水稻萌发期激素信号转导和谷胱甘肽代谢转录分析

展开
  • 1华南农业大学 国家植物航天育种工程技术研究中心,广州 510642
    2广东海洋大学 滨海农业学院,广东 湛江 524088
*通信联系人, E-mail: chenlin@scau.edu.cn; heredity24@126.com

收稿日期: 2020-09-23

  修回日期: 2021-03-04

  网络出版日期: 2021-11-10

基金资助

国家自然科学基金资助项目(31872885);广东省重点领域研发计划项目(2020B020219004);国家重点研发计划资助项目(2017YFD0100100)

Transcriptome Analysis of Hormone Signal Transduction and Glutathione Metabolic Pathway in Rice Seeds at Germination Stage

Expand
  • 1National Engineering Research Center of Plant Space Breeding, South China Agricultural University, Guangzhou 510642, China
    2 Binhai Agricultural College, Guangdong Ocean University, Zhanjiang 524088, China
*Corresponding author, E-mail: chenlin@scau.edu.cn; heredity24@126.com

Received date: 2020-09-23

  Revised date: 2021-03-04

  Online published: 2021-11-10

摘要

【目的】利用转录组测序技术,探究水稻萌发过程中激素信号转导和细胞内部氧化还原平衡的调控机理,以期增加对萌发过程中复杂调控机制的理解,促进萌发期基因组转录调控网络的构建,并挖掘调控种子萌发的相关基因,为水稻直播稻新品种选育提供理论参考。【方法】利用萌发0、24和48 h的种子进行动态转录组测序分析,以差异倍数≥2、错误发现率≤0.05为阈值筛选差异基因,并利用Gene Ontology(GO)和KEGG Pathway数据库对萌发不同阶段的差异基因进行分析注释;同时利用实时荧光定量PCR对测序结果进行验证;最后运用String蛋白互作数据库以combined_score≥0.9为阈值分析差异基因的蛋白互作网络。【结果】在种子萌发前期鉴定到8719个差异基因,而在萌发后期仅鉴定到3480个。GO和KEGG富集结果均显示与激素信号转导相关的基因主要在萌发前期被诱导,特别是生长素信号转导途径中的GH3家族基因在萌发前期均受到显著诱导;而谷胱甘肽代谢途径中的基因在萌发后期转录更为活跃,其中谷胱甘肽-S-转移酶基因富集最多。此外,两个异柠檬酸脱氢酶基因在萌发过程中被显著诱导,经蛋白互作预测发现两个异柠檬酸脱氢酶基因与GH3家族基因可能存在相互作用。【结论】在种子萌发前期,生长素信号转导途径中的GH3家族基因可能在减弱生长素信号以及降低生长素活性方面发挥着重要作用,其高表达能降低生长素对种子的休眠作用,促进萌发启动;在种子萌发后期,谷胱甘肽代谢途径中的谷胱甘肽-S-转移酶基因可能在细胞抵抗氧化胁迫中发挥主要作用;此外,在整个萌发过程中,GH3和异柠檬酸脱氢酶家族基因的相互作用可能在实现激素转导途径和谷胱甘肽代谢途径的交互串联作用、共同调控种子萌发方面具有重要意义。

本文引用格式

崔欢, 高巧丽, 罗立新, 杨靖, 陈淳, 郭涛, 刘永柱, 黄永相, 王慧, 陈志强, 肖武名 . 水稻萌发期激素信号转导和谷胱甘肽代谢转录分析[J]. 中国水稻科学, 2021 , 35(6) : 554 -564 . DOI: 10.16819/j.1001-7216.2021.200915

