Establishment of Q-PCR method for qualitative testing of the presence or absence of KIR genes
Autor: | Yunan LI, Jianxin ZHEN, Shuang LIANG, Qiong YU, Zhihui DENG |
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Jazyk: | čínština |
Rok vydání: | 2024 |
Předmět: | |
Zdroj: | Zhongguo shuxue zazhi, Vol 37, Iss 6, Pp 660-665 (2024) |
Druh dokumentu: | article |
ISSN: | 1004-549X 1004-549x |
DOI: | 10.13303/j.cjbt.issn.1004-549x.2024.06.009&lang=en |
Popis: | Objective To establish a method for qualitative detection of the presence or absence of all KIR genes by quantitative polymerase chain reaction(Q-PCR). Methods Based on the polymorphism of high-resolution level KIR alleles in Chinese population and the IPD-KIR database, KIR gene-specific primers were designed to amplify all the 16 KIR genes and 2DS4-Normal and 2DS4-Deleted subtypes by Q-PCR. Meanwhile, one negative control and one positive control specific amplifying human growth hormone (HGH) gene fragment were set to monitor the false positive and false negative results in PCR amplification, respectively. A total of 302 samples with known KIR genotype previously identified by KIR PCR-SSP commercial kit were randomly selected for blind inspection to verify the reliability of KIR Q-PCR method established by authors. Results The results of 300 samples detected by our KIR Q-PCR method were consistent with the known results, but two samples showed inconsistent results. One sample was negative for 2DS5 by Q-PCR but positive by PCR-SSP, another sample was positive for 2DS1 by Q-PCR but negative by PCR-SSP. The two doubtful samples were genotyped by sequencing-based typing (PCR-SBT) for 2DS5 and 2DS1, respectively. PCR-SBT results confirmed that the results of Q-PCR test was correct. Conclusion The KIR Q-PCR method established in this paper can provide accurate and reliable results for testing the presence or absence of KIR genes. |
Databáze: | Directory of Open Access Journals |
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