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Functional analysis of sense organ specification in the Tribolium castaneum larva reveals divergent mechanisms in insects
ABSTRACT: Insects and other arthropods utilise external sensory structures for mechanosensory, olfactory, and gustatory reception. These sense organs have characteristic shapes related to their function, and in many cases are distributed in a fixed pattern so that they are identifiable individually....
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7866635/ https://www.ncbi.nlm.nih.gov/pubmed/33546687 http://dx.doi.org/10.1186/s12915-021-00948-y |
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author | Klann, Marleen Schacht, Magdalena Ines Benton, Matthew Alan Stollewerk, Angelika |
author_facet | Klann, Marleen Schacht, Magdalena Ines Benton, Matthew Alan Stollewerk, Angelika |
author_sort | Klann, Marleen |
collection | PubMed |
description | ABSTRACT: Insects and other arthropods utilise external sensory structures for mechanosensory, olfactory, and gustatory reception. These sense organs have characteristic shapes related to their function, and in many cases are distributed in a fixed pattern so that they are identifiable individually. In Drosophila melanogaster, the identity of sense organs is regulated by specific combinations of transcription factors. In other arthropods, however, sense organ subtypes cannot be linked to the same code of gene expression. This raises the questions of how sense organ diversity has evolved and whether the principles underlying subtype identity in D. melanogaster are representative of other insects. Here, we provide evidence that such principles cannot be generalised, and suggest that sensory organ diversification followed the recruitment of sensory genes to distinct sensory organ specification mechanism. RESULTS: We analysed sense organ development in a nondipteran insect, the flour beetle Tribolium castaneum, by gene expression and RNA interference studies. We show that in contrast to D. melanogaster, T. castaneum sense organs cannot be categorised based on the expression or their requirement for individual or combinations of conserved sense organ transcription factors such as cut and pox neuro, or members of the Achaete-Scute (Tc ASH, Tc asense), Atonal (Tc atonal, Tc cato, Tc amos), and neurogenin families (Tc tap). Rather, our observations support an evolutionary scenario whereby these sensory genes are required for the specification of sense organ precursors and the development and differentiation of sensory cell types in diverse external sensilla which do not fall into specific morphological and functional classes. CONCLUSIONS: Based on our findings and past research, we present an evolutionary scenario suggesting that sense organ subtype identity has evolved by recruitment of a flexible sensory gene network to the different sense organ specification processes. A dominant role of these genes in subtype identity has evolved as a secondary effect of the function of these genes in individual or subsets of sense organs, probably modulated by positional cues. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12915-021-00948-y. |
format | Online Article Text |
id | pubmed-7866635 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-78666352021-02-08 Functional analysis of sense organ specification in the Tribolium castaneum larva reveals divergent mechanisms in insects Klann, Marleen Schacht, Magdalena Ines Benton, Matthew Alan Stollewerk, Angelika BMC Biol Research Article ABSTRACT: Insects and other arthropods utilise external sensory structures for mechanosensory, olfactory, and gustatory reception. These sense organs have characteristic shapes related to their function, and in many cases are distributed in a fixed pattern so that they are identifiable individually. In Drosophila melanogaster, the identity of sense organs is regulated by specific combinations of transcription factors. In other arthropods, however, sense organ subtypes cannot be linked to the same code of gene expression. This raises the questions of how sense organ diversity has evolved and whether the principles underlying subtype identity in D. melanogaster are representative of other insects. Here, we provide evidence that such principles cannot be generalised, and suggest that sensory organ diversification followed the recruitment of sensory genes to distinct sensory organ specification mechanism. RESULTS: We analysed sense organ development in a nondipteran insect, the flour beetle Tribolium castaneum, by gene expression and RNA interference studies. We show that in contrast to D. melanogaster, T. castaneum sense organs cannot be categorised based on the expression or their requirement for individual or combinations of conserved sense organ transcription factors such as cut and pox neuro, or members of the Achaete-Scute (Tc ASH, Tc asense), Atonal (Tc atonal, Tc cato, Tc amos), and neurogenin families (Tc tap). Rather, our observations support an evolutionary scenario whereby these sensory genes are required for the specification of sense organ precursors and the development and differentiation of sensory cell types in diverse external sensilla which do not fall into specific morphological and functional classes. CONCLUSIONS: Based on our findings and past research, we present an evolutionary scenario suggesting that sense organ subtype identity has evolved by recruitment of a flexible sensory gene network to the different sense organ specification processes. A dominant role of these genes in subtype identity has evolved as a secondary effect of the function of these genes in individual or subsets of sense organs, probably modulated by positional cues. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12915-021-00948-y. BioMed Central 2021-02-05 /pmc/articles/PMC7866635/ /pubmed/33546687 http://dx.doi.org/10.1186/s12915-021-00948-y Text en © The Author(s) 2021 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/. 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 in a credit line to the data. |
spellingShingle | Research Article Klann, Marleen Schacht, Magdalena Ines Benton, Matthew Alan Stollewerk, Angelika Functional analysis of sense organ specification in the Tribolium castaneum larva reveals divergent mechanisms in insects |
title | Functional analysis of sense organ specification in the Tribolium castaneum larva reveals divergent mechanisms in insects |
title_full | Functional analysis of sense organ specification in the Tribolium castaneum larva reveals divergent mechanisms in insects |
title_fullStr | Functional analysis of sense organ specification in the Tribolium castaneum larva reveals divergent mechanisms in insects |
title_full_unstemmed | Functional analysis of sense organ specification in the Tribolium castaneum larva reveals divergent mechanisms in insects |
title_short | Functional analysis of sense organ specification in the Tribolium castaneum larva reveals divergent mechanisms in insects |
title_sort | functional analysis of sense organ specification in the tribolium castaneum larva reveals divergent mechanisms in insects |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7866635/ https://www.ncbi.nlm.nih.gov/pubmed/33546687 http://dx.doi.org/10.1186/s12915-021-00948-y |
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