major histocompatibility complex (human), class I, B46
Alleles B*4601
Structure (See HLA-B)
Symbol(s) HLA-B
EBI-HLA B*4601
Locus chr.6 6p21.31

HLA-B46 (B46) is an HLA-B serotype. The serotype identifies the gene products of HLA-B*4601 allele.[1] B*4601 resulted from a rare, interlocus, gene conversion between B62, probably B*1501, and a HLA-C allele.[2] B*4601 is the most common HLA-B allele that does not have an origin within Africa, and estimated 400 million people in Eastern Asia carry a B46 allele. When found B*4601 segregates with only 2 HLA-Cw alleles, A limited number of HLA-A and HLA-DRB1 alleles suggesting that the allele recently expanded from a limited sized group within SE Asia. Extremely low frequencies outside of Eastern Asia are indicators of a recent expansion of B46 from a recently small population. The frequency distribution suggests the ancestral B46 population was in SE China, or, potentially Burma (Myanmar or Laos, untested). B46 in Asia correlates with wet-rice farming. The exceptions are notable, it has been found in the Nivkhi on north-eastern Sakalin Island, the Ainu, and the Nivkhi-related (genetically) Tlinglet population of Alaska at trace levels.

Serotype

B46 serotype recognition of Some HLA B*46 allele-group gene products[3]
B*46B46 OtherSample
allele % %size (N)
460159291487

The serotyping is poor for B*4601 and it is preferable to use SSP-PCR. B*46:01 is one of the four B alleles that reacts with neither Bw4 nor Bw6. The others are B*18:06, B*55:03 and B*73:01.[4]

B*4601 Allele Frequencies

HLA B*4601 frequencies
freq
ref.Population(%)
[5]Buyei (China)21.6
[5]Miao (China)18.4
[6]Han (2) (Yunnan, China)17.9
[6]Thai (in Singapore)17.2
[6]Southern Chinese (in Taiwan)17.2
[6]Chinese (in Hong Kong)16.3
[6]Hakka (2)(Taiwan)15.6
[6]Guangzhou (China)15.5
[6]Northeastern Thailand15.1
[6]Minnan (Avg 1 & 2) (Taiwan)15.0
[6]Middle' Chinese (in Taiwan)15.0
[6]Hakka (Taiwan)13.6
[6]Wuhan (China)13.5
[6]Maonan (Guangxi, China)13.4
[6]Chinese (in Singapore)13.4
[5]Vietnamese13.2
[6]Southern Han (China)11.5
[6]Shanghai (China)11.2
[6]Meizhou Han (Guangdong, China)10.0
[6]Shijiazhuang Tianjian Han (Beijing)9.6
[6]Guangzhou Han (China)9.4
[6]Thailand9.2
[6]Nu (Yunnan, China)9.0
[6]Northern Chinese (in Taiwan)8.6
[6]Pazeh (Taiwan)8.2
[6]Aichi (Japan)7.6
[6]Lisu (Yunnan, China)7.2
[6]Beijing (China)6.8
[6]Naxi (Yunnan, China)6.1
[6]Hui (Qinghai, China)5.9
[6]Northern Han (China)5.7
[6]Japan (3)5.0
[6]Hyogo (Japan)4.7
[6]South Korea (3)4.4
[6]Man (Harbin City, China)4.1
[6]Siraya (Taiwan)3.9
[6]Central Japan3.6
[6]Linqu County (Shandong, China)3.3
[6]Timorese2.6
[6]Inner Mongolia (China)2.0
[6]Javanese (in Singapore)2.0
[6]Oold (Mongolia)1.9
[6]Nivkhi (Sakhalin I, Russia) sland1.9
[6]Thao (Taiwan)1.7
[6]Riau Malay (in Singapore)1.5
[6]Tuva (2) (Russia)1.4
[6]Tibetan (China)1.3
[6]Khalkh (Ulaanbaatar, Mongolia)1.2
[6]Ainu (Hokkaidō, Japan)1.0
[6]Okinawa (in Hawaii, USA)1.0
[6]Indigenous (Taiwan)0.9
[6]Khalkha (Mongolia)0.5
[6]Brahui (Pakistan)0.5
HLA-B*4601 abundance
Dark Red = 7% or greater
Red = 3 to 7%
Orange = 1 to 3%
Green = O to 1%
Black = regions not typed

