4株SARS冠状病毒基因组5’端序列的分析与比较  

Comparative Analysis of Genomic Organization of the 5' and of Four Strain SARS-associated Coronaviruses

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作  者:常国辉[1] 彭文明[1] 刘伯华[1] 范宝昌[1] 刘洪[1] 邓永强[1] 吕富双[1] 杨保安[1] 秦鄂德[1] 祝庆余[1] 

机构地区:[1]军事医学科学院微生物流行病研究所,北京100071

出  处:《中国病毒学》2003年第4期330-334,共5页Virologica Sinica

基  金:国家863计划项目基金(2003AA208201)

摘  要:利用5′RACE试剂盒对从中国不同地区、不同SARS患者体中分离的SARS-CoV基因组5′端序列进行RT-PCR扩增,并将扩增产物克隆至T easy vector。扩增片段的序列测定结果表明:所分离的4株SARS-CoV基因组5′端非编码区的核苷酸序列和其他国家和地区报道的序列基本一致,而且所形成二级结构也完全相同,但与已知普通冠状病毒的差别较大。同时发现在依赖于RNA的RNA聚合酶起始密码子上游-197 nt处有冠状病毒典型的转录调控核心保守序列5′-CUAAAC-3′。The viral RNAs were isolated from the infected Vero-E6 cells, then the templates were produced by reverse transcription reaction.Two pairs of primers were used to amplify the 5'-ends of four strains of SARS-associated coronavirus(SARS-CoV)by RACE,cDNA fragments with the length of about 420 bp were amplified. The fragments were then purified and sequenced. The sequences of 5' -UTRs of SARS -CoV isolated in China were the same as those isolated in other countries and regions, such as Tor2 strain, Urbani strain, HKU-Sul0 strain, CUHK-W1 strain, SIN2500 strain and SIN2677 strain. The secondary structures formed by 5'-UTRs of all known SARS-CoV were almost identical, but significantly different from other known non-SARS coronaviruses. Sequence analysis indicated that the conserved core sequence(5'-CUAAAC-3') of transcription regulating sequence in some coronaviruses was about - 197 nt upstream from the start codon.

关 键 词:SARS 冠状病毒 基因组 5′端序列 序列分析 转录调控序列 

分 类 号:R373[医药卫生—病原生物学] R511[医药卫生—基础医学]

 

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