Showing 2 results for S. Esmaeilkhanian
M. H. Banabazi, S. Esmaeilkhanian, S. R. Miraei Ashtiani, M. Moradi Shahrbabak,
Volume 10, Issue 4 (winter 2007)
Abstract
Genetic variation within and between five Iranian sheep populations including Sanjabi (SAN), Kordi Kordistan (KKO), Kordi Khorasan (KKH), Mehraban (MEH) and Moghani (MOG) was assessed using six microsatellite markers (McMA2, McMA26, MAF64, OarAE64, OarCP26 and OarFCB304). The PCR reactions were successfully perfomed with all primers except OarAE64. All locus-population combinations were at Hardy-Weinberg equilibrium except McMA2 in MOG population (P<0.005). Polymorphism criteria showed that the five studied loci were polymorphic in all populations. The lowest DA genetic distance (0.234) was observed between KKH and KKO and the highest (0.388) between SAN and MOG populations. The dendrograms based on DA distances were drawn using unweighted pair-group method using an arithmetic average (UPGMA) and neighbor-joining (NJ) method. KKO, KKH and SAN were grouped together at one cluster and MEH and MOG at another by both methods. The average expected heterozygosity for each populations (as interpopulation variation) ranged from 0.744 to 0.847 for KKH and MEH, respectively. The estimated time of divergence for two Kordi populations (KKO and KKH) was 445 years that complies with historical evidences. The findings of this research confirmed that microsatellite variation could be a useful tool for screening of investigating biodiversity among domestic animals.
A.r. Khanahmadi, Gh. Rahimi, A. Nejati-Javaremi, S. Esmaeilkhanian,
Volume 11, Issue 40 (summer 2007)
Abstract
In order to detect genetic variation of native fowls in Mazandaran native Fowls breeding station, blood samples were collected from 100 male and female of birds (1:11). The DNA of the blood samples was extracted according to an optimized salting out protocol. The extracted DNA was amplified through polymerase chain reaction (PCR). Of the twenty random primers (10 mer) were used in this study, fourteen yielded satisfactory PCR. The total 63 polymorphic and 77 monomorphic bands were detected for the 14 primers. The number of bands displayed for each primer ranged from 4 to 16 with 200-2100 base pairs. The highest and lowest percentages of polymorphism band were observed for primer 9 (72%) and primer 14 (16%) respectively. The band sharing frequency was calculated for each primer, which ranged from 79 to 96. The genetic similarity within population and genetic variation were estimated as 89 and 11 percentage respectively. In conclusion, the existence of high level of polymorphism after ten generation of selection may indicate the accuracy of genetic evaluation program, suitable selection strategies and also large enough effective population size in this breeding flock.
