López-Carrasco Amparo, Gago-Zachert Selma, Mileti Giuseppe, Minoia Sofia, Flores Ricardo, Delgado Sonia
a Instituto de Biología Molecular y Celular de Plantas (IBMCP), Universidad Politécnica de Valencia-Consejo Superior de Investigaciones Científicas , Valencia , Spain.
b Department of Molecular Signal Processing , Leibniz Institute of Plant Biochemistry , Halle ( Saale ), Germany.
RNA Biol. 2016;13(1):83-97. doi: 10.1080/15476286.2015.1119365.
Eggplant latent viroid (ELVd), like other members of family Avsunviroidae, replicates in plastids through a symmetric rolling-circle mechanism in which elongation of RNA strands is most likely catalyzed by a nuclear-encoded polymerase (NEP) translocated to plastids. Here we have addressed where NEP initiates transcription of viroid strands. Because this step is presumably directed by sequence/structural motifs, we have previously determined the conformation of the monomeric linear (+) and (-) RNAs of ELVd resulting from hammerhead-mediated self-cleavage. In silico predictions with 3 softwares led to similar bifurcated conformations for both ELVd strands. In vitro examination by non-denaturing PAGE showed that they migrate as prominent single bands, with the ELVd (+) RNA displaying a more compact conformation as revealed by its faster electrophoretic mobility. In vitro SHAPE analysis corroborated the ELVd conformations derived from thermodynamics-based predictions in silico. Moreover, sequence analysis of 94 full-length natural ELVd variants disclosed co-variations, and mutations converting canonical into wobble pairs or vice versa, which confirmed in vivo most of the stems predicted in silico and in vitro, and additionally helped to introduce minor structural refinements. Therefore, results from the 3 experimental approaches were essentially consistent among themselves. Application to RNA preparations from ELVd-infected tissue of RNA ligase-mediated rapid amplification of cDNA ends, combined with pretreatments to modify the 5' ends of viroid strands, mapped the transcription initiation sites of ELVd (+) and (-) strands in vivo at different sequence/structural motifs, in contrast with the situation previously observed in 2 other members of the family Avsunviroidae.
茄子潜隐类病毒(ELVd)与鳄梨潜隐类病毒科的其他成员一样,通过对称滚环机制在质体中复制,其中RNA链的延伸很可能由转运至质体的核编码聚合酶(NEP)催化。在此,我们研究了NEP在何处启动类病毒链的转录。由于这一步骤可能由序列/结构基序指导,我们之前已确定了锤头介导的自我切割产生的ELVd单体线性(+)和(-)RNA的构象。使用3种软件进行的计算机模拟预测得出,ELVd两条链的构象类似,均为分叉状。非变性聚丙烯酰胺凝胶电泳的体外检测表明,它们迁移为明显的单一条带,ELVd(+)RNA显示出更紧密的构象,这可通过其更快的电泳迁移率得以揭示。体外SHAPE分析证实了源自基于热力学的计算机模拟预测的ELVd构象。此外,对94个全长天然ELVd变体的序列分析揭示了共变现象,以及将标准碱基对转换为摆动碱基对或反之的突变,这在体内证实了计算机模拟和体外预测的大多数茎环结构,此外还有助于引入细微的结构优化。因此,这3种实验方法的结果彼此基本一致。将RNA连接酶介导的cDNA末端快速扩增应用于ELVd感染组织的RNA制备,并结合预处理以修饰类病毒链的5'末端,在体内将ELVd(+)和(-)链的转录起始位点定位在不同的序列/结构基序处,这与鳄梨潜隐类病毒科其他2个成员先前观察到的情况不同。