Vos P, Jaegle M, Wellink J, Verver J, Eggen R, Van Kammen A, Goldbach R
Department of Molecular Biology, Agricultural University, Wageningen, The Netherlands.
Virology. 1988 Jul;165(1):33-41. doi: 10.1016/0042-6822(88)90655-1.
A set of full-length DNA copies of both M and B RNA of cowpea mosaic virus (CPMV) was cloned downstream of a phage T7 promoter. Upon in vitro transcription using T7 RNA polymerase, M and B RNA-like transcripts were obtained from these DNA copies with only two additional nucleotides at the 5' end and five extra nucleotides at the 3' end in comparison to natural viral RNA. In cowpea protoplasts the transcripts of several cDNA clones of B RNA were able to replicate leading to detectable synthesis of viral RNA and proteins. Transcripts of M cDNA clones inoculated together with these B RNA transcripts were also expressed, although the number of protoplasts in which both transcripts were expressed was very low. Preliminary infectivity tests with mutagenized RNA transcripts indicate essential roles of the B RNA-encoded 24K and 32K polypeptides in viral RNA replication.
将豇豆花叶病毒(CPMV)的M和B RNA的一组全长DNA拷贝克隆到噬菌体T7启动子的下游。使用T7 RNA聚合酶进行体外转录后,从这些DNA拷贝中获得了M和B RNA样转录本,与天然病毒RNA相比,其5'端仅多了两个核苷酸,3'端多了五个额外的核苷酸。在豇豆原生质体中,B RNA的几个cDNA克隆的转录本能够复制,导致可检测到病毒RNA和蛋白质的合成。与这些B RNA转录本一起接种的M cDNA克隆的转录本也能表达,尽管两种转录本都表达的原生质体数量非常少。对诱变RNA转录本的初步感染性测试表明,B RNA编码的24K和32K多肽在病毒RNA复制中起着重要作用。