Rümenapf T, Unger G, Strauss J H, Thiel H J
Division of Biology, California Institute of Technology, Pasadena 91125.
J Virol. 1993 Jun;67(6):3288-94. doi: 10.1128/JVI.67.6.3288-3294.1993.
The genomic RNA of pestiviruses is translated into a large polyprotein that is cleaved into a number of proteins. The structural proteins are N terminal in this polyprotein and include three glycoproteins called E0, E1, and E2 on the basis of the order in which they appear in the polyprotein. Using pulse-chase experiments, we show that a pestiviral glycoprotein precursor, E012, is formed that is processed into E0, E1, and E2 in an ordered fashion. Processing is initiated by a nascent cleavage between the capsid and the translocated E012 followed by cleavage at the C terminus of E2. E012 is then rapidly cleaved to form E01 and E2. After E2 is released from the precursor, E01 is processed into E0 and E1. To identify the sites of cleavage, the N termini of the glycoproteins of the pestivirus classical swine fever virus (formerly termed hog cholera virus) were sequenced after expression in the vaccinia virus system. The N termini are Glu-268 for E0 (gp44/48), Leu-495 for E1 (gp33) and Arg-690 for E2 (gp55). The sequences around the cleavage sites capsid/E0 and E1/E2 conform to the rules known for cellular signal proteases, as does the sequence at the presumed C terminus of E2. The sequence upstream of the E0/E1 cleavage site also shows sequence characteristics of signalase processing sites but lacks the typical hydrophobic signal peptide; this cleavage site has characteristics in common with a site in flaviviruses that is also cleaved in a delayed fashion. The absence of any membrane-spanning region results in the shedding of E0 by infected cells, and E0 can be detected in the virus-free supernatant. Comparison of the sequences around the cleavage sites of pestiviruses suggests a general processing scheme for the structural glycoproteins. Comparison of the pesti- and flaviviral structural glycoproteins suggests analogies between E012 and prM-E.
瘟病毒的基因组RNA被翻译为一个大的多聚蛋白,该多聚蛋白随后被切割为多个蛋白质。结构蛋白位于该多聚蛋白的N端,根据它们在多聚蛋白中出现的顺序,包括三种糖蛋白,分别称为E0、E1和E2。通过脉冲追踪实验,我们发现形成了一种瘟病毒糖蛋白前体E012,它以有序的方式被加工为E0、E1和E2。加工过程首先是衣壳与易位的E012之间发生新生切割,随后在E2的C端进行切割。然后E012迅速被切割形成E01和E2。E2从前体释放后,E01被加工为E0和E1。为了确定切割位点,在痘苗病毒系统中表达后,对瘟病毒经典猪瘟病毒(以前称为猪霍乱病毒)糖蛋白的N端进行了测序。E0(gp44/48)的N端是Glu-268,E1(gp33)的N端是Leu-495,E2(gp55)的N端是Arg-690。衣壳/E0和E1/E2切割位点周围的序列符合细胞信号蛋白酶已知的规则,E2假定C端的序列也是如此。E0/E1切割位点上游的序列也显示出信号肽酶加工位点的序列特征,但缺乏典型的疏水信号肽;该切割位点与黄病毒中一个也以延迟方式切割的位点具有共同特征。由于不存在任何跨膜区域,感染细胞会释放E0,并且可以在无病毒的上清液中检测到E0。瘟病毒切割位点周围序列的比较表明了结构糖蛋白的一般加工方案。瘟病毒和黄病毒结构糖蛋白的比较表明E012和prM-E之间存在相似性。