Wickner R B, Icho T, Fujimura T, Widner W R
Section on the Genetics of Simple Eukaryotes, National Institute of Diabetes and Digestive and Kidney Diseases, Bethesda, Maryland 20892.
J Virol. 1991 Jan;65(1):155-61. doi: 10.1128/JVI.65.1.155-161.1991.
The plus strand of the L-A double-stranded RNA virus of Saccharomyces cerevisiae has two large open reading frames, ORF1, which encodes the major coat protein, and ORF2, which encodes a single-stranded RNA-binding protein having a sequence diagnostic of viral RNA-dependent RNA polymerases. ORF2 is expressed only as a Gag-Pol-type fusion protein with ORF1. We have constructed a plasmid which expresses these proteins from the yeast PGK1 promoter. We show that this plasmid can support the replication of the killer toxin-encoding M1 satellite virus in the absence of an L-A double-stranded RNA helper virus itself. This requires ORF2 expression, providing a potential in vivo assay for the RNA polymerase and single-stranded RNA-binding activities of the fusion protein determined by ORF2. ORF1 expression, like a host ski- mutation, can suppress the usual requirement of M1 for the MAK11, MAK18, and MAK27 genes and allow a defective L-A (L-A-E) to support M1 replication. These results suggest that expression of ORF1 from the vector makes the cell a ski- phenocopy. Indeed, expression of ORF1 in a wild-type killer makes it a superkiller, suggesting that a target of the SKI antiviral system may be the major coat protein.
酿酒酵母的L-A双链RNA病毒的正链有两个大的开放阅读框,即ORF1,其编码主要衣壳蛋白;以及ORF2,其编码一种单链RNA结合蛋白,该蛋白具有病毒RNA依赖性RNA聚合酶的序列诊断特征。ORF2仅作为与ORF1的Gag-Pol型融合蛋白表达。我们构建了一个从酵母PGK1启动子表达这些蛋白的质粒。我们表明,在没有L-A双链RNA辅助病毒本身的情况下,该质粒可以支持编码杀伤毒素的M1卫星病毒的复制。这需要ORF2表达,从而为ORF2所确定的融合蛋白的RNA聚合酶和单链RNA结合活性提供了一种潜在的体内检测方法。ORF1的表达,就像宿主ski-突变一样,可以抑制M1通常对MAK11、MAK18和MAK27基因的需求,并允许有缺陷的L-A(L-A-E)支持M1复制。这些结果表明,从载体表达的ORF1使细胞成为ski-表型模拟物。事实上,在野生型杀伤细胞中表达ORF1会使其成为超级杀伤细胞,这表明SKI抗病毒系统的一个靶点可能是主要衣壳蛋白。