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作物学报 ›› 2011, Vol. 37 ›› Issue (02): 286-293.doi: 10.3724/SP.J.1006.2011.00286

• 作物遗传育种·种质资源·分子遗传学 • 上一篇    下一篇

棉花CBF基因的克隆及其转基因烟草的抗寒性分析

郭惠明, 李召春, 张晗, 信月芝, 程红梅   

  1. 中国农业科学院生物技术研究所,北京 100081
  • 收稿日期:2010-08-02 修回日期:2010-10-09 出版日期:2011-02-12 网络出版日期:2010-12-15
  • 基金资助:

    本研究由国家科技重大专项转基因专项(2008ZX08005-004)和国家烟草专卖局(110200601010)项目支持资助。

Cloning of Cotton CBF Gene and Its Cold Tolerance Expression in Transgenic Tobacco

GUO Hui-Ming,LI Zhao-Chun,ZHANG Han,XIN Yue-Zhi,CHENG Hong-Mei*   

  1. Biotechnology Research Institute, Chinese Academy of Agricultural Sciences, Beijing100081, China
  • Received:2010-08-02 Revised:2010-10-09 Published:2011-02-12 Published online:2010-12-15

摘要: 从中棉12 (Gh12)、中棉36 (Gh36)和海岛棉7124 (Gb7124)品种中克隆并鉴定了棉花的CBF基因,该基因编码一个由184个氨基酸组成的蛋白CBF,该蛋白具有CBF转录因子典型的序列标签“PKRRAGRKKFQETRHP”和“FADSAW”。Southern杂交表明,CBF基因在3个棉花品种中均以基因家族的形式存在。围绕海岛棉7124的CBF基因(GbCBF1)开展的逆境表达谱分析表明,GbCBF1基因受低温、干旱、盐和ABA等多种逆境条件的诱导表达。将GbCBF1基因构建到由强启动子35S和弱启动子NOS这2种启动子控制的植物表达载体pCambia2301上并转化烟草NC89,经过筛选及PCR鉴定,共获得26株转基因烟草。对部分T1代植株进行的PCR和RT-PCR检测表明,GbCBF1基因可以在烟草中正常转录并遗传。分析表明,在低温下,转基因烟草的电解质渗漏率普遍低于野生型烟草,而游离脯氨酸含量和可溶性糖含量均高于野生型烟草,说明转GbCBF1基因提高了烟草的耐寒性。

关键词: 棉花, 转基因烟草, CBF, 转录因子, 抗寒性

Abstract: Low temperature is an adverse environment condition affecting the growth and productivity of crops, it is also one of limiting factors for cotton yeild and quality in China.CBF is a kind of transcription factor that can regulate expression of a number of genes related with abiotic stresses. Therefore, it is important to study the characteristics of cotton CBFs and their response to abiotic stresses. In this study, CBF gene was isolated from the genomic DNA of cotton cultivars Gh12, Gh36 and Gb7124. Cotton CBF gene encodes 184 amino acids, containing CBF-family signature “PKRRAGRKKFQETRHP” and “FADSAW”. Southern blotting result showed that CBF genes were presented as the form of gene family in the genome of cotton. Northern blotting result indicated that GbCBF1 gene was induced by low temperature, drought, salt and ABA. GbCBF1 was constructed into plant expression vector pCambia2301, in which the gene was driven by 35S and NOS promoters separately. Plant expression vectors were then transferred into tobacco NC89 using Agrobacterium-mediated transformation method. Twenty six trangentic tobacco lines were obtained after kanamycin screening and PCR detection. PCR and Reverse tanscription PCR methods were used to analyze part of T1 transgenic tobacco, the results showed that GbCBF1gene could be transcripted and inherit in offspring normally. The analytical result demonstrateted that the electrolytic leakage rate of transgenic tobacco was lower than that of wild type tobacco generally, however, free proline content and soluble sugar content of transgenic tobacco were higher than those of wild type tobacco under low temperature stress. In conclusion, GbCBF1 enhances cold tolerance in transgenic tobacco.

