Published August 17, 2020 | Version v1
Journal article Open

A comparison of humans and baboons suggests germline mutation rates do not track cell divisions

  • 1. Columbia University
  • 2. University of Oklahoma
  • 3. Wake Forest University
  • 4. University of Chicago
  • 5. University of California, San Francisco

Description

In humans, most germline mutations are inherited from the father. This observation has been widely interpreted as reflecting the replication errors that accrue during spermatogenesis. If so, the male bias in mutation should be substantially lower in a closely related species with similar rates of spermatogonial stem cell divisions but a shorter mean age of reproduction. To test this hypothesis, we resequenced two 3–4 generation nuclear families (totaling 29 individuals) of olive baboons (Papio anubis), who reproduce at approximately 10 years of age on average, and analyzed the data in parallel with three 3-generation human pedigrees (26 individuals). We estimated a mutation rate per generation in baboons of 0.57×10−8 per base pair, approximately half that of humans. Strikingly, however, the degree of male bias in germline mutations is approximately 4:1, similar to that of humans—indeed, a similar male bias is seen across mammals that reproduce months, years, or decades after birth. These results mirror the finding in humans that the male mutation bias is stable with parental ages and cast further doubt on the assumption that germline mutations track cell divisions. Our mutation rate estimates for baboons raise a further puzzle, suggesting a divergence time between apes and Old World monkeys of 65 million years, too old to be consistent with the fossil record; reconciling them now requires not only a slowdown of the mutation rate per generation in humans but also in baboons.

Data availability

Pedigree and de novo mutation data are available within S2 TableS3 Table, and S1 Data. Whole genome sequence data are available through the NCBI database of Genotypes and Phenotypes, (dbGaP study id phs000185, https://www.ncbi.nlm.nih.gov/gap/) and the NCBI Sequence Read Archive (BioProject accession number PRJNA433868, https://www.ncbi.nlm.nih.gov/bioproject/PRJNA433868); accession numbers are included in S1 Data. Data underlying the figure panels are available in S2 Data. Code for reproducing the figures and analyses is available at https://github.com/flw88/baboon_dnms.

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Additional details

Identifiers

DOI
10.1371/journal.pbio.3000838
Other
oai:uchicago.tind.io:6146

Funding

National Institute of General Medical Sciences
R01GM122975
Burroughs Wellcome Fund
Career at the Scientific Interface award
Alfred P. Sloan Foundation
Fellowship
Eunice Kennedy Shriver National Institute of Child Health and Human Development
R01HD21244
National Heart, Lung, and Blood Institute
R01HL085197
National Institutes of Health
R24OD017859
National Institute of General Medical Sciences
T32GM008224

UChicago Information

Division(s)
Biological Sciences Division
Department(s)
Human Genetics