Computational Biology Group, Institute of Infectious Diseases and Molecular Medicine, University of Cape Town, Observatory, South Africa.
PLoS Pathog. 2011 Sep;7(9):e1002203. doi: 10.1371/journal.ppat.1002203. Epub 2011 Sep 15.
Genetic recombination is an important process during the evolution of many virus species and occurs particularly frequently amongst begomoviruses in the single stranded DNA virus family, Geminiviridae. As in many other recombining viruses it is apparent that non-random recombination breakpoint distributions observable within begomovirus genomes sampled from nature are the product of variations both in basal recombination rates across genomes and in the over-all viability of different recombinant genomes. Whereas factors influencing basal recombination rates might include local degrees of sequence similarity between recombining genomes, nucleic acid secondary structures and genomic sensitivity to nuclease attack or breakage, the viability of recombinant genomes could be influenced by the degree to which their co-evolved protein-protein and protein-nucleotide and nucleotide-nucleotide interactions are disreputable by recombination. Here we investigate patterns of recombination that occur over 120 day long experimental infections of tomato plants with the begomoviruses Tomato yellow leaf curl virus and Tomato leaf curl Comoros virus. We show that patterns of sequence exchange between these viruses can be extraordinarily complex and present clear evidence that factors such as local degrees of sequence similarity but not genomic secondary structure strongly influence where recombination breakpoints occur. It is also apparent from our experiment that over-all patterns of recombination are strongly influenced by selection against individual recombinants displaying disrupted intra-genomic interactions such as those required for proper protein and nucleic acid folding. Crucially, we find that selection favoring the preservation of co-evolved longer-range protein-protein and protein DNA interactions is so strong that its imprint can even be used to identify the exact sequence tracts involved in these interactions.
遗传重组是许多病毒物种进化过程中的一个重要过程,特别是在单链 DNA 病毒家族 Geminiviridae 中的 begomoviruses 中频繁发生。与许多其他重组病毒一样,很明显,从自然界中采样的 begomovirus 基因组中可观察到的非随机重组断点分布是基因组间基本重组率变化以及不同重组基因组总体生存力变化的产物。虽然影响基本重组率的因素可能包括重组基因组之间局部序列相似性、核酸二级结构和基因组对核酸酶攻击或断裂的敏感性,但重组基因组的生存力可能会受到其共进化的蛋白-蛋白、蛋白-核酸和核酸-核酸相互作用因重组而受到多大程度破坏的影响。在这里,我们研究了番茄黄卷叶病毒和番茄卷叶科摩罗病毒在番茄植物长达 120 天的实验感染中发生的重组模式。我们表明,这些病毒之间的序列交换模式可以非常复杂,并提供了明确的证据表明,局部序列相似性等因素而不是基因组二级结构强烈影响重组断点的位置。从我们的实验中也可以明显看出,总体重组模式强烈受到对显示出破坏内部基因组相互作用的单个重组体的选择的影响,例如对正确的蛋白质和核酸折叠所必需的相互作用。至关重要的是,我们发现,有利于保存共进化的长程蛋白-蛋白和蛋白-DNA 相互作用的选择非常强烈,以至于它的印记甚至可以用于识别涉及这些相互作用的确切序列片段。