Exploiting selection at linked sites to infer the rate and strength of adaptation.

Abstract

Genomic data encodes past evolutionary events and has the potential to reveal the strength, rate, and biological drivers of adaptation. However, jointly estimating adaptation rate (a) and adaptation strength remains challenging because evolutionary processes such as demography, linkage, and non-neutral polymorphism can confound inference. Here, we exploit the influence of background selection to reduce the fixation rate of weakly-beneficial alleles to jointly infer the strength and rate of adaptation. We develop an MK-based method (ABC-MK) to infer adaptation rate and strength, and estimate α = 0.135 in human protein-coding sequences, 72% of which is contributed by weakly-adaptive variants. We show that in this adaptation regime α is reduced ≈ 25% by linkage genome-wide. Moreover, we show that virus-interacting proteins (VIPs) undergo adaptation that is both stronger and nearly twice as frequent as the genome average (α = 0.224, 56% due to strongly-beneficial alleles). Our results suggest that while most adaptation in human proteins is weakly-beneficial, adaptation to viruses is often strongly-beneficial. Our method provides a robust framework for estimating adaptation rate and strength across species.