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aristaless1 has a dual role in appendage formation and wing color specification during butterfly development

BACKGROUND: Highly diverse butterfly wing patterns have emerged as a powerful system for understanding the genetic basis of phenotypic variation. While the genetic basis of this pattern variation is being clarified, the precise developmental pathways linking genotype to phenotype are not well unders...

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Autores principales: Bayala, Erick X., VanKuren, Nicholas, Massardo, Darli, Kronforst, Marcus R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10161628/
https://www.ncbi.nlm.nih.gov/pubmed/37143075
http://dx.doi.org/10.1186/s12915-023-01601-6
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author Bayala, Erick X.
VanKuren, Nicholas
Massardo, Darli
Kronforst, Marcus R.
author_facet Bayala, Erick X.
VanKuren, Nicholas
Massardo, Darli
Kronforst, Marcus R.
author_sort Bayala, Erick X.
collection PubMed
description BACKGROUND: Highly diverse butterfly wing patterns have emerged as a powerful system for understanding the genetic basis of phenotypic variation. While the genetic basis of this pattern variation is being clarified, the precise developmental pathways linking genotype to phenotype are not well understood. The gene aristaless, which plays a role in appendage patterning and extension, has been duplicated in Lepidoptera. One copy, aristaless1, has been shown to control a white/yellow color switch in the butterfly Heliconius cydno, suggesting a novel function associated with color patterning and pigmentation. Here we investigate the developmental basis of al1 in embryos, larvae, and pupae using new antibodies, CRISPR/Cas9, RNAi, qPCR assays of downstream targets, and pharmacological manipulation of an upstream activator. RESULTS: We find that Al1 is expressed at the distal tips of developing embryonic appendages consistent with its ancestral role. In developing wings, we observe Al1 accumulation within developing scale cells of white H. cydno during early pupation while yellow scale cells exhibit little Al1 at this time point. Reduced Al1 expression is also associated with yellow scale development in al1 knockouts and knockdowns. We propose that Al1 expression in future white scales might be related to an observed downregulation of the enzyme Cinnabar and other genes that synthesize and transport the yellow pigment, 3–hydroxykynurenine (3-OHK). Finally, we provide evidence that Al1 activation is under the control of Wnt signaling. CONCLUSIONS: We propose a model in which high levels of Al1 during early pupation, which are mediated by Wnt, are important for melanic pigmentation and specifying white portions of the wing while reduced levels of Al1 during early pupation promote upregulation of proteins needed to move and synthesize 3-OHK, promoting yellow pigmentation. In addition, we discuss how the ancestral role of aristaless in appendage extension may be relevant in understanding the cellular mechanism behind color patterning in the context of the heterochrony hypothesis. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12915-023-01601-6.
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spelling pubmed-101616282023-05-06 aristaless1 has a dual role in appendage formation and wing color specification during butterfly development Bayala, Erick X. VanKuren, Nicholas Massardo, Darli Kronforst, Marcus R. BMC Biol Research Article BACKGROUND: Highly diverse butterfly wing patterns have emerged as a powerful system for understanding the genetic basis of phenotypic variation. While the genetic basis of this pattern variation is being clarified, the precise developmental pathways linking genotype to phenotype are not well understood. The gene aristaless, which plays a role in appendage patterning and extension, has been duplicated in Lepidoptera. One copy, aristaless1, has been shown to control a white/yellow color switch in the butterfly Heliconius cydno, suggesting a novel function associated with color patterning and pigmentation. Here we investigate the developmental basis of al1 in embryos, larvae, and pupae using new antibodies, CRISPR/Cas9, RNAi, qPCR assays of downstream targets, and pharmacological manipulation of an upstream activator. RESULTS: We find that Al1 is expressed at the distal tips of developing embryonic appendages consistent with its ancestral role. In developing wings, we observe Al1 accumulation within developing scale cells of white H. cydno during early pupation while yellow scale cells exhibit little Al1 at this time point. Reduced Al1 expression is also associated with yellow scale development in al1 knockouts and knockdowns. We propose that Al1 expression in future white scales might be related to an observed downregulation of the enzyme Cinnabar and other genes that synthesize and transport the yellow pigment, 3–hydroxykynurenine (3-OHK). Finally, we provide evidence that Al1 activation is under the control of Wnt signaling. CONCLUSIONS: We propose a model in which high levels of Al1 during early pupation, which are mediated by Wnt, are important for melanic pigmentation and specifying white portions of the wing while reduced levels of Al1 during early pupation promote upregulation of proteins needed to move and synthesize 3-OHK, promoting yellow pigmentation. In addition, we discuss how the ancestral role of aristaless in appendage extension may be relevant in understanding the cellular mechanism behind color patterning in the context of the heterochrony hypothesis. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12915-023-01601-6. BioMed Central 2023-05-04 /pmc/articles/PMC10161628/ /pubmed/37143075 http://dx.doi.org/10.1186/s12915-023-01601-6 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research Article
Bayala, Erick X.
VanKuren, Nicholas
Massardo, Darli
Kronforst, Marcus R.
aristaless1 has a dual role in appendage formation and wing color specification during butterfly development
title aristaless1 has a dual role in appendage formation and wing color specification during butterfly development
title_full aristaless1 has a dual role in appendage formation and wing color specification during butterfly development
title_fullStr aristaless1 has a dual role in appendage formation and wing color specification during butterfly development
title_full_unstemmed aristaless1 has a dual role in appendage formation and wing color specification during butterfly development
title_short aristaless1 has a dual role in appendage formation and wing color specification during butterfly development
title_sort aristaless1 has a dual role in appendage formation and wing color specification during butterfly development
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10161628/
https://www.ncbi.nlm.nih.gov/pubmed/37143075
http://dx.doi.org/10.1186/s12915-023-01601-6
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