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Journal of Heredity Advance Access originally published online on October 26, 2005
Journal of Heredity 2005 96(6):679-687; doi:10.1093/jhered/esi117
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© The American Genetic Association. 2005. All rights reserved. For permissions, please email: journals.permissions@oxfordjournals.org.

Noninvasive Genotyping and Mendelian Analysis of Microsatellites in African Savannah Elephants

J. B. A. Okello, G. Wittemyer, H. B. Rasmussen, I. Douglas-Hamilton, S. Nyakaana, P. Arctander, and H. R. Siegismund

From the Molecular Biology Laboratory, Makerere University Institute of Environment and Natural Resources, P. O. Box 7298, Kampala, Uganda (Okello, Nyakaana); the Department of Environmental Science, Policy and Management, 201 Wellman Hall, University of California at Berkeley, CA 94720–3112 (Wittemyer); the Animal Behaviour Research Group, Department of Zoology, University of Oxford, South Park Road, Oxford OX1 3PS, UK (Rasmussen); Save the Elephants, PO Box 54667, Nairobi 00200, Kenya (Wittemyer, Rasmussen, Douglas-Hamilton); and the Department of Evolutionary Biology, University of Copenhagen, Universitetsparken 15 DK-2100 Copenhagen Ø, Denmark (Arctander, Siegismund)

Address correspondence to J. B. A. Okello at the address above, or e-mail: jbaokello{at}muienr.mak.ac.ug.

We obtained fresh dung samples from 202 (133 mother-offspring pairs) savannah elephants (Loxodonta africana) in Samburu, Kenya, and genotyped them at 20 microsatellite loci to assess genotyping success and errors. A total of 98.6% consensus genotypes was successfully obtained, with allelic dropout and false allele rates at 1.6% (n = 46) and 0.9% (n = 37) of heterozygous and total consensus genotypes, respectively, and an overall genotyping error rate of 2.5% based on repeat typing. Mendelian analysis revealed consistent inheritance in all but 38 allelic pairs from mother-offspring, giving an average mismatch error rate of 2.06%, a possible result of null alleles, mutations, genotyping errors, or inaccuracy in maternity assignment. We detected no evidence for large allele dropout, stuttering, or scoring error in the dataset and significant Hardy-Weinberg deviations at only two loci due to heterozygosity deficiency. Across loci, null allele frequencies were low (range: 0.000–0.042) and below the 0.20 threshold that would significantly bias individual-based studies. The high genotyping success and low errors observed in this study demonstrate reliability of the method employed and underscore the application of simple pedigrees in noninvasive studies. Since none of the sires were included in this study, the error rates presented are just estimates.


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