4.2 Article

The skeletome of the red coral Corallium rubrum indicates an independent evolution of biomineralization process in octocorals

期刊

BMC ECOLOGY AND EVOLUTION
卷 21, 期 1, 页码 -

出版社

BMC
DOI: 10.1186/s12862-020-01734-0

关键词

Corallium rubrum; Biomineralization; Axial skeleton; Sclerites; Organic matrix; Proteomics; Evolution

资金

  1. Centre Scientifique de Monaco (Government of Principality of Monaco) [500/685229]
  2. Centre Scientifique de Monaco research program - Government of Principality of Monaco
  3. Fondation Paul HAMEL

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The study examined the organic matrix composition of the red coral axial skeleton and sclerites, revealing that the difference between the two biominerals is due to the modeling of the matrix network rather than specific structural components. The red coral organic matrix contains a high proportion of collagen-like proteins and proteins with sugar-binding domains.
BackgroundThe process of calcium carbonate biomineralization has arisen multiple times during metazoan evolution. In the phylum Cnidaria, biomineralization has mostly been studied in the subclass Hexacorallia (i.e. stony corals) in comparison to the subclass Octocorallia (i.e. red corals); the two diverged approximately 600 million years ago. The precious Mediterranean red coral, Corallium rubrum, is an octocorallian species, which produces two distinct high-magnesium calcite biominerals, the axial skeleton and the sclerites. In order to gain insight into the red coral biomineralization process and cnidarian biomineralization evolution, we studied the protein repertoire forming the organic matrix (OM) of its two biominerals.ResultsWe combined High-Resolution Mass Spectrometry and transcriptome analysis to study the OM composition of the axial skeleton and the sclerites. We identified a total of 102 OM proteins, 52 are found in the two red coral biominerals with scleritin being the most abundant protein in each fraction. Contrary to reef building corals, the red coral organic matrix possesses a large number of collagen-like proteins. Agrin-like glycoproteins and proteins with sugar-binding domains are also predominant. Twenty-seven and 23 proteins were uniquely assigned to the axial skeleton and the sclerites, respectively. The inferred regulatory function of these OM proteins suggests that the difference between the two biominerals is due to the modeling of the matrix network, rather than the presence of specific structural components. At least one OM component could have been horizontally transferred from prokaryotes early during Octocorallia evolution.ConclusionOur results suggest that calcification of the red coral axial skeleton likely represents a secondary calcification of an ancestral gorgonian horny axis. In addition, the comparison with stony coral skeletomes highlighted the low proportion of similar proteins between the biomineral OMs of hexacorallian and octocorallian corals, suggesting an independent acquisition of calcification in anthozoans.

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