Aix-Marseille University, CNRS, EFS, ADES, "Biologie des Groupes Sanguins," Marseille, France.
Etablissement Français du Sang PACA Corse, Marseille, France.
J Immunol. 2022 Jan 1;208(1):49-53. doi: 10.4049/jimmunol.2100358. Epub 2021 Dec 6.
The biological relevance of genes initially categorized as "pseudogenes" is slowly emerging, notably in innate immunity. In the HLA region on chromosome 6, is one such pseudogene; yet, it is transcribed, and its variation is associated with immune properties. Furthermore, two alleles, * and , putatively encode a complete, membrane-bound HLA protein. Here we thus hypothesized that HLA-H contributes to immune homeostasis similarly to tolerogenic molecules HLA-G, -E, and -F. We tested if * encodes a membrane-bound protein that can inhibit the cytotoxicity of effector cells. We used an HLA-null human erythroblast cell line transduced with * cDNA to demonstrate that HLA-H02:07 encodes a membrane-bound protein. Additionally, using a cytotoxicity assay, our results support that K562 * inhibits human effector IL-2-activated PBMCs and human IL-2-independent NK92-MI cell line activity. Finally, through in silico genotyping of the Denisovan genome and haplotypic association with Denisovan-derived *, we also show that * is of archaic origin. Hence, admixture with archaic humans brought a functional allele into modern European and Asian populations.
最初被归类为“假基因”的基因的生物学相关性正在慢慢显现,特别是在先天免疫中。在染色体 6 上的 HLA 区域, 就是这样一个假基因;然而,它被转录,其变异与免疫特性有关。此外,两个 等位基因,和,可能编码完整的、膜结合的 HLA 蛋白。因此,我们假设 HLA-H 与免疫耐受分子 HLA-G、-E 和 -F 相似,有助于免疫稳态。我们测试了是否编码一种可以抑制效应细胞细胞毒性的膜结合蛋白。我们使用转导了 cDNA 的 HLA 缺失的人类红系母细胞系来证明 HLA-H02:07 编码一种膜结合蛋白。此外,通过细胞毒性测定,我们的结果支持 K562抑制人类效应 IL-2 激活的 PBMCs 和人类 IL-2 非依赖的 NK92-MI 细胞系活性。最后,通过对丹尼索瓦基因组进行基因分型和与丹尼索瓦衍生的的单倍型关联,我们还表明具有古老的起源。因此,与古人类的混合将一个功能性*等位基因带入了现代欧洲和亚洲人群。