IDENTIFICATION OF NEW DRB1-ASTERISK-07 (DRB1-ASTERISK-0703), DRB1-ASTERISK-08 (DRB1-ASTERISK-0817) AND 2 DRB3-ASTERISK (DRB3-ASTERISK-0302 AND DRB3-ASTERISK-01014) ALLELES
S. Hashemitavoularis et al., IDENTIFICATION OF NEW DRB1-ASTERISK-07 (DRB1-ASTERISK-0703), DRB1-ASTERISK-08 (DRB1-ASTERISK-0817) AND 2 DRB3-ASTERISK (DRB3-ASTERISK-0302 AND DRB3-ASTERISK-01014) ALLELES, Tissue antigens, 51(5), 1998, pp. 577-581
We report here the identification of four novel DRB alleles using a re
verse hybridization (CANTYPE) assay. Molecular cloning and sequencing
confirmed the initial unusual hybridization patterns, All four new all
eles were detected during routine HLA typing for the Canadian Unrelate
d Bone Marrow Donor Registry. DRB10703 is identical to DRB1*0701 exce
pt for a single nucleotide substitution (AGA-->AGT), changing codon 29
from Arg to Ser, a so far undetected DRB polymorphism. DRB10817 diff
ers from DRB1'0801 by a single nucleotide substitution (TAC-->TTC), c
hanging codon 47 from Tyr to Phe. This polymorphism has not, until now
been identified in DRB108 alleles. Compared with DRB3*0301, DRB3*030
2 contains a single nucleotide substitution (TAC-->CAC) at codon 30, c
hanging the encoded Tyr to His. This polymorphism is typical for DRB3
02 alleles. DRB301014 is identical to DRB3*0101 except for a single s
ilent nucleotide substitution (GGG-->GGA) at codon 84. This polymorphi
sm has previously only been described for the DRB115012 allele. DRB1*
0817, DRB30302 and DRB3*01014 may have arisen from gene conversion, b
ut DRB10703 most likely nas generated by a point mutation event. The
DRB30302 allele was detected in two unrelated subjects, while the oth
er three have each only been detected once.