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Genetic profile of KIR and HLA in southern Chinese Han population

机译:中国南方汉族人群KIR和HLA的遗传特征

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KIR and their HLA ligands are encoded by two of the most diverse gene families in the human genome. The function of KIR on the NK cell is highly dependent on the normal expression of class I HLA on the target cell. Previous population studies in southern Chinese have been focused on the KIR framework genes and genotypes but little is known about the compound profiles of KIR/HLA. The present study examined 503 unrelated individuals from southern Chinese Han population for the polymorphism of KIR and class I HLA genes. All 16 KIR genes were detected in the study population and the four framework genes KIR3DL2, 3DL3, 3DP1, and 2DL4 were present in all individuals. Thirty unique KIR gene profiles were found reflecting a rather limited number of KIR haplotypes in this population. KIRAA1 was the most common profile observed in 54.7% of the samples. Among the AA1 individuals, 15.6% were homozygous for the deleted KIR2DS4. Haplotype A (74.8%) was more common than haplotype B (25.2%). HLA-C1 was a much more common ligand for 2D KIRs than C2. Bw4-80I, Bw4-80T, and the Bw4-bearing HLA-A alleles were detected at similar frequencies. The matched KIR+HLA pairs 2DL2/3+C1 (98.1%), 3DL1+Bw4 (73.3%), 3DL2+A3/11 (60.0%) were the most common ones whereas 3DS1+Bw4-80I was the least common (9.4%). A total of 193 unique compound profiles of KIR-HLA were identified in 480 informative individuals, 130 of the profiles being detected only once. The study provided a comprehensive analysis of the KIR/HLA profiles in southern Chinese in regards of the presence/absence of KIR genes, HLA ligands, matched KIR+HLA pairs, and KIR/HLA compound profiles. The results could help to better understand the role played by KIR/HLA interaction in associated diseases and clinical transplantation in southern Chinese.
机译:KIR及其HLA配体由人类基因组中两个最多样化的基因家族编码。 KIR在NK细胞上的功能高度依赖于I类HLA在靶细胞上的正常表达。先前在华南地区进行的人口研究一直集中在KIR框架基因和基因型上,但对KIR / HLA的化合物概况了解甚少。本研究检查了来自中国南方汉族人群的503个无关个体的KIR和I类HLA基因多态性。在研究人群中检测到所有16个KIR基因,并且所有个体中都存在四个框架基因KIR3DL2、3DL3、3DP1和2DL4。发现了三十种独特的KIR基因图谱,反映了该种群中相当有限的KIR单倍型。 KIRAA1是在54.7%的样品中观察到的最常见的曲线。在AA1个体中,缺失的KIR2DS4是纯合子的15.6%。单倍型A(74.8%)比单倍型B(25.2%)更常见。 HLA-C1是2D KIR较C2更为常见的配体。在相似的频率下检测到Bw4-80I,Bw4-80T和带有Bw4的HLA-A等位基因。匹配的KIR + HLA对2DL2 / 3 + C1(98.1%),3DL1 + Bw4(73.3%),3DL2 + A3 / 11(60.0%)是最常见的,而3DS1 + Bw4-80I是最不常见的(9.4 %)。在480名信息丰富的个体中共鉴定出193种独特的KIR-HLA化合物谱,其中130种谱仅被检测到一次。该研究针对是否存在KIR基因,HLA配体,匹配的KIR + HLA对以及KIR / HLA复合图,对华南地区的KIR / HLA图进行了全面分析。结果可能有助于更好地了解KIR / HLA相互作用在华南地区相关疾病和临床移植中的作用。

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