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Updated: Mar 28, 2026

Characterizing Mutational Load and Clonal Composition of Human Blood
Published on: July 11, 2019
Distance from sub-Saharan Africa predicts mutational load in diverse human genomes
Brenna M Henn1, Laura R Botigué2, Stephan Peischl3
1Department of Ecology and Evolution, Stony Brook University, The State University of New York, Stony Brook, NY 11794; brenna.henn@stonybrook.edu cdbustam@stanford.edu.
Abstract:
The Out-of-Africa (OOA) dispersal ∼ 50,000 y ago is characterized by a series of founder events as modern humans expanded into multiple continents. Population genetics theory predicts an increase of mutational load in populations undergoing serial founder effects during range expansions. To test this hypothesis, we have sequenced full genomes and high-coverage exomes from seven geographically divergent human populations from Namibia, Congo, Algeria, Pakistan, Cambodia, Siberia, and Mexico. We find that individual genomes vary modestly in the overall number of predicted deleterious alleles. We show via spatially explicit simulations that the observed distribution of deleterious allele frequencies is consistent with the OOA dispersal, particularly under a model where deleterious mutations are recessive. We conclude that there is a strong signal of purifying selection at conserved genomic positions within Africa, but that many predicted deleterious mutations have evolved as if they were neutral during the expansion out of Africa. Under a model where selection is inversely related to dominance, we show that OOA populations are likely to have a higher mutation load due to increased allele frequencies of nearly neutral variants that are recessive or partially recessive.
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