Nishikawa Y, Xuan X, Otsuka H
Department of Global Agricultural Sciences, Graduate School of Agricultural and Life Science, The University of Tokyo, Japan.
Virus Res. 1998 Jul;56(1):77-92. doi: 10.1016/s0168-1702(98)00062-8.
We have determined the sequence of the gE and gI genes of canine herpesvirus (CHV), DFD-6 strain. The gE ORF codes for a 522 a.a. polypeptide with a signal sequence at the amino-terminus and a trans-membrane domain at the carboxy-terminus. The gI ORF codes for a 259 a.a. polypeptide with a signal sequence but no trans-membrane domain. Comparison with another line of CHV indicated that the DFD-6 gI gene underwent a frame-shift mutation which caused the loss of the trans-membrane domain. Antibodies against the gE and gI polypeptides detected a 94 kDa gE and a broad band of gI (55-62 kDa) in DFD-6 infected cells, respectively. The precursor of DFD-6 gE is modified to the mature form by N-linked glycosylation only in the presence of gI. Together with the fact that the gI- mutant of DFD-6 produced smaller plaques, it is suggested that the truncated DFD-6 gI is functional. The precursor of DFD-6 gI is modified to the mature form by N-linked glycosylation only in the presence of gE.
我们已经确定了犬疱疹病毒(CHV)DFD - 6株gE和gI基因的序列。gE开放阅读框编码一个含522个氨基酸的多肽,其氨基末端有一个信号序列,羧基末端有一个跨膜结构域。gI开放阅读框编码一个含259个氨基酸的多肽,有一个信号序列但没有跨膜结构域。与另一株CHV的比较表明,DFD - 6的gI基因发生了移码突变,导致跨膜结构域缺失。针对gE和gI多肽的抗体分别在DFD - 6感染的细胞中检测到一条94 kDa的gE条带和一条gI的宽带(55 - 62 kDa)。DFD - 6 gE的前体仅在gI存在的情况下通过N - 连接糖基化修饰为成熟形式。再加上DFD - 6的gI突变体产生较小的噬斑这一事实,表明截短的DFD - 6 gI具有功能。DFD - 6 gI的前体仅在gE存在的情况下通过N - 连接糖基化修饰为成熟形式。