Integrative Biology, University of Texas at Austin, Austin, Texas, United States of America.
PLoS One. 2011 Feb 9;6(2):e14645. doi: 10.1371/journal.pone.0014645.
One of the goals of biology is to bridge levels of organization. Recent technological advances are enabling us to span from genetic sequence to traits, and then from traits to ecological dynamics. The quantitative genetics parameter heritability describes how quickly a trait can evolve, and in turn describes how quickly a population can recover from an environmental change. Here I propose that we can link the details of the genetic architecture of a quantitative trait--i.e., the number of underlying genes and their relationships in a network--to population recovery rates by way of heritability. I test this hypothesis using a set of agent-based models in which individuals possess one of two network topologies or a linear genotype-phenotype map, 16-256 genes underlying the trait, and a variety of mutation and recombination rates and degrees of environmental change. I find that the network architectures introduce extensive directional epistasis that systematically hides and reveals additive genetic variance and affects heritability: network size, topology, and recombination explain 81% of the variance in average heritability in a stable environment. Network size and topology, the width of the fitness function, pre-change additive variance, and certain interactions account for ∼75% of the variance in population recovery times after a sudden environmental change. These results suggest that not only the amount of additive variance, but importantly the number of loci across which it is distributed, is important in regulating the rate at which a trait can evolve and populations can recover. Taken in conjunction with previous research focused on differences in degree of network connectivity, these results provide a set of theoretical expectations and testable hypotheses for biologists working to span levels of organization from the genotype to the phenotype, and from the phenotype to the environment.
生物学的目标之一是弥合组织层次之间的差距。最近的技术进步使我们能够跨越遗传序列到特征,然后从特征到生态动态。定量遗传学参数遗传力描述了一个特征可以进化多快,进而描述了一个种群从环境变化中恢复的速度有多快。在这里,我提出我们可以通过遗传力将数量性状的遗传结构细节(即,网络中潜在基因的数量及其关系)与种群恢复率联系起来。我使用一组基于代理的模型来测试这个假设,其中个体具有两种网络拓扑结构之一或线性基因型-表型图,16-256 个基因是性状的基础,以及各种突变和重组率以及环境变化的程度。我发现网络结构引入了广泛的方向性上位性,系统地隐藏和揭示了加性遗传方差,并影响了遗传力:网络大小、拓扑结构和重组解释了稳定环境中平均遗传力方差的 81%。网络大小和拓扑结构、适应度函数的宽度、预变加性方差以及某些相互作用解释了环境突然变化后种群恢复时间方差的 75%左右。这些结果表明,不仅加性方差的数量,而且重要的是其分布的基因座数量,对于调节特征可以进化以及种群可以恢复的速度都很重要。与之前专注于网络连接程度差异的研究相结合,这些结果为从事从基因型到表型以及从表型到环境跨越组织层次的生物学家提供了一组理论预期和可测试的假设。