Pfeiffer P, Jung J L, Heitzler J, Keith G
Institut de Biologie Moléculaire des Plantes, Strasbourg, France.
J Gen Virol. 1993 Jun;74 ( Pt 6):1167-73. doi: 10.1099/0022-1317-74-6-1167.
The 16.7 kbp dsRNA specific to the '447' cytoplasmic male sterility (CMS) line of Vicia faba was labelled in vitro with [alpha-32P]ATP and poly(A) polymerase, and by T4 RNA ligase-mediated addition of [32P]pCp. Analysis of the reaction products under denaturing conditions revealed in both cases extensive labelling of a 4.5 kb ssRNA, already detected in previous experiments in which the RNA-dependent RNA polymerase associated with the dsRNA was allowed to pursue RNA synthesis on preinitiated complexes. Mobility shift analysis of total pCp-labelled dsRNA revealed not two but three different 3' termini. The most prominent sequencing pattern corresponded to the 4.5 kb ssRNA, indicating that this RNA species has a preferentially accessible, free 3' OH extremity. Northern blot analysis of the denatured dsRNA confirmed that the 4.5 kb ssRNA is a subgenomic mRNA and detected its counterpart of about 12 kb. Nearly all 16.7 kbp dsRNA molecules featured an interrupted positive-sense strand, indicating a marked prevalence of transcription over replication complexes. This unusual strategy of transcription by a strand displacement mechanism, following initiation at an internal discontinuity, is compared with that of other dsRNA viruses or defective viruses, and is discussed in relation to the expression of the CMS trait.
用[α-32P]ATP和多聚(A)聚合酶,以及通过T4 RNA连接酶介导添加[32P]pCp,对蚕豆“447”细胞质雄性不育(CMS)系特异的16.7 kbp双链RNA进行体外标记。在变性条件下对反应产物进行分析,结果显示在这两种情况下,均有一条4.5 kb单链RNA被大量标记,在之前的实验中就已检测到该RNA,当时允许与双链RNA相关的RNA依赖性RNA聚合酶在预起始复合物上进行RNA合成。对总pCp标记的双链RNA进行迁移率变动分析,结果显示并非有两个而是有三个不同的3'末端。最显著的测序模式对应于4.5 kb单链RNA,表明该RNA种类具有优先可及的游离3' OH末端。对变性双链RNA进行Northern印迹分析,证实4.5 kb单链RNA是一种亚基因组mRNA,并检测到其约12 kb的对应物。几乎所有16.7 kbp双链RNA分子的正义链都有中断,表明转录在复制复合物中明显占优势。这种在内部间断处起始后通过链置换机制进行转录的不同寻常策略,与其他双链RNA病毒或缺陷病毒的策略进行了比较,并就CMS性状的表达进行了讨论。