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 |
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Format: | Artikel |
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. |
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ISSN: | 0042-9007 1423-0410 |
DOI: | 10.1111/vox.12642 |