A2-Cw11(1)-B46

This haplotype is unique in several regards, first and most importantly the B46 serotype is not from Africa, this distinguishes it from every other known B serotype. It is the result of a recombination event between B62(B*1501) and an HLA-C allele within Asia. This event happened recently as there is only one major allele and minor alleles are at trace frequencies. There has been some recombination between this haplotype, A24 and A11 bearing alleles, probably in a local (or tribal population). B46 is found wherever Asian wet-rice farming peoples have traveled and is found at low frequencies in non-farming indigenous groups. The one exception is the Ninhvet of Siberia and the Eastern Tlinglet of Alaska. This B46 contribution appears to have been recent. Because of the numbers of people represented by the sample groups, and its relative high frequency in those group A2-B46 is one of the most frequent, if not the most frequent A-B haplotype in the world, even though it is absent from the indigenous populations of most peoples in the world.

HLA A2-B46 haplotype frequencies
freqRank in
ref.Population(%)Pop.
[5] Buyi16.611
[5] Miao13.61
[5] Singapore
(Chinese)		11.42
[7] Chaoshan10.11
[5] Southern Han7.82
[5] VietNam7.81
[5] Thai7.21
[5] Thai Chinese4.0
[5] Japanese3.34
[5] Li3.0
[5] Korea2.8
[5] Uygar2.7
[5] Manchu2.6
[5] Inner Mong.1.9
[5] Northern Han1.8
1 highest freq. A-B hap in Asia.

This haplotype is unique in several regards, first and most importantly the B46 serotype is not from Africa, this distinguishes it from every other major B serotype except B*48. It is the result of a recombination event between B62(B*1501) and an HLA-C allele within Asia. This event happened recently as there is only one major allele and minor alleles are at trace frequencies. There has been some recombination between this haplotype, A24 and A11 bearing alleles, probably in a local (or tribal population). B46 is found wherever Asian wet-rice farming peoples have traveled and is found at low frequencies in non-farming indigenous groups. The one exception is the Ninhvet of Siberia and the Eastern Tlinglet of Alaska. This B46 contribution appears to have been recent. Because of the numbers of people represented by the sample groups, and its relative high frequency in those group A2-B46 is one of the most frequent, if not the most frequent A-B haplotype in the world, even though it is absent from the indigenous populations of most peoples in the world.

The most common haplotype, and probably the ancestral haplotype given its distribution from the Ninhivet to Indonesia is:

A*0207 : C*0102 : B*4601 : DRB1*0901 : DQA1*0302 : DQB1*0303

A different haplotype that is more common in Korea and Japan is

A*0207 : C*0102 : B*4601 : DRB1*0803 : DQA1*0103 : DQB1*0601

B46, or a closely linked allele may have been under positive selection in rice farmers of Asia.

References

  1. ↑ 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.
  2. ↑ Hildebrand WH, Domena JD, Shen SY, et al. (1994). "HLA-B15: a widespread and diverse family of HLA-B alleles". Tissue Antigens. 43 (4): 209–18. doi:10.1111/j.1399-0039.1994.tb02327.x. PMID 7521976.
  3. ↑ Allele Query Form IMGT/HLA – European Bioinformatics Institute
  4. ↑ Voorter, CE; van der Vlies, S; Kik, M; van den Berg-Loonen, EM (October 2000). "Unexpected Bw4 and Bw6 reactivity patterns in new alleles". Tissue Antigens. 56 (4): 363–70. doi:10.1034/j.1399-0039.2000.560409.x. PMID 11098937.
  5. 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 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 [Oxfordshire]: Oxford University Press. ISBN 978-0-19-262390-4.
  6. 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 Middleton D, Menchaca L, Rood H, Komerofsky R (2003). "New allele frequency database: http://www.allelefrequencies.net". Tissue Antigens. 61 (5): 403–7. doi:10.1034/j.1399-0039.2003.00062.x. PMID 12753660. {{cite journal}}: External link in |title= (help)
  7. ↑ Hu SP, Luan JA, Li B, et al. (2007). "Genetic link between Chaoshan and other Chinese Han populations: Evidence from HLA-A and HLA-B allele frequency distribution". Am. J. Phys. Anthropol. 132 (1): 140–50. doi:10.1002/ajpa.20460. PMID 16883565.
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