欢迎访问作物学报，今天是
作物学报

作物学报 ›› 2010, Vol. 36 ›› Issue (1): 147-153.doi: 10.3724/SP.J.1006.2010.00147

• 耕作栽培·生理生化 • 上一篇    下一篇

转PvP5CS1基因拟南芥植株对干旱和盐胁迫的反应

陈吉宝1,2，赵丽英2，毛新国1，王述民1,*，景蕊莲1,*   

  1. 1中国农业科学院作物科学研究所/农作物基因资源与基因改良国家重大科学工程/农业部作物种质资源与生物技术重点实验室，北京100081；2南阳师范学院生命科学与技术学院，河南南阳473061
  • 收稿日期:2009-09-05 修回日期:2009-09-01 出版日期:2010-01-12 网络出版日期:2009-11-17
  • 通讯作者: 王述民, E-mail: smwang@mail.caas.net.cn, Tel: 010-82108567; 景蕊莲, E-mail: jingrl@caas.net.cn, Tel: 010-62186706
  • 基金资助:

    本研究由车窗科技支撑计划项目（2006BAD13B05）资助。

Response of PvP5CS1 Transgenic Arabidopsis Plants to Drought-and Salt-Stress

CHEN Ji-Bao1,2,ZHAO Li-Ying2,MAO Xin-Guo1,WANG Shu-Min1,*,JING Rui-Lian1   

  1. 1National Key Facility for Crop Gene resources and Genetic Improvement/Key Laboratory of Crop Germplasm & Biotechnology,Ministry of Agriculture/Institute of Crop Sciences,Chinese Academy of Agricultural Sciences,Beijing 100081,China;2School of Life Science and Technology,Nanyang Normal University,Nanyang 473061,China
  • Received:2009-09-05 Revised:2009-09-01 Published:2010-01-12 Published online:2009-11-17
  • Contact: WANG Shu-Min, E-mail: smwang@mail.caas.net.cn, Tel: 010-82108567; 景蕊莲, E-mail: jingrl@caas.net.cn, Tel: 010-62186706

PDF

3766

被引次数

28

摘要：

为探索普通菜豆脯氨酸合成酶基因P5CS1在植物渗透胁迫中的作用，本研究应用农杆菌介导法，将PvP5CS1基因转入拟南芥，获得6株阳性转基因株系；通过检测转基因植株与野生型植株在干旱和盐胁迫下种子发芽率，幼苗脯氨酸含量、株系电导率、相对根长和成株死亡率，分析了PvP5CS1基因的表达对改善拟南芥抗渗透胁迫的效应。结果表明，在150 mmol L-1 NaCl和150 mmol L-1甘露醇渗透胁迫下，转基因植株平均相对发芽率分别是野生型的1.6倍和1.62倍；150、250 mmol L-1甘露醇和150 mmol L-1 NaCl处理下，转基因拟南芥植株平均脯氨酸含量分别是野生型的2.68、1.30和1.30倍；平均相对电导率分别是野生型植株的85%、77%和85%；平均相对根长分别是野生型植株的1.2、1.3和1.2倍；300 mmol L-1 NaCl处理下，转基因植株的平均死亡率为42%，显著低于野生型(90%)(P<0.05)；干旱胁迫下，转基因植株的平均死亡率为56%，显著低于野生型(70%)(P<0.05)，说明PvP5CS1基因在拟南芥中的表达明显改善了转基因植株的抗旱性和耐盐性。

关键词: PvP5CS1, 脯氨酸, 干旱胁迫, 盐胁迫

Abstract:

Under adverse environment, many plants increase their cell osmotic potential through accumulation of intracellular organic osmolytes-proline. The proline accumulation in plants can not only increase cell osmotic potential but also stabilize proteins, membranes, and subcellular structures as well as protect cells against oxidative damage by reactive oxygen species. Pyrroline- 5-carboxylate synthetase (P5CS), a rate-limiting enzyme involved in the biosynthesis of proline in higher plants, is encoded by P5CS gene. The full length cDNA sequence of PvP5CS1 gene was subcloned into pCHF3 vector and transformed into wild Arabidopsis via Agrobacterium tumefaciens. A total of six positive transgenic plants were obtained. The result of RT-PCR showed that the PvP5CS1 gene was normally expressed in transgenic plants. The T4 generation purified lines of transgenic plants and wild Arabidopsis were used for osmotic stress experiment. Seed relative germination rates of transgenic plants under treatment or non-treatment conditions were all significantly higher than those of wild plants under stress conditions (P<0.001). The average seed relative germination rate of transgenic seedlings was 1.62 times and 1.6 times higher than those of wild plants treated with 150 mmol L-1 mannitol and 150 mmol L-1 NaCl, respectively. Proline content, conductivity rate and root length of eight-day transgenic seedlings under osmatic stress were determined. The results showed that introduction of PvP5CS1 gene into Arabidopsis resulted in significant accumulation of proline. The relative proline content in transgenic plants under stress non-treated conditions were all significantly higher than those in wild type plants (P<0.05). Under four treatments (CK, 150, 250 mmol L-1 mannitol and 150 mmol L-1 NaCl), the average relative proline contents in transgenic plants were 1.38, 2.68, 1.30 and 1.30 times of those in wild type plants. The transgenic plants had longer root and less cell damage than wild plants under osmotic stress conditions. Under 150, 250 mmol L-1 mannitol- and 150 mmol L-1 NaCl-stress conditions, average relative conductivity rate in transgenic plants were 85%,77%, and 85% of that in wild type plants, respectively. The average relative root length in transgenic plants was 1.2,1.3, and 1.2 times of that in wild type plants, respectively. After 300 mmol L-1 NaCl treatment for 15 days, the seedling death rate was 42% and 90% for transgenic and wild type plants, respectively. In the condition of drought stress for 25 days and following by re-watering for 5 days, the seedling death rate of transgenic plants was also significantly lower than that of wild types (P<0.05), which was 56% for transgenic plants and 70% for wild plants. These results indicated that over-expression of PvP5CS1 in transgenic Arabidopsis plants increased plants tolerance to salt and drought stresses.

