Sanjuán Rafael, Moya Andrés, Elena Santiago F
Institut Cavanilles de Biodiversitat i Biologia Evolutiva, Universitat de Valencia, P.O. Box 22085, 46071 Valencia, Spain.
Proc Natl Acad Sci U S A. 2004 Oct 26;101(43):15376-9. doi: 10.1073/pnas.0404125101. Epub 2004 Oct 18.
The tendency for genetic architectures to exhibit epistasis among mutations plays a central role in the modern synthesis of evolutionary biology and in theoretical descriptions of many evolutionary processes. Nevertheless, few studies unquestionably show whether, and how, mutations typically interact. Beneficial mutations are especially difficult to identify because of their scarcity. Consequently, epistasis among pairs of this important class of mutations has, to our knowledge, never before been explored. Interactions among genome components should be of special relevance in compacted genomes such as those of RNA viruses. To tackle these issues, we first generated 47 genotypes of vesicular stomatitis virus carrying pairs of nucleotide substitution mutations whose separated and combined deleterious effects on fitness were determined. Several pairs exhibited significant interactions for fitness, including antagonistic and synergistic epistasis. Synthetic lethals represented 50% of the latter. In a second set of experiments, 15 genotypes carrying pairs of beneficial mutations were also created. In this case, all significant interactions were antagonistic. Our results show that the architecture of the fitness depends on complex interactions among genome components.
遗传结构在突变间表现出上位性的趋势,在进化生物学的现代综合理论以及许多进化过程的理论描述中起着核心作用。然而,很少有研究能明确表明突变是否以及如何发生典型的相互作用。有益突变因其稀缺性而特别难以识别。因此,据我们所知,这类重要突变对之间的上位性此前从未被探究过。基因组成分之间的相互作用在诸如RNA病毒等紧凑基因组中应具有特殊的相关性。为了解决这些问题,我们首先构建了47种携带核苷酸取代突变对的水疱性口炎病毒基因型,确定了这些突变对适应性的单独和联合有害影响。几对突变对适应性表现出显著的相互作用,包括拮抗上位性和协同上位性。合成致死突变占后者的50%。在第二组实验中,还构建了15种携带有益突变对的基因型。在这种情况下,所有显著的相互作用都是拮抗的。我们的结果表明,适应性的结构取决于基因组成分之间的复杂相互作用。