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      A rapid and efficient method of genotyping zebrafish mutants.

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

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          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. (c) 2009 Wiley-Liss, Inc.

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