Weaver T A, Talbot K J, Panganiban A T
McArdle Laboratory for Cancer Research, University of Wisconsin-Madison 53706.
J Virol. 1990 Jun;64(6):2642-52. doi: 10.1128/JVI.64.6.2642-2652.1990.
The nature of spleen necrosis virus pol gene expression and the role of gag and gag-pol polyproteins in virion assembly was investigated. The DNA sequence of the gag-pol junction revealed that the two genes occupy the same open reading frame but are separated by an in-frame amber stop codon. Biochemical analysis of gag-pol translational readthrough in vitro and in Escherichia coli suggests that, in a manner similar to that in other mammalian type C retroviruses, amber stop codon suppression is required for pol gene expression. Removal of the gag stop codon had little or no effect on synthesis or cleavage of the polyprotein but interrupted particle assembly. This block could be overcome by complementation with wild-type gag protein.
研究了脾坏死病毒pol基因表达的性质以及gag和gag-pol多聚蛋白在病毒粒子组装中的作用。gag-pol连接区的DNA序列显示,这两个基因占据相同的开放阅读框,但被一个框内琥珀色终止密码子隔开。对体外和大肠杆菌中gag-pol翻译通读的生化分析表明,与其他哺乳动物C型逆转录病毒类似,pol基因表达需要琥珀色终止密码子抑制。去除gag终止密码子对多聚蛋白的合成或切割影响很小或没有影响,但会中断颗粒组装。通过与野生型gag蛋白互补可以克服这种阻断。