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Wade, E. E.

Publications and source records attributed to Wade, E. E..

2 recordsLinked to original sources

Robustness of the inference of the distribution of fitness effects to selective sweeps

The distribution of fitness effects (DFE) describes the proportion of new mutations with certain selective strengths. It is a crucial quantity for the study of complex disease and evolutionary genetics. Population genetics approaches infer the DFE using the site frequency spectrum (SFS), which summarizes allele frequencies within a sample. These approaches first fit a demographic model to an SFS of putatively neutral sites, then infer the DFE from an SFS of selected sites conditional on that demographic model. This approach assumes that sites are independent and that population size changes affect selected and neutral sites equally. Selective sweeps may violate these assumptions. As a beneficial mutation rises in frequency, nearby sites hitchhike alongside the beneficial mutation. This distortion might differ between neutral and selected sites. Here, we evaluate the performance of the DFE inference method, fitdadi, in the presence of selective sweeps. We simulate genomic segments containing neutral and deleterious mutations drawn from a known DFE under varying selective sweep conditions, and test whether fitdadi can recover the true DFE with a flexible demographic model. When SFS are sampled immediately after fixation of a beneficial mutation, the demographic models absorb the sweep's effect as a population expansion, and the DFE is recovered relatively well. Performance declines at lower recombination rates and when using the unfolded SFS, leading to an overestimation of the strength of purifying selection. We then model recurrent selective sweeps at rates consistent with human polymorphism and divergence data. The demographic model captures these distortions, and the DFE is unbiased. Our results suggest that DFE inferences are unlikely to be substantially biased by selective sweeps, but that future studies should consider using the folded SFS and excluding regions of low recombination rate.

evolutionary biology↗

Quantifying the fraction of new mutations that are recessive lethal

The presence and impact of recessive lethal mutations has been widely documented in diploid outcrossing species. However, precise estimates in different species of the proportion of mutations that are recessive lethal remain limited. Here, we attempt to quantify the fraction of new mutations that are recessive lethal using Fit{partial}a{partial}i, a commonly-used method for inferring the distribution of fitness effects (DFE) using the site frequency spectrum. Using simulations, we demonstrate that Fit{partial}a{partial}i cannot accurately estimate the fraction of recessive lethal mutations, as expected given that Fit{partial}a{partial}i assumes that all mutations are additive by default. Consistent with the idea that mis-specification of the dominance model can explain this performance, we find that Fit{partial}a{partial}i can accurately infer the fraction of additive lethal mutations. Moreover, we demonstrate that in both additive and recessive cases, inference of the deleterious non-lethal portion of the DFE is minimally impacted by a small proportion (<10%) of lethal mutations. Finally, as an alternative approach to estimate the proportion of mutations that are recessive lethal, we employ models of mutation-selection-drift balance using existing genomic parameters and segregating recessive lethals estimates for humans and Drosophila melanogaster. In both species, we find that the segregating recessive lethal load can be explained by a very small fraction (<1%) of new nonsynonymous mutations being recessive lethal. Our results refute recent assertions of a much higher recessive lethal mutation fraction (4-5%), while highlighting the need for additional information on the joint distribution of selection and dominance coefficients.

evolutionary biology↗