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Probing the conserved roles of cut in the development and function of optically different insect compound eyes

Astonishing functional diversity exists among arthropod eyes, yet eye development relies on deeply conserved genes. This phenomenon is best understood for early events, whereas fewer investigations have focused on the influence of later transcriptional regulators on diverse eye organizations and the...

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Autores principales: Rathore, Shubham, Meece, Michael, Charlton-Perkins, Mark, Cook, Tiffany A., Buschbeck, Elke K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10102356/
https://www.ncbi.nlm.nih.gov/pubmed/37065850
http://dx.doi.org/10.3389/fcell.2023.1104620
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author Rathore, Shubham
Meece, Michael
Charlton-Perkins, Mark
Cook, Tiffany A.
Buschbeck, Elke K.
author_facet Rathore, Shubham
Meece, Michael
Charlton-Perkins, Mark
Cook, Tiffany A.
Buschbeck, Elke K.
author_sort Rathore, Shubham
collection PubMed
description Astonishing functional diversity exists among arthropod eyes, yet eye development relies on deeply conserved genes. This phenomenon is best understood for early events, whereas fewer investigations have focused on the influence of later transcriptional regulators on diverse eye organizations and the contribution of critical support cells, such as Semper cells (SCs). As SCs in Drosophila melanogaster secrete the lens and function as glia, they are critical components of ommatidia. Here, we perform RNAi-based knockdowns of the transcription factor cut (CUX in vertebrates), a marker of SCs, the function of which has remained untested in these cell types. To probe for the conserved roles of cut, we investigate two optically different compound eyes: the apposition optics of D. melanogaster and the superposition optics of the diving beetle Thermonectus marmoratus. In both cases, we find that multiple aspects of ocular formation are disrupted, including lens facet organization and optics as well as photoreceptor morphogenesis. Together, our findings support the possibility of a generalized role for SCs in arthropod ommatidial form and function and introduces Cut as a central player in mediating this role.
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spelling pubmed-101023562023-04-15 Probing the conserved roles of cut in the development and function of optically different insect compound eyes Rathore, Shubham Meece, Michael Charlton-Perkins, Mark Cook, Tiffany A. Buschbeck, Elke K. Front Cell Dev Biol Cell and Developmental Biology Astonishing functional diversity exists among arthropod eyes, yet eye development relies on deeply conserved genes. This phenomenon is best understood for early events, whereas fewer investigations have focused on the influence of later transcriptional regulators on diverse eye organizations and the contribution of critical support cells, such as Semper cells (SCs). As SCs in Drosophila melanogaster secrete the lens and function as glia, they are critical components of ommatidia. Here, we perform RNAi-based knockdowns of the transcription factor cut (CUX in vertebrates), a marker of SCs, the function of which has remained untested in these cell types. To probe for the conserved roles of cut, we investigate two optically different compound eyes: the apposition optics of D. melanogaster and the superposition optics of the diving beetle Thermonectus marmoratus. In both cases, we find that multiple aspects of ocular formation are disrupted, including lens facet organization and optics as well as photoreceptor morphogenesis. Together, our findings support the possibility of a generalized role for SCs in arthropod ommatidial form and function and introduces Cut as a central player in mediating this role. Frontiers Media S.A. 2023-03-31 /pmc/articles/PMC10102356/ /pubmed/37065850 http://dx.doi.org/10.3389/fcell.2023.1104620 Text en Copyright © 2023 Rathore, Meece, Charlton-Perkins, Cook and Buschbeck. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Cell and Developmental Biology
Rathore, Shubham
Meece, Michael
Charlton-Perkins, Mark
Cook, Tiffany A.
Buschbeck, Elke K.
Probing the conserved roles of cut in the development and function of optically different insect compound eyes
title Probing the conserved roles of cut in the development and function of optically different insect compound eyes
title_full Probing the conserved roles of cut in the development and function of optically different insect compound eyes
title_fullStr Probing the conserved roles of cut in the development and function of optically different insect compound eyes
title_full_unstemmed Probing the conserved roles of cut in the development and function of optically different insect compound eyes
title_short Probing the conserved roles of cut in the development and function of optically different insect compound eyes
title_sort probing the conserved roles of cut in the development and function of optically different insect compound eyes
topic Cell and Developmental Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10102356/
https://www.ncbi.nlm.nih.gov/pubmed/37065850
http://dx.doi.org/10.3389/fcell.2023.1104620
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