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Five HLA‐B22 group alleles in Japanese
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HLA‐B22‐group alleles in Japanese were identified using PCR‐single‐strand conformation polymorphism (SSCP) and sequence analyses. We analyzed genomic DNAs obtained from Japanese individuals positive for HLA‐B22 group antigens (HLA‐B54, B55, B56) including two locally proposed splits (B55.2, and B22N). In the SSCP analysis of both exons 2 and 3, we discriminated five different B22‐group alleles. Each allelic pattern corresponded to each serological split antigen. Direct sequencing analysis of exon 2 and exon 3 showed that alleles encoding B54, B55.1 and B56 antigens in Japanese are encoded by B*5401, B*5502 and B*5601, respectively, and those encoding B55.2 and B22N antigens are previously unidentified alleles, B*5504 and B*5603, respectively. Full‐length cDNA sequencing showed that the B*5603 sequence is identical to those of B*5501, B*5502, B*5601, and B*5602 in exons 1 to 2 except for a synonymous substitution at nucleotide position 165 in exon 2. On the other hand, the sequence of exons 3 to 7 was identical to those of some B15 and B46 alleles, suggesting that B*5603 was generated by a recombination event between one of the B55 and B56 alleles and one of the B15 and B46 alleles in intron 2. As for B*5504, the entire exon 1 to 7 sequence is identical to that of B*5502 except that the 5‐half of the exon 3 sequence is identical to those of some B7, B27, B40 and B48 alleles, suggesting that an event such as gene conversion, segmental exchange, or double recombination occurred in this region.
Title: Five HLA‐B22 group alleles in Japanese
Description:
HLA‐B22‐group alleles in Japanese were identified using PCR‐single‐strand conformation polymorphism (SSCP) and sequence analyses.
We analyzed genomic DNAs obtained from Japanese individuals positive for HLA‐B22 group antigens (HLA‐B54, B55, B56) including two locally proposed splits (B55.
2, and B22N).
In the SSCP analysis of both exons 2 and 3, we discriminated five different B22‐group alleles.
Each allelic pattern corresponded to each serological split antigen.
Direct sequencing analysis of exon 2 and exon 3 showed that alleles encoding B54, B55.
1 and B56 antigens in Japanese are encoded by B*5401, B*5502 and B*5601, respectively, and those encoding B55.
2 and B22N antigens are previously unidentified alleles, B*5504 and B*5603, respectively.
Full‐length cDNA sequencing showed that the B*5603 sequence is identical to those of B*5501, B*5502, B*5601, and B*5602 in exons 1 to 2 except for a synonymous substitution at nucleotide position 165 in exon 2.
On the other hand, the sequence of exons 3 to 7 was identical to those of some B15 and B46 alleles, suggesting that B*5603 was generated by a recombination event between one of the B55 and B56 alleles and one of the B15 and B46 alleles in intron 2.
As for B*5504, the entire exon 1 to 7 sequence is identical to that of B*5502 except that the 5‐half of the exon 3 sequence is identical to those of some B7, B27, B40 and B48 alleles, suggesting that an event such as gene conversion, segmental exchange, or double recombination occurred in this region.
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