HLA-DQ4 (DQ4) is a serotype subgroup within HLA-DQ(DQ) serotypes. The serotype is determined by the antibody recognition of β4 subset of DQ β-chains. The β-chain of DQ is encoded by HLA-DQB1 locus and DQ4 are encoded by the HLA-DQB104 allele group. This group currently contains 2 common alleles, DQB10401 and DQB10402. HLA-DQ4 and HLA-DQB104 are almost synonymous in meaning. DQ4 β-chains combine with α-chains, encoded by genetically linked HLA-DQA1 alleles, to form the cis-haplotype isoforms. These isoforms, nicknamed DQ4.3 and DQ4.4, are also encoded by the DQA10303 and DQA10401 genes, respectively.

Serotype

Alleles

DQB1*0401

DQB1*0402

Haplotypes

DQ4.3

DQA10303:DQB10401 is linked to DRB10405 and is common on the west Pacific rim, from Indonesia to Japan and inland areas of Eastern Asia. In Japan it confers susceptibility to juvenile diabetes likely via the DR4 gene. **DQA10303:DQB10402** is primarily found in Northeastern Asia and the west Pacific rim. It is similar to DQA10303:DQB1*0402.

DQ4.2

DQA10401:DQB10402 has a trimodal global distribution. The highest frequencies are found in the highland regions of the new world, peaking in NW Mexico and in the Andes. It is also found at high levels in Namibia and Botswana. Between these two population it is moderately high in the Ainu of northern Japan.

DQ4 and Disease

DQ4 is associated with: The DR8-DQ4 haplotype is associated with DR4-DQ4(DRB10405:DQB10401) is associated with: The DQA10303:DQB104 haplotype is associated with: Other diseases mentioned are high-altitude pulmonary edema, Vogt–Koyanagi–Harada disease (DRB1*0405, see above table for Japanese), HIV resistance in the US, and haemophilia A (anti-FVIII inhibitor response).

DQ4 distribution

The table to the left shows the values of Japanese (values converted from phenotype frequencies to haplotype frequencies for sake of consistency) DR-DQ types. This table is presented here because of the diversity of DQ4 types in the Japanese population not seen elsewhere. DQ4 is typically rare most of the world but where it appears more frequently is something of interest. The node of DQ4 is with the DQA10401:DQB10402 (DQ4.24 for this page) haplotype in Northwestern Mexico and the highland region of western South America reaching 40% haplotype frequencies in that area. Outside of the Indigenous American population DQ4.24 is elevated at 10% in the Ainu of Hokkaidō, Japan. There are a number of other A-B haplotypes that suggest a connection between the Ainu and the Meso-American and Andean populations as well as Lakota Sioux all have DQ4 levels higher than the Ainu. The linkage of DQ4 in Asia appears to be heaviest with DR8 (DR0801, DR0802, DR0804) for DQ4.24 and the frequency is elevated from the Ryukyu Islands to Okhotsk, Ulchi, Negidal, Tofalar at approximately 10% falling off in the Mansi at 4% and punctate levels in between. Haplotype diversity of DQB10402 appears to be centered around the Amur River/Japanese Island Chain, and diversity of DQB10401 very roughly follows a similar pattern. DQ4.24 is also high in the Swedes however this may be due to east to west gene flow traceable at other HLA loci. Since DQA10401:DQB10402 is found in the !Kung, one reasonably assumes it evolved in Africa and migrated with one of several potential waves, probably the earliest. Tracing the migration route is excessively difficult, but it appears that a possible second node of expansion in Central Asia and not the West Pacific Rim/Austro-Indic route postulated as the early human distribution. The most common haplotypes in the !Kung (for example Cw-B) that also appear in Eurasia appear to have been associated with the earliest migration, and is suggestive of a coastal migration; however the relatively high frequencies in the Ainu and Amur basin suggest a migration through the Transbaikal that is consistent with archaeology from about 18 kya. One expects with such a route that Korean would be higher than Japanese and Japanese higher the Ryukyuans still higher than Taiwan aboriginals. From the west gene frequencies in the Levant and Black Sea region are at 'diffusive' levels whereas there are pockets of increased frequency in the Zoroastrians of Yadz region (DQA10401 and DQB10402). Thus the DR8-DQ4.24 haplotype is probably one of western origin. The DR4-DQA10303:DQB1040X can be found at high frequencies in PNG highland groups but not DQ4.24. The DR0405 and DR410 are found specifically associated with these DQ types and there is some haplotype diversity. So that it appears the presence of the DQA103:DQB1*04 is of West Pacific Rim origins in Japanese and proximal Siberians, but unfortunately there is no current typing of these haplotypes in the Taiwan aboriginal population. The presence in Indonesia may be the result of retrograde gene flow that can be established by other HLA types as well as mtDNA.