Author/Authors :
Eftekhari Shahroudi, Feridoun ferdowsi university of mashhad, مشهد, ايران , Nassiry, Mohammad Reza ferdowsi university of mashhad, مشهد, ايران , Valizadh, Reza ferdowsi university of mashhad, مشهد, ايران , Heravi Moussavi, Alireza ferdowsi university of mashhad, مشهد, ايران , Tahmoores Pour, Mojtaba ferdowsi university of mashhad, مشهد, ايران , Ghiasi, Heydar ferdowsi university of mashhad, مشهد, ايران
Abstract :
Genotypes for melatonin receptor type 1A (MTNR1A) and Calpastatin (CAST) were determined by enzymatic digestion of PCR products and Calpain(CAPN) genotype detected by PCR-SSCP method in Iranian Karakul sheep. Blood samples were collected from 100 purebred Karakul sheep. The extraction of genomic DNA was based on guanidinium thio-cyanate-silica gel method. PCR amplicons were digested with restriction enzymes Mnll and Mspl for MTNR1A and CAST genes, respectively The MTNR1A locus had two alle-les with frequencies of 0.79 for (+) and 0.21 for (-) alleles. Allelic frequencies for CAST locus were 0.85 for M and 0.15 for N. In addition, Calpain had two alleles A and B with respective frequencies of 0.79 and 0.21. The observed het-erozygosity values for MTNR1A, Calpastatin and Calpain locus were 0.42, 0.29 and 0.35, respectively The X2 test confirmed the existence of Hardy-Weinberg equilibrium for the three loci in the population. The data showed a large variation in studied genes. The genetic polymorphism could be regarded as useful tool for selection programs based on marker- assisted selection between different genotypes of those loci.
Keywords :
MTNR1A , Calpastatin , Calpain , Polymorphism , PCR , RFLP , SSCP , Karakul Sheep.