二氧化碳调控番茄成熟的转录组学分析

Decis. Sci. Pub Date : 2023-06-30 DOI:10.3390/sci5030026
J. Bobokalonov, Yanhong Liu, Karley K. Mahalak, Jenni Firrman, S. Sheen, Siyuan Zhou, Linshu Liu
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引用次数: 0

摘要

西红柿是一种易腐烂的时令水果,具有很高的经济效益。在其他几种试剂中,二氧化碳(CO2)用于延长番茄的保质期,并在冷藏或包装期间保持其质量。为了深入了解番茄成熟过程中的二氧化碳胁迫,研究人员对绿成熟后期的番茄进行了两种CO2输送方法之一的调节:5% CO2 14天(T1)或100% CO2 3小时(T2)。常规理化表征发现,T1或T2诱导的CO2在颜色变化、硬度和碳水化合物溶解方面延迟了番茄的成熟。然而,T1有更持久的效果。此外,CO2在T1阶段抑制了乙烯的生成,在T2阶段促进了乙烯的生成。这些物理观察结果通过全基因组水平的RNA-Seq分析进一步评估,包括参与乙烯合成、信号转导和类胡萝卜素生物合成的基因。转录组学分析表明,通过T1方法引入CO2可下调果实成熟相关基因;相比之下,即使存在大量乙烯,T2也上调了负责S1乙烯合成酶ACS6的基因编码,这表明T1和T2通过不同的机制调节番茄成熟。采用实时荧光定量PCR (qRT-PCR)进行验证,证实了RNA-Seq数据。本研究的结果提供了在全基因组水平上对番茄成熟过程中二氧化碳基因调控的见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Transcriptomics Analysis of Tomato Ripening Regulated by Carbon Dioxide
Tomatoes are a perishable and seasonal fruit with a high economic impact. Carbon dioxide (CO2), among several other reagents, is used to extend the shelf-life and preserve the quality of tomatoes during refrigeration or packaging. To obtain insight into CO2 stress during tomato ripening, tomatoes at the late green mature stage were conditioned with one of two CO2 delivery methods: 5% CO2 for 14 days (T1) or 100% CO2 for 3 h (T2). Conventional physical and chemical characterization found that CO2 induced by either T1 or T2 delayed tomato ripening in terms of color change, firmness, and carbohydrate dissolution. However, T1 had longer-lasting effects. Furthermore, ethylene production was suppressed by CO2 in T1, and promoted in T2. These physical observations were further evaluated via RNA-Seq analysis at the whole-genome level, including genes involved in ethylene synthesis, signal transduction, and carotenoid biosynthesis. Transcriptomics analysis revealed that the introduction of CO2 via the T1 method downregulated genes related to fruit ripening; in contrast, T2 upregulated the gene encoding for ACS6, the enzyme responsible for S1 ethylene synthesis, even though there was a large amount of ethylene present, indicating that T1 and T2 regulate tomato ripening via different mechanisms. Quantitative real-time PCR assays (qRT-PCR) were used for validation, which substantiated the RNA-Seq data. The results of the present research provide insight into gene regulation by CO2 during tomato ripening at the whole-genome level.
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