Etessami P, Callis R, Ellwood S, Stanley J
Department of Virus Research, John Innes Institute, Norwich, UK.
Nucleic Acids Res. 1988 Jun 10;16(11):4811-29. doi: 10.1093/nar/16.11.4811.
Insertion and deletion mutagenesis of both extended open reading frames (ORFs) of cassava latent virus DNA 2 destroys infectivity. Infectivity is restored by coinoculating constructs that contain single mutations within different ORFs. Although frequent intermolecular recombination produces dominant parental-type virus, mutants can be retained within the virus population indicating that they are competent for replication and suggesting that rescue can occur by complementation of trans acting gene products. By cloning specific fragments into DNA 1 coat protein deletion vectors we have delimited the DNA 2 coding regions and provide substantive evidence that both are essential for virus infection. Although a DNA 2 component is unique to whitefly-transmitted geminiviruses, the results demonstrate that neither coding region is involved solely in insect transmission. The requirement for a bipartite genome for whitefly-transmitted geminiviruses is discussed.
木薯潜隐病毒DNA 2的两个延伸开放阅读框(ORF)的插入和缺失诱变会破坏其感染性。通过共接种在不同ORF内含有单突变的构建体可恢复感染性。尽管频繁的分子间重组产生了显性亲本型病毒,但突变体可保留在病毒群体中,这表明它们具有复制能力,并提示可通过反式作用基因产物的互补作用实现拯救。通过将特定片段克隆到DNA 1外壳蛋白缺失载体中,我们确定了DNA 2的编码区域,并提供了确凿证据,证明两者对于病毒感染均至关重要。尽管DNA 2组分是粉虱传播双生病毒所特有的,但结果表明,两个编码区域均不单独参与昆虫传播。本文讨论了粉虱传播双生病毒对二分体基因组的需求。