A rapid and efficient method of genotyping zebrafish mutants

Dev Dyn. 2009 Dec;238(12):3168-74. doi: 10.1002/dvdy.22143.

Abstract

In order to facilitate high throughput genotyping of zebrafish, we have developed a novel technique that uses High Resolution Melting Analysis (HRMA) to distinguish wild-type, heterozygous mutants and homogyzous mutants. This one hour technique removes the need for restriction enzymes and agarose gels. The generated melting curve profiles are sensitive enough to detect non-specific PCR products. We have been able to reliably genotype three classes of mutations in zebrafish, including point mutants, apc(hu745) (apc(mcr)), and p53(zy7) (p53(I166T)), a small deletion mutant (bap28(y75)) and a retroviral insertion mutant (wdr43(hi821a)). This technique can genotype individual zebrafish embryos and adults (by tail-clip) and is applicable to other model organisms.

Publication types

  • Evaluation Study
  • Research Support, N.I.H., Extramural

MeSH terms

  • Animals
  • Animals, Genetically Modified
  • Base Sequence
  • Cytogenetic Analysis / methods*
  • DNA Mutational Analysis / methods*
  • Efficiency
  • Embryo, Nonmammalian
  • Gene Deletion
  • Genotype
  • Molecular Sequence Data
  • Mutagenesis, Insertional
  • Mutant Proteins / analysis
  • Mutant Proteins / genetics
  • Polymorphism, Single Nucleotide
  • Retroviridae / genetics
  • Retroviridae / physiology
  • Time Factors
  • Zebrafish / embryology
  • Zebrafish / genetics*
  • Zebrafish / growth & development
  • Zebrafish / metabolism

Substances

  • Mutant Proteins