Wellink J, Verver J, van Kammen A
Department of Molecular Biology, Agricultural University, Wageningen, The Netherlands.
Biochimie. 1993;75(8):741-7. doi: 10.1016/0300-9084(93)90105-2.
The involvement of the AUG codons at positions 115, 161, 512 and 524 in translation and infectivity of cowpea mosaic virus M RNA was studied. Mutations were introduced in each of these codons in a full length cDNA clone of M RNA and the effect of the mutations was examined by translation from in vitro transcripts of these mutant cDNAs in rabbit reticulocyte lysates and by checking the replication of these transcripts in the presence of B RNA in cowpea protoplasts and plants. It was found that AUG115, at the beginning of an open reading frame (ORF) for a putative 2-kDa protein, can be used in vitro to initiate translation, but mutation of this AUG codon in the M RNA does not affect the ability of the virus to infect cowpea plants. AUG161, located at the beginning of the large ORF, was shown to be essential for expression of the large 105-kDa polyprotein and for replication of M RNA. Translation of the second 95-kDa polyprotein was found to start at AUG512. Upon mutation of this AUG codon efficient initiation of translation occurred at AUG524. Results with M RNAs that lack AUG512 and/or 524 indicate that an intact 95-kDa polyprotein is not required for replication of M RNA but that this protein has an essential function in cell-to-cell movement of the virus.
研究了豇豆花叶病毒M RNA中第115、161、512和524位的AUG密码子在翻译和感染性中的作用。在M RNA的全长cDNA克隆中,对每个密码子进行了突变,并通过在兔网织红细胞裂解物中从这些突变cDNA的体外转录本进行翻译,以及检查这些转录本在豇豆原生质体和植物中B RNA存在下的复制情况,来检测突变的影响。结果发现,位于假定的2 kDa蛋白开放阅读框(ORF)起始处的AUG115可在体外用于起始翻译,但M RNA中该AUG密码子的突变并不影响病毒感染豇豆植物的能力。位于大ORF起始处的AUG161被证明对于105 kDa大聚蛋白的表达和M RNA的复制至关重要。发现第二个95 kDa聚蛋白的翻译起始于AUG512。该AUG密码子突变后,翻译在AUG524处高效起始。对缺乏AUG512和/或524的M RNA的研究结果表明,完整的95 kDa聚蛋白对于M RNA的复制不是必需的,但该蛋白在病毒的细胞间移动中具有重要功能。