Integrated analysis of sequence evolution and population history using hypervariable compound haplotypes

• Published in: Human molecular genetics 2000-11, Vol.9 (18), p.2675-2681
• Main Authors: ROGERS, Emma J, SHONE, Angela C, ALONSO, Santos, MAY, Celia A, ARMOUR, John A. L
• Format: Article
• Language: English
• Subjects: Africa; Animals; Asia; Base Sequence; Biological and medical sciences; chromosome 16; Chromosomes, Human, Pair 16 - genetics; DNA - genetics; Europe; Evolution, Molecular; Fundamental and applied biological sciences. Psychology; Gene Conversion - genetics; Genetic Variation - genetics; Genetics of eukaryotes. Biological and molecular evolution; Gorilla gorilla - genetics; Haplotypes - genetics; Human; Humans; Microsatellite Repeats - genetics; Mutation - genetics; Pan troglodytes - genetics; Phylogeny; Polymorphism, Genetic - genetics; Pongo pygmaeus - genetics; Population genetics, reproduction patterns; Time Factors
• ISSN: 0964-6906; 1460-2083; 1460-2083
• DOI: 10.1093/hmg/9.18.2675

We have examined compound haplotypes from a highly informative region of human chromosome 16, in which information from the rapid evolution of a highly unstable minisatellite is integrated with data on the longer-term evolution of this segment from 10 flanking substitutional polymorphisms. Combined with sequence data from non-human primates, analysis of relationships between these compound haplotypes allows the reconstruction of a rooted network of the evolutionary pathways between them. Most relationships can be explained via simple substitutional mutations, although the origins of some haplotypes involve recurrent events at a hotspot for substitutional mutation and/or gene conversion. For compound haplotypes including the minisatellite array, the network found in a range of world-wide populations constitutes a highly informative data set for the analysis of population history (437 different compound haplotypes were discriminated among 658 studied). Since the mutation rates and processes of the minisatellite array are known from direct studies, ages for individual lineages have been estimated using associated minisatellite diversity. These analyses suggest that the higher information content and sampling depth of these compound haplotypes may allow more precise calibration of lineage ages than is possible using coalescent analysis of DNA sequence. Using this method we have dated the oldest Eurasian lineage as 52,000-66,000 years and the oldest European specific lineage as 37,600-56,200 years.