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A novel DRB3 allele (DRB3*0208), a new allelic variant of DRB1*1502 (DRB1*15023) and two new DQB1 (DQB1*03012 and DQB1*0614) alleles
被引:5
|作者:
Hashemi-Tavoularis, S
Ouellet, S
Sengar, DPS
Buyse, IM
机构:
[1] Canadian Red Cross Soc, HLA Lab, Natl Off, Ottawa, ON K1G 4J5, Canada
[2] Univ Ottawa, Fac Med, Dept Med, Ottawa, ON, Canada
[3] Univ Ottawa, Fac Med, Dept Pathol & Lab Med, Ottawa, ON, Canada
[4] Univ Ottawa, Fac Med, Dept Microbiol & Immunol, Ottawa, ON, Canada
来源:
关键词:
DQB1*03012;
DQB1*0614 alleles;
DRB1*15023;
DRB3*0208;
reverse hybridization assay;
D O I:
10.1111/j.1399-0039.1998.tb03047.x
中图分类号:
Q2 [细胞生物学];
学科分类号:
071009 ;
090102 ;
摘要:
Four novel HLA Class II alleles were identified using CANTYPE reverse hybridization assay. The initial unusual SSO hybridization patterns were confirmed by cloning and sequencing analysis. DRB3*0208 allele is identical to DRB3*0202 except for three nucleotide substitutions (GAT-->AGC) changing codon 57 from Asp to Scr. This polymorphism has so far been undetected in DRB3 alleles DRB1*15023 differs from DRB1*15021 by a single silent nucleotide substitution (AAC-->AAT, both encoding fur Asn) at codon 33. This polymorphism has not, until now, been identified in DRB alleles Compared with DQB1*03011, the novel DQB1*03012 contains a single silent nucleotide substitution (GCA-->GCG, both encoding for Ala) at codon 38. Finally, DQB1*0614 allele is identical to DQB1*0603 except for a single nucleotide substitution (TAC-->TTC), changing codon 9 from Tyr to Phe. Polymorphisms observed here in the DQB1*03012 and DQB1*0614 alleles are present in several of the known DQB1 alleles. DRB3*0208, DQB1*03012 and DQB1*0614 may have arisen from gene conversion, but the DRB1*15023 most likely was generated by a point mutation event. DQB1*0614 was detected in three related subjects, while each of the other three new alleles has only been detected once.
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页码:294 / 299
页数:6
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