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Carbonic anhydrase IV in lizard chemical signals

The evolution of chemical signals is subject to environmental constraints. A multicomponent signal may combine semiochemical molecules with supporting compounds able to enhance communication efficacy. Carbonic anhydrases (CAs) are ubiquitous enzymes catalysing the reversible hydration of carbon diox...

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Autores principales: Mangiacotti, Marco, Fumagalli, Marco, Casali, Claudio, Biggiogera, Marco, Forneris, Federico, Sacchi, Roberto
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10465503/
https://www.ncbi.nlm.nih.gov/pubmed/37644071
http://dx.doi.org/10.1038/s41598-023-41012-9
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author Mangiacotti, Marco
Fumagalli, Marco
Casali, Claudio
Biggiogera, Marco
Forneris, Federico
Sacchi, Roberto
author_facet Mangiacotti, Marco
Fumagalli, Marco
Casali, Claudio
Biggiogera, Marco
Forneris, Federico
Sacchi, Roberto
author_sort Mangiacotti, Marco
collection PubMed
description The evolution of chemical signals is subject to environmental constraints. A multicomponent signal may combine semiochemical molecules with supporting compounds able to enhance communication efficacy. Carbonic anhydrases (CAs) are ubiquitous enzymes catalysing the reversible hydration of carbon dioxide, a reaction involved in a variety of physiological processes as it controls the chemical environment of the different tissues or cellular compartments, thus contributing to the overall system homeostasis. CA-IV isoform has been recently identified by mass spectrometry in the femoral gland secretions (FG) of the marine iguana, where it has been hypothesized to contribute to the chemical stability of the signal, by regulating blend pH. Lizards, indeed, use FG to communicate by delivering the waxy secretion on bare substrate, where it is exposed to environmental stressors. Therefore, we expect that some molecules in the mixture may play supporting functions, enhancing the stability of the chemical environment, or even conferring homeostatic properties to the blend. CA-IV may well represent an important candidate to this hypothesized supporting/homeostatic function, and, therefore, we can expect it to be common in FG secretions of other lizard species. To evaluate this prediction and definitely validate CA identity, we analysed FG secretions of eight species of wall lizards (genus Podarcis), combining mass spectrometry, immunoblotting, immunocytochemistry, and transmission electron microscopy. We demonstrate CA-IV to actually occur in the FG of seven out of the eight considered species, providing an immunochemistry validation of mass-spectrometry identifications, and localizing the enzyme within the secretion mass. The predicted structure of the identified CA is compatible with the known enzymatic activity of CA-IV, supporting the hypothesis that CA play a signal homeostasis function and opening to new perspective about the role of proteins in vertebrate chemical communication.
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spelling pubmed-104655032023-08-31 Carbonic anhydrase IV in lizard chemical signals Mangiacotti, Marco Fumagalli, Marco Casali, Claudio Biggiogera, Marco Forneris, Federico Sacchi, Roberto Sci Rep Article The evolution of chemical signals is subject to environmental constraints. A multicomponent signal may combine semiochemical molecules with supporting compounds able to enhance communication efficacy. Carbonic anhydrases (CAs) are ubiquitous enzymes catalysing the reversible hydration of carbon dioxide, a reaction involved in a variety of physiological processes as it controls the chemical environment of the different tissues or cellular compartments, thus contributing to the overall system homeostasis. CA-IV isoform has been recently identified by mass spectrometry in the femoral gland secretions (FG) of the marine iguana, where it has been hypothesized to contribute to the chemical stability of the signal, by regulating blend pH. Lizards, indeed, use FG to communicate by delivering the waxy secretion on bare substrate, where it is exposed to environmental stressors. Therefore, we expect that some molecules in the mixture may play supporting functions, enhancing the stability of the chemical environment, or even conferring homeostatic properties to the blend. CA-IV may well represent an important candidate to this hypothesized supporting/homeostatic function, and, therefore, we can expect it to be common in FG secretions of other lizard species. To evaluate this prediction and definitely validate CA identity, we analysed FG secretions of eight species of wall lizards (genus Podarcis), combining mass spectrometry, immunoblotting, immunocytochemistry, and transmission electron microscopy. We demonstrate CA-IV to actually occur in the FG of seven out of the eight considered species, providing an immunochemistry validation of mass-spectrometry identifications, and localizing the enzyme within the secretion mass. The predicted structure of the identified CA is compatible with the known enzymatic activity of CA-IV, supporting the hypothesis that CA play a signal homeostasis function and opening to new perspective about the role of proteins in vertebrate chemical communication. Nature Publishing Group UK 2023-08-29 /pmc/articles/PMC10465503/ /pubmed/37644071 http://dx.doi.org/10.1038/s41598-023-41012-9 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Mangiacotti, Marco
Fumagalli, Marco
Casali, Claudio
Biggiogera, Marco
Forneris, Federico
Sacchi, Roberto
Carbonic anhydrase IV in lizard chemical signals
title Carbonic anhydrase IV in lizard chemical signals
title_full Carbonic anhydrase IV in lizard chemical signals
title_fullStr Carbonic anhydrase IV in lizard chemical signals
title_full_unstemmed Carbonic anhydrase IV in lizard chemical signals
title_short Carbonic anhydrase IV in lizard chemical signals
title_sort carbonic anhydrase iv in lizard chemical signals
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10465503/
https://www.ncbi.nlm.nih.gov/pubmed/37644071
http://dx.doi.org/10.1038/s41598-023-41012-9
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