Abstract

【Objective】By using transcriptome sequencing technology, we explored the regulation mechanism of hormone signal transduction and redox balance inside cells during rice germination, as a way to increase the understanding of and construct the complex regulatory network of germination. At the same time, mining the genes that regulate seed germination could lay a theoretical basis for direct-seeded rice breeding.【Method】Dynamic transcriptome sequencing analysis was performed using seeds at 0, 24, and 48 hours after imbibition as materials. Differentially expressed genes (DEGs) were screened with the threshold of Fold Change≥2 and False Discovery Rate≤ 0.05. Gene Ontology and KEGG Pathway databases were used to analyze and annotate the DEGs at different stages of germination and real-time quantitative PCR was conducted to verify the sequencing results. Finally, the protein interaction network of DEGs was analyzed using the String protein interaction database under the threshold of combined_score≥0.9.【Result】8719 DEGs were identified in the early stage of seed germination, but only 3480 DEGs in the late stage of germination. The results of GO and KEGG enrichment analysis showed that the DEGs related to hormone signal transduction were mainly induced in the early stage, especially the GH3 (Gretchen Hagen 3) family genes in the auxin signal transduction pathway were all significantly induced after imbibition. While the DEGs involved in the glutathione metabolism pathway were more active during the late germination period, and the glutathione-S-transferase genes were the most enriched in this pathway. In addition, two isocitrate dehydrogenase (ICDH) genes were significantly induced throughout the germination process. According to protein interaction prediction, the two ICDH genes may interact with the GH3 family genes.【Conclusion】The GH3 family genes in the AUX signal transduction pathway may play an important role in attenuating the AUX signal and reducing the AUX activity in the early stage of seed germination. Their high expression levels reduce the regulatory effect of auxin on seed dormancy and promote seed germination. In the glutathione metabolism pathway, GST genes may play a major role in resistance to cell oxidative stress in the late stage of seed germination. In addition, the interaction between GH3 and ICDH family genes during the germination process may have important significance in realizing the tandem effect of hormone transduction pathway and glutathione metabolism pathway and co-regulating seed germination.

