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Venomics Reveals a Non-Compartmentalised Venom Gland in the Early Diverged Vermivorous Conus distans
The defensive use of cone snail venom is hypothesised to have first arisen in ancestral worm-hunting snails and later repurposed in a compartmentalised venom duct to facilitate the dietary shift to molluscivory and piscivory. Consistent with its placement in a basal lineage, we demonstrate that the...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8949452/ https://www.ncbi.nlm.nih.gov/pubmed/35324723 http://dx.doi.org/10.3390/toxins14030226 |
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author | Prashanth, Jutty Rajan Dutertre, Sebastien Rai, Subash Kumar Lewis, Richard J. |
author_facet | Prashanth, Jutty Rajan Dutertre, Sebastien Rai, Subash Kumar Lewis, Richard J. |
author_sort | Prashanth, Jutty Rajan |
collection | PubMed |
description | The defensive use of cone snail venom is hypothesised to have first arisen in ancestral worm-hunting snails and later repurposed in a compartmentalised venom duct to facilitate the dietary shift to molluscivory and piscivory. Consistent with its placement in a basal lineage, we demonstrate that the C. distans venom gland lacked distinct compartmentalisation. Transcriptomics revealed C. distans expressed a wide range of structural classes, with inhibitory cysteine knot (ICK)-containing peptides dominating. To better understand the evolution of the venom gland compartmentalisation, we compared C. distans to C. planorbis, the earliest diverging species from which a defence-evoked venom has been obtained, and fish-hunting C. geographus from the Gastridium subgenus that injects distinct defensive and predatory venoms. These comparisons support the hypothesis that venom gland compartmentalisation arose in worm-hunting species and enabled repurposing of venom peptides to facilitate the dietary shift from vermivory to molluscivory and piscivory in more recently diverged cone snail lineages. |
format | Online Article Text |
id | pubmed-8949452 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-89494522022-03-26 Venomics Reveals a Non-Compartmentalised Venom Gland in the Early Diverged Vermivorous Conus distans Prashanth, Jutty Rajan Dutertre, Sebastien Rai, Subash Kumar Lewis, Richard J. Toxins (Basel) Article The defensive use of cone snail venom is hypothesised to have first arisen in ancestral worm-hunting snails and later repurposed in a compartmentalised venom duct to facilitate the dietary shift to molluscivory and piscivory. Consistent with its placement in a basal lineage, we demonstrate that the C. distans venom gland lacked distinct compartmentalisation. Transcriptomics revealed C. distans expressed a wide range of structural classes, with inhibitory cysteine knot (ICK)-containing peptides dominating. To better understand the evolution of the venom gland compartmentalisation, we compared C. distans to C. planorbis, the earliest diverging species from which a defence-evoked venom has been obtained, and fish-hunting C. geographus from the Gastridium subgenus that injects distinct defensive and predatory venoms. These comparisons support the hypothesis that venom gland compartmentalisation arose in worm-hunting species and enabled repurposing of venom peptides to facilitate the dietary shift from vermivory to molluscivory and piscivory in more recently diverged cone snail lineages. MDPI 2022-03-19 /pmc/articles/PMC8949452/ /pubmed/35324723 http://dx.doi.org/10.3390/toxins14030226 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Prashanth, Jutty Rajan Dutertre, Sebastien Rai, Subash Kumar Lewis, Richard J. Venomics Reveals a Non-Compartmentalised Venom Gland in the Early Diverged Vermivorous Conus distans |
title | Venomics Reveals a Non-Compartmentalised Venom Gland in the Early Diverged Vermivorous Conus distans |
title_full | Venomics Reveals a Non-Compartmentalised Venom Gland in the Early Diverged Vermivorous Conus distans |
title_fullStr | Venomics Reveals a Non-Compartmentalised Venom Gland in the Early Diverged Vermivorous Conus distans |
title_full_unstemmed | Venomics Reveals a Non-Compartmentalised Venom Gland in the Early Diverged Vermivorous Conus distans |
title_short | Venomics Reveals a Non-Compartmentalised Venom Gland in the Early Diverged Vermivorous Conus distans |
title_sort | venomics reveals a non-compartmentalised venom gland in the early diverged vermivorous conus distans |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8949452/ https://www.ncbi.nlm.nih.gov/pubmed/35324723 http://dx.doi.org/10.3390/toxins14030226 |
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