摘要
用 R T P C R技术从 C S F V H C L V 株 F482 代感染兔脾的细胞总 R N A 中分段扩增出了 C S F V E2 基因特异的3 个部分重叠的 D N A 片段(大小分别为 499 bp、572 bp 和 245 bp),并将之分别克隆到p G E M T 载体上 经核苷酸序列测定和片段重叠完成了包含 E2 全长基因的 1 144 bp 序列的测定,其 G C含量为49.0% :核苷酸序列与国外报道的各株病毒的 E2 基因同源性分别为83.5% ~97.5% ;其推导的氨基酸序列的同源性也分别为89.3%~96.2% ,变异主要分布在 E2 蛋白的 N
Three partly overlapped fragments encompassing CSFV E 2 gene was amplified from the total cellular RNA of the CSFV strain HCLV infected rabbit spleen by reverse transcription polymerase chain reaction(RT PCR) and was inserted into the pGEM T vector seperately. The target rejion encompassing CSFV E 2 gene was sequenced completely to be 1144bp with 49.0% of the G+C content. The nucleotide sequence of the E 2 gene of the CSFV strain HCLV was homologous to that of other strains by 83.5% ~97.5%, respectively, and the corresponding deduced amino acid sequence was homologous by 89.3% ~96.2%, respectively. The amino acid variation distributed mainly in the N half of the the glycoprotein E 2, in which the major antigenic domains located.
出处
《武汉大学学报(自然科学版)》
CSCD
1999年第4期509-512,共4页
Journal of Wuhan University(Natural Science Edition)
基金
国家攀登计划( B 类)课题
关键词
猪瘟病毒
囊膜糖蛋白E2
核苷酸序列
抗原漂变
classical swine fever virus
glycoprotein E 2
nucleotide sequence
antigenic shift