Genome-wide identification and characterization of the thioredoxin (TRX) gene family in tomato (Solanum lycopersicum) and a functional analysis of SlTRX2 under salt stress.

IF 6.1 2区 生物学 Q1 PLANT SCIENCES
Xiaoyu Cui, Jiamao Gu, Pengkun Liu, Ruiqin Lu, Zhen Ren, Yueqi Zhang, Feng Wang, Mingfang Qi, Yufeng Liu, Tianlai Li
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Abstract

Thioredoxin is a multifunctional acidic protein widely presented in organisms that regulates intracellular redox processes, participating in a series of biochemical reactions in cells to affect the growth and development of plants. Although the thioredoxin (TRX) gene family has been widespread recognized across various plant species, and the tomato genome has been sequenced for years now, of tomato (Solanum lycopersicum) has remained largely uncharted in terms of identifying and unraveling the functional intricacies of is TRX genes. In this study, 53 SlTRX genes were identified, unevenly distributed across 11 of the 12 tomato chromosomes. These 53 SlTRX genes were categorized into 4 distinct subfamilies based on their evolutionary kinship and phylogenetic development. Expression profiling reveals that most of SlTRX genes exhibited distinct expression patterns across various tissues and developmental stages. In addition, the gene structure, conserved protein motifs and cis-elements of 53 SlTRX genes were analyzed simultaneously. In our rigorous in silico expression analysis, 8 SlTRX genes were meticulously selected for subsequent experiments. Subcellular localization indicated that these 8 SlTRX genes were localized in chloroplasts. Furthermore, these 8 SlTRX genes were responsive to abiotic stress (salt, drought and cold stress) under the qRT-PCR analysis, and their different expression patterns under diverse types of treatments indicated their possible roles in stress tolerance in tomato. Based on these results, SlTRX2, whose expression level continued to increase under salt stress, was selected for silencing to further investigate its function, and furthermore, silencing SlTRX2 inhibited plant growth and led to a significant reduction in photosynthesis under salt stress. Yeast two-hybrid and luciferase complementation imaging assays demonstrated that SlTRX2 may regulate tomato salt resistance by affecting related photosynthetic genes. Thus, our study establishes a valuable resource for further analysis on biological functions of SlTRX genes and will provide important insights in the mechanism of action under stress.

番茄硫氧还蛋白(TRX)基因家族的全基因组鉴定及SlTRX2基因在盐胁迫下的功能分析
硫氧还蛋白是一种广泛存在于生物体中的多功能酸性蛋白,调节细胞内氧化还原过程,参与细胞内的一系列生化反应,影响植物的生长发育。虽然硫氧还蛋白(TRX)基因家族已经在各种植物物种中被广泛认识,并且番茄基因组已经测序多年,但番茄(Solanum lycopersicum)在鉴定和揭示其TRX基因功能复杂性方面仍处于未知状态。在这项研究中,鉴定了53个SlTRX基因,不均匀地分布在12条番茄染色体中的11条上。根据SlTRX基因的进化亲缘关系和系统发育,将这53个SlTRX基因分为4个不同的亚家族。表达谱显示,大多数SlTRX基因在不同组织和发育阶段表现出不同的表达模式。同时分析了53个SlTRX基因的基因结构、保守蛋白基序和顺式元件。在我们严格的硅表达分析中,精心选择了8个SlTRX基因用于后续实验。亚细胞定位表明这8个SlTRX基因定位于叶绿体中。qRT-PCR分析表明,这8个SlTRX基因对非生物胁迫(盐胁迫、干旱胁迫和冷胁迫)均有响应,在不同处理条件下的不同表达模式表明它们可能在番茄抗逆性中起作用。基于以上结果,我们选择在盐胁迫下表达水平持续升高的SlTRX2进行沉默,进一步研究其功能,结果表明,沉默SlTRX2抑制了盐胁迫下植物的生长,导致光合作用显著降低。酵母双杂交和荧光素酶互补成像实验表明,SlTRX2可能通过影响相关光合基因调控番茄耐盐性。因此,我们的研究为进一步分析SlTRX基因的生物学功能建立了宝贵的资源,并将为研究应激作用机制提供重要的见解。
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来源期刊
Plant Physiology and Biochemistry
Plant Physiology and Biochemistry 生物-植物科学
CiteScore
11.10
自引率
3.10%
发文量
410
审稿时长
33 days
期刊介绍: Plant Physiology and Biochemistry publishes original theoretical, experimental and technical contributions in the various fields of plant physiology (biochemistry, physiology, structure, genetics, plant-microbe interactions, etc.) at diverse levels of integration (molecular, subcellular, cellular, organ, whole plant, environmental). Opinions expressed in the journal are the sole responsibility of the authors and publication does not imply the editors'' agreement. Manuscripts describing molecular-genetic and/or gene expression data that are not integrated with biochemical analysis and/or actual measurements of plant physiological processes are not suitable for PPB. Also "Omics" studies (transcriptomics, proteomics, metabolomics, etc.) reporting descriptive analysis without an element of functional validation assays, will not be considered. Similarly, applied agronomic or phytochemical studies that generate no new, fundamental insights in plant physiological and/or biochemical processes are not suitable for publication in PPB. Plant Physiology and Biochemistry publishes several types of articles: Reviews, Papers and Short Papers. Articles for Reviews are either invited by the editor or proposed by the authors for the editor''s prior agreement. Reviews should not exceed 40 typewritten pages and Short Papers no more than approximately 8 typewritten pages. The fundamental character of Plant Physiology and Biochemistry remains that of a journal for original results.
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