Takamatsu N, Watanabe Y, Iwasaki T, Shiba T, Meshi T, Okada Y
Laboratory of Molecular Biology, School of Hygienic Sciences, Kitasato University, Kanagawa, Japan.
J Virol. 1991 Mar;65(3):1619-22. doi: 10.1128/JVI.65.3.1619-1622.1991.
To determine the sequences essential for viral multiplication in the 5' untranslated leader sequence of tobacco mosaic virus RNA, mutant TMV-L (a tomato strain) RNAs which carry several deletions in this 71-nucleotide sequence were constructed by an in vitro transcription system and their multiplication was analyzed by introducing mutant RNA into tobacco protoplasts by electroporation. Large deletions of the sequence from nucleotides 9 to 47 or 25 to 71 abolished viral multiplication; when about 10-nucleotide deletions were introduced throughout this 5' leader sequence, only deletion of the sequence from nucleotides 2 to 8 abolished detectable viral multiplication. This mutant RNA, however, directed the synthesis of the 130,000-molecular-weight protein in a rabbit reticulocyte lysate in vitro translation system, and consequently this 5'-proximal portion appears likely to be essential for replication.
为了确定烟草花叶病毒RNA 5'非翻译前导序列中病毒增殖所必需的序列,利用体外转录系统构建了在这个71个核苷酸序列中有多个缺失的突变型TMV-L(番茄株系)RNA,并通过电穿孔将突变型RNA导入烟草原生质体来分析它们的增殖情况。从核苷酸9至47或25至71的序列发生大的缺失会使病毒增殖消失;当在整个这个5'前导序列中引入约10个核苷酸的缺失时,只有从核苷酸2至8的序列缺失会使可检测到的病毒增殖消失。然而,这种突变型RNA在兔网织红细胞裂解物体外翻译系统中指导了130,000分子量蛋白的合成,因此这个5'近端部分似乎对复制至关重要。