Crops ›› 2025, Vol. 41 ›› Issue (2): 66-73.doi: 10.16035/j.issn.1001-7283.2025.02.009

Previous Articles     Next Articles

Identification and Bioinformatics Analysis of the Typical Thioredoxin (TRX) Gene Family in Barley

Chen Hu(), Gao Yuan, Sun Jiameng, Yu Peng, Xiao Hongwu, Zhang Haitao()   

  1. College of Agronomy, Anhui Agricultural University, Hefei 230036, Anhui, China
  • Received:2024-01-15 Revised:2024-03-19 Online:2025-04-15 Published:2025-04-16

Abstract:

The chromosome location, physical and chemical properties, gene structure, conserved domain and promoter were predicted and analyzed by online tools such as TBtools, ExPASy, BUSCA, MEME and PlantCARE at the genome-wide level of cultivated barley MOREX. Using the published RNA-seq data, the expression patterns of typical TRX gene family members in different periods and different tissues of barley and their expression profiles under drought stress were analyzed. The results showed that there were 15 members in the typical TRX gene family of barley, which were unevenly distributed on six chromosomes (except 6H chromosome). Promoter cis-acting elements predicted that the typical TRX gene family of barley played a role in growth and development, hormonal regulation, and abiotic stress. The 15 typical TRX genes were expressed in different tissues such as seeds, roots, stems, leaves and flowers, and at different periods.

Key words: Barley (Hordeum vulgare L.), TRX gene family, System evolution, Expression analysis, Bioinformatics

Fig.1

Location of typical TRX genes in barley on chromosomes"

Table 1

Basic information of typical HvTRX genes identified in barley"

基因名称
Gene name
基因ID
Gene ID
位置
Position
氨基酸数
Number of
amino acids
理论等电点
Theoretical
pI
分子质量
Molecular
weight
总平均亲水性
Grand average
hydropathicity
亚细胞定位
Subcellular
localization
HvTRX1 HORVU.MOREX.r3.1HG0026030 1H 131 5.15 14.48 -0.270 细胞质
HvTRX2 HORVU.MOREX.r3.1HG0070830 1H 143 4.54 15.98 -0.331 细胞核
HvTRX3 HORVU.MOREX.r3.1HG0076510 1H 122 5.12 13.17 0.319 细胞核
HvTRX4 HORVU.MOREX.r3.2HG0149410 2H 118 5.09 12.75 0.089 细胞质
HvTRX5 HORVU.MOREX.r3.2HG0168580 2H 184 8.89 20.26 -0.224 线粒体
HvTRX6 HORVU.MOREX.r3.2HG0183850 2H 240 9.56 25.72 -0.343 叶绿体
HvTRX7 HORVU.MOREX.r3.2HG0194850 2H 577 4.78 63.54 -0.228 细胞质
HvTRX8 HORVU.MOREX.r3.2HG0210290 2H 172 6.74 18.71 -0.058 叶绿体
HvTRX9 HORVU.MOREX.r3.3HG0325100 3H 162 8.40 17.86 -0.200 叶绿体
HvTRX10 HORVU.MOREX.r3.4HG0341820 4H 186 6.32 20.62 -0.308 叶绿体
HvTRX11 HORVU.MOREX.r3.5HG0451950 5H 175 8.52 19.28 0.031 线粒体
HvTRX12 HORVU.MOREX.r3.5HG0479110 5H 319 5.93 35.58 -0.504 细胞核
HvTRX13 HORVU.MOREX.r3.5HG0520730 5H 131 5.89 14.47 -0.065 细胞核
HvTRX14 HORVU.MOREX.r3.7HG0738080 7H 176 9.48 19.35 -0.199 线粒体
HvTRX15 HORVU.MOREX.r3.7HG0749460 7H 173 8.55 18.44 -0.106 叶绿体

Fig.2

Phylogenetic relationship (a), conserved motif (b), and gene structure (c) of typical HvTRX genes family in barley (a) The different letters represent the seven subtypes of typical HvTRX. (b) The different colors represent 10 different conserved motifs. (c) The yellow and green rectangles represent coding sequences (CDS) and non coding sequences (UTR), respectively, while the black lines represent introns. The length of CDS, UTR and introns of each typical HvTRX gene were displayed proportionally."

Fig.3

Cis-elements analysis of the typical HvTRX gene promoters in barley"

Fig.4

Phylogenetic tree of typical TRX proteins using the Maximum Likelihood method , and indicate the proteins of barley, rice and Arabidopsis, respectively."

