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Endothelin signalling in iridophore development and stripe pattern formation of zebrafish

Colour patterns of adult fish are composed of several different types of pigment cells distributing in the skin during juvenile development. The zebrafish, Danio rerio, displays a striking pattern of dark stripes of melanophores interspersed with light stripes of xanthophores. A third cell type, sil...

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Autores principales: Krauss, Jana, Frohnhöfer, Hans Georg, Walderich, Brigitte, Maischein, Hans-Martin, Weiler, Christian, Irion, Uwe, Nüsslein-Volhard, Christiane
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Company of Biologists 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4058085/
https://www.ncbi.nlm.nih.gov/pubmed/24857848
http://dx.doi.org/10.1242/bio.20148441
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author Krauss, Jana
Frohnhöfer, Hans Georg
Walderich, Brigitte
Maischein, Hans-Martin
Weiler, Christian
Irion, Uwe
Nüsslein-Volhard, Christiane
author_facet Krauss, Jana
Frohnhöfer, Hans Georg
Walderich, Brigitte
Maischein, Hans-Martin
Weiler, Christian
Irion, Uwe
Nüsslein-Volhard, Christiane
author_sort Krauss, Jana
collection PubMed
description Colour patterns of adult fish are composed of several different types of pigment cells distributing in the skin during juvenile development. The zebrafish, Danio rerio, displays a striking pattern of dark stripes of melanophores interspersed with light stripes of xanthophores. A third cell type, silvery iridophores, contributes to both stripes and plays a crucial role in adult pigment pattern formation. Several mutants deficient in iridophore development display similar adult phenotypes with reduced numbers of melanophores and defects in stripe formation. This indicates a supporting role of iridophores for melanophore development and maintenance. One of these mutants, rose (rse), encodes the Endothelin receptor b1a. Here we describe a new mutant in zebrafish, karneol (kar), which has a phenotype similar to weak alleles of rse with a reduction in iridophore numbers and defects of adult pigment patterning. We show that, unlike rse, kar is not required in iridophores. The gene defective in the kar mutant codes for an endothelin-converting enzyme, Ece2, which activates endothelin ligands by proteolytic cleavage. By morpholino-mediated knockdown, we identify Endothelin 3b (Edn3b) as the ligand for endothelin receptor signalling in larval iridophores. Thus, Endothelin signalling is involved in iridophore development, proliferation and stripe morphogenesis in larvae as well as adult zebrafish. In mammals the pathway is required for melanocyte development; therefore, our results indicate a previously unrecognized close evolutionary relationship between iridophores in zebrafish and melanocytes in mammals.
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spelling pubmed-40580852014-07-15 Endothelin signalling in iridophore development and stripe pattern formation of zebrafish Krauss, Jana Frohnhöfer, Hans Georg Walderich, Brigitte Maischein, Hans-Martin Weiler, Christian Irion, Uwe Nüsslein-Volhard, Christiane Biol Open Research Article Colour patterns of adult fish are composed of several different types of pigment cells distributing in the skin during juvenile development. The zebrafish, Danio rerio, displays a striking pattern of dark stripes of melanophores interspersed with light stripes of xanthophores. A third cell type, silvery iridophores, contributes to both stripes and plays a crucial role in adult pigment pattern formation. Several mutants deficient in iridophore development display similar adult phenotypes with reduced numbers of melanophores and defects in stripe formation. This indicates a supporting role of iridophores for melanophore development and maintenance. One of these mutants, rose (rse), encodes the Endothelin receptor b1a. Here we describe a new mutant in zebrafish, karneol (kar), which has a phenotype similar to weak alleles of rse with a reduction in iridophore numbers and defects of adult pigment patterning. We show that, unlike rse, kar is not required in iridophores. The gene defective in the kar mutant codes for an endothelin-converting enzyme, Ece2, which activates endothelin ligands by proteolytic cleavage. By morpholino-mediated knockdown, we identify Endothelin 3b (Edn3b) as the ligand for endothelin receptor signalling in larval iridophores. Thus, Endothelin signalling is involved in iridophore development, proliferation and stripe morphogenesis in larvae as well as adult zebrafish. In mammals the pathway is required for melanocyte development; therefore, our results indicate a previously unrecognized close evolutionary relationship between iridophores in zebrafish and melanocytes in mammals. The Company of Biologists 2014-05-23 /pmc/articles/PMC4058085/ /pubmed/24857848 http://dx.doi.org/10.1242/bio.20148441 Text en © 2014. Published by The Company of Biologists Ltd http://creativecommons.org/licenses/by/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0), which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed.
spellingShingle Research Article
Krauss, Jana
Frohnhöfer, Hans Georg
Walderich, Brigitte
Maischein, Hans-Martin
Weiler, Christian
Irion, Uwe
Nüsslein-Volhard, Christiane
Endothelin signalling in iridophore development and stripe pattern formation of zebrafish
title Endothelin signalling in iridophore development and stripe pattern formation of zebrafish
title_full Endothelin signalling in iridophore development and stripe pattern formation of zebrafish
title_fullStr Endothelin signalling in iridophore development and stripe pattern formation of zebrafish
title_full_unstemmed Endothelin signalling in iridophore development and stripe pattern formation of zebrafish
title_short Endothelin signalling in iridophore development and stripe pattern formation of zebrafish
title_sort endothelin signalling in iridophore development and stripe pattern formation of zebrafish
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4058085/
https://www.ncbi.nlm.nih.gov/pubmed/24857848
http://dx.doi.org/10.1242/bio.20148441
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