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番茄脱水素基因SlDHN2b的克隆与表达分析

Cloning and Characterization of Dehydrins Gene SlDHN2b in Tomato

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【作者】 郭鹏张士刚金华邹吉祥董燕姜国斌

【Author】 GUO Peng 1 ,ZHANG Shi-gang 2 ,JIN Hua 1 ,ZOU Ji-xiang 1 ,DONG Yan 3 ,and JIANG Guo-bin 1,* ( 1 College of Environment and Resources,Dalian Nationalities University,Dalian,Liaoning 116600,China; 2 Tai’an Municipal Bureau of Agriculture,Tai’an,Shandong 271018,China; 3 Liaoning Forestry Vocational and Technical College, Shenyang 110101,China)

【机构】 大连民族学院环境与资源学院生物技术系山东泰安市农业局辽宁林业职业技术学院

【摘要】 利用RT-PCR从番茄叶片中获得脱水素基因(dehydrins)的cDNA序列,命名为SlDHN2b。该基因开放阅读框1140bp,编码380个氨基酸。蛋白序列分析表明该蛋白高度亲水。Real-timePCR分析表明该基因受盐、脱水、ABA诱导表达。通过染色体步移技术获得SlDHN2b基因的启动子,PLACE数据库分析预测SlDHN2b启动子序列中含有多种逆境相关的作用元件。Northern杂交表明该基因在叶片中表达量最高,果实、花、茎中次之,根中最少。

【Abstract】 In present study,a cDNA clone,designated SlDHN2b,was isolated from tomato by RT-PCR. The ORF of SlDHN2b was 1 140 bp and contained 380 amino acid residues. Protein sequence analysis showed that the SlDHN2b was high hydrophilic. Real-time PCR analysis indicated that mRNA accumulation of SlDHN2b was induced by salt stress,abscisic acid(ABA)and dehydration. Analysis of the promoter of PdEPF1 revealed the presence of stress-responsive elements by genome walking kit. Tissue-specific expression indicated that SlDHN2b was mainly expressed in leaves,weakly expressed in bud,flower,stem and the lowest in roots. Analysis of the promoter of SlDHN2b revealed the presence of stress-responsive elements.

【关键词】 番茄SlDHN2b克隆逆境启动子
【Key words】 tomatoSlDHN2bcloningabiotic stresspromoter
【基金】 国家自然科学基金项目(31100489);辽宁省重点农业攻关计划项目(2008207001);中央高校基本科研业务费资助项目(DC12010204)
  • 【文献出处】 园艺学报 ,Acta Horticulturae Sinica , 编辑部邮箱 ,2012年10期
  • 【分类号】S641.2
  • 【被引频次】8
  • 【下载频次】254
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