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

被引:1
|
作者
Tao, Sudan [1 ]
You, Xuan [1 ]
Wang, Jielin [1 ]
Zhang, Wei [1 ]
He, Ji [1 ]
Zhu, Faming [1 ]
机构
[1] Blood Ctr Zhejiang Prov, Key Lab Blood Safety Res Zhejiang Prov, Hangzhou, Zhejiang, Peoples R China
基金
中国国家自然科学基金;
关键词
KIR; Real-time quantitative PCR; Natural killer cells; Genetic polymorphism; CELL-RECEPTOR GENES; ORGANIZATION; DIVERSITY;
D O I
10.1007/s00251-023-01331-7
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
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(-triangle 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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页码:137 / 143
页数:7
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