The Population-Specific Impact of Neandertal Introgression on Human Disease

Genome Biol Evol. 2021 Jan 7;13(1):evaa250. doi: 10.1093/gbe/evaa250.

Abstract

Since the discovery of admixture between modern humans and Neandertals, multiple studies investigated the effect of Neandertal-derived DNA on human disease and nondisease phenotypes. These studies have linked Neandertal ancestry to skin- and hair-related phenotypes, immunity, neurological, and behavioral traits. However, these inferences have so far been limited to cohorts with participants of European ancestry. Here, I analyze summary statistics from 40 disease GWAS (genome-wide association study) cohorts of ∼212,000 individuals provided by the Biobank Japan Project for phenotypic effects of Neandertal DNA. I show that Neandertal DNA is associated with autoimmune diseases, prostate cancer and type 2 diabetes. Many of these disease associations are linked to population-specific Neandertal DNA, highlighting the importance of studying a wider range of ancestries to characterize the phenotypic legacy of Neandertals in people today.

Keywords: Neandertal admixture; disease; genome-wide association studies; human evolution; population genetics.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alleles
  • Animals
  • Diabetes Mellitus, Type 2 / genetics
  • Disease / genetics*
  • Evolution, Molecular
  • Female
  • Fossils
  • Genetic Variation
  • Genome, Human*
  • Genome-Wide Association Study*
  • Humans
  • Japan
  • Male
  • Neanderthals / genetics*
  • Phenotype
  • Polymorphism, Single Nucleotide
  • White People / genetics