Determination for KIR genotype and allele copy number via real-time quantitative PCR method.

IF 2.9 4区 医学 Q2 GENETICS & HEREDITY Immunogenetics Pub Date : 2024-04-01 Epub Date: 2024-01-11 DOI:10.1007/s00251-023-01331-7
Sudan Tao, Xuan You, Jielin Wang, Wei Zhang, Ji He, Faming Zhu
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Abstract

Killer cell immunoglobulin-like receptor (KIR) and human leukocyte antigen (HLA) play crucial roles in regulating NK cell activity. Here, we report a real-time quantitative PCR (qPCR) to genotype all KIR genes and their copy numbers simultaneously. With 18 pairs of locus-specific primers, we identified KIR genes by Ct values and determined KIR copy number using the 2-∆Ct method. Haplotypes were assigned based on KIR gene copy numbers. The real-time qPCR results were consistent with the NGS method, except for one sample with KIR2DL5 discrepancy. qPCR is a multiplex method that can identify KIR copy number, which helps obtain a relatively accurate haplotype structure, facilitating increased KIR research in laboratories where NGS or other high-resolution methods are not available.

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通过实时定量 PCR 方法确定 KIR 基因型和等位基因拷贝数。
杀伤细胞免疫球蛋白样受体(KIR)和人类白细胞抗原(HLA)在调节 NK 细胞活性方面起着至关重要的作用。在此,我们报告了一种实时定量 PCR(qPCR)方法,可同时对所有 KIR 基因及其拷贝数进行基因分型。利用 18 对基因座特异性引物,我们通过 Ct 值确定了 KIR 基因,并用 2-∆Ct 法确定了 KIR 拷贝数。根据 KIR 基因拷贝数分配单倍型。实时 qPCR 的结果与 NGS 方法一致,只有一个样本的 KIR2DL5 存在差异。qPCR 是一种可识别 KIR 拷贝数的多重方法,有助于获得相对准确的单倍型结构,从而有助于在无法使用 NGS 或其他高分辨率方法的实验室开展更多的 KIR 研究。
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来源期刊
Immunogenetics
Immunogenetics 医学-免疫学
CiteScore
6.20
自引率
6.20%
发文量
48
审稿时长
1 months
期刊介绍: Immunogenetics publishes original papers, brief communications, and reviews on research in the following areas: genetics and evolution of the immune system; genetic control of immune response and disease susceptibility; bioinformatics of the immune system; structure of immunologically important molecules; and immunogenetics of reproductive biology, tissue differentiation, and development.
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