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A simple method for genotyping the bovine growth hormone gene
Author(s) -
Chikuni K,
Tanabe R,
Muroya S,
Fukumoto Y,
Ozawa S
Publication year - 1997
Publication title -
animal genetics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.756
H-Index - 81
eISSN - 1365-2052
pISSN - 0268-9146
DOI - 10.1111/j.1365-2052.1997.00095.x
Subject(s) - biology , multiplex polymerase chain reaction , genotyping , primer (cosmetics) , genotype , microbiology and biotechnology , allele , genetics , polymerase chain reaction , gene , agarose gel electrophoresis , locus (genetics) , variants of pcr , bovine somatotropin , oligonucleotide , exon , recombinant dna , chemistry , organic chemistry
An allele‐specific polymerase chain reaction (PCR) amplification method was developed to determine the genotypes at the bovine growth hormone locus that result from two nucleotide substitutions in exon 5 of the gene. This method was a multiplex PCR (ASM–PCR) employing a common primer pair and two allele‐specific reverse primers. The common primer pair was designed to amplify a target region containing two substitution points from the three variants of the bovine growth hormone gene. The allele‐specific primers were designed to be mismatched with other genotypes at the 3' end of oligonucleotides. When the common and allele‐specific reverse primers competed with each other, the shorter allele‐specific fragments were amplified preferentially. Consequently, the PCR products of the variant‐specific fragments were 347, 483 and 656 bp for alleles A, B and C, respectively, of the bovine growth hormone gene. Genotypes of the bovine growth hormone gene were easily identified by agarose gel electrophoresis of PCR products. The results suggested that this multiplex PCR method would be useful for identification of genetic variants caused by point mutations.