Abstract
We report the development of a fast and reliable PCR-based method for sex identification of tiger DNA designed to be incorporated into fluorescent short tandem repeat (STR) profiling. A single primer pair, consisting of a fluorescently-labelled forward primer and an unlabelled reverse primer, is used to co-amplify homologous fragments of a zinc finger (ZF) protein intron which exhibits size polymorphism between the X and Y chromosomes. The ZFX and ZFY amplicons differ in size by 12 bp and can thus be differentiated by capillary electrophoresis.
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Acknowledgments
This work is part of a collaboration funded by the Darwin Initiative with the purpose of developing DNA techniques to monitor and enforce against the illegal trade of protected species in South East Asia. The authors thank the zoo organisations for reference tiger samples, and in particular to Sarah Christie (ZSL). Thanks are also due to the Programme Coordination Unit of ASEAN WEN and TRAFFIC SE Asia.
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McEwing, R., Ouitavon, K., Rovie-Ryan, J.J. et al. Molecular sexing of tigers, Panthera tigris . Conservation Genet Resour 4, 299–301 (2012). https://doi.org/10.1007/s12686-011-9529-x
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DOI: https://doi.org/10.1007/s12686-011-9529-x