The B allele with a 5·8 kb deletion in intron 1 of the ABO gene is the major allele in Japanese individuals with B m and A 1 B m phenotypes

B and A B phenotypes are the most frequent ABO variants in the Japanese population. The B antigen on B red blood cells is only detectable by adsorption and elution tests, and plasma B-transferase activity is usually detected at half or less levels compared with that of common B. Recently, a B allele...

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Veröffentlicht in:Vox sanguinis 2018-05, Vol.113 (4), p.393-396
Hauptverfasser: Ogasawara, K, Miyazaki, T, Ito, S, Yabe, R, Uchikawa, M, Enomoto, T, Yokoya, N, Hori, Y, Kumamoto, M, Watanabe, S, Satake, M
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Sprache:eng
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Zusammenfassung:B and A B phenotypes are the most frequent ABO variants in the Japanese population. The B antigen on B red blood cells is only detectable by adsorption and elution tests, and plasma B-transferase activity is usually detected at half or less levels compared with that of common B. Recently, a B allele lacking an erythroid cell-specific transcription enhancer in intron 1 of the ABO gene was identified from individuals with B and A B phenotypes, which could explain the unique serologic properties of B . In the Japanese Red Cross Society, eight Blood Centers tested blood samples from donors throughout Japan and collected blood samples from 888 B and 415 A B individuals. DNA analysis revealed that 1300 of 1303 (99·77%) individuals had the B allele with a 5·8 kb deletion (c.28 + 5110_10889del), which included the enhancer element.
ISSN:0042-9007
1423-0410
DOI:10.1111/vox.12642