Abstract

The aim of this study was to analyze the distribution of killer-cell immunoglobulin-like receptor (KIR) genes and their human leucocyte antigen (HLA) ligand combinations in different original ethnic populations in China, and thus, to provide relevant genomic diversity data for the future study of viral infections, autoimmune diseases, and reproductive fitness. A total of 1119 unrelated individuals from 11 ethnic populations—including Hani, Jinuo, Lisu, Nu, Bulang, Wa, Dai, Maonan, Zhuang, Tu, and Yugu—from four original groups, were included. The presence/absence of the 16 KIR loci were detected, and the KIR gene’s phenotype, genotype, and haplotype A and B frequencies, as well as KIR ligand’s HLA allotype and KIR–HLA pairs for each population, were calculated. Principal component analysis and phylogenetic trees were constructed to compare the characteristics of the KIR and KIR–HLA pair distributions of these 11 populations. In total, 92 KIR genotypes were identified, including six new genotypes. The KIR and its HLA ligands had a distributed diversity in 11 ethnic populations in China, and each group had its specific KIR and KIR–HLA pair profile. The difference among the KIR–HLA pairs between northern and southern groups, but not among the four original groups, may reflect strong pressure from previous or ongoing infectious diseases, which have a significant impact on KIR and its HLA combination repertoires.

Highlights

  • Segregated in different chromosomes, 6p21 and 19q13.4, human leucocyte antigen (HLA) and killer-cell immunoglobulin-like receptor (KIR) genes, respectively, exhibit diverse polymorphisms and their molecular expressions interact with each other as receptor ligands to ensure the proper role of nature killer (NK) cells in modulating an immune response [1,2]

  • Principal component analysis (PCA) and phylogenetic trees were constructed to compare the characteristics of the KIR and KIR–HLA pair distributions in the 11 populations

  • The extensive diversity of HLA and KIR genes and their interactive roles in the immune response make these genes coevolve in genotypic combination

Read more

Summary

Introduction

Segregated in different chromosomes, 6p21 and 19q13.4, human leucocyte antigen (HLA) and killer-cell immunoglobulin-like receptor (KIR) genes, respectively, exhibit diverse polymorphisms and their molecular expressions interact with each other as receptor ligands to ensure the proper role of nature killer (NK) cells in modulating an immune response [1,2]. Several studies on the coinheritance of these two genetic systems have indicated that carrying the appropriate KIR–HLA combination is important for human survival [3,4]. During human migration outward from Africa and the successive colonization worldwide, the cooperative KIR haplotypes and activating KIR–HLA pairs are important for humans to adapt to quickly changing environments and to increase population reproduction [5,6]. HLA polymorphism has been well studied in worldwide populations, which makes it a genetic marker for tracing a population’s origin, migration, and admixture [7,8]. Among 16 identified KIR genes, 2DL1, 2DL2, KIR2DS5, and 3DS1 belong to activating KIR genes, and KIR2DL4 has both inhibitory and activating

Objectives
Methods
Results
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call