学方法来剖析番茄(Solanum lycopersicum)植物对多达六种低强度非生物胁迫源的MFSC的反应。我们的分析揭示了番茄中一个复杂性依赖的分子程序。转录组学分析确定了194个核心转录本,这些转录本在所有应激条件下都发生了普遍的改变,以及155个转录因子(tf)在高复杂性条件下(4-、5-和6-应激组合)特异性调节。关注热相关MFSC反应,我们鉴定了103个转录本,这些转录本对这些条件有独特的反应,包括两个TF(锌指TF 32和B3家族蛋白),它们可能是所有热相关MFSC的主要调节因子。代谢组学分析显示,MFSC下的初级代谢发生了明显的重编程,其特征是三羧酸中间体水平下降,糖、γ-氨基丁酸(GABA)和支链氨基酸的积累,这表明在能量密集型过程中,一种有利于渗透保护和氧化还原稳态的权衡。对番茄、拟南芥、衣藻、水稻和大豆的比较分析强调了与MFSC相关的保守分子特征。整合组学相关分析揭示了植物激素信号、光合效率和关键mfsc相关转录物和代谢枢纽之间的功能联系。总之,我们揭示了番茄中协调和复杂依赖的分子程序,为植物对MFSC的适应提供了见解,并为工程适应气候的作物确定了候选的调控和代谢标记。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Multi-omics-based insights into tomato adaptation to multifactorial stress combination
Multifactorial stress combination (MFSC) is emerging as a major constraint to crop productivity under different climate change scenarios. While the physiological impacts of MFSC have been previously characterized in different plant species, the molecular and metabolic effects of MFSC remain poorly defined. Here, we used an integrative multi-omics approach to dissect the response of tomato (Solanum lycopersicum) plants to a MFSC of up to six low-intensity abiotic stressors. Our analysis uncovered a complexity-dependent molecular program in tomato. Transcriptomic analysis identified a core set of 194 transcripts commonly altered across all stress conditions, along with 155 transcription factors (TFs) specifically regulated under high-complexity conditions (4-, 5-, and 6-stress combinations). Focusing on heat-associated MFSC responses, we identified 103 transcripts uniquely responsive to these conditions, including two TFs (Zinc finger TF 32 and a B3 family protein) that may act as master regulators of all heat-associated MFSCs. Metabolomic profiling revealed a pronounced reprogramming of primary metabolism under MFSC, marked by decreased levels of tricarboxylic acid intermediates and accumulation of sugars, γ-aminobutyric acid (GABA), and branched-chain amino acids, suggesting a trade-off that favors osmoprotection and redox homeostasis over energy-intensive processes. Comparative analyses across tomato, Arabidopsis, Chlamydomonas, rice, and soybean highlighted a conserved molecular signature associated with MFSC. Integrated omics correlation analysis uncovered functional links among phytohormone signaling, photosynthetic efficiency, and key MFSC-related transcripts and metabolic hubs. Together, we reveal a coordinated and complexity-dependent molecular program in tomato, offering insights into plant adaptation to MFSC and identifying candidate regulatory and metabolic markers for engineering climate-resilient crops.
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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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