Genome-wide identification and characterization of the thioredoxin (TRX) gene family in tomato (Solanum lycopersicum) and a functional analysis of SlTRX2 under salt stress.
{"title":"Genome-wide identification and characterization of the thioredoxin (TRX) gene family in tomato (Solanum lycopersicum) and a functional analysis of SlTRX2 under salt stress.","authors":"Xiaoyu Cui, Jiamao Gu, Pengkun Liu, Ruiqin Lu, Zhen Ren, Yueqi Zhang, Feng Wang, Mingfang Qi, Yufeng Liu, Tianlai Li","doi":"10.1016/j.plaphy.2025.109478","DOIUrl":null,"url":null,"abstract":"<p><p>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.</p>","PeriodicalId":20234,"journal":{"name":"Plant Physiology and Biochemistry","volume":"220 ","pages":"109478"},"PeriodicalIF":6.1000,"publicationDate":"2025-01-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Plant Physiology and Biochemistry","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1016/j.plaphy.2025.109478","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"PLANT SCIENCES","Score":null,"Total":0}
引用次数: 0
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.
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.