Verbeek A, Tijssen P
Institut Armand-Frappier, Université du Québec, Laval-des-Rapides, Canada.
J Gen Virol. 1991 Jul;72 ( Pt 7):1659-66. doi: 10.1099/0022-1317-72-7-1659.
The 3' end of the turkey coronavirus (TCV) genome and the gene encoding the nucleocapsid protein (N) were cloned and sequenced. The gene encoding the membrane protein (M) was obtained by cloning a polymerase chain reaction (PCR)-amplified fragment obtained using bovine coronavirus (BCV)-specific primers. Furthermore, five TCV DNA fragments, obtained by PCR on RNA from clinical specimens and corresponding to either the N terminus of the M protein or the complete M protein were also cloned and sequenced. The sequence revealed a 3' non-coding region of 291 bases, an open reading frame (ORF) encoding the N protein with a predicted size of 448 amino acids, or an Mr of 49K, and an ORF encoding the M protein with a predicted size of 230 amino acids and an Mr of 26K. A third ORF, encoding a hypothetical protein of 207 amino acids with an Mr of 23K was found within the N gene sequence. The amino acid sequences of both the N and M proteins were more than 99% similar to those published for BCV. Extensive similarity was also observed between the amino acid sequences of the TCV N protein and those of murine hepatitis virus (MHV) (70%) and human respiratory coronavirus strain OC43 (HCV-OC43) (98%) and between the amino acid sequences of the predicted M proteins of TCV and MHV (86%). Such striking identity suggests that BCV, TCV and HCV-OC43 must have diverged from each other only recently. A potential N-glycosylation site was found at the N terminus of the TCV M protein and is situated at the same location in BCV, MHV and transmissible gastroenteritis virus.
克隆并测序了火鸡冠状病毒(TCV)基因组的3'末端以及编码核衣壳蛋白(N)的基因。通过克隆使用牛冠状病毒(BCV)特异性引物扩增得到的聚合酶链反应(PCR)片段,获得了编码膜蛋白(M)的基因。此外,还克隆并测序了通过对临床标本RNA进行PCR获得的五个TCV DNA片段,这些片段对应于M蛋白的N末端或完整M蛋白。序列显示有一个291个碱基的3'非编码区、一个编码N蛋白的开放阅读框(ORF),预测大小为448个氨基酸,分子量为49K,以及一个编码M蛋白的ORF,预测大小为230个氨基酸,分子量为26K。在N基因序列中发现了第三个ORF,编码一个预测分子量为23K、含207个氨基酸的假设蛋白。N蛋白和M蛋白的氨基酸序列与已发表的BCV氨基酸序列相似度均超过99%。在TCV N蛋白的氨基酸序列与鼠肝炎病毒(MHV)(70%)和人呼吸道冠状病毒OC43株(HCV-OC43)(98%)的氨基酸序列之间,以及在TCV和MHV预测的M蛋白的氨基酸序列之间也观察到广泛的相似性。这种显著的一致性表明,BCV、TCV和HCV-OC43彼此之间的分化肯定是最近才发生的。在TCV M蛋白的N末端发现了一个潜在的N-糖基化位点,该位点在BCV、MHV和传染性胃肠炎病毒中的位置相同。