Key words: Cotton, Transgenic tobacco, CBF, Transcription factor, Cold tolerance

[1]Bray E A. Plant responses to water deficit. Trends Plant Sci, 1997, 2: 48–54
[2]Gilmour S J, Zarka D G, Stockinger E J, Salazar M P, Houghton J M, Thomashow M F. Low temperature regulation of the Arabidopsis CBF family of AP2 transcriptional activators as an early step in cold induced COR gene expression. Plant J, 1998, 16: 433–442
[3]Baker S S, Wilhelm K S, Thomashow M F. The 5'-region of Arabidopsis thaliana corl5a has cis-acting elements that confer cold-, drought- and ABA-regulated gene expression. Plant Mol Biol, 1994, 24: 701–713
[4]Dubouzet J G, Sakuma Y, Ito Y, Kasuga M, Dubouzet E G, Miura S, Seki M, Shinozaki K, Yamaguchi-Shinozaki K. OsDREB genes in rice, Oryza sativa L., encode transcription activators that function in drought-, high-salt- and cold-responsive gene expression. Plant J, 2003, 33: 751–763
[5]Fan Y-L(樊亚利). Reviewing sixty years’ development of cotton industry in Xinjiang. Finance & Economics of Xinjiang (新疆财经), 2009, (5): 18–23 (in Chinese with English abstract)
[6]Artus N N, Uemura M, Steponkus P L, Gilmour S J, Lin C T, Thomashow F. Constitutive expression of the cold regulated Arabidopsis thaliana COR15a gene affects both chloroplast and protoplast freezing to lerance. Proc Natl Acad Sci USA, 1996, 93: 13404–13409
[7]Monroy A F, Castonguay Y, Laberge S, Sarhan F, Vezina L P, Dhindsa R S. A new cold-induced alfalfa gene is associated with enhanced hardening at subzero temperature. Plant Physiol, 1993, 120: 873–879
[8]Thomashow M F. Plant cold acclimation: Freezing tolerance genes and regulation mechanisms. Annu Rev Plant Physiol Plant Mol Biol, 1999, 50: 571–599
[9]Stockinger E J, Gilmour S J, Thomashow M F. Arabidopsis thaliana CBF1 encodes an AP2 domain-containing transcriptional activator that binds to the C-repeat/DRE, a cis-acting DNA regulatory element that stimulates transcription in response to low temperature and water deficit. Proc Natl Acad Sci USA, 1997, 94: 1035–1040
[10]Liu Q, Kasuga M, Sakuma Y, Abe H, Miura S, Yamaguchi-Shinozaki K, Shinozaki K. Two transcription factors, DREB1 and DREB2, with an EREBP/AP2 DNA binding domain separate two cellular signal transduction pathways in drought and low temperature responsive gene expression, respectively, in Arabidopsis. Plant Cell, 1998, 10: 1391–1406
[11]Gilmour S J, Fowle S G. Thomashow M F. Arabidopsis transcriptional activators CBF1, CBF2, and CBF3 have matching functional activities. Plant Mol Biol, 2004, 54: 767–781
[12]Ito Y, Katsura K, Maruyama K, Taji T, Kobayashi M, Seki M, Shinozaki K, Yamaguchi-Shinozaki K. Functional analysis of rice DREB1/CBF-type transcription factors involved in cold-responsive gene expression in transgenic rice. Plant Cell Physiol, 2006, 47: 141–153
[13]Qin F, Sakuma Y, Li J, Liu Q, Li Y Q, Shinozaki K, Yamaguchi-Shinozaki K. Cloning and functional analysis of a novel DREB1/CBF transcription factor involved in cold responsive gene expression in Zea mays L. Plant Cell Physiol, 2004, 45: 1042–1052
[14]Zhang X, Fowler S G, Cheng H M, Lou Y G, Rhee S Y, Stockinger E J, Thomashow M F. Freezing-sensitive tomato has a functional CBF cold response pathway, but a CBF regulon that differs from that of freezing tolerant Arabidopsis. Plant J, 2004, 39: 905–919
[15]Xiong Y W, Fei S Z. Functional and phylogenetic analysis of a DREB/CBF-like gene in perennial ryegrass (Lolium perenne L.). Planta, 2006, 224: 878–888
[16]Wang G-L(王关林), Fang H-J(方宏筠). Plant Genetic Engineering (植物基因工程), 2nd edn. Beijing: Scientific and Technical Publishers, 2002 (in Chinese)
[17]Hunag W-K(黄文坤), Cheng H-M(程红梅), Guo J-Y(郭建英), Gao B-D(高必达), Wan F-H(万方浩). Method of RNA extraction from different tissues of invasive alien weed Eupatorium adenophorum. Biotech Bull (生物技术通报), 2007, 2: 147–150 (in Chinese with English abstract)
[18]Gong M, Li Y J, Chen S Z. Abscisic acid-induced thermotolerance in maize seedling is mediated by calcium and associated with antioxidant systems. J Plant Physiol, 1998, 153: 488–496
[19]Bates L S, Waldren R P, Teare I D. Rapid determination of free proline for water stress studies. Plant Soil, 1973, 39: 205–207
[20]Irigoyen J J, Emerich D W, Sánchez-Díaz M. Water stress induced changes in concentrations of praline and total soluble sugars in nodulated alfalfa (Medicago sativa) plants. Physiol Plant, 1992, 84: 55–60
[21]Abe H, Yamaguchi-Shinozaki K, Urao T, Iwasaki T, Hosokawa D, Shinozaki K. Role of Arabidopsis MYC and MYB homoloys in drought and abscisic acid-regulated gene expression. Plant Cell, 1997, 9: 1859–1868
[22]Guy C L. Cold acclimation and freezing stress tolerance: role of protein metabolism. Annu Rev Plant Physiol Plant Mol Biol, 1990, 41: 187–223
[23]Delauney A J. Verma D P S. Proline biosynthesis and osmo regulation in plants. Plant J, 1993, 4: 215–223
[24]Gilmour S, Sebolt A M, Salazar M P, Everard J D, Thomashow M F. Overexpression of the Arabidopsis CBF3 transcriptional activator mimics multiple biochemical changes associated with cold acclimation. Plant Physiol, 2000, 124: 1854–1865
[25]Cholewa E, Cholewinski A J, Shelp B J, Snedden W A, Bown A W. Cold shock stimulated Caminobutyric acid synthesis ismediated by an increase incytosolic Ca2+, not by an increase in cytosolic H+. Can J Bot, 1997, 75: 375–382
[26]Wanner L A, Junttila O. Cold induced freezing tolerance in Arabidopsis. Plant Physiol, 1999, 120: 391–400
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