De novo rates of aTrypanosoma-resistant mutation in two human populations

Abstract

Until recently, mutation rates have only been measured as averages across many genomic positions. Recently, a method to measure mutation rates at the single-mutation resolution was applied to a narrow region in the human hemoglobin subunit beta (HBB) gene containing the site of the hemoglobin S (HbS) mutation as well as to a paralogous hemoglobin subunit delta (HBD) region, in sperm samples from sub-Saharan African and northern European donors. The HbS mutation, which protects against malaria while causing sickle-cell anemia in homozygotes originated de novo significantly more frequently in theHBBgene in Africans compared to the other three test cases combined (the EuropeanHBBgene and the European and AfricanHBDgene). Here, we apply this approach to the human apolipopro-tein L1 (APOL1) gene containing the site of the G1 1024A→G mutation, which protects against African sleeping sickness caused byTrypanosoma brucei gambiensewhile causing a substantially increased risk of chronic kidney disease (CKD) in homozygotes. We find that the 1024A→G mutation is the mutation of highest de novo origination rate and deviates most from the genome-wide average rate for its type (A→G) compared to all other observable mutations in the region, and that it originates de novo significantly more frequently in Africans than in Europeans—i.e., in the population where it is of adaptive significance. The results are inconsistent with the notion that the probability of a specific mutational event is independent of its value to the organism and underscore the importance of studying mutation rates at the single-mutation resolution.