SYBR green dye-based probe-free SNP genotyping: introduction of T-Plex real-time PCR assay

Anal Biochem. 2013 Oct 15;441(2):225-31. doi: 10.1016/j.ab.2013.07.007. Epub 2013 Jul 16.

Abstract

Single-nucleotide polymorphism (SNP) genotyping is widely used in genetic association studies to characterize genetic factors underlying inherited traits. Despite many recent advances in high-throughput SNP genotyping, inexpensive and flexible methods with reasonable throughput levels are still needed. Real-time PCR methods for discovering and genotyping SNPs are becoming increasingly important in various fields of biology. In this study, we introduce a new, single-tube strategy that combines the tetra-primer ARMS PCR assay, SYBR Green I-based real-time PCR, and melting-point analysis with primer design strategies to detect the SNP of interest. This assay, T-Plex real-time PCR, is based on the T(m) discrimination of the amplified allele-specific amplicons in a single tube. The specificity, sensitivity, and robustness of the assay were evaluated for common mutations in the FV, PII, MTHFR, and FGFR3 genes. We believe that T-Plex real-time PCR would be a useful alternative for either individual genotyping requests or large epidemiological studies.

Keywords: FVL; MTHFR; SNP; SYBR green; T-Plex real-time PCR; Tetra-primer ARMS PCR.

Publication types

  • Evaluation Study

MeSH terms

  • Alleles
  • Base Sequence
  • Benzothiazoles
  • DNA Primers / genetics
  • Diamines
  • Genotype
  • Humans
  • Organic Chemicals / analysis*
  • Polymorphism, Single Nucleotide*
  • Quinolines
  • Real-Time Polymerase Chain Reaction / instrumentation*
  • Sensitivity and Specificity

Substances

  • Benzothiazoles
  • DNA Primers
  • Diamines
  • Organic Chemicals
  • Quinolines
  • SYBR Green I