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CaDREB3启动子分离及其缺失体转基因烟草的获得
引用本文:蔡金森,王博,杨晟,石兰平,文嘉瑜,史玮,刘志钦,贺俐,吴杨,何水林.CaDREB3启动子分离及其缺失体转基因烟草的获得[J].热带作物学报,2014,35(7):1368-1373.
作者姓名:蔡金森  王博  杨晟  石兰平  文嘉瑜  史玮  刘志钦  贺俐  吴杨  何水林
作者单位:1 福建农林大学作物遗传育种与综合利用教育部重点实验室 2 福建农林大学生命科学学院;1 福建农林大学作物遗传育种与综合利用教育部重点实验室 2 福建农林大学生命科学学院;1 福建农林大学作物遗传育种与综合利用教育部重点实验室 2 福建农林大学生命科学学院;1 福建农林大学作物遗传育种与综合利用教育部重点实验室 2 福建农林大学生命科学学院;1 福建农林大学作物遗传育种与综合利用教育部重点实验室 3 福建农林大学作物科学学院;1 福建农林大学作物遗传育种与综合利用教育部重点实验室 3 福建农林大学作物科学学院;1 福建农林大学作物遗传育种与综合利用教育部重点实验室 2 福建农林大学生命科学学院;井冈山大学生命科学学院;井冈山大学生命科学学院;1 福建农林大学作物遗传育种与综合利用教育部重点实验室 2 福建农林大学生命科学学院
基金项目:国家自然科学基金项目(No. 31060263、31260482)。
摘    要:CaDREB3是辣椒DREB家族中1个成员,为明确CaDREB3受逆境胁迫诱导表达的分子机制,从辣椒基因组DNA中分离获得了CaDREB3上游的启动子,利用生物信息学软件进行顺式作用元件的分析,结果表明该启动子的TATA框为起始密码子ATG上游-89 bp至-86 bp的TATA,同时含有多种与逆境胁迫相关的顺式作用元件,如ABRE、HSE、MYB和TCA等,并使用Gateway技术构建了启动子6个缺失体的GUS融合载体,获得了6个缺失体的烟草转基因植株,这些结果为将来分析该启动子应答逆境胁迫的调控区域奠定了一定的基础。

关 键 词:DREB转录因子  Genome  Walking  启动子

Isolation of Promoter and Acquisition of Transgenic Tobacco Plants for Its 5' Deletion Mutation Analysis
CAI Jinsen,WANG Bo,YANG Sheng,SHI Lanping,WEN Jiayu,SHI Wei,LIU Zhiqin,HE Li,WU Yang and HE Shuilin.Isolation of Promoter and Acquisition of Transgenic Tobacco Plants for Its 5'' Deletion Mutation Analysis[J].Chinese Journal of Tropical Crops,2014,35(7):1368-1373.
Authors:CAI Jinsen  WANG Bo  YANG Sheng  SHI Lanping  WEN Jiayu  SHI Wei  LIU Zhiqin  HE Li  WU Yang and HE Shuilin
Institution:1 Key Laboratory of Ministry of Education for Genetics, Breeding and Multiple Utilization of Crops,Fujian Agriculture and Forestry University 2 College of Life Science, Fujian Agriculture and Forestry University;1 Key Laboratory of Ministry of Education for Genetics, Breeding and Multiple Utilization of Crops,Fujian Agriculture and Forestry University 2 College of Life Science, Fujian Agriculture and Forestry University;1 Key Laboratory of Ministry of Education for Genetics, Breeding and Multiple Utilization of Crops,Fujian Agriculture and Forestry University 2 College of Life Science, Fujian Agriculture and Forestry University;1 Key Laboratory of Ministry of Education for Genetics, Breeding and Multiple Utilization of Crops,Fujian Agriculture and Forestry University 2 College of Life Science, Fujian Agriculture and Forestry University;1 Key Laboratory of Ministry of Education for Genetics, Breeding and Multiple Utilization of Crops,Fujian Agriculture and Forestry University 3 College of Crop Science, Fujian Agriculture and Forestry University;1 Key Laboratory of Ministry of Education for Genetics, Breeding and Multiple Utilization of Crops,Fujian Agriculture and Forestry University 3 College of Crop Science, Fujian Agriculture and Forestry University;1 Key Laboratory of Ministry of Education for Genetics, Breeding and Multiple Utilization of Crops,Fujian Agriculture and Forestry University 3 College of Crop Science, Fujian Agriculture and Forestry University;College of Life Science, Jinggangshan University;College of Life Science, Jinggangshan University;1 Key Laboratory of Ministry of Education for Genetics, Breeding and Multiple Utilization of Crops,Fujian Agriculture and Forestry University 2 College of Life Science, Fujian Agriculture and Forestry University
Abstract:CaDREB3 is a member of the DREB family in pepper. In order to further clarify the molecular mechanism of the stress-induced expression of CaDREB3, we isolated the upstream promoter of CaDREB3 from pepper genomic DNA. Bioinformatics analysis illustrated that the TATA box located from -89 bp to -86 bp, upstream from start codon(ATG), and a variety of stress-associated cis-acting elements were included, such as ABRE, HSE, MYB and TCA, etc. Five deletions fused to GUS--reported gene of CaDREB3 promoter were constructed via Gateway technology and transgenic plants of the six deletions were generated. Taken together, the results above lay the foundation to determine the regulatory region of the promoter response to stress.
Keywords:
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