大白菜DREB类转录因子cDNA的克隆及植物表达载体的构建  

Cloning the cDNA of DREB-like Transcription Factor from Chinese Cabbage and Construction of Plant Expression Vector

作　　者：李妍[1] 申书兴[1] 轩淑欣[1] 李晓峰[1] 王彦华[1] 

机构地区：[1]河北农业大学园艺学院,河北保定071001

出　　处：《华北农学报》2009年第1期69-73,共5页Acta Agriculturae Boreali-Sinica

基　　金：河北省自然科学基金(C2006000416);河北农业大学博士启动基金

摘　　要：以干旱处理的大白菜自交系85-1为材料,利用RT-PCR技术获得了大白菜DREB类转录因子基因的cDNA编码序列,命名为BcDREB1(GenBank登录号为:EU924266)。序列分析表明,BcDREB1核苷酸序列长663 bp,编码214个氨基酸,含有一个典型的AP2结构域,具有DREB转录因子的典型特征。将该基因的cDNA编码序列连接到植物表达载体pCAMBIA2301中,成功构建了大白菜BcDREB1基因的植物表达载体pCAM-BcDREB1,为进一步通过转基因技术研究该基因的功能奠定了基础。The cDNA of DREB transcription factor named BcDREB1 （C, enBank accession number EU924266）was obtained from Chinese cabbage inbred line 85-1 under the drought stress by RT-PCR method.The sequence analysis indicated that the clone was consisted of 663 nucleotides（nt）, coding 214 amino acids. The deduced primary structure of BcDREB1 contained a single AP2 domain and showed the typical characteristics of DREB gene family. A plant expression vector of the BcDREB1 gene was constructed and named pCAM BcDREB1 ,in which the CDS sequence of BcDREB1 was controlled by the CaMV 35S promoter. This work laid the foundations for future transgenic research on BcDREB1 gene function.

关 键 词：大白菜 DREB转录因子 基因克隆 植物表达载体 

分 类 号：Q785[生物学—分子生物学]