Fig.5

The collinearity of typical TRX genes among barley, rice and Arabidopsis Gray lines indicate all collinearity blocks within barley and other crop genomes and the duplicated TRX gene pairs are highlighted by black lines. The numerals represent the chromosome numbers of the genomes of the above three crops."

Fig.6

Expression patterns of typical TRX genes in barley in different tissues"

Fig.7

The expression heat map of typical HvTRX genes in leaves (a) and roots (b) of barley under drought stress CK1, D1: control and drought treatment of drought-tolerant materials; CK2, D2: control and drought treatment of drought-sensitive materials; CK: control; WD: water shortage treatment."

[1] Haas M, Schreiber M, Mascher M. Domestication and crop evolution of wheat and barley: Genes, genomics, and future directions. Journal of Integrative Plant Biology, 2019, 61(3):204-225.
doi: 10.1111/jipb.12737
[2] Geng L, Li M D, Zhang G D, et al. Barley: a potential cereal for producing healthy and functional foods. Food Quality and Safety, 2022, 6(2):142-154.
[3] Sakellariou M, Mylona P V. New uses for traditional crops: the case of barley biofortification. Agronomy, 2020, 10(12):1964.
[4] Lemaire S D, Miginiac-Maslow M. The thioredoxin superfamily in Chlamydomonas reinhardtii. Photosynthesis Research, 2004,82:203-220.
[5] Arnér E S J, Holmgren A. Physiological functions of thioredoxin and thioredoxin reductase. European Journal of Biochemistry, 2000, 267(20):6102-6109.
doi: 10.1046/j.1432-1327.2000.01701.x pmid: 11012661
[6] Liu J, Liu B, Feng D R, et al. Evidence for a role of chloroplastic m-type thioredoxins in the biogenesis of photosystem II in Arabidopsis. Plant Physiology, 2013, 163(4):1710-1728.
doi: 10.1104/pp.113.228353 pmid: 24151299
[7] Zhou J F, Song T Q, Zhou H W, et al. Genome-wide identification, characterization, evolution, and expression pattern analyses of the typical thioredoxin gene family in wheat (Triticum aestivum L.). Frontiers in Plant Science, 2022,13:1020584.
[8] Jacquot J P, Vidal J, Gadal P, et al. Evidence for the existence of several enzyme-specific thioredoxins in plants. FEBS Letters, 1978, 96(2):243-246.
[9] Wolosiuk R A, Buchanan B B. Thioredoxin and glutathione regulate photosynthesis in chloroplasts. Nature, 1977, 266(5602):565-567.
[10] Okegawa Y, Motohashi K. Chloroplastic thioredoxin m functions as a major regulator of Calvin cycle enzymes during photosynthesis in vivo. The Plant Journal, 2015, 84(5):900-913.
doi: 10.1111/tpj.13049 pmid: 26468055
[11] Barajas-López J D, Serrato A J, Cazalis R, et al. Circadian regulation of chloroplastic f and m thioredoxins through control of the CCA 1 transcription factor. Journal of Experimental Botany, 2011, 62(6):2039-2051.
doi: 10.1093/jxb/erq394 pmid: 21196476
[12] Buchanan B B. The path to thioredoxin and redox regulation in chloroplasts. Annual Review of Plant Biology, 2016,67:1-24.
[13] Gelhaye E, Rouhier N, Gérard J, et al. A specific form of thioredoxin h occurs in plant mitochondria and regulates the alternative oxidase. Proceedings of the National Academy of Sciences of the United States of America, 2004, 101(40):14545-14550.
[14] Laloi C, Rayapuram N, Chartier Y, et al. Identification and characterization of a mitochondrial thioredoxin system in plants. Proceedings of the National Academy of Sciences of the United States of America, 2001, 98(24):14144-14149.
[15] Collin V, Issakidis-Bourguet E, Marchand C, et al. The Arabidopsis plastidial thioredoxins: new functions and new insights into specificity. Journal of Biological Chemistry, 2003, 278(26):23747-23752.
