Pomeroy Robert S, Balamurugan Kuppareddi, Wong Helena, Duncan George
Department of Chemistry and Biochemistry, University of California, San Diego, CA, USA.
Electrophoresis. 2014 Nov;35(21-22):3020-7. doi: 10.1002/elps.201400143. Epub 2014 Oct 20.
High-resolution melt (HRM) analysis of the VNTR region of the human D1S80 locus, a 16-bp repeat minisatellite from approximately 400 to over 700 bp in length, was investigated. A Qiagen Rotor-Gene Q using the Type-it PCR HRM kit was used to acquire HRM curves for 14 single, and 16 biallelic, dsDNA samples. The HRM analysis was applicable over a range of DNA concentrations; however the characteristics of the melt curve did depend on the forward and reverse primer ratio. Despite the large amplicon size and the similarities of the repeat sequences, it was possible to discriminate different genotypes. Heterozygotes were clearly different from the homozygous variants and even small differences in the repeat sequence could be differentiated. However, the melt analysis requires a high-resolution system with temperature resolution of 0.02°C or better in order to sort out differences in these large amplicons of near identical GC content (in this case 56%). HRM analysis of amplicons with large repeat sequences can be used as a means of comparing DNA fragments. Examination of multiple sequences can be used to differentiate DNA samples and demonstrate the potential of HRM analysis as a rapid and inexpensive prescreening technique in forensic applications.
对人类D1S80基因座的VNTR区域进行了高分辨率熔解(HRM)分析,该区域是一个长度约为400至700 bp以上的16 bp重复微卫星。使用Qiagen Rotor-Gene Q和Type-it PCR HRM试剂盒获取了14个单链和16个双链DNA样本的HRM曲线。HRM分析适用于一系列DNA浓度;然而,熔解曲线的特征确实取决于正向和反向引物比例。尽管扩增子大小较大且重复序列相似,但仍有可能区分不同的基因型。杂合子与纯合变体明显不同,甚至重复序列中的微小差异也可以区分。然而,熔解分析需要一个温度分辨率为0.02°C或更高的高分辨率系统,以便区分这些GC含量近乎相同(在这种情况下为56%)的大扩增子中的差异。对具有大重复序列的扩增子进行HRM分析可作为比较DNA片段的一种方法。对多个序列的检测可用于区分DNA样本,并证明HRM分析作为法医应用中一种快速且廉价的预筛选技术的潜力。