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作物学报 ›› 2018, Vol. 44 ›› Issue (01): 24-31.doi: 10.3724/SP.J.1006.2018.00024

• 作物遗传育种·种质资源·分子遗传学 • 上一篇    下一篇

水稻ABA生物合成基因OsNCED3响应干旱胁迫

徐学中,汪婷,万旺,李思慧 ,朱国辉*   

  1. 华南农业大学生命科学学院,广东广州 510642
  • 收稿日期:2016-11-30 修回日期:2017-09-10 出版日期:2018-01-12 网络出版日期:2017-10-27
  • 基金资助:

    本研究由国家自然科学基金项目(31171466, 31570250)和国家重点基础研究发展计划(2012CB114306)资助。

ABA Biosynthesis Gene OsNCED3 Confers Drought Stress Tolerance in Rice

XU Xue-Zhong,WANG Ting,WAN Wang,LI Si-Hui,ZHU Guo-Hui*   

  1. College of Life Sciences, South China Agricultural University, Guangzhou 510642, Guangdong, China
  • Received:2016-11-30 Revised:2017-09-10 Published:2018-01-12 Published online:2017-10-27
  • Supported by:

    This study was supported by the National Natural Science Foundation of China (31171466) and the National Basic Research Program of China (2012CB114306).

摘要:

9-顺-环氧类胡萝卜素双加氧酶(NCED)是植物内源脱落酸(ABA)生物合成的限速酶,由NCED基因家族编码,水稻中响应干旱胁迫并以此调节ABA水平的OsNCED基因尚见未报道。本研究发现在水稻已报道的5个OsNCED基因中,OsNCED3的表达受干旱胁迫诱导,复水处理后其表达快速下调,其表达模式与此过程中内源ABA含量变化趋势一致。OsNCED3的RNAi转基因植株表现为干旱敏感,且生物量下降;而过量表达OsNCED3基因增加了水稻的抗旱性。干旱胁迫下过量表达OsNCED3的转基因株系有较高的ABA水平,同时其抗氧化酶超氧化物歧化酶(SOD)、过氧化物酶(POD)和过氧化氢酶(CAT)活性,以及逆境响应基因脱水素蛋白(Dehydrin)和胚胎发育晚期丰富蛋白(LEA)转录表达均高于野生型。下调表达OsNCED3的转基因株系则呈现相反的变化趋势。因此,OsNCED3是水稻干旱胁迫响应基因,调节了干旱环境下ABA水平和抗逆性。

关键词: OsNCED3基因, 干旱胁迫, 脱落酸, 水稻

Abstract:

NCED (9-cis-epoxycarotenoid dioxygenase), encoded by NCED gene family, is a rate limited enzyme responsible for the ABA biosynthesis in plants. It remains unknown whether OsNCED genes are responsible for controlling ABA levels during drought stress in rice. Among the five OsNCED genes, we found that OsNCED3 mRNA level was promptly induced by PEG-mimic drought stress and decreased by re-watering, with a tendency of well consistent with the variation of ABA content. Down-regulating of OsNCED3 gene expression in RNA interference (RNAi)-transgenic plants decreased the total biomass and showed a hypersensitive phenotype subjecting to drought stress, while the overexpression (OE)-transgenic seedlings increased the drought stress tolerance compared with the wild-type (WT). ABA contents in OsNCED3-OE leaves were higher than those in WT, meanwhile, OsNCED3-OE lines also increased the activities of anti-oxidative enzyme including superoxide dismutase (SOD), peroxidase (POD), catalase (CAT), and expressions of stress/drought-related genes, i.e. dehydrin protein, LEA protein under drought stress. OsNCED3-RNAi lines showed an opposite tendency with the OsNCED3-OE plants. We therefore conclude that OsNCED3 gene plays an important role in controlling ABA level and drought stress resistance in rice.

