Using Xenopus to analyze neurocristopathies like Kabuki syndrome.

Janina Schwenty-Lara, Silke Pauli, Annette Borchers

Genesis (New York, N.Y. : 2000) 2021 Feb

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Neurocristopathies are human congenital syndromes that arise from defects in neural crest (NC) development and are typically associated with malformations of the craniofacial skeleton. Genetic analyses have been very successful in identifying pathogenic mutations, however, model organisms are required to characterize how these mutations affect embryonic development thereby leading to complex clinical conditions. The African clawed frog Xenopus laevis provides a broad range of in vivo and in vitro tools allowing for a detailed characterization of NC development. Due to the conserved nature of craniofacial morphogenesis in vertebrates, Xenopus is an efficient and versatile system to dissect the morphological and cellular phenotypes as well as the signaling events leading to NC defects. Here, we review a set of techniques and resources how Xenopus can be used as a disease model to investigate the pathogenesis of Kabuki syndrome and neurocristopathies in a wider sense. © 2020 The Authors. Genesis published by Wiley Periodicals LLC.

Citation

Janina Schwenty-Lara, Silke Pauli, Annette Borchers. Using Xenopus to analyze neurocristopathies like Kabuki syndrome. Genesis (New York, N.Y. : 2000). 2021 Feb;59(1-2):e23404