de Groot R J, Maduro J, Lenstra J A, Horzinek M C, van der Zeijst B A, Spaan W J
Institute of Virology, Veterinary Faculty, State University, Utrecht, The Netherlands.
J Gen Virol. 1987 Oct;68 ( Pt 10):2639-46. doi: 10.1099/0022-1317-68-10-2639.
The peplomer gene of feline infectious peritonitis virus (FIPV) strain 79-1146 was isolated from a genomic cDNA library by differential hybridization with RNA 2 and 3 as probes. From the nucleotide sequence a primary translation product of 1452 residues (Mr 160,472) was predicted, containing an N-terminal signal sequence, a C-terminal transmembrane segment and 35 potential N-linked glycosylation sites. By S1 nuclease analysis the 5' end of the presumptive RNA 2 body was located at about 30 nucleotides upstream from the initiating AUG codon. At approximately the same position a nine nucleotide sequence ACUAAACUU was found, which was also present 37 nucleotides downstream from the open reading frame. Comparison of the sequences of the FIPV, murine hepatitis virus and infectious bronchitis virus peplomer proteins showed about 27% overall homology, with most conservation in the C-terminal half.
通过以RNA 2和RNA 3为探针进行差异杂交,从基因组cDNA文库中分离出猫传染性腹膜炎病毒(FIPV)79 - 1146株的纤突蛋白基因。根据核苷酸序列预测,其初级翻译产物有1452个氨基酸残基(分子量160472),包含一个N端信号序列、一个C端跨膜片段和35个潜在的N - 连接糖基化位点。通过S1核酸酶分析,推测的RNA 2主体的5'端位于起始AUG密码子上游约30个核苷酸处。在大致相同位置发现了一个九核苷酸序列ACUAAACUU,该序列在开放阅读框下游37个核苷酸处也存在。比较FIPV、鼠肝炎病毒和传染性支气管炎病毒纤突蛋白的序列,发现总体同源性约为27%,在C端一半区域保守性最高。