Abstract :
This research developed two real-time PCR assays, employing high-resolution melt and allele-specific analysis to accurately
genotype the F94L mutation in cattle. This mutation (g.433C.A) in the growth differentiation factor 8 or myostatin gene has
recently been shown to be functionally associated with increased muscle mass and carcass yield in cattle. The F94L mutation is
not, like other myostatin mutations, associated with reduced fertility and dystocia. It is therefore a candidate for introgression
into other breeds to improve retail beef yield and the development of a simple and accurate test to genotype this specific
mutation is warranted. Variations in the efficiency of enzyme cleavage compromised the accuracy of genotyping by published
methods, potentially resulting in an overestimation of the frequency of the mutant allele. The frequency of the F94L mutation
was determined by real-time PCR in 1140 animals from 15 breeds of cattle in Australia. The mutation was present in
Simmental (0.8%), Piedmontese (2%), Droughtmaster (4%) and Limousin (94.2%) but not found in Salers, Angus, Poll Hereford,
Hereford, Gelbvieh, Charolais, Jersey, Brahman, Holstein, Shorthorn or Maine Anjou. The low prevalence of F94L in all beef
breeds except Limousin indicates the significant potential for this mutation to improve retail yield in Australian beef cattle.
Keywords :
marker-assisted selection , Myostatin , beef cattle , F94L , Real-time PCR