非裔美国人HLA-A, -B, -C, -DRB1等位基因和单倍型频率

B Tu, S J Mack, A Lazaro, A Lancaster, G Thomson, K Cao, M Chen, G Ling, R Hartzman, J Ng, C K Hurley
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引用次数: 53

摘要

基于序列的分型用于鉴定人类白细胞抗原(HLA)-A、-B、-C和-DRB1等位基因,这些等位基因来自564名非裔美国志愿者,他们被招募参加一个不相关的造血干细胞登记。HLA-A、HLA-B 67、HLA-C 33和HLA-DRB1 44个等位基因在每个位点上鉴定出的已知等位基因数为42个。鉴定了6个在初始序列特异性寡核苷酸探针检测中未发现的新等位基因(A*260104、A*7411、Cw*0813、Cw*1608、Cw*1704和DRB1*130502)。平衡选择的作用,塑造比预期更“均匀”的等位基因频率分布,被推断为所有四个基因座,特别是HLA-A和DRB1基因座。使用期望最大化算法估计2、3和4位点单倍型。与来自非洲和欧洲的其他人群的比较表明,尽管也注意到HLA-A:B单倍型频率与先前对非洲裔美国人个体的研究相似,但此处描述的非洲裔美国人人群中的欧洲人混合程度低于先前报道的其他非洲裔美国人人群。
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HLA-A, -B, -C, -DRB1 allele and haplotype frequencies in an African American population.

Sequence-based typing was used to identify human leukocyte antigen (HLA)-A, -B, -C, and -DRB1 alleles from 564 consecutively recruited African American volunteers for an unrelated hematopoietic stem cell registry. The number of known alleles identified at each locus was 42 for HLA-A, HLA-B 67, HLA-C 33, and HLA-DRB1 44. Six novel alleles (A*260104, A*7411, Cw*0813, Cw*1608, Cw*1704, and DRB1*130502) not observed in the initial sequence-specific oligonucleotide probe testing were characterized. The action of balancing selection, shaping more 'even' than expected allele frequency distributions, was inferred for all four loci and significantly so for the HLA-A and DRB1 loci. Two-, three-, and four-locus haplotypes were estimated using the expectation maximization algorithm. Comparisons with other populations from Africa and Europe suggest that the degree of European admixture in the African American population described here is lower than that in other African American populations previously reported, although HLA-A:B haplotype frequencies similar to those in previous studies of African American individuals were also noted.

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Tissue antigens
Tissue antigens 医学-病理学
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审稿时长
6 months
期刊最新文献
Identification of a novel HLA-DRB1*14 allele, HLA-DRB1*14:143, by sequence-based typing. Identification of the novel HLA-A allele, HLA-A*24:96, in a Chinese individual. CCR5 gene polymorphism is a genetic risk factor for radiographic severity of rheumatoid arthritis. A HLA-A null allele (A*24:132N) with a stop codon in exon 3 generated by a point mutation. Detection of complement-fixing and non-fixing antibodies specific for endothelial precursor cells and lymphocytes using flow cytometry.
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