From gels to chips: "minisequencing" primer extension for analysis of point mutations and single nucleotide polymorphisms

Hum Mutat. 1999;13(1):1-10. doi: 10.1002/(SICI)1098-1004(1999)13:1<1::AID-HUMU1>3.0.CO;2-I.

Abstract

In the minisequencing primer extension reaction, a DNA polymerase is used specifically to extend a primer that anneals immediately adjacent to the nucleotide position to be analyzed with a single labeled nucleoside triphospate complementary to the nucleotide at the variant site. The reaction allows highly specific detection of point mutations and single nucleotide polymorphisms (SNPs). Because all SNPs can be analyzed with high specificity at the same reaction conditions, minisequencing is a promising reaction principle for multiplex high-throughput genotyping assays. It is also a useful tool for accurate quantitative PCR-based analysis. This review discusses the different approaches, ranging from traditional gel-based formats to multiplex detection on microarrays that have been developed and applied to minisequencing assays.

Publication types

  • Review

MeSH terms

  • Amino Acid Substitution
  • DNA Mutational Analysis / methods*
  • DNA Primers / isolation & purification
  • DNA Primers / metabolism*
  • DNA-Directed DNA Polymerase / metabolism
  • Electrophoresis, Agar Gel
  • Enzyme-Linked Immunosorbent Assay
  • Genotype
  • Humans
  • Nucleotides / analysis
  • Point Mutation / genetics*
  • Polymerase Chain Reaction
  • Sensitivity and Specificity

Substances

  • DNA Primers
  • Nucleotides
  • DNA-Directed DNA Polymerase