Molecular Characterization of New Zealand White and APAU Black Rabbits using Microsatellite Markers

Genetic diversity among two genetic groups (New Zealand White andAPAU Black) was investigated with a set of20 microsatellite markers in the present study. The results showed that out of 20 microsatellites, 12 rabbit specific markers were successfully amplified by PCR which were highly polymorphic. A...

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Bibliographic Details
Published inJournal of Animal Research Vol. 6; no. 4; p. 597
Main Authors Sagar, N. Govardhana, Reddy, S. Sai, Gupta, B. Ramesh, Mahendar, M.
Format Journal Article
LanguageEnglish
Published New Delhi New Delhi Publishers 01.08.2016
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Summary:Genetic diversity among two genetic groups (New Zealand White andAPAU Black) was investigated with a set of20 microsatellite markers in the present study. The results showed that out of 20 microsatellites, 12 rabbit specific markers were successfully amplified by PCR which were highly polymorphic. A total of 257 alleles were observed across the 12 loci amplified. Number of alleles ranged from 5 to 14 and 5 to 16 in New Zealand White and APAU Black populations, respectively. The overall mean values of observed heterozygosity (0.554 in New Zealand White and 0.556 in APAU Black), expected heterozygosity (0.870 in New Zealand White and 0.875 in APAU Black), Polymorphic Information Content (0.856 in New Zealand White and 0.862 in APAU Black) and the mean effective number of alleles (8.629 in New Zealand White and 8.876 in APAU Black) of these two genetic groups were high. Out of the 12 amplified loci 7 loci deviated significantly from Hardy - Weinberg equilibrium in New Zealand White and 5 loci deviated in case of APAU Black which may be due to selection followed. The mean F^sub IS^, F^sub IT^ and F^sub ST^ values over all the population were found to be 0.377, 0.402 and 0.040, respectively. The results suggested that the 12 amplified rabbit specific microsatellite loci were effective markers for analysis of genetic relationships among rabbit populations.
ISSN:2249-5290
2249-6629
2277-940X
DOI:10.5958/2277-940X.2016.00069.3