Abstract

Hybridization between humans and Neanderthals has resulted in a low level of Neanderthal ancestry scattered across the genomes of many modern-day humans. After hybridization, on average, selection appears to have removed Neanderthal alleles from the human population. Quantifying the strength and causes of this selection against Neanderthal ancestry is key to understanding our relationship to Neanderthals and, more broadly, how populations remain distinct after secondary contact. Here, we develop a novel method for estimating the genome-wide average strength of selection and the density of selected sites using estimates of Neanderthal allele frequency along the genomes of modern-day humans. We confirm that East Asians had somewhat higher initial levels of Neanderthal ancestry than Europeans even after accounting for selection. We find that the bulk of purifying selection against Neanderthal ancestry is best understood as acting on many weakly deleterious alleles. We propose that the majority of these alleles were effectively neutral—and segregating at high frequency—in Neanderthals, but became selected against after entering human populations of much larger effective size. While individually of small effect, these alleles potentially imposed a heavy genetic load on the early-generation human–Neanderthal hybrids. This work suggests that differences in effective population size may play a far more important role in shaping levels of introgression than previously thought.

Highlights

  • The recent sequencing of ancient genomic DNA has greatly expanded our knowledge of the relationship to our closest evolutionary cousins, the Neanderthals [1,2,3,4,5]

  • One hypothesis is that the underlying alleles were not deleterious in Neanderthals, but rather represent genetic incompatibilities that became deleterious only once they were introduced to the human population

  • We show that observed patterns of Neanderthal ancestry in modern humans can be explained as a PLOS Genetics | DOI:10.1371/journal.pgen

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Summary

Introduction

The recent sequencing of ancient genomic DNA has greatly expanded our knowledge of the relationship to our closest evolutionary cousins, the Neanderthals [1,2,3,4,5]. While some introgressed archaic alleles appear to have been adaptive in anatomically modern human (AMH) populations [12,13,14], on average selection has been suggested to act against Neanderthal DNA from modern humans. This can be seen from the non-uniform distribution of Neanderthal alleles along the human genome [9, 13]. A pattern of lower levels of Denisovan ancestry near genes and on the X chromosome in modern humans have recently been reported [18, 19]

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