放大器
基因分型
分子反转探针
高分辨率熔体
分子生物学
荧光
生物
熔化曲线分析
基因型
单核苷酸多态性
SNP基因分型
遗传学
SNP公司
聚合酶链反应
基因
作者
Qian Wang,Yiping Wen,Minghui Shen,M. A. Knepper,Lina Gao
出处
期刊:Chinese Journal of Laboratory Medicine
[Chinese Medical Association]
日期:2017-02-11
卷期号:40 (2): 88-94
标识
DOI:10.3760/cma.j.issn.1009-9158.2017.02.004
摘要
Objective
To evaluate the utility of fluorescent dye SYTO13 for high-resolution melting (HRM) detection in single nucleotide polymorphism (SNP) genotyping and its clinical application.
Methods
This is a performance verification study. 36 genotype defined samples were divided into three groups: SNP rs3125734 C>T (class Ⅰ SNP) , rs255758 A>C (class ⅡSNP) and rs688C>T. These samples were used to evaluate SYTO13′s SNP genotyping capability of class Ⅰ SNP, class Ⅱ SNP, and two PCR products of different lengths (52 and 107 bp) covering the same SNP of rs688C>T. The commercial HRM dye of LCGreen Plus was used as the control. The genotyping capability is indicated by the Tm difference(ΔTm) between wild type and homozygous mutant genotypes. The Tm differences between wild genotype and homozygous mutant genotype were compared using the Independent Samples t test. Paired t test was used to evaluate genotyping capability of the two dyes. The clinical applicability is evaluated by synchronously performing PCR amplification and HRM analysis on thirty-five randomly selected DNA samples with known genotypes of the three SNPs.
Results
The SNPs of class Ⅰ and class Ⅱ can be genotyped directly and clearly with SYTO13 (ΔTmclassⅠ=0.36±0.05, tclassⅠ =14.827, PclassⅠ=0.000; ΔTm classⅡ=0.42±0.110, tclassⅡ=9.539, PclassⅡ=0.000). The classⅠSNP genotyping results was better using SYTO13 (ΔTmSYTO13=0.39±0.027), while the SNP genotyping for small amplicon did not discriminated clearly in this study. Long amplicons of class Ⅰ and Ⅱ SNPs can be identified directly except for several samples which can be genotyped accurately after having performed reexamination.
Conclusion
SYTO13 can apply for HRM analysis of genotyping classⅠ and Ⅱ SNPs with long amplicon and for clinical routine detection.(Chin J Lab Med, 2017, 40: 88-94)
Key words:
Polymorphism, single nucleotide; Genotyping techniques; Fluorescent dyes; High resolution melting
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