参考文献

[1] Wei F, Droc G, Guiderdoni E, Hsing Y C.International consortium of rice mutagenesis: Resources and beyond[J]. Rice, 2013, 6: 39.
[2] Mahender A, Anandan A, Pradhan S K.Early seedling vigour, an imperative trait for direct-seeded rice: An overview on physio-morphological parameters and molecular markers[J]. Planta, 2015, 241(5): 1027-1050.
[3] Miura K, Lin S Y, Araki H, Nagamine T, Kuroki M, Shimizu H, Ando I, Yano M.Genetical studies on germination of seed and seedling establishment for breeding of improved rice varieties suitable for direct seeding culture[J]. Jarq-Japan Agricultural Research Quarterly, 2004, 38(1): 1-5.
[4] Hsu S, Tung C.Genetic mapping of anaerobic Germination-associated QTLs controlling coleoptile elongation in rice[J]. Rice, 2015, 8: 38.
[5] Wang Z, Wang J, Bao Y, Wu Y, Zhang H.Quantitative trait loci controlling rice seed germination under salt stress[J]. Euphytica, 2011, 178(3): 297-307.
[6] Dametto A, Sperotto R A, Adamski J M, Blasi E A R, Cargnelutti D, de Oliveira L F V, Ricachenevsky F K, Fregonezi J N, Mariath J E A, Da Cruz R P, Margis R, Fett J P. Cold tolerance in rice germinating seeds revealed by deep RNAseq analysis of contrasting indica genotypes[J]. Plant Science, 2015, 238: 1-12.
[7] Mccormac A C, Keefe P D.Cauliflower(Brassica oleracea L.) seed vigour: imbibition effects[J]. Journal of Experimental Botany, 1990(7): 893-899.
[8] Weitbrecht K, Mueller K, Leubner-Metzger G.First off the mark: Early seed germination[J]. Journal of Experimental Botany, 2011, 62(10): 3289-3309.
[9] Yang P, Li X, Wang X, Chen H, Chen F, Shen S.Proteomic analysis of rice (Oryza sativa) seeds during germination[J]. Proteomics, 2007, 7(18): 3358-3368.
[10] He D, Han C, Yang P.Gene expression profile changes in germinating rice[J]. Journal of Integrative Plant Biology, 2011, 53(10): 835-844.
[11] He D, Han C, Yao J, Shen S, Yang P.Constructing the metabolic and regulatory pathways in germinating rice seeds through proteomic approach[J]. Proteomics, 2011, 11(13): 2693-2713.
[12] He D, Yang P.Proteomics of rice seed germination[J]. Frontiers in Plant Science, 2013, 4: 246. Doi: 10.3389/fpls.2013.00246.
[13] Sano N, Ono H, Murata K, Yamada T, Hirasawa T, Kanekatsu M.Accumulation of long-lived mRNAs associated with germination in embryos during seed development of rice[J]. Journal of Experimental Botany, 2015, 66(13): 4035-4046.
[14] Wei T, He Z, Tan X, Liu X, Yuan X, Luo Y, Hu S.An integrated RNA-Seq and network study reveals a complex regulation process of rice embryo during seed germination[J]. Biochemical and Biophysical Research Communications, 2015, 464(1): 176-181.
[15] Chen C, Letnik I, Hacham Y, Dobrev P, Ben-Daniel B, Vankova R, Amir R, Miller G.ASCORBATE PEROXIDASE6 protects arabidopsis desiccating and germinating seeds from stress and mediates cross talk between reactive oxygen species, abscisic acid, and auxin[J]. Plant Physiology, 2014, 166(1): 370-383.
[16] He Y, Zhao J, Feng D, Huang Z, Liang J, Zheng Y, Cheng J, Ying J, Wang Z.RNA-Seq study reveals AP2-Domain-Containing signalling regulators involved in initial imbibition of seed germination in rice[J]. Rice Science, 2020, 27(4): 302-314.
[17] Penfield S.Seed dormancy and germination[J]. Current Biology, 2017, 27(17): R874-R878.
[18] Gimeno-Gilles C, Lelievre E, Viau L, Malik-Ghulam M, Ricoult C, Niebel A, Leduc N, Limami A M.ABA-Mediated inhibition of germination is related to the inhibition of genes encoding Cell-Wall biosynthetic and architecture: Modifying enzymes and structural proteins in medicago truncatula embryo axis[J]. Molecular Plant, 2009, 2(1): 108-119.
[19] Wang Y, Hou Y, Qiu J, Wang H, Wang S, Tang L, Tong X, Zhang J.Abscisic acid promotes jasmonic acid biosynthesis via a 'SAPK10-bZIP72-AOC' pathway to synergistically inhibit seed germination in rice (Oryza sativa)[J]. New Phytologist, 2020, 228(4): 1336-1353.
[20] Shu K, Liu X, Xie Q, He Z.Two faces of one seed: Hormonal regulation of dormancy and germination[J]. Molecular Plant, 2016, 9(1): 34-45.
[21] Umezawa T, Nakashima K, Miyakawa T, Kuromori T, Tanokura M, Shinozaki K, Yamaguchi-Shinozaki K.Molecular basis of the core regulatory network in ABA responses: Sensing, signaling and transport[J]. Plant and Cell Physiology, 2010, 51(11): 1821-1839.
