Immunogenetics and Histocompatibility, Instituto de Investigación Sanitaria Puerta de Hierro Segovia de Arana, Madrid, Spain.
Hospital del Mar Medical Research Institute (IMIM), Barcelona, Spain.
Front Immunol. 2020 Mar 17;11:440. doi: 10.3389/fimmu.2020.00440. eCollection 2020.
Inhibitory Killer-cell Immunoglobulin-like Receptors (KIR) specific for HLA class I molecules enable human natural killer cells to monitor altered antigen presentation in pathogen-infected and tumor cells. genes display extensive copy-number variation and allelic polymorphism. They organize in a series of variable arrangements, designated haplotypes, which derive from duplications of ancestral genes and sequence diversification through point mutation and unequal crossing-over events. Genomic studies have established the organization of multiple haplotypes-many of them are fixed in most human populations, whereas variants of those have less certain distributions. Whilst -gene diversity of many populations and ethnicities has been explored superficially (frequencies of individual genes and presence/absence profiles), less abundant are in-depth analyses of how such diversity emerges from -haplotype structures. We characterize here the genetic diversity of KIR in a sample of 414 Spanish individuals. Using a parsimonious approach, we manage to explain all 38 observed -gene profiles by homo- or heterozygous combinations of six fixed centromeric and telomeric motifs; of six variant gene arrangements characterized previously by us and others; and of two novel haplotypes never detected before in Caucasoids. Associated to the latter haplotypes, we also identified the novel transcribed allele, and a chimeric / gene (designated ) that challenges current criteria for classification and nomenclature of genes and haplotypes.
抑制性杀伤细胞免疫球蛋白样受体 (KIR) 特异性识别 HLA Ⅰ类分子,使人类自然杀伤细胞能够监测病原体感染和肿瘤细胞中抗原呈递的改变。KIR 基因显示出广泛的拷贝数变异和等位基因多态性。它们以一系列可变的排列方式组织,称为单倍型,这些单倍型源自祖先基因的重复和通过点突变和不等交换事件的序列多样化。基因组研究已经确定了多个 KIR 单倍型的组织,其中许多在大多数人群中是固定的,而那些变体的分布则不太确定。虽然已经对许多人群和种族的 KIR 基因多样性进行了表面探索(单个基因的频率和存在/缺失谱),但对于这种多样性如何从 KIR 单倍型结构中产生的深入分析却很少。我们在这里对 414 名西班牙个体样本中的 KIR 遗传多样性进行了表征。通过一种简约的方法,我们成功地解释了所有 38 种观察到的 KIR 基因谱,这些基因谱是由六个固定的着丝粒和端粒基序的纯合或杂合组合、我们以前和其他人以前表征的六个变体基因排列以及两个以前在白种人中从未检测到的新单倍型来解释的。与后两种单倍型相关,我们还鉴定了新的转录 KIR 等位基因,以及一种嵌合 / 基因(命名为 ),这对 KIR 基因和单倍型的分类和命名标准提出了挑战。