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Distinct genetic origins of eumelanin intensity and barring patterns in cichlid fishes
Pigment patterns are incredibly diverse across vertebrates and are shaped by multiple selective pressures from predator avoidance to mate choice. A common pattern across fishes, but for which we know little about the underlying mechanisms, is repeated melanic vertical bars. In order to understand ge...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Cold Spring Harbor Laboratory
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10349982/ https://www.ncbi.nlm.nih.gov/pubmed/37461734 http://dx.doi.org/10.1101/2023.07.02.547430 |
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author | Brandon, A. Allyson Michael, Cassia Carmona Baez, Aldo Moore, Emily C. Ciccotto, Patrick J. Roberts, Natalie B. Roberts, Reade B. Powder, Kara E. |
author_facet | Brandon, A. Allyson Michael, Cassia Carmona Baez, Aldo Moore, Emily C. Ciccotto, Patrick J. Roberts, Natalie B. Roberts, Reade B. Powder, Kara E. |
author_sort | Brandon, A. Allyson |
collection | PubMed |
description | Pigment patterns are incredibly diverse across vertebrates and are shaped by multiple selective pressures from predator avoidance to mate choice. A common pattern across fishes, but for which we know little about the underlying mechanisms, is repeated melanic vertical bars. In order to understand genetic factors that modify the level or pattern of vertical barring, we generated a genetic cross of 322 F(2) hybrids between two cichlid species with distinct barring patterns, Aulonocara koningsi and Metriaclima mbenjii. We identify 48 significant quantitative trait loci that underlie a series of seven phenotypes related to the relative pigmentation intensity, and four traits related to patterning of the vertical bars. We find that genomic regions that generate variation in the level of eumelanin produced are largely independent of those that control the spacing of vertical bars. Candidate genes within these intervals include novel genes and those newly-associated with vertical bars, which could affect melanophore survival, fate decisions, pigment biosynthesis, and pigment distribution. Together, this work provides insights into the regulation of pigment diversity, with direct implications for an animal’s fitness and the speciation process. |
format | Online Article Text |
id | pubmed-10349982 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Cold Spring Harbor Laboratory |
record_format | MEDLINE/PubMed |
spelling | pubmed-103499822023-07-17 Distinct genetic origins of eumelanin intensity and barring patterns in cichlid fishes Brandon, A. Allyson Michael, Cassia Carmona Baez, Aldo Moore, Emily C. Ciccotto, Patrick J. Roberts, Natalie B. Roberts, Reade B. Powder, Kara E. bioRxiv Article Pigment patterns are incredibly diverse across vertebrates and are shaped by multiple selective pressures from predator avoidance to mate choice. A common pattern across fishes, but for which we know little about the underlying mechanisms, is repeated melanic vertical bars. In order to understand genetic factors that modify the level or pattern of vertical barring, we generated a genetic cross of 322 F(2) hybrids between two cichlid species with distinct barring patterns, Aulonocara koningsi and Metriaclima mbenjii. We identify 48 significant quantitative trait loci that underlie a series of seven phenotypes related to the relative pigmentation intensity, and four traits related to patterning of the vertical bars. We find that genomic regions that generate variation in the level of eumelanin produced are largely independent of those that control the spacing of vertical bars. Candidate genes within these intervals include novel genes and those newly-associated with vertical bars, which could affect melanophore survival, fate decisions, pigment biosynthesis, and pigment distribution. Together, this work provides insights into the regulation of pigment diversity, with direct implications for an animal’s fitness and the speciation process. Cold Spring Harbor Laboratory 2023-07-03 /pmc/articles/PMC10349982/ /pubmed/37461734 http://dx.doi.org/10.1101/2023.07.02.547430 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which allows reusers to copy and distribute the material in any medium or format in unadapted form only, for noncommercial purposes only, and only so long as attribution is given to the creator. |
spellingShingle | Article Brandon, A. Allyson Michael, Cassia Carmona Baez, Aldo Moore, Emily C. Ciccotto, Patrick J. Roberts, Natalie B. Roberts, Reade B. Powder, Kara E. Distinct genetic origins of eumelanin intensity and barring patterns in cichlid fishes |
title | Distinct genetic origins of eumelanin intensity and barring patterns in cichlid fishes |
title_full | Distinct genetic origins of eumelanin intensity and barring patterns in cichlid fishes |
title_fullStr | Distinct genetic origins of eumelanin intensity and barring patterns in cichlid fishes |
title_full_unstemmed | Distinct genetic origins of eumelanin intensity and barring patterns in cichlid fishes |
title_short | Distinct genetic origins of eumelanin intensity and barring patterns in cichlid fishes |
title_sort | distinct genetic origins of eumelanin intensity and barring patterns in cichlid fishes |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10349982/ https://www.ncbi.nlm.nih.gov/pubmed/37461734 http://dx.doi.org/10.1101/2023.07.02.547430 |
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