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Systemic paralogy and function of retinal determination network homologs in arachnids

BACKGROUND: Arachnids are important components of cave ecosystems and display many examples of troglomorphisms, such as blindness, depigmentation, and elongate appendages. Little is known about how the eyes of arachnids are specified genetically, let alone the mechanisms for eye reduction and loss i...

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Autores principales: Gainett, Guilherme, Ballesteros, Jesús A., Kanzler, Charlotte R., Zehms, Jakob T., Zern, John M., Aharon, Shlomi, Gavish-Regev, Efrat, Sharma, Prashant P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7681978/
https://www.ncbi.nlm.nih.gov/pubmed/33225889
http://dx.doi.org/10.1186/s12864-020-07149-x
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author Gainett, Guilherme
Ballesteros, Jesús A.
Kanzler, Charlotte R.
Zehms, Jakob T.
Zern, John M.
Aharon, Shlomi
Gavish-Regev, Efrat
Sharma, Prashant P.
author_facet Gainett, Guilherme
Ballesteros, Jesús A.
Kanzler, Charlotte R.
Zehms, Jakob T.
Zern, John M.
Aharon, Shlomi
Gavish-Regev, Efrat
Sharma, Prashant P.
author_sort Gainett, Guilherme
collection PubMed
description BACKGROUND: Arachnids are important components of cave ecosystems and display many examples of troglomorphisms, such as blindness, depigmentation, and elongate appendages. Little is known about how the eyes of arachnids are specified genetically, let alone the mechanisms for eye reduction and loss in troglomorphic arachnids. Additionally, duplication of Retinal Determination Gene Network (RDGN) homologs in spiders has convoluted functional inferences extrapolated from single-copy homologs in pancrustacean models. RESULTS: We investigated a sister species pair of Israeli cave whip spiders, Charinus ioanniticus and C. israelensis (Arachnopulmonata, Amblypygi), of which one species has reduced eyes. We generated embryonic transcriptomes for both Amblypygi species, and discovered that several RDGN homologs exhibit duplications. We show that duplication of RDGN homologs is systemic across arachnopulmonates (arachnid orders that bear book lungs), rather than being a spider-specific phenomenon. A differential gene expression (DGE) analysis comparing the expression of RDGN genes in field-collected embryos of both species identified candidate RDGN genes involved in the formation and reduction of eyes in whip spiders. To ground bioinformatic inference of expression patterns with functional experiments, we interrogated the function of three candidate RDGN genes identified from DGE using RNAi in the spider Parasteatoda tepidariorum. We provide functional evidence that one of these paralogs, sine oculis/Six1 A (soA), is necessary for the development of all arachnid eye types. CONCLUSIONS: Our work establishes a foundation to investigate the genetics of troglomorphic adaptations in cave arachnids, and links differential gene expression to an arthropod eye phenotype for the first time outside of Pancrustacea. Our results support the conservation of at least one RDGN component across Arthropoda and provide a framework for identifying the role of gene duplications in generating arachnid eye diversity.
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spelling pubmed-76819782020-11-23 Systemic paralogy and function of retinal determination network homologs in arachnids Gainett, Guilherme Ballesteros, Jesús A. Kanzler, Charlotte R. Zehms, Jakob T. Zern, John M. Aharon, Shlomi Gavish-Regev, Efrat Sharma, Prashant P. BMC Genomics Research Article BACKGROUND: Arachnids are important components of cave ecosystems and display many examples of troglomorphisms, such as blindness, depigmentation, and elongate appendages. Little is known about how the eyes of arachnids are specified genetically, let alone the mechanisms for eye reduction and loss in troglomorphic arachnids. Additionally, duplication of Retinal Determination Gene Network (RDGN) homologs in spiders has convoluted functional inferences extrapolated from single-copy homologs in pancrustacean models. RESULTS: We investigated a sister species pair of Israeli cave whip spiders, Charinus ioanniticus and C. israelensis (Arachnopulmonata, Amblypygi), of which one species has reduced eyes. We generated embryonic transcriptomes for both Amblypygi species, and discovered that several RDGN homologs exhibit duplications. We show that duplication of RDGN homologs is systemic across arachnopulmonates (arachnid orders that bear book lungs), rather than being a spider-specific phenomenon. A differential gene expression (DGE) analysis comparing the expression of RDGN genes in field-collected embryos of both species identified candidate RDGN genes involved in the formation and reduction of eyes in whip spiders. To ground bioinformatic inference of expression patterns with functional experiments, we interrogated the function of three candidate RDGN genes identified from DGE using RNAi in the spider Parasteatoda tepidariorum. We provide functional evidence that one of these paralogs, sine oculis/Six1 A (soA), is necessary for the development of all arachnid eye types. CONCLUSIONS: Our work establishes a foundation to investigate the genetics of troglomorphic adaptations in cave arachnids, and links differential gene expression to an arthropod eye phenotype for the first time outside of Pancrustacea. Our results support the conservation of at least one RDGN component across Arthropoda and provide a framework for identifying the role of gene duplications in generating arachnid eye diversity. BioMed Central 2020-11-23 /pmc/articles/PMC7681978/ /pubmed/33225889 http://dx.doi.org/10.1186/s12864-020-07149-x Text en © The Author(s) 2020 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
Gainett, Guilherme
Ballesteros, Jesús A.
Kanzler, Charlotte R.
Zehms, Jakob T.
Zern, John M.
Aharon, Shlomi
Gavish-Regev, Efrat
Sharma, Prashant P.
Systemic paralogy and function of retinal determination network homologs in arachnids
title Systemic paralogy and function of retinal determination network homologs in arachnids
title_full Systemic paralogy and function of retinal determination network homologs in arachnids
title_fullStr Systemic paralogy and function of retinal determination network homologs in arachnids
title_full_unstemmed Systemic paralogy and function of retinal determination network homologs in arachnids
title_short Systemic paralogy and function of retinal determination network homologs in arachnids
title_sort systemic paralogy and function of retinal determination network homologs in arachnids
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7681978/
https://www.ncbi.nlm.nih.gov/pubmed/33225889
http://dx.doi.org/10.1186/s12864-020-07149-x
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