Zebrafish pigmentation mutations and the processes of neural crest development

Robert N. Kelsh(Max Planck Society), Michael Brand(Max Planck Society), Yun‐Jin Jiang(Max Planck Society), Carl‐Philipp Heisenberg(Max Planck Society), Shuo Lin(Max Planck Society), Pascal Haffter(Max Planck Society), Jörg Odenthal(Max Planck Society), Mary C. Mullins(Max Planck Society), Fredericus J. M. van Eeden(Max Planck Society), Makoto Furutani‐Seiki(Max Planck Society), Michael Granato(Max Planck Society), Matthias Hammerschmidt(Max Planck Society), Donald A. Kane(Max Planck Society), Rachel M. Warga(Max Planck Society), Dirk Beuchle(Max Planck Society), Elisabeth Vogelsang(Max Planck Society), Christiane Nüsslein‐Volhard(Max Planck Society)
Development
December 1, 1996
Cited by 472

Abstract

Neural crest development involves cell-fate specification, proliferation, patterned cell migration, survival and differentiation. Zebrafish neural crest derivatives include three distinct chromatophores, which are well-suited to genetic analysis of their development. As part of a large-scale mutagenesis screen for embryonic/early larval mutations, we have isolated 285 mutations affecting all aspects of zebrafish larval pigmentation. By complementation analysis, we define 94 genes. We show here that comparison of their phenotypes permits classification of these mutations according to the types of defects they cause, and these suggest which process of neural crest development is probably affected. Mutations in eight genes affect the number of chromatophores: these include strong candidates for genes necessary for the processes of pigment cell specification and proliferation. Mutations in five genes remove part of the wild-type pigment pattern, and suggest a role in larval pigment pattern formation. Mutations in five genes show ectopic chromatophores in distinct sites, and may have implications for chromatophore patterning and proliferation. 76 genes affect pigment or morphology of one or more chromatophore types: these mutations include strong candidates for genes important in various aspects of chromatophore differentiation and survival. In combination with the embryological advantages of zebrafish, these mutations should permit cellular and molecular dissection of many aspects of neural crest development.


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