Key words: PvP5CS1, Proline, Drought stress, Salt stress

[1] Bohnert H J, Jensen R G. Strategies for engineering water stress tolerance in plants. Trends Biotechnol, 1996, 14: 89-97

[2] Schat H, Sharma S S, Vooijs R. Heavy metal induced accumulation of free proline in a metal-tolerant and a non-tolerant ecotype of Silene vulgaris. Physiol Plant, 1997, 101: 477-482


 



[3] Trotel P, Bouchereau A, Niogret M F, Larher F. The fate of osmo-regulated proline in leaf discs of rape (Brassica napus L.) incubated in a medium of low osmolarity. Plant Sci, 1996, 118: 31-45



[4] Zhu B, Su J, Chang M, Verma D P S, Fan U L, Wu R. Overexpression of a Δ1-pyrroline-5-carboxylate synthetase gene and analysis of tolerance to water-and salt-stress in transgenic rice. Plant Sci, 1998, 139: 41-48



[5] Igarashi Y, Yoshiba Y, Sanada Y, Yamaguchi-Shinozaki K, Wada K, Shinozaki K. Characterization of the gene for Δ1- pyrroline-5-carboxylate synthetase and correlation between the expression of the gene and salt tolerance in Oryza sativa. Plant Mol Biol, 1997, 33: 857-865



[6] Sawahel W A, Hassan A H. Generation of transgenic wheat plants producing high levels of the osmoprotectant proline. Biotechnol Lett, 2002, 24: 721-725



[7] Han K H, Hwang C H. Salt tolerance enhanced by transformation of a P5CS gene in carrot. J Plant Biotechnol, 2003, 5: 149-153



[8] Chen J-B(陈吉宝). Cloning, Function Analysis and Single Nucleotide Polymorphism of Common Bean (Phaseoleae vulgaris L.) P5CS Gene. PhD Dissertation of Chinese Academy and Agricultural Sciences,2008 (in Chinese with English abstract)



[9] Chen J B, Wang S M, Jing R L, Mao X G. Cloning the PvP5CS gene from common bean (Phaseolus vulgaris) and its expression patterns under abiotic stresses. J Plant Physiol, 2009, 166: 12-19



[10] Chen J-B(陈吉宝), Jing R-L(景蕊莲), Mao X-G(毛新国), Chang X-P(昌小平), Wang S-M(王述民). A response of PvP5CS2 gene to abiotic stresses in common bean. Acta Agron Sin (作物学报), 2008, 34(7): 1121-1127 (in Chinese with English abstract)



[11] Xu C-Y(徐重益), Jing R-L(景蕊莲). Isolation, location and functional analysis of drought-response gene TaPP2Ac/a from wheat (Triticum aestivum L.). PhD Dissertation of Chinese Academy and Agricultural Sciences,2007



[12] Kavi-Kishor P B, Sangam S, Amrutha R N, Laxmi P S, Naidu K R, Rao K R S S, Rao S, Reddy K J, Theriappan P, Sreenivasulu N. Regulation of proline biosynthesis, degradation, uptake and transport in higher plants: Its implications in plant growth and abiotic stress tolerance. Curr Sci, 2005, 88: 424-438



[13] Verslues P E, Agarwal M, Katiyar-Agarwal S, Zhu J, Zhu J K.Methods and concepts in quantifying resistance to drought, salt and freezing, abiotic stresses that affect plant water status. Plant J, 2006, 45: 523-539



[14] Armengaud P, Thiery L, Buhot N, Grenier-De March G, Savouré A. Transcriptional regulation of proline biosynthesis in Medicago truncatula reveals developmental and environmental specific features. Physiol Plant, 2004, 120: 442-450



[15] Kavi-Kishor P B, Hong Z, Miao G H, Hu C A A, Verma D P S. Over expression of Δ1-pyrroline-5-carboxylate synthetase increases proline overproduction and confers osmtolerance in transgenic plants. Plant Physiol, 1995, 108: 1387-1394



