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Calcareous sponge genomes reveal complex evolution of α-carbonic anhydrases and two key biomineralization enzymes

BACKGROUND: Calcium carbonate biominerals form often complex and beautiful skeletal elements, including coral exoskeletons and mollusc shells. Although the ability to generate these carbonate structures was apparently gained independently during animal evolution, it sometimes involves the same gene...

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Autores principales: Voigt, Oliver, Adamski, Marcin, Sluzek, Kasia, Adamska, Maja
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4265532/
https://www.ncbi.nlm.nih.gov/pubmed/25421146
http://dx.doi.org/10.1186/s12862-014-0230-z
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author Voigt, Oliver
Adamski, Marcin
Sluzek, Kasia
Adamska, Maja
author_facet Voigt, Oliver
Adamski, Marcin
Sluzek, Kasia
Adamska, Maja
author_sort Voigt, Oliver
collection PubMed
description BACKGROUND: Calcium carbonate biominerals form often complex and beautiful skeletal elements, including coral exoskeletons and mollusc shells. Although the ability to generate these carbonate structures was apparently gained independently during animal evolution, it sometimes involves the same gene families. One of the best-studied of these gene families comprises the α- carbonic anhydrases (CAs), which catalyse the reversible transformation of CO(2) to HCO(3)(−) and fulfill many physiological functions. Among Porifera –the oldest animal phylum with the ability to produce skeletal elements– only the class of calcareous sponges can build calcitic spicules, which are the extracellular products of specialized cells, the sclerocytes. Little is known about the molecular mechanisms of their synthesis, but inhibition studies suggest an essential role of CAs. In order to gain insight into the evolution and function of CAs in biomineralization of a basal metazoan species, we determined the diversity and expression of CAs in the calcareous sponges Sycon ciliatum and Leucosolenia complicata by means of genomic screening, RNA-Seq and RNA in situ hybridization expression analysis. Active biomineralization was located with calcein-staining. RESULTS: We found that the CA repertoires of two calcareous sponge species are strikingly more complex than those of other sponges. By characterizing their expression patterns, we could link two CAs (one intracellular and one extracellular) to the process of calcite spicule formation in both studied species. The extracellular biomineralizing CAs seem to be of paralogous origin, a finding that advises caution against assuming functional conservation of biomineralizing genes based upon orthology assessment alone. Additionally, calcareous sponges possess acatalytic CAs related to human CAs X and XI, suggesting an ancient origin of these proteins. Phylogenetic analyses including CAs from genomes of all non-bilaterian phyla suggest multiple gene losses and duplications and presence of several CAs in the last common ancestor of metazoans. CONCLUSIONS: We identified two key biomineralization enzymes from the CA-family in calcareous sponges and propose their possible interaction in spicule formation. The complex evolutionary history of the CA family is driven by frequent gene diversification and losses. These evolutionary patterns likely facilitated the numerous events of independent recruitment of CAs into biomineralization within Metazoa. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12862-014-0230-z) contains supplementary material, which is available to authorized users.
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spelling pubmed-42655322014-12-15 Calcareous sponge genomes reveal complex evolution of α-carbonic anhydrases and two key biomineralization enzymes Voigt, Oliver Adamski, Marcin Sluzek, Kasia Adamska, Maja BMC Evol Biol Research Article BACKGROUND: Calcium carbonate biominerals form often complex and beautiful skeletal elements, including coral exoskeletons and mollusc shells. Although the ability to generate these carbonate structures was apparently gained independently during animal evolution, it sometimes involves the same gene families. One of the best-studied of these gene families comprises the α- carbonic anhydrases (CAs), which catalyse the reversible transformation of CO(2) to HCO(3)(−) and fulfill many physiological functions. Among Porifera –the oldest animal phylum with the ability to produce skeletal elements– only the class of calcareous sponges can build calcitic spicules, which are the extracellular products of specialized cells, the sclerocytes. Little is known about the molecular mechanisms of their synthesis, but inhibition studies suggest an essential role of CAs. In order to gain insight into the evolution and function of CAs in biomineralization of a basal metazoan species, we determined the diversity and expression of CAs in the calcareous sponges Sycon ciliatum and Leucosolenia complicata by means of genomic screening, RNA-Seq and RNA in situ hybridization expression analysis. Active biomineralization was located with calcein-staining. RESULTS: We found that the CA repertoires of two calcareous sponge species are strikingly more complex than those of other sponges. By characterizing their expression patterns, we could link two CAs (one intracellular and one extracellular) to the process of calcite spicule formation in both studied species. The extracellular biomineralizing CAs seem to be of paralogous origin, a finding that advises caution against assuming functional conservation of biomineralizing genes based upon orthology assessment alone. Additionally, calcareous sponges possess acatalytic CAs related to human CAs X and XI, suggesting an ancient origin of these proteins. Phylogenetic analyses including CAs from genomes of all non-bilaterian phyla suggest multiple gene losses and duplications and presence of several CAs in the last common ancestor of metazoans. CONCLUSIONS: We identified two key biomineralization enzymes from the CA-family in calcareous sponges and propose their possible interaction in spicule formation. The complex evolutionary history of the CA family is driven by frequent gene diversification and losses. These evolutionary patterns likely facilitated the numerous events of independent recruitment of CAs into biomineralization within Metazoa. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12862-014-0230-z) contains supplementary material, which is available to authorized users. BioMed Central 2014-11-25 /pmc/articles/PMC4265532/ /pubmed/25421146 http://dx.doi.org/10.1186/s12862-014-0230-z Text en © Voigt et al.; licensee BioMed Central Ltd. 2014 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. 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
Voigt, Oliver
Adamski, Marcin
Sluzek, Kasia
Adamska, Maja
Calcareous sponge genomes reveal complex evolution of α-carbonic anhydrases and two key biomineralization enzymes
title Calcareous sponge genomes reveal complex evolution of α-carbonic anhydrases and two key biomineralization enzymes
title_full Calcareous sponge genomes reveal complex evolution of α-carbonic anhydrases and two key biomineralization enzymes
title_fullStr Calcareous sponge genomes reveal complex evolution of α-carbonic anhydrases and two key biomineralization enzymes
title_full_unstemmed Calcareous sponge genomes reveal complex evolution of α-carbonic anhydrases and two key biomineralization enzymes
title_short Calcareous sponge genomes reveal complex evolution of α-carbonic anhydrases and two key biomineralization enzymes
title_sort calcareous sponge genomes reveal complex evolution of α-carbonic anhydrases and two key biomineralization enzymes
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4265532/
https://www.ncbi.nlm.nih.gov/pubmed/25421146
http://dx.doi.org/10.1186/s12862-014-0230-z
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