Key words: OsNCED3 gene, drought stress, abscisic acid, Oryza sativa

[1]Hu H, Xiong L. Genetic engineering and breeding of drought-resistant crops. Annu Rev Plant Biol, 2014, 65: 715–741 [2]Zhu J K. Salt and drought stress signal transduction in plants. Annu Rev Plant Biol, 2002, 53: 247–273 [3]Shinozaki K, Yamaguchi-Shinozaki K. Gene networks involved in drought stress response and tolerance. J Exp Bot, 2007, 58: 221–227 [4]Nambara E, Marion-Poll A. Abscisic acid biosynthesis and catabolism. Annu Rev Plant Biol, 2005, 56: 165–185 [5]Qin X, Zeevaart J A. The 9-cis-epoxycarotenoid cleavage reaction is the key regulatory step of abscisic acid biosynthesis in water-stressed bean. Proc Natl Acad Sci USA, 1999, 96: 15354–15361 [6]Zhu G, Ye N, Zhang J. Glucose-induced delay of seed germination in rice is mediated by the suppression of ABA catabolism rather than an enhancement of ABA biosynthesis. Plant Cell Physiol, 2009, 50: 644–651 [7]Zhu G, Ye N, Yang J, Peng X, Zhang J. Regulation of expression of starch synthesis genes by ethylene and ABA in relation to the development of rice inferior and superior spikelets. J Exp Bot, 2011, 62: 3907–3916 [8]Hwang S, Chen H, Huang W, Chu Y, Shii C, Cheng W. Ectopic expression of rice OsNCED3 in Arabidopsis increases ABA level and alters leaf morphology. Plant Sci, 2010, 178: 12–22 [9]李合生. 植物生理生化实验原理和技术. 北京: 高等教育出版社, 2000. pp 261–263 Li H S. Experimental Principle and Technology of Plant Physiology and Biochemistry. Beijing: Higher Education Press, 2000. pp 261–263 [10]Priya R, Siva R. Analysis of phylogenetic and functional diverge in plant nine-cis epoxycarotenoid dioxygenase gene family. J Plant Res, 2015, 128: 519–534 [11]Tan B C, Joseph L M, Deng W T, Liu L, Li Q B, Cline K, Mccarty D R. Molecular characterization of the Arabidopsis 9-cis epoxycarotenoid dioxygenase gene family. Plant J, 2003, 35: 44–56 [12]Iuchi S, Kobayashi M, Taji T, Naramoto M, Seki M, Kato T, Tabata S, Kakubari Y, Yamaguchi-Shinozaki K, Shinozaki K. Regulation of drought tolerance by gene manipulation of 9-cis-epoxycarotenoid dioxygenase, a key enzyme in abscisic acid biosynthesis in Arabidopsis. Plant J, 2001, 27: 325–333 [13]Ruggiero B, Koiwa H, Manabe Y, Quist T M, Inan G, Saccardo F, Joly R J, Hasegawa P M, Bressan R A, Maggio A. Uncoupling the effects of abscisic acid on plant growth and water relations. Analysis of sto1/nced3, an abscisic acid-deficient but salt stress-tolerant mutant in Arabidopsis. Plant Physiol, 2004, 136: 3134–3147 [14]Lefebvre V, North H, Frey A, Sotta B, Seo M, Okamoto M, Nambara E, Marion-Poll A. Functional analysis of Arabidopsis NCED6 and NCED9 genes indicates that ABA synthesized in the endosperm is involved in the induction of seed dormancy. Plant J, 2006, 45: 309–319 [15]Hu X, Zhang A, Zhang J, Jiang M. Abscisic acid is a key inducer of hydrogen peroxide production in leaves of maize plants exposed to water stress. Plant Cell Physiol, 2006, 47: 1484–1495 [16]Esterbauer H, Schaur R J, Zollner H. Chemistry and biochemistry of 4-hydroxynonenal, malonaldehyde and related aldehydes. Free Radic Biol Med, 1991, 11: 81–128 [17]Apel K, Hirt H. Reactive oxygen species: metabolism, oxidative stress, and signal transduction. Annu Rev Plant Biol, 2004, 55: 373–399 [18]Xiang Y, Tang N, Du H, Ye H, Xiong L. Characterization of OsbZIP23 as a key player of the basic leucine zipper transcription factor family for conferring abscisic acid sensitivity and salinity and drought tolerance in rice. Plant Physiol, 2008, 148: 1938–1952 [19]Hundertmark M, Hincha D K. LEA (late embryogenesis abundant) proteins and their encoding genes in Arabidopsis thaliana. BMC Genomics, 2008, 9: 1–22

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