Evolutionary origin and development of snake fangs

Freek J. Vonk, Jeroen F. Admiraal, Kate Jackson, Ram Reshef, Merijn A.G. De Bakker, Kim Vanderschoot, Iris Van Den Berge, Marit Van Atten, Erik Burgerhout, Andrew Beck, Peter J. Mirtschin, Elazar Kochva, Frans Witte, Bryan G. Fry, Anthony E. Woods, Michael K. Richardson

Research output: Contribution to journalArticlepeer-review


Many advanced snakes use fangs - specialized teeth associated with a venom gland - to introduce venom into prey or attacker. Various front- and rear-fanged groups are recognized, according to whether their fangs are positioned anterior (for example cobras and vipers) or posterior (for example grass snakes) in the upper jaw. A fundamental controversy in snake evolution is whether or not front and rear fangs share the same evolutionary and developmental origin. Resolving this controversy could identify a major evolutionary transition underlying the massive radiation of advanced snakes, and the associated developmental events. Here we examine this issue by visualizing the tooth-forming epithelium in the upper jaw of 96 snake embryos, covering eight species. We use the sonic hedgehog gene as a marker, and three-dimensionally reconstruct the development in 41 of the embryos. We show that front fangs develop from the posterior end of the upper jaw, and are strikingly similar in morphogenesis to rear fangs. This is consistent with their being homologous. In front-fanged snakes, the anterior part of the upper jaw lacks sonic hedgehog expression, and ontogenetic allometry displaces the fang from its posterior developmental origin to its adult front position - consistent with an ancestral posterior position of the front fang. In rear-fanged snakes, the fangs develop from an independent posterior dental lamina and retain their posterior position. In light of our findings, we put forward a new model for the evolution of snake fangs: a posterior subregion of the tooth-forming epithelium became developmentally uncoupled from the remaining dentition, which allowed the posterior teeth to evolve independently and in close association with the venom gland, becoming highly modified in different lineages. This developmental event could have facilitated the massive radiation of advanced snakes in the Cenozoic era, resulting in the spectacular diversity of snakes seen today.

Original languageEnglish
Pages (from-to)630-633
Number of pages4
Issue number7204
StatePublished - 31 Jul 2008
Externally publishedYes

Bibliographical note

Funding Information:
Acknowledgements We thank the following persons and institutions who helped us or contributed material used in this study: J. W. Arntzen, M. Brittijn, M. de Boer, R. van Deutekom, N. Dunstan, K. Van Egmond, P. L. Y. Fung, I. Gavrilov, W. Getreuer, J. Hanken, E. Heida, I. Ineich, T. de Jong, K. V. Kardong, M. Lautenbach, J. Losos, D. Millar, C. Pepermans, J. M. Richman, J. Rosado, R. de Ruiter, P. Schilperoord, M. M. Smith, S. Soubzmaigne, N. Vidal, E. M. Wielhouwer, J. Woltering, National Museum of Natural History Naturalis Leiden, Reptilezoo Serpo, Muséum National d’Histoire Naturelle Paris, AQIS, DEH, APCG and DWLBC (Australia). This work received funding from the following sources: a Toptalent grant from the Netherlands Organization for Scientific Research (NWO; F.J.V.), a Smart Mix grant from the Dutch government (M.K.R.), a Valorisation grant from the Dutch Technology Foundation (STW; M.K.R., F.J.V., B.G.F.), the Curatoren fund (F.J.V.), the LUSTRA fund (F.J.V.), the Australian Research Council and the Australian Academy of Science (B.G.F.), DEST-ISL (B.G.F.), Whitman College (K.J.), a NWO visitors grant (M.K.R., B.G.F.) and the Leiden University Fund (F.J.V.).

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  • General


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