[22] Nee G, Kramer K, Nakabayashi K, Yuan B, Xiang Y, Miatton E, Finkemeier I, Soppe W J J. DELAY of GERMINATION1 requires PP2C phosphatases of the ABA signalling pathway to control seed dormancy[J]. Nature Communications, 2017, 8: 72.
[23] Song S, Wang G, Wu H, Fan X, Liang L, Zhao H, Li S, Hu Y, Liu H, Ayaad M, Xing Y.OsMFT2 is involved in the regulation of ABA signaling-mediated seed germination through interacting with OsbZIP23/66/72 in rice[J]. Plant Journal, 2020, 103(2): 532-546.
[24] Liu X, Zhang H, Zhao Y, Feng Z, Li Q, Yang H, Luan S, Li J, He Z.Auxin controls seed dormancy through stimulation of abscisic acid signaling by inducing ARF-mediated ABI3 activation in Arabidopsis[J]. Proceedings of the National Academy of Sciences of the United States of America, 2013, 110(38): 15485-15490.
[25] He Y, Zhao J, Yang B, Sun S, Peng L, Wang Z.Indole-3-acetate beta-glucosyltransferase OsIAGLU regulates seed vigour through mediating crosstalk between auxin and abscisic acid in rice[J]. Plant Biotechnology Journal, 2020, 18(9): 1933-1945.
[26] Corbineau F, Xia Q, Bailly C, El-Maarouf-Bouteau H. Ethylene, a key factor in the regulation of seed dormancy[J]. Frontiers in Plant Science, 2014, 5: 539.
[27] Livak K J, Schmittgen T D.Analysis of relative gene expression data using Real-Time quantitative PCR and the 2-ΔΔCT method[J]. Methods, 2001, 25(4): 402-408.
[28] Dharmasiri N, Dharmasiri S, Estelle M.The F-box protein TIR1 is an auxin receptor[J]. Nature, 2005, 435(7041): 441-445.
[29] Soon F, Ng L, Zhou X E, West G M, Kovach A, Tan M H E, Suino-Powell K M, He Y, Xu Y, Chalmers M J, Brunzelle J S, Zhang H, Yang H, Jiang H, Li J, Yong E, Cutler S, Zhu J, Griffin P R, Melcher K, Xu H E. Molecular mimicry regulates ABA signaling by SnRK2 kinases and PP2C phosphatases[J]. Science, 2012, 335(6064): 85-88.
[30] Cutler S R, Rodriguez P L, Finkelstein R R, Abrams S R.Abscisic acid: Emergence of a core signaling network[J]. Annual Review of Plant Biology, 2010: 651-679.
[31] Chapman E J, Estelle M.Mechanism of Auxin-Regulated gene expression in plants[J]. Annual Review of Genetics, 2009, 43(1): 265-285.
[32] Jain M, Kaur N, Tyagi A K, Khurana J P.The auxin-responsive GH3 gene family in rice (Oryza sativa)[J]. Functional & Integrative Genomics, 2006, 6(1): 36-46.
[33] Zagorchev L, Seal C E, Kranner I, Odjakova M.A central role for thiols in plant tolerance to abiotic stress[J]. International Journal of Molecular Sciences, 2013, 14(4): 7405-7432.
[34] Chi Y, Cheng Y, Vanitha J, Kumar N, Ramamoorthy R, Ramachandran S, Jiang S.Expansion mechanisms and functional divergence of the glutathione S-Transferase family in sorghum and other higher plants[J]. DNA Research, 2011, 18(1): 1-16.
[35] Jo S H, Lee S H, Chun H S, Lee S M, Koh H J, Lee S E, Chun J S, Park J W, Huh T L.Cellular defense against UVB-induced phototoxicity by cytosolic NADP(+)- dependent isocitrate dehydrogenase[J]. Biochemical and Biophysical Research Communications, 2002, 292(2): 542-549.
[36] Jo S, Son M, Koh H, Lee S, Song I, Kim Y, Lee Y, Jeong K, Kim W B, Park J, Song B J, Huhe T.Control of mitochondrial redox balance and cellular defense against oxidative damage by mitochondrial NADP+-dependent isocitrate dehydrogenase[J]. Journal of Biological Chemistry, 2001, 276(19): 16168-16176.
[37] Noctor G, Mhamdi A, Chaouch S, Han Y, Neukermans J, Marquez-Garcia B, Queval G, Foyer C H.Glutathione in plants: An integrated overview[J]. Plant Cell and Environment, 2012, 35(2SI): 454-484.
[38] Moons A.Regulatory and functional interactions of plant growth regulators and plant glutathione S-transferases (GSTS)[J]// Vitamins and Hormones, 2005,72: 155-202.
[39] Miller G.Reactive oxygen signaling and abiotic stress[J]. Physiologia Plantarum, 2010, 133(3): 481-489.
[40] Murata Y, Pei Z M, Mori I C, Schroeder J.Abscisic acid activation of plasma membrane Ca2+ channels in guard cells requires cytosolic NAD(P)H and is differentially disrupted upstream and downstream of reactive oxygen species production in abi1-1 and abi2-1 protein phosphatase 2C mutants[J]. Plant Cell, 2002, 14(1): 287.
[41] Kusumi K, Yaeno T, Kojo K, Hirayama M, Hirokawa D, Yara A, Iba K.The role of salicylic acid in the glutathione-mediated protection against photooxidative stress in rice[J]. Physiologia Plantarum, 2006, 128(4): 651-661.
文章导航

/

浙ICP备05004719号-5
公安备案号:33010302003356
地址:浙江省杭州市富阳区水稻所路28号 邮编:311400 电话:0571-63370278 E-mail:cjrs@263.net
本系统由北京玛格泰克科技发展有限公司设计开发
总访问量: 今日访问: 在线人数: