40 This is also true when populations from Taiwan (TW), OCE, and NAM and SAM, which exhibit a very high degree of diversification probably because of rapid genetic drift, are excluded. Significant correlations Small molecule library with geography are also obtained at the global scale when genetic distances

are estimated by weighting them by the molecular distances (i.e. the nucleotide differences) among the alleles.51 This result is therefore robust and leads to the conclusion that human migrations were a primary force in the evolution of HLA variation worldwide, in addition to demographic expansions (contributing to allelic diversification) and contractions (contributing to population diversification). Genetic signatures of the history

of modern humans are even more detectable when one focuses on the HLA genetic patterns within specific continental areas. The following examples are illustrative. In Africa, linguistic differentiations among populations speaking languages of each of the four main African linguistic phyla – Niger-Congo (NC), Nilo-Saharan (NS), Afro-Asiatic (AA) and Khoisan (KH) – are excellent predictors of HLA genetic differentiations: according to a recent analysis of HLA-DRB1 variation in Africa,63 AA populations from Ethiopia (i.e. Amhara and Oromo, which exhibit a very high frequency of DRB1*13:02, but also elevated *07:01 and *03:01 frequencies) cluster with AA populations from North Africa, whereas the Nyangatom, a NS population, also from Ethiopia, show a peculiar genetic profile and share some similarities

(high frequencies of *11:01) with NC, the buy Y-27632 latter being further differentiated into West Africans (high frequencies of *13:04) and Central-South Africans (high frequencies of *15:03). Therefore, although the HLA genetic patterns of African populations appear to be geographically structured according to South, West, East and North differentiations,64 a close relationship is also found for the DRB1 locus between genetic and linguistic variation in Africa. This confirms the conclusions drawn from the study of other genetic markers like GM (as described in an earlier section), RH and the Y chromosome:13,14,65 at least for these polymorphisms, present oxyclozanide African genetic patterns are mostly explained by recent migrations (i.e. within the last ∼ 15 000 years) corresponding to the expansion of the main linguistic families in this continent. At loci HLA-C and -DRB1 (and this is also the case for GM, as stated above), the HLA genetic structure of Europeans reveals marked variation between West-Central and North populations, on one hand, and Southeast populations, on the other (with elevated frequencies of DRB1*11:04, DRB1*11:01 and C*04:01 compared with the other regions), a sharp genetic boundary being detected approximately at the level of the Alps.