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Physiological demands and signaling associated with snake venom production and storage illustrated by transcriptional analyses of venom glands

Despite the extensive body of research on snake venom, many facets of snake venom systems, such as the physiology and regulation of the venom gland itself, remain virtually unstudied. Here, we use time series gene expression analyses of the rattlesnake venom gland in comparison with several non-veno...

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Autores principales: Perry, Blair W., Schield, Drew R., Westfall, Aundrea K., Mackessy, Stephen P., Castoe, Todd A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7582160/
https://www.ncbi.nlm.nih.gov/pubmed/33093509
http://dx.doi.org/10.1038/s41598-020-75048-y
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author Perry, Blair W.
Schield, Drew R.
Westfall, Aundrea K.
Mackessy, Stephen P.
Castoe, Todd A.
author_facet Perry, Blair W.
Schield, Drew R.
Westfall, Aundrea K.
Mackessy, Stephen P.
Castoe, Todd A.
author_sort Perry, Blair W.
collection PubMed
description Despite the extensive body of research on snake venom, many facets of snake venom systems, such as the physiology and regulation of the venom gland itself, remain virtually unstudied. Here, we use time series gene expression analyses of the rattlesnake venom gland in comparison with several non-venom tissues to characterize physiological and cellular processes associated with venom production and to highlight key distinctions of venom gland cellular and physiological function. We find consistent evidence for activation of stress response pathways in the venom gland, suggesting that mitigation of cellular stress is a crucial component of venom production. Additionally, we demonstrate evidence for an unappreciated degree of cellular and secretory activity in the steady state venom gland relative to other secretory tissues and identify vacuolar ATPases as the likely mechanisms driving acidification of the venom gland lumen during venom production and storage.
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spelling pubmed-75821602020-10-23 Physiological demands and signaling associated with snake venom production and storage illustrated by transcriptional analyses of venom glands Perry, Blair W. Schield, Drew R. Westfall, Aundrea K. Mackessy, Stephen P. Castoe, Todd A. Sci Rep Article Despite the extensive body of research on snake venom, many facets of snake venom systems, such as the physiology and regulation of the venom gland itself, remain virtually unstudied. Here, we use time series gene expression analyses of the rattlesnake venom gland in comparison with several non-venom tissues to characterize physiological and cellular processes associated with venom production and to highlight key distinctions of venom gland cellular and physiological function. We find consistent evidence for activation of stress response pathways in the venom gland, suggesting that mitigation of cellular stress is a crucial component of venom production. Additionally, we demonstrate evidence for an unappreciated degree of cellular and secretory activity in the steady state venom gland relative to other secretory tissues and identify vacuolar ATPases as the likely mechanisms driving acidification of the venom gland lumen during venom production and storage. Nature Publishing Group UK 2020-10-22 /pmc/articles/PMC7582160/ /pubmed/33093509 http://dx.doi.org/10.1038/s41598-020-75048-y Text en © The Author(s) 2020 Open Access This 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/.
spellingShingle Article
Perry, Blair W.
Schield, Drew R.
Westfall, Aundrea K.
Mackessy, Stephen P.
Castoe, Todd A.
Physiological demands and signaling associated with snake venom production and storage illustrated by transcriptional analyses of venom glands
title Physiological demands and signaling associated with snake venom production and storage illustrated by transcriptional analyses of venom glands
title_full Physiological demands and signaling associated with snake venom production and storage illustrated by transcriptional analyses of venom glands
title_fullStr Physiological demands and signaling associated with snake venom production and storage illustrated by transcriptional analyses of venom glands
title_full_unstemmed Physiological demands and signaling associated with snake venom production and storage illustrated by transcriptional analyses of venom glands
title_short Physiological demands and signaling associated with snake venom production and storage illustrated by transcriptional analyses of venom glands
title_sort physiological demands and signaling associated with snake venom production and storage illustrated by transcriptional analyses of venom glands
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7582160/
https://www.ncbi.nlm.nih.gov/pubmed/33093509
http://dx.doi.org/10.1038/s41598-020-75048-y
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