摘要
利用RT-PCR技术对番鸭源新城疫病毒FP1/02株的F蛋白基因进行分段扩增、定向克隆到pMD 18-T SimpleVector质粒载体,然后测定其核苷酸序列,拼接出F基因全序列,并推导出其相应的氨基酸序列.FP1/02株的F蛋白基因全长1690 bp,编码553个氨基酸,其裂解位点的氨基酸序列为112R-R-Q-K-R-F117,具有强毒株特有的氨基酸序列结构特征.核苷酸序列分析结果表明,FP1/02株与其他不同源新城疫病毒毒株之间的核苷酸序列同源性为87.2%~93.3%.
Full-length F protein gene of the FP1/02 strain of Newcastle disease virus(NDV) isolated from muscovy duck was amplified by using reverse transcription polymerase chain reaction(RT-PCR) and cloned into pMD 18-T simple vector. The sequence of F protein gene of FP1/02 strain was determined with its full-length of 1690 bp coding 553 amino acid(AA). The amino acid sequence in the cleavage site of the deduced peptide is ^112R-R-Q-K-R-F^112,which exists only in a virulent NDV strain. The result of sequence analysis of F protein gene in full-length indicated that the homology between FP1/02 isolate and other NDV strains would be from 87.2% to 93. 3%.
出处
《中国兽医学报》
CAS
CSCD
北大核心
2005年第6期578-580,共3页
Chinese Journal of Veterinary Science
关键词
番鸭
新城疫病毒F蛋白基因
克隆
序列分析
muscovy duck
Newcastle disease virus
F protein gene
cloning
sequence analysis