TY - JOUR
T1 - Identification of a new HLA-DRB1 allele (DRB1*0318) in three members of a Caucasian spanish family
AU - Ercilla, M. G.
AU - Guardia, A.
AU - Suárez, B.
AU - Arias, M. T.
AU - Fabregat, V.
AU - Costa, M.
AU - Salinas, I.
AU - Martorell, Jaume
AU - Vives, J.
AU - Lozano, F.
AU - Bosch Merino, Maria Assumpcio
PY - 2001/1/1
Y1 - 2001/1/1
N2 - This communication reports the identification of a new allele HLA-DRB1*03 in three members of a Caucasian Spanish family. The new allele has been officially named HLA-DRB1*0318 by the World Health Organization Nomenclature Committee. The exon 2 sequence of this new allele is identical to that of DRB1*03011 except for the first nucleotide of codon 45. The nucleotide change (C replacing G) leads to the amino acid substitution of glycine to arginine (GGG→CGG) at position 45. This position of the β1 domain shows very little polymorphism among DRB1* alleles (nucleotide changes at this position have only been reported for DRB1*1436 and DRB1*0105) and locates in the vicinity of the highly polymorphic position 47, which is a constituent of the groove's pocket interacting with the amino acid position 7 of the antigen peptide. The familial study showed that the new allele was maternally transmitted into the HLA-A*3002, -B*1801, -Cw*0501, -DRB1*0318, -DRB3*0202, -DQB1*0201 haplotype. Interestingly, the two siblings of the family, which were HLA identical and suffered of insulin-dependent diabetes mellitus (IDDM), were carriers of the two HLA haplotypes (DRB1*03/DQB1*0201 and DRB1*04/DQB1*0302) reported as susceptibility markers to IDDM in Caucasians.
AB - This communication reports the identification of a new allele HLA-DRB1*03 in three members of a Caucasian Spanish family. The new allele has been officially named HLA-DRB1*0318 by the World Health Organization Nomenclature Committee. The exon 2 sequence of this new allele is identical to that of DRB1*03011 except for the first nucleotide of codon 45. The nucleotide change (C replacing G) leads to the amino acid substitution of glycine to arginine (GGG→CGG) at position 45. This position of the β1 domain shows very little polymorphism among DRB1* alleles (nucleotide changes at this position have only been reported for DRB1*1436 and DRB1*0105) and locates in the vicinity of the highly polymorphic position 47, which is a constituent of the groove's pocket interacting with the amino acid position 7 of the antigen peptide. The familial study showed that the new allele was maternally transmitted into the HLA-A*3002, -B*1801, -Cw*0501, -DRB1*0318, -DRB3*0202, -DQB1*0201 haplotype. Interestingly, the two siblings of the family, which were HLA identical and suffered of insulin-dependent diabetes mellitus (IDDM), were carriers of the two HLA haplotypes (DRB1*03/DQB1*0201 and DRB1*04/DQB1*0302) reported as susceptibility markers to IDDM in Caucasians.
KW - HLA-DRB103 alleles
KW - Insulin-dependent diabetes mellitus
KW - Sequence-based typing
U2 - 10.1034/j.1399-0039.2001.057005489.x
DO - 10.1034/j.1399-0039.2001.057005489.x
M3 - Article
SN - 0001-2815
VL - 57
SP - 489
EP - 491
JO - Tissue Antigens
JF - Tissue Antigens
ER -