Weiland J J, Dreher T W
Department of Agricultural Chemistry, Oregon State University, Corvallis 97331-6502.
Nucleic Acids Res. 1989 Jun 26;17(12):4675-87. doi: 10.1093/nar/17.12.4675.
Full-length cDNA of the 6.3 kb turnip yellow mosaic virus (TYMV) genome was placed between a T7 promoter and a unique Hind III site. In vitro transcription of Hind III-linearized DNA of clone pTYMC yielded full-length RNA transcripts. In inoculations of Chinese cabbage protoplasts and plants, capped transcripts and virion RNA had similar specific infectivities and produced similar systemic symptoms. We have used the pTYMC clone in studies of the expression of two overlapping open reading frames (1.9 kb and 5.5 kb ORFs) by making mutants with alterations in the initiation codons. Evidence is presented from in vitro translations of mutant and wild type RNAs that both ORFs are expressed from TYMV RNA. A mutant in the initiation codon of the 5.5 kb ORF did not replicate in protoplasts, while mutants in the initiation codon of the 1.9 kb ORF replicated at low levels. The two groups of mutants were not able to complement each other.
将6.3kb芜菁黄花叶病毒(TYMV)基因组的全长cDNA置于T7启动子和一个独特的 Hind III位点之间。对克隆pTYMC的Hind III线性化DNA进行体外转录,产生了全长RNA转录本。在接种大白菜原生质体和植株时,加帽转录本和病毒粒子RNA具有相似的比感染性,并产生相似的系统症状。我们通过对起始密码子进行改变来构建突变体,利用pTYMC克隆研究了两个重叠开放阅读框(1.9kb和5.5kb ORF)的表达。从突变体和野生型RNA的体外翻译结果表明,两个ORF均由TYMV RNA表达。5.5kb ORF起始密码子的突变体在原生质体中不能复制,而1.9kb ORF起始密码子的突变体则以低水平复制。这两组突变体不能相互互补。