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Comparative analyses of glycerotoxin expression unveil a novel structural organization of the bloodworm venom system
BACKGROUND: We present the first molecular characterization of glycerotoxin (GLTx), a potent neurotoxin found in the venom of the bloodworm Glycera tridactyla (Glyceridae, Annelida). Within the animal kingdom, GLTx shows a unique mode of action as it can specifically up-regulate the activity of Ca(v...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5336659/ https://www.ncbi.nlm.nih.gov/pubmed/28259138 http://dx.doi.org/10.1186/s12862-017-0904-4 |
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author | Richter, Sandy Helm, Conrad Meunier, Frederic A. Hering, Lars Campbell, Lahcen I. Drukewitz, Stephan H. Undheim, Eivind A. B. Jenner, Ronald A. Schiavo, Giampietro Bleidorn, Christoph |
author_facet | Richter, Sandy Helm, Conrad Meunier, Frederic A. Hering, Lars Campbell, Lahcen I. Drukewitz, Stephan H. Undheim, Eivind A. B. Jenner, Ronald A. Schiavo, Giampietro Bleidorn, Christoph |
author_sort | Richter, Sandy |
collection | PubMed |
description | BACKGROUND: We present the first molecular characterization of glycerotoxin (GLTx), a potent neurotoxin found in the venom of the bloodworm Glycera tridactyla (Glyceridae, Annelida). Within the animal kingdom, GLTx shows a unique mode of action as it can specifically up-regulate the activity of Ca(v)2.2 channels (N-type) in a reversible manner. The lack of sequence information has so far hampered a detailed understanding of its mode of action. RESULTS: Our analyses reveal three ~3.8 kb GLTx full-length transcripts, show that GLTx represents a multigene family, and suggest it functions as a dimer. An integrative approach using transcriptomics, quantitative real-time PCR, in situ hybridization, and immunocytochemistry shows that GLTx is highly expressed exclusively in four pharyngeal lobes, a previously unrecognized part of the venom apparatus. CONCLUSIONS: Our results overturn a century old textbook view on the glycerid venom system, suggesting that it is anatomically and functionally much more complex than previously thought. The herein presented GLTx sequence information constitutes an important step towards the establishment of GLTx as a versatile tool to understand the mechanism of synaptic function, as well as the mode of action of this novel neurotoxin. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12862-017-0904-4) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5336659 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-53366592017-03-07 Comparative analyses of glycerotoxin expression unveil a novel structural organization of the bloodworm venom system Richter, Sandy Helm, Conrad Meunier, Frederic A. Hering, Lars Campbell, Lahcen I. Drukewitz, Stephan H. Undheim, Eivind A. B. Jenner, Ronald A. Schiavo, Giampietro Bleidorn, Christoph BMC Evol Biol Research Article BACKGROUND: We present the first molecular characterization of glycerotoxin (GLTx), a potent neurotoxin found in the venom of the bloodworm Glycera tridactyla (Glyceridae, Annelida). Within the animal kingdom, GLTx shows a unique mode of action as it can specifically up-regulate the activity of Ca(v)2.2 channels (N-type) in a reversible manner. The lack of sequence information has so far hampered a detailed understanding of its mode of action. RESULTS: Our analyses reveal three ~3.8 kb GLTx full-length transcripts, show that GLTx represents a multigene family, and suggest it functions as a dimer. An integrative approach using transcriptomics, quantitative real-time PCR, in situ hybridization, and immunocytochemistry shows that GLTx is highly expressed exclusively in four pharyngeal lobes, a previously unrecognized part of the venom apparatus. CONCLUSIONS: Our results overturn a century old textbook view on the glycerid venom system, suggesting that it is anatomically and functionally much more complex than previously thought. The herein presented GLTx sequence information constitutes an important step towards the establishment of GLTx as a versatile tool to understand the mechanism of synaptic function, as well as the mode of action of this novel neurotoxin. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12862-017-0904-4) contains supplementary material, which is available to authorized users. BioMed Central 2017-03-04 /pmc/articles/PMC5336659/ /pubmed/28259138 http://dx.doi.org/10.1186/s12862-017-0904-4 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. 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. |
spellingShingle | Research Article Richter, Sandy Helm, Conrad Meunier, Frederic A. Hering, Lars Campbell, Lahcen I. Drukewitz, Stephan H. Undheim, Eivind A. B. Jenner, Ronald A. Schiavo, Giampietro Bleidorn, Christoph Comparative analyses of glycerotoxin expression unveil a novel structural organization of the bloodworm venom system |
title | Comparative analyses of glycerotoxin expression unveil a novel structural organization of the bloodworm venom system |
title_full | Comparative analyses of glycerotoxin expression unveil a novel structural organization of the bloodworm venom system |
title_fullStr | Comparative analyses of glycerotoxin expression unveil a novel structural organization of the bloodworm venom system |
title_full_unstemmed | Comparative analyses of glycerotoxin expression unveil a novel structural organization of the bloodworm venom system |
title_short | Comparative analyses of glycerotoxin expression unveil a novel structural organization of the bloodworm venom system |
title_sort | comparative analyses of glycerotoxin expression unveil a novel structural organization of the bloodworm venom system |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5336659/ https://www.ncbi.nlm.nih.gov/pubmed/28259138 http://dx.doi.org/10.1186/s12862-017-0904-4 |
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