[16] Collin V, Lamkemeyer P, Miginiac-Maslow M, et al. Characterization of plastidial thioredoxins from Arabidopsis belonging to the new y-type. Plant Physiology, 2004, 136(4):4088-4095.
[17] Arsova B, Hoja U, Wimmelbacher M, et al. Plastidial thioredoxin z interacts with two fructokinase-like proteins in a thiol- dependent manner: evidence for an essential role in chloroplast development in Arabidopsis and Nicotiana benthamiana. The Plant Cell, 2010, 22(5):1498-1515.
[18] Geigenberger P, Thormählen I, Daloso D M, et al. The unprecedented versatility of the plant‎ thioredoxin system. Trends in Plant Science, 2017, 22(3):249-262.
doi: S1360-1385(16)30221-7 pmid: 28139457
[19] Nikkanen L, Rintamäki E. Chloroplast thioredoxin systems dynamically regulate photosynthesis in plants. Biochemical Journal, 2019, 476(7):1159-1172.
doi: 10.1042/BCJ20180707 pmid: 30988137
[20] Laughner B J, Sehnke P C, Ferl R J. A novel nuclear member of the thioredoxin superfamily. Plant Physiology, 1998, 118(3):987-996.
pmid: 9808743
[21] Funato Y, Hayashi T, Irino Y, et al. Nucleoredoxin regulates glucose metabolism via phosphofructokinase 1. Biochemical and Biophysical Research Communications, 2013, 440(4):737-742.
doi: 10.1016/j.bbrc.2013.09.138 pmid: 24120946
[22] Chen C J, Chen H, Zhang Y, et al. TBtools:an integrative toolkit developed for interactive analyses of big biological data. Molecular Plant, 2020, 13(8):1194-1202.
[23] Sun L J, Ren H Y, Liu R X, et al. An h-type thioredoxin functions in tobacco defense responses to two species of viruses and an abiotic oxidative stress. Molecular Plant-Microbe Interactions, 2010, 23(11):1470-1485.
doi: 10.1094/MPMI-01-10-0029 pmid: 20923353
[24] Havelda Z, Várallyay É, Válóczi A, et al. Plant virus infection‐induced persistent host gene downregulation in systemically infected leaves. The Plant Journal, 2008, 55(2):278-288.
doi: 10.1111/j.1365-313X.2008.03501.x pmid: 18397378
[25] Valerio C, Costa A, Marri L, et al.Thioredoxin-regulated β-amylase (BAM1) triggers diurnal starch degradation in guard cells, and in mesophyll cells under osmotic stress. Journal of Experimental Botany, 2011, 62(2):545-555.
[26] Moon H, Lee B, Choi G, et al. NDP kinase 2 interacts with two oxidative stress-activated MAPKs to regulate cellular redox state and enhances multiple stress tolerance in transgenic plants. Proceedings of the National Academy of Sciences of the United States of America, 2003, 100(1):358-363.
[27] Xie G, Kato H, Sasaki K, et al. A cold-induced thioredoxin h of rice, OsTrx23, negatively regulates kinase activities of OsMPK3 and OsMPK6 in vitro. FEBS Letters, 2009, 583(17):2734-2738.
doi: 10.1016/j.febslet.2009.07.057 pmid: 19665023
[28] Zhang S X, Yu Y, Song T Q, et al. Genome-wide identification of foxtail millet’s TRX family and a functional analysis of SiNRX1 in response to drought and salt stresses in transgenic Arabidopsis. Frontiers in Plant Science, 2022,13:946037.
[29] Nuruzzaman M, Sharoni A M, Satoh K, et al. The thioredoxin gene family in rice: Genome-wide identification and expression profiling under different biotic and abiotic treatments. Biochemical and Biophysical Research Communications, 2012, 423(2):417-423.
doi: 10.1016/j.bbrc.2012.05.142 pmid: 22683629
[30] Elasad M, Wei H L, Wang H T, et al. Genome-wide analysis and characterization of the TRX gene family in upland cotton. Tropical Plant Biology, 2018, 11(3/4):119-130.
[31] Zhang J R, Zhao T, Yan F D, et al. Genome-wide identification and expression analysis of Thioredoxin (Trx) genes in seed development of vitis vinifera. Journal of Plant Growth Regulation, 2022, 41(7):3030-3045.
[32] Li X, Su G J, Ntambiyukuri A, et al. Genome-wide identification and expression analysis of the AhTrx family genes in peanut. Biologia Plantarum, 2022, 66(1):112-122.
