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作 者:伍欣星[1] 赵文先[1] 丁晓华[1] 丁红珍[2] 甘人宝[2]
机构地区:[1]湖北医科大学病毒研究所,武汉430071 [2]中科院上海生化所
出 处:《中华微生物学和免疫学杂志》1996年第6期395-398,共4页Chinese Journal of Microbiology and Immunology
基 金:湖北省科委"八五"重点科技项目基金
摘 要:从湖北地区一宫颈癌活检组织中提取DNA,采取加端聚合酶链反应(PCR)技术,获得了人乳头瘤病毒16型E7基因(HPV16E7)。将该基因克隆于载体pUC18后,进行了该基因一级结构顺序分析。完整的HPV16E7湖北株基因(HPV16E7-HB)全长294bp,与已发表的德国株(GS)大小一致,但其核苷酸顺序中有2处发生了变异,均为C→T变异。A complete E7 gene of HPV16 was isolated from a cervical carcinoma biopsy DNA from Hubei province of China by Add-on PCR. After cloning into plasmid pUC18 , the total nucleotide sequence of HPVl6 E7 was determined. The entire HPV16 E7 gene has 294 nucleotides. It was the same as the German strain. But there were two mutations in sequences. Both of them were C→T mutation. A nonsense mutation was identified at coden 43,a Gln codon (CAA) was converted into TAA ,the stop codon, A 0. 3kb fragment of HPV16 E7-HB was inserted into experssed vector pWR590-1. When E coli JM 109 was transformed by recombinant expression plasmid and induced by IPTG, a fusion protein product with the expected molecutar weight 69kD was observed , which was approximately 30% of the total bacterial proteins. It was comfirmed that virus polypeptiedes by E7 encoded stoped in advance because of nonsense mutation of HPVl6 E7-HB. The results showed: there were gene structure and polypeptide difference of HPV16 E7 in different country and/or area. This is the first report of HPV16 E7 primary structure of China.
关 键 词:人乳头瘤病毒 16型 核苷酸 序列分析 宫颈肿瘤
分 类 号:R373.11[医药卫生—病原生物学] R737.330.2[医药卫生—基础医学]
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