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Bar, stripe and spot development in sand-dwelling cichlids from Lake Malawi

BACKGROUND: Melanic patterns such as horizontal stripes, vertical bars and spots are common among teleost fishes and often serve roles in camouflage or mimicry. Extensive research in the zebrafish model has shown that the development of horizontal stripes depends on complex cellular interactions bet...

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Autores principales: Hendrick, Laura A., Carter, Grace A., Hilbrands, Erin H., Heubel, Brian P., Schilling, Thomas F., Le Pabic, Pierre
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6691528/
https://www.ncbi.nlm.nih.gov/pubmed/31417669
http://dx.doi.org/10.1186/s13227-019-0132-7
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author Hendrick, Laura A.
Carter, Grace A.
Hilbrands, Erin H.
Heubel, Brian P.
Schilling, Thomas F.
Le Pabic, Pierre
author_facet Hendrick, Laura A.
Carter, Grace A.
Hilbrands, Erin H.
Heubel, Brian P.
Schilling, Thomas F.
Le Pabic, Pierre
author_sort Hendrick, Laura A.
collection PubMed
description BACKGROUND: Melanic patterns such as horizontal stripes, vertical bars and spots are common among teleost fishes and often serve roles in camouflage or mimicry. Extensive research in the zebrafish model has shown that the development of horizontal stripes depends on complex cellular interactions between melanophores, xanthophores and iridophores. Little is known about the development of horizontal stripes in other teleosts, and even less is known about bar or spot development. Here, we compare chromatophore composition and development of stripes, bars and spots in two cichlid species of sand-dwellers from Lake Malawi—Copadichromis azureus and Dimidiochromis compressiceps. RESULTS: (1) In D. compressiceps, stripes are made of dense melanophores underlaid by xanthophores and overlaid by iridophores. Melanophores and xanthophores are either loose or absent in interstripes, and iridophores are dense. In C. azureus, spots and bars are composed of a chromatophore arrangement similar to that of stripes but are separated by interbars where density of melanophores and xanthophores is only slightly lower than in stripes and iridophore density appears slightly greater. (2) Stripe, bar and spot chromatophores appear in the skin at metamorphosis. Stripe melanophores directly differentiate along horizontal myosepta into the adult pattern. In contrast, bar number and position are dynamic throughout development. As body length increases, new bars appear between old ones or by splitting of old ones through new melanophore appearance, not migration. Xanthophore and iridophore distributions follow melanophore patterns. (3) Metamorphic pigmentation arises in cichlids in a fashion similar to that described in zebrafish: melanophore progenitors derived from the medial route of neural crest migration migrate from the vicinity of the neural tube to the skin during metamorphosis. CONCLUSION: The three pigment cell types forming stripes, bars and spots arise in the skin at metamorphosis. Stripes develop by differentiation of melanophores along horizontal myosepta, while bars do not develop along patent anatomical boundaries and increase in number in relation with body size. We propose that metamorphic melanophore differentiation and migratory arrest upon arrival to the skin lead to stripe formation, while bar formation must be supported by extensive migration of undifferentiated melanophores in the skin.
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spelling pubmed-66915282019-08-15 Bar, stripe and spot development in sand-dwelling cichlids from Lake Malawi Hendrick, Laura A. Carter, Grace A. Hilbrands, Erin H. Heubel, Brian P. Schilling, Thomas F. Le Pabic, Pierre EvoDevo Research BACKGROUND: Melanic patterns such as horizontal stripes, vertical bars and spots are common among teleost fishes and often serve roles in camouflage or mimicry. Extensive research in the zebrafish model has shown that the development of horizontal stripes depends on complex cellular interactions between melanophores, xanthophores and iridophores. Little is known about the development of horizontal stripes in other teleosts, and even less is known about bar or spot development. Here, we compare chromatophore composition and development of stripes, bars and spots in two cichlid species of sand-dwellers from Lake Malawi—Copadichromis azureus and Dimidiochromis compressiceps. RESULTS: (1) In D. compressiceps, stripes are made of dense melanophores underlaid by xanthophores and overlaid by iridophores. Melanophores and xanthophores are either loose or absent in interstripes, and iridophores are dense. In C. azureus, spots and bars are composed of a chromatophore arrangement similar to that of stripes but are separated by interbars where density of melanophores and xanthophores is only slightly lower than in stripes and iridophore density appears slightly greater. (2) Stripe, bar and spot chromatophores appear in the skin at metamorphosis. Stripe melanophores directly differentiate along horizontal myosepta into the adult pattern. In contrast, bar number and position are dynamic throughout development. As body length increases, new bars appear between old ones or by splitting of old ones through new melanophore appearance, not migration. Xanthophore and iridophore distributions follow melanophore patterns. (3) Metamorphic pigmentation arises in cichlids in a fashion similar to that described in zebrafish: melanophore progenitors derived from the medial route of neural crest migration migrate from the vicinity of the neural tube to the skin during metamorphosis. CONCLUSION: The three pigment cell types forming stripes, bars and spots arise in the skin at metamorphosis. Stripes develop by differentiation of melanophores along horizontal myosepta, while bars do not develop along patent anatomical boundaries and increase in number in relation with body size. We propose that metamorphic melanophore differentiation and migratory arrest upon arrival to the skin lead to stripe formation, while bar formation must be supported by extensive migration of undifferentiated melanophores in the skin. BioMed Central 2019-08-12 /pmc/articles/PMC6691528/ /pubmed/31417669 http://dx.doi.org/10.1186/s13227-019-0132-7 Text en © The Author(s) 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Hendrick, Laura A.
Carter, Grace A.
Hilbrands, Erin H.
Heubel, Brian P.
Schilling, Thomas F.
Le Pabic, Pierre
Bar, stripe and spot development in sand-dwelling cichlids from Lake Malawi
title Bar, stripe and spot development in sand-dwelling cichlids from Lake Malawi
title_full Bar, stripe and spot development in sand-dwelling cichlids from Lake Malawi
title_fullStr Bar, stripe and spot development in sand-dwelling cichlids from Lake Malawi
title_full_unstemmed Bar, stripe and spot development in sand-dwelling cichlids from Lake Malawi
title_short Bar, stripe and spot development in sand-dwelling cichlids from Lake Malawi
title_sort bar, stripe and spot development in sand-dwelling cichlids from lake malawi
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6691528/
https://www.ncbi.nlm.nih.gov/pubmed/31417669
http://dx.doi.org/10.1186/s13227-019-0132-7
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