- Author:
Chao-xia LU
1
;
Na ZHU
;
Qian ZHANG
;
Hong HUANG
;
Bing-shen KE
;
Huai-shui HOU
;
Bai-jun SHEN
Author Information
- Publication Type:Journal Article
- MeSH: Alleles; Base Sequence; Cloning, Molecular; Genotype; HLA-B Antigens; chemistry; genetics; Humans; Molecular Sequence Data; Polymerase Chain Reaction; Sequence Analysis, DNA
- From: Chinese Journal of Medical Genetics 2011;28(1):88-91
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVETo investigate the molecular basis for a novel human leukocyte antigen (HLA) allele B*5827.
METHODSDNA from the proband was analyzed by polymerase chain reaction-sequence specific oligonucleotide (PCR-SSO) typing. The amplified product was sequenced bidirectionally.
RESULTSAbnormal HLA-B locus was observed and its nucleotide sequence was different from the known HLA-B allele sequences, with highest homology to HLA-B*5820 allele. It differs from HLA-B*5820 by 8 nucleotide substitutions in exon 3, i.e., nt 290 (G > C), nt 346 (T > A), nt 390 (A > C), nt 404 (G > C), nt 413 (C > G), nt 471 (A > G), nt 486 (A > G) and nt 487 (C > A), resulting in an amino acid change from ser > arg at nt 97, phe >tyr at nt 115, ser > arg at nt 130, thr > ala at nt 157 and thr > glu at nt 162. Nucleotide differences of nt 404 (G > C) and nt 413( C > G) did not change amino acid.
CONCLUSIONThe sequences of the novel allele have been submitted to GenBank (access No.GU071234). A novel HLA class I allele B*5827 has been officially assigned by the WHO HLA Nomenclature Committee in Jan. 2010.