MacLean R Craig, Buckling Angus
Department of Zoology, University of Oxford, Oxford, United Kingdom.
PLoS Genet. 2009 Mar;5(3):e1000406. doi: 10.1371/journal.pgen.1000406. Epub 2009 Mar 6.
Understanding how beneficial mutations affect fitness is crucial to our understanding of adaptation by natural selection. Here, using adaptation to the antibiotic rifampicin in the opportunistic pathogen Pseudomonas aeruginosa as a model system, we investigate the underlying distribution of fitness effects of beneficial mutations on which natural selection acts. Consistent with theory, the effects of beneficial mutations are exponentially distributed where the fitness of the wild type is moderate to high. However, when the fitness of the wild type is low, the data no longer follow an exponential distribution, because many beneficial mutations have large effects on fitness. There is no existing population genetic theory to explain this bias towards mutations of large effects, but it can be readily explained by the underlying biochemistry of rifampicin-RNA polymerase interactions. These results demonstrate the limitations of current population genetic theory for predicting adaptation to severe sources of stress, such as antibiotics, and they highlight the utility of integrating statistical and biophysical approaches to adaptation.
了解有益突变如何影响适应性对于我们理解自然选择导致的适应性至关重要。在此,我们以机会致病菌铜绿假单胞菌对利福平的适应性作为模型系统,研究自然选择所作用的有益突变的适应性效应的潜在分布。与理论一致,当野生型适应性处于中等至高时,有益突变的效应呈指数分布。然而,当野生型适应性较低时,数据不再遵循指数分布,因为许多有益突变对适应性有很大影响。目前尚无种群遗传学理论来解释这种对大效应突变的偏向,但利福平与RNA聚合酶相互作用的潜在生物化学可以很容易地解释这一现象。这些结果证明了当前种群遗传学理论在预测对诸如抗生素等严重应激源的适应性方面的局限性,并且突出了整合统计和生物物理方法来研究适应性的实用性。