[33] Bhurta R, Hurali D T, Tyagi S, et al. Genome-wide identification and expression analysis of the thioredoxin (trx) gene family reveals its role in leaf rust resistance in wheat (Triticum aestivum L.). Frontiers in Genetics, 2022,13:563.
[34] Hägglund P, Björnberg O, Navrot N, et al. The barley grain thioredoxin system-an update. Frontiers in Plant Science, 2013,4:151.
[1] Zhang Jun, Cai Suyun, Xu Zihao, Hou Lei, He Runli, Yin Guifang, Wang Lihua, Wang Yanqing, Lu Wenjie, Sun Daowang. Cloning, Bioinformatics and Expression Analysis of FtERF Gene in Fagopyrum tataricum [J]. Crops, 2024, 40(2): 23-29.
[2] Zhang Qian, Ren Wen, Zhao Bingbing, Zhou Miaoyi, Li Hanshuai, Liu Ya, Du Hewei. Cloning and Bioinformatics Analysis of ZmMAPKKK21 Gene in Maize [J]. Crops, 2024, 40(2): 30-39.
[3] Zhang Yu, Yang Wenjing, Liu Xuan, Nie Fengjie, Zhang Li, Shi Lei, Zhang Guohui, Guo Zhiqian, Gong Lei. Cloning and Expression Analysis of Potato StCWIN1 Gene Promoter and Its Role under Drought Stress [J]. Crops, 2024, 40(2): 54-61.
[4] Lü Baolian, Yang Yuxin, Cui Licao, Shi Feng, Ma Liang, Kong Xiuying, Zhang Lichao, Ni Zhiyong. Identification of bHLH Family Transcription Factors of Wheat and Expression Analysis under Salt Stress [J]. Crops, 2024, 40(1): 65-72.
[5] Wu Ying, Hu Die, Li Ting, Duan Qianyuan, Wei Ningning, Zhang Xinghua, Xu Shutu, Xue Jiquan. Analysis of WRKY Transcription Factor IIc Subfamily in Maize and Its Expression Profile under Drought [J]. Crops, 2024, 40(1): 80-89.
[6] Zhao Pengpeng, Li Luhua, Ren Mingjian, An Chang, Hong Dingli, Li Xin, Xu Ruhong. Bioinformatics and Expression Analysis of GzCIPK7-5B Gene in Wheat [J]. Crops, 2023, 39(4): 77-84.
[7] Qiu Kaihua, Fang Shumei, Liang Xilong. Functional Analysis of SRRM1-Like Transcription Factor of Magnaporthe grisea [J]. Crops, 2023, 39(3): 246-253.
[8] Meng Yaxuan, Yao Xuhang, Sun Yingqi, Zhao Xinyue, Wang Fengxia, Weng Qiaoyun, Liu Yinghui. Identification and Bioinformatics Analysis of DGAT Gene Family in Cereal Crops [J]. Crops, 2023, 39(1): 20-29.
[9] Zhou Fei. Bioinformatics and Expression Analysis of HaLACS7 Gene in Sunflower [J]. Crops, 2022, 38(3): 104-108.
[10] Yang Xiaolin, Duan Ying, Cai Suyun, He Runli, Yin Guifang, Wang Yanqing, Lu Wenjie, Sun Daowang, Wang Lihua. Molecular Cloning and Bioinformatics Analyzing of Laccase in Fagopyrum tataricum [J]. Crops, 2022, 38(3): 73-79.
[11] Lu Ping, Kang Qingfang, Zhao Mengyao, Zhang Fengjie, Wu Qiangqiang, Ma Fangfang, Wang Yushen, Han Yuanhuai, Wang Xingchun, Li Xueyin. Identification and Functional Analysis of miR169 Family and Its Target Genes in Setaria italica [J]. Crops, 2022, 38(2): 54-63.
[12] Yin Guifang, Duan Ying, Yang Xiaolin, Cai Suyun, Wang Yanqing, Lu Wenjie, Sun Daowang, He Runli, Wang Lihua. Cloning and Bioinformatics Analysis of FtC4H Gene from Tartary Buckwheat [J]. Crops, 2022, 38(1): 77-83.
[13] Wang Zhilong, Xue Yinghong, Hao Yueru, Liu Baoling, Yuan Lixia, Xue Jin'ai, Li Runzhi. Identification and Expression Analysis of Oil-Related Transcription actor CsLEC2 Gene Family in Camelina sativa (L.) Crantz [J]. Crops, 2020, 36(5): 23-32.
[14] Xu Yuanyuan, Zhao Peng, Hong Quanchun, Zhu Xiaoqin, Pei Dongli. Isolation and Expression Analysis of Transcription Factor Gene TaMYB70 in Wheat [J]. Crops, 2020, 36(4): 84-90.
[15] Zhao Xunchao,Xu Jingyu,Gai Shengnan,Wei Yulei,Xu Xiaoxuan,Ding Dong,Liu Meng,Zhang Jinjie,Shao Wenjing. Identification of Stearyl -ACP Desaturase Gene (SbSAD) Family and Their Expression Analysis at Different Developmental Stages in Sorghum [J]. Crops, 2020, 36(2): 20-27.
Viewed
Full text


Abstract

Cited

  Shared   
  Discussed   
No Suggested Reading articles found!