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The calcitonin-like system is an ancient regulatory system of biomineralization

Biomineralization is the process by which living organisms acquired the capacity to accumulate minerals in tissues. Shells are the biomineralized exoskeleton of marine molluscs produced by the mantle but factors that regulate mantle shell building are still enigmatic. This study sought to identify c...

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Autores principales: Cardoso, João C. R., Félix, Rute C., Ferreira, Vinícius, Peng, MaoXiao, Zhang, Xushuai, Power, Deborah M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7200681/
https://www.ncbi.nlm.nih.gov/pubmed/32371888
http://dx.doi.org/10.1038/s41598-020-64118-w
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author Cardoso, João C. R.
Félix, Rute C.
Ferreira, Vinícius
Peng, MaoXiao
Zhang, Xushuai
Power, Deborah M.
author_facet Cardoso, João C. R.
Félix, Rute C.
Ferreira, Vinícius
Peng, MaoXiao
Zhang, Xushuai
Power, Deborah M.
author_sort Cardoso, João C. R.
collection PubMed
description Biomineralization is the process by which living organisms acquired the capacity to accumulate minerals in tissues. Shells are the biomineralized exoskeleton of marine molluscs produced by the mantle but factors that regulate mantle shell building are still enigmatic. This study sought to identify candidate regulatory factors of molluscan shell mineralization and targeted family B G-protein coupled receptors (GPCRs) and ligands that include calcium regulatory factors in vertebrates, such as calcitonin (CALC). In molluscs, CALC receptor (CALCR) number was variable and arose through lineage and species-specific duplications. The Mediterranean mussel (Mytilus galloprovincialis) mantle transcriptome expresses six CALCR-like and two CALC-precursors encoding four putative mature peptides. Mussel CALCR-like are activated in vitro by vertebrate CALC but only receptor CALCRIIc is activated by the mussel CALCIIa peptide (EC(50) = 2.6 ×10(−5) M). Ex-vivo incubations of mantle edge tissue and mantle cells with CALCIIa revealed they accumulated significantly more calcium than untreated tissue and cells. Mussel CALCIIa also significantly decreased mantle acid phosphatase activity, which is associated with shell remodelling. Our data indicate the CALC-like system as candidate regulatory factors of shell mineralization. The identification of the CALC system from molluscs to vertebrates suggests it is an ancient and conserved calcium regulatory system of mineralization.
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spelling pubmed-72006812020-05-12 The calcitonin-like system is an ancient regulatory system of biomineralization Cardoso, João C. R. Félix, Rute C. Ferreira, Vinícius Peng, MaoXiao Zhang, Xushuai Power, Deborah M. Sci Rep Article Biomineralization is the process by which living organisms acquired the capacity to accumulate minerals in tissues. Shells are the biomineralized exoskeleton of marine molluscs produced by the mantle but factors that regulate mantle shell building are still enigmatic. This study sought to identify candidate regulatory factors of molluscan shell mineralization and targeted family B G-protein coupled receptors (GPCRs) and ligands that include calcium regulatory factors in vertebrates, such as calcitonin (CALC). In molluscs, CALC receptor (CALCR) number was variable and arose through lineage and species-specific duplications. The Mediterranean mussel (Mytilus galloprovincialis) mantle transcriptome expresses six CALCR-like and two CALC-precursors encoding four putative mature peptides. Mussel CALCR-like are activated in vitro by vertebrate CALC but only receptor CALCRIIc is activated by the mussel CALCIIa peptide (EC(50) = 2.6 ×10(−5) M). Ex-vivo incubations of mantle edge tissue and mantle cells with CALCIIa revealed they accumulated significantly more calcium than untreated tissue and cells. Mussel CALCIIa also significantly decreased mantle acid phosphatase activity, which is associated with shell remodelling. Our data indicate the CALC-like system as candidate regulatory factors of shell mineralization. The identification of the CALC system from molluscs to vertebrates suggests it is an ancient and conserved calcium regulatory system of mineralization. Nature Publishing Group UK 2020-05-05 /pmc/articles/PMC7200681/ /pubmed/32371888 http://dx.doi.org/10.1038/s41598-020-64118-w 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Cardoso, João C. R.
Félix, Rute C.
Ferreira, Vinícius
Peng, MaoXiao
Zhang, Xushuai
Power, Deborah M.
The calcitonin-like system is an ancient regulatory system of biomineralization
title The calcitonin-like system is an ancient regulatory system of biomineralization
title_full The calcitonin-like system is an ancient regulatory system of biomineralization
title_fullStr The calcitonin-like system is an ancient regulatory system of biomineralization
title_full_unstemmed The calcitonin-like system is an ancient regulatory system of biomineralization
title_short The calcitonin-like system is an ancient regulatory system of biomineralization
title_sort calcitonin-like system is an ancient regulatory system of biomineralization
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7200681/
https://www.ncbi.nlm.nih.gov/pubmed/32371888
http://dx.doi.org/10.1038/s41598-020-64118-w
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