Diversity of Lactase Persistence Alleles in Ethiopia: Signature of a Soft Selective Sweep

• Published in: American journal of human genetics 2013-09, Vol.93 (3), p.538-544
• Main Authors: Jones, Bryony L., Raga, Tamiru O., Liebert, Anke, Zmarz, Pawel, Bekele, Endashaw, Danielsen, E. Thomas, Olsen, Anders Krüger, Bradman, Neil, Troelsen, Jesper T., Swallow, Dallas M.
• Format: Article
• Language: English
• Subjects: Alleles; Base Sequence; Caco-2 Cells; Cell Cycle Proteins - genetics; Cohort Studies; Demography; Enhancer Elements, Genetic - genetics; Ethiopia; Genetic diversity; Genetic Variation; Haplotypes; Haplotypes - genetics; Humans; Introns - genetics; Lactase - genetics; Milk; Minichromosome Maintenance Complex Component 6; Minority & ethnic groups; Mutation; Selection, Genetic; Sequence Analysis, DNA; Transfection
• ISSN: 0002-9297; 1537-6605
• DOI: 10.1016/j.ajhg.2013.07.008

The persistent expression of lactase into adulthood in humans is a recent genetic adaptation that allows the consumption of milk from other mammals after weaning. In Europe, a single allele (−13910∗T, rs4988235) in an upstream region that acts as an enhancer to the expression of the lactase gene LCT is responsible for lactase persistence and appears to have been under strong directional selection in the last 5,000 years, evidenced by the widespread occurrence of this allele on an extended haplotype. In Africa and the Middle East, the situation is more complicated and at least three other alleles (−13907∗G, rs41525747; −13915∗G, rs41380347; −14010∗C, rs145946881) in the same LCT enhancer region can cause continued lactase expression. Here we examine the LCT enhancer sequence in a large lactose-tolerance-tested Ethiopian cohort of more than 350 individuals. We show that a further SNP, −14009T>G (ss 820486563), is significantly associated with lactose-digester status, and in vitro functional tests confirm that the −14009∗G allele also increases expression of an LCT promoter construct. The derived alleles in the LCT enhancer region are spread through several ethnic groups, and we report a greater genetic diversity in lactose digesters than in nondigesters. By examining flanking markers to control for the effects of mutation and demography, we further describe, from empirical evidence, the signature of a soft selective sweep.