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胶质细胞源性神经营养因子基因的克隆及其在大肠杆菌中的高效表达
引用本文:王金惠,王嘉玺,彭善云,段聚宝,邹民吉.胶质细胞源性神经营养因子基因的克隆及其在大肠杆菌中的高效表达[J].军事医学科学院院刊,1999(4).
作者姓名:王金惠  王嘉玺  彭善云  段聚宝  邹民吉
作者单位:军事医学科学院基础医学研究所!北京100850
摘    要:目的:分离胶质细胞源性神经营养因子(glial cell line-derived neurotrophic factor,GDNF)基因,并在E.coli中获得表达。方法:从人多形性成胶质细胞瘤细胞株BT325 中提取总RNA ,利用RT-PCR技术分离GDNF基因,构建表达载体pBV-GDNF,转化大肠杆菌,温控诱导GDNF的表达。结果与结论:分离得到的人GDNF基因,在大肠杆菌中得到高效表达,表达产物占全菌总蛋白的24.7% ,初步纯化后纯度达90% 以上。

关 键 词:胶质细胞源性神经营养因子  基因表达

Isolation of the gene encoding glial cell line derived neurotrophic factor and its high expression in E.coli
Wang Jinhui,Wang Jiaxi,Peng Shanyun,Duan Jubao,Zou Minji Institute of Basic Medical Sciences,Academy of Military Medical Sciences,Beijing.Isolation of the gene encoding glial cell line derived neurotrophic factor and its high expression in E.coli[J].Bulletin of the Academy of Military Medical Sciences,1999(4).
Authors:Wang Jinhui  Wang Jiaxi  Peng Shanyun  Duan Jubao  Zou Minji Institute of Basic Medical Sciences  Academy of Military Medical Sciences  Beijing
Affiliation:Wang Jinhui,Wang Jiaxi,Peng Shanyun,Duan Jubao,Zou Minji Institute of Basic Medical Sciences,Academy of Military Medical Sciences,Beijing 100850
Abstract:Objective: To isolate the coding region of the glial cell line derived neurotrophic factor(GDNF) gene and to express it in E.coli. Methods: The GDNF coding sequence from the total RNA of human astrocytoma cell line BT325 was amplified. The isolated fragment was sequenced by dideoxy method, recombined in vitro with plasmid pBV220, and transformed into E.coli cells. Results and Conclusion: The GDNF coding the sequence and an E.coli strain high expressing GDNF were successfully obtained. The expressed GDNF amounted to 24.7% of the total bacterial protein. The GDNF amounted to at least 90% after purification.
Keywords:glial cell line  derived neurotrophic factor  gene expression
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