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Spicule formation in calcareous sponges: Coordinated expression of biomineralization genes and spicule-type specific genes
The ability to form mineral structures under biological control is widespread among animals. In several species, specific proteins have been shown to be involved in biomineralization, but it is uncertain how they influence the shape of the growing biomineral and the resulting skeleton. Calcareous sp...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5390275/ https://www.ncbi.nlm.nih.gov/pubmed/28406140 http://dx.doi.org/10.1038/srep45658 |
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author | Voigt, Oliver Adamska, Maja Adamski, Marcin Kittelmann, André Wencker, Lukardis Wörheide, Gert |
author_facet | Voigt, Oliver Adamska, Maja Adamski, Marcin Kittelmann, André Wencker, Lukardis Wörheide, Gert |
author_sort | Voigt, Oliver |
collection | PubMed |
description | The ability to form mineral structures under biological control is widespread among animals. In several species, specific proteins have been shown to be involved in biomineralization, but it is uncertain how they influence the shape of the growing biomineral and the resulting skeleton. Calcareous sponges are the only sponges that form calcitic spicules, which, based on the number of rays (actines) are distinguished in diactines, triactines and tetractines. Each actine is formed by only two cells, called sclerocytes. Little is known about biomineralization proteins in calcareous sponges, other than that specific carbonic anhydrases (CAs) have been identified, and that uncharacterized Asx-rich proteins have been isolated from calcitic spicules. By RNA-Seq and RNA in situ hybridization (ISH), we identified five additional biomineralization genes in Sycon ciliatum: two bicarbonate transporters (BCTs) and three Asx-rich extracellular matrix proteins (ARPs). We show that these biomineralization genes are expressed in a coordinated pattern during spicule formation. Furthermore, two of the ARPs are spicule-type specific for triactines and tetractines (ARP1 or SciTriactinin) or diactines (ARP2 or SciDiactinin). Our results suggest that spicule formation is controlled by defined temporal and spatial expression of spicule-type specific sets of biomineralization genes. |
format | Online Article Text |
id | pubmed-5390275 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-53902752017-04-14 Spicule formation in calcareous sponges: Coordinated expression of biomineralization genes and spicule-type specific genes Voigt, Oliver Adamska, Maja Adamski, Marcin Kittelmann, André Wencker, Lukardis Wörheide, Gert Sci Rep Article The ability to form mineral structures under biological control is widespread among animals. In several species, specific proteins have been shown to be involved in biomineralization, but it is uncertain how they influence the shape of the growing biomineral and the resulting skeleton. Calcareous sponges are the only sponges that form calcitic spicules, which, based on the number of rays (actines) are distinguished in diactines, triactines and tetractines. Each actine is formed by only two cells, called sclerocytes. Little is known about biomineralization proteins in calcareous sponges, other than that specific carbonic anhydrases (CAs) have been identified, and that uncharacterized Asx-rich proteins have been isolated from calcitic spicules. By RNA-Seq and RNA in situ hybridization (ISH), we identified five additional biomineralization genes in Sycon ciliatum: two bicarbonate transporters (BCTs) and three Asx-rich extracellular matrix proteins (ARPs). We show that these biomineralization genes are expressed in a coordinated pattern during spicule formation. Furthermore, two of the ARPs are spicule-type specific for triactines and tetractines (ARP1 or SciTriactinin) or diactines (ARP2 or SciDiactinin). Our results suggest that spicule formation is controlled by defined temporal and spatial expression of spicule-type specific sets of biomineralization genes. Nature Publishing Group 2017-04-13 /pmc/articles/PMC5390275/ /pubmed/28406140 http://dx.doi.org/10.1038/srep45658 Text en Copyright © 2017, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Voigt, Oliver Adamska, Maja Adamski, Marcin Kittelmann, André Wencker, Lukardis Wörheide, Gert Spicule formation in calcareous sponges: Coordinated expression of biomineralization genes and spicule-type specific genes |
title | Spicule formation in calcareous sponges: Coordinated expression of biomineralization genes and spicule-type specific genes |
title_full | Spicule formation in calcareous sponges: Coordinated expression of biomineralization genes and spicule-type specific genes |
title_fullStr | Spicule formation in calcareous sponges: Coordinated expression of biomineralization genes and spicule-type specific genes |
title_full_unstemmed | Spicule formation in calcareous sponges: Coordinated expression of biomineralization genes and spicule-type specific genes |
title_short | Spicule formation in calcareous sponges: Coordinated expression of biomineralization genes and spicule-type specific genes |
title_sort | spicule formation in calcareous sponges: coordinated expression of biomineralization genes and spicule-type specific genes |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5390275/ https://www.ncbi.nlm.nih.gov/pubmed/28406140 http://dx.doi.org/10.1038/srep45658 |
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