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HLA-Cw*16 (Cw*16) is an HLA-C allele-group. The serotype identifies the more common HLA-Cw*16 gene products. This allele group is most commonly found in West Africa, but A single Haplotype of Cw16 is found in Western Europe at unusually high frequencies. There is no useful serology for Cw*16.

Alleles

Cw*1601

While Cw*1601 probably did not evolve in Western Africa, it has certainly seen an expansion and it is a region in which most of the haplotype diversity is seen. As the frequency table for Cw*1601 reveals that highest frequencies for a given latitude north, more or less, follows the 0th meridian from Western Africa to the United Kingdom, the exception, an antinode, in Western France, indicating a displacement in those regions or the core of the Cw*16 bearing migration along the Eastern Region. There is a secondary node in the Basques of Spain, however given very little haplotype diversification (See A29-Cw*16-B44 haplotype, this page) indicates that this is the result of asymmetric expansion or selection within the Basque for the allele.
The Mandinka of Senegal are related to Bandiagara of Mali because the Malian Empire settled Senegal. The Bubi are found on the islands off the coast of Equatorial Guinea (Click on map to enlarge to full size to see islands)

Other alleles and haplotypes follow a similar pattern. The DR7-DQ2, DR3-DQ2 and A*2901 follow a similar pattern of apparent gene flow from Africa to Western Europe. Although for DR3-DQ2 the migration appears to be associated with B8 and probably occurred in the early AMH settlement of Europe.

Haplotypes

A29-Cw*16-B44

A29-Cw16-B44(A*2902:Cw*1601:B*4403) appears to have originated in West Africa were Cw*16 frequency is highest and has undergone more linkage equilibrium. Cw*16 decline slowly heading north and more rapidly to the east and northeast, with the highest frequency/latitude north generally along Eastern Spain into the British Ilses, some flow up the channel but haplotype frequency drops in the interior of Europe.

This haplotype can generally be extended from A- to -DQ as A29-Cw16-B44-DR7-DQ2.2:

A*2901 : Cw*1601 : B*4403 : DRB1*0701 : DQA1*0201 : DQB1*0202

And, the Cw16 component is in strong linkage disequilibrium with the DR7-DQ2.2 component suggesting that since the haplotypes introduction into Europe there has not been adequate time for equilibration, supporting its recent introduction into Europe. This particular haplotype supports theories of migration that are more numerous than those supported by mtDNA or Y chromosomal information, many such 'smaller' migrations are evident with HLA haplotypes, suggesting a much greater complexity to human population than haploid loci make evident.

References

1. Cianetti L, Testa U, Scotto L, et al. (1989). "Three new class I HLA alleles: structure of mRNAs and alternative mechanisms of processing". Immunogenetics. 29 (2): 80–91. doi:10.1007/BF00395855. PMID 2914713. S2CID 21766147.
2. Marsh, S. G.; Albert, E. D.; Bodmer, W. F.; Bontrop, R. E.; Dupont, B.; Erlich, H. A.; Fernández-Viña, M.; Geraghty, D. E.; Holdsworth, R.; Hurley, C. K.; Lau, M.; Lee, K. W.; Mach, B.; Maiers, M.; Mayr, W. R.; Müller, C. R.; Parham, P.; Petersdorf, E. W.; Sasazuki, T.; Strominger, J. L.; Svejgaard, A.; Terasaki, P. I.; Tiercy, J. M.; Trowsdale, J. (2010). "Nomenclature for factors of the HLA system, 2010". Tissue Antigens. 75 (4): 291–455. doi:10.1111/j.1399-0039.2010.01466.x. PMC 2848993. PMID 20356336.
3. ^ Middleton D, Menchaca L, Rood H, Komerofsky R (2003). "New allele frequency database". Tissue Antigens. 61 (5): 403–7. doi:10.1034/j.1399-0039.2003.00062.x. PMID 12753660.
4. ^ Sasazuki, Takehiko; Tsuji, Kimiyoshi; Aizawa, Miki (1992). HLA 1991: proceedings of the eleventh International Histocompatibility Workshop and Conference, held in Yokohama, Japan, 6–13 November 1991. Oxford : Oxford University Press. ISBN 978-0-19-262390-4.

• HLA-C alleles