甘薯Ran基因的克隆和表达分析  

Cloning and Expression Analysis of Ran Gene in Sweet Potato

作　　者：范乾程[1] 王亚[1] 隋炯明[1] 毕英娜 刘媛 王晶珊[1] 

机构地区：[1]青岛农业大学生命科学学院/山东省高校植物生物技术重点实验室,山东青岛266109 [2]威海恩特花木有限公司,山东威海264205 [3]莱西市农业局,山东莱西266600

出　　处：《农学学报》2013年第3期4-9,共6页Journal of Agriculture

基　　金：青岛农业大学大学生创新项目"条斑紫菜抗逆基因Rab的克隆及其功能验证"(631121)

摘　　要：Ran蛋白是小GTP结合蛋白家族成员之一,控制着蛋白和RNA分子的运输过程。研究发现有些Ran基因受多种逆境胁迫的诱导表达。为了获得甘薯Ran基因,本试验通过RT-PCR克隆了1个甘薯Ran基因。测序结果显示其含有长666bp的完整开放阅读框,编码的蛋白含221个氨基酸,推测分子量为25.15kDa。比对分析发现甘薯与多种生物的Ran蛋白的氨基酸序列同源性都超过90%,荧光定量PCR研究表明IbRan基因受低温、PEG、盐和植物激素ABA的诱导表达。这为利用基因工程手段调控甘薯的抗逆性奠定了基础。Ran protein is a member of small GTP-binding protein family controlling the transport of protein and RNA, some of them are found to be responsive to different environmental stresses. In order to obtain Ran gene in sweet potato, Ran gene from sweet potato （IbRan） was amplified successfully by RT-PCR. Sequencing result indicated that the cloned cDNA contained a continuous complete open reading frame （ORF） of 666 bp encoding a polypeptide of 221 amino acids with a calculated molecular mass of 25.15 kDa. Sequence comparison of the IbRan showed very high homology to the Ran subfamily from other species, with over 90% homology. Transcription of IbRan gene was differentially regulated by different environmental stimuli such as cold, PEG, NaCl and the plant hormone ABA using real-time PCR. This gene can be used to regulate stresses resistance of sweet potato by genetic engineerinz.

关 键 词：甘薯 Ran基因 进化树 表达分析 

分 类 号：Q781[生物学—分子生物学]