[16] Yamada M, Morishita M, Urano K, Shiozaki N, Yamaguchi-Shinozaki K, Shinozaki K, Yoshiba Y. Effects of free proline accumulation in petunias under drought stress. J Exp Bot, 2005, 56: 1975-1981



[17] Su J, Wu R. Stress-inducible synthesis of proline in transgenic rice confers faster growth under stress conditions than that with constitutive synthesis. Plant Sci, 2004, 166: 941-948
[1] 邹仪妹, 徐敏, 汪海洋, 姚辉, 王加峰, 刘浩, 任代胜. 两系不育系水稻幼苗根系响应盐胁迫的转录因子调控网络鉴定[J]. 作物学报, 2026, 52(6): 1728-1742.
[2] 宋裕祯, Bheel Chander Kumar, 王跃, 张颖星, 郭娟, Khound Rituraj, Santra Dipak Kumar, 曹晓宁, 王瑞云. 糜子AP2亚家族全基因组鉴定及PmAP2-1和PmAP2-9耐盐功能分析[J]. 作物学报, 2026, 52(4): 1127-1139.
[3] 覃奕琰, 付瑶, 苏畅, 李娜, 徐静茹, 程笑然, 张琪, 赵明辉. OsST41调控水稻苗期耐盐性的功能分析[J]. 作物学报, 2026, 52(3): 802-812.
[4] 张晴, 杨昱, 郭茜, 岳霈尧, 殷丛丛, 牛景萍, 赵晋忠, 杜维俊, 岳爱琴. 大豆GmARA6a的克隆及响应盐胁迫的功能分析[J]. 作物学报, 2026, 52(2): 480-493.
[5] 杨飚, 杜帅康, 张继旺, 石瑛, 张丽莉. 马铃薯III类POD基因家族的全基因组鉴定及其表达谱分析[J]. 作物学报, 2026, 52(2): 405-420.
[6] 刘吉昌, 李思烨, 李雪婷, 王洪章, 刘鹏, 张吉旺, 赵斌, 任佰朝, 任昊. 盐胁迫对不同耐盐型夏玉米品种根系生长及养分吸收效率的影响[J]. 作物学报, 2026, 52(2): 565-577.
[7] 刘海波, 张蕾, 王立琦, 石晓丽, 周文莹, 崔国贤, 佘玮. 苎麻BnGCL1基因响应干旱胁迫的功能研究[J]. 作物学报, 2026, 52(1): 14-27.
[8] 王雅致, 杨飚, 季香林, 石瑛, 张丽莉. 二倍体马铃薯抗旱资源鉴定及抗旱基因初步筛选[J]. 作物学报, 2026, 52(1): 72-84.
[9] 孔娜, 刘涛, 刘文婷, 陈刚, 文利超, 邓智超, 郭梅, 李伟, 郭永峰. 烟草NtCEP7基因克隆及其编码小肽在苗期抗旱中的作用分析[J]. 作物学报, 2026, 52(1): 249-261.
[10] 胡城祯, 高维东, 孔斌雪, 王建飞, 车卓, 杨德龙, 陈涛. 小麦TaAPC11基因家族鉴定及TaAPC11-5B参与干旱胁迫的生物学功能研究[J]. 作物学报, 2026, 52(1): 148-164.
[11] 何鹏旭, 姚立蓉, 陈远玲, 闫妍, 张宏, 汪军成, 李葆春, 杨轲, 司二静, 孟亚雄, 马小乐, 王化俊. 大麦干旱胁迫萌发生理及分子机理的差异性与相关性研究[J]. 作物学报, 2025, 51(9): 2412-2432.
[12] 陆雯佳, 汪军成, 姚立蓉, 张宏, 司二静, 杨轲, 孟亚雄, 李葆春, 马小乐, 王化俊. 大麦PRX基因家族全基因组鉴定及其干旱胁迫下的表达分析[J]. 作物学报, 2025, 51(5): 1198-1214.
[13] 潘炬忠, 韦萍, 朱德平, 邵胜雪, 陈珊珊, 韦雅倩, 高维维. 水稻转录因子OsERF104的克隆和功能研究[J]. 作物学报, 2025, 51(4): 900-913.
[14] 王林, 陈晓雨, 张文梦龙, 汪思琦, 程冰云, 程靖秋, 潘锐, 张文英. 大麦HvMYB2分子特性及响应干旱胁迫的功能分析[J]. 作物学报, 2025, 51(4): 873-887.
[15] 李雪婷, 任昊, 王洪章, 张吉旺, 赵斌, 任佰朝, 刘莹, 姚海燕, 刘鹏. 盐胁迫对不同耐盐型玉米品种叶片光合性能和干物质积累与分配的影响[J]. 作物学报, 2025, 51(4): 1091-1101.
Viewed
Full text


Abstract

Cited
  Shared   
  Discussed   
No Suggested Reading articles found!
京ICP备15008789号-2