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Comparative Proteomics of Octocoral and Scleractinian Skeletomes and the Evolution of Coral Calcification

机译:八孔和辛辛胺骨骼骨骼组的比较蛋白质组学及珊瑚钙化的演变

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摘要

Corals are the ecosystem engineers of coral reefs, one of the most biodiverse marine ecosystems. The ability of corals to form reefs depends on the precipitation of calcium carbonate (CaCO3) under biological control. However, several mechanisms underlying coral biomineralization remain elusive, for example, whether corals employ different molecular machineries to deposit different CaCO3 polymorphs (i.e., aragonite or calcite). Here, we used tandem mass spectrometry (MS/MS) to compare the proteins occluded in the skeleton of three octocoral and one scleractinian species: Tubipora musica and Sinularia cf. cruciata (calcite sclerites), the blue coral Heliopora coerulea (aragonitic skeleton), and the scleractinian aragonitic Montipora digitata. Reciprocal Blast analysis revealed extremely low overlap between aragonitic and calcitic species, while a core set of proteins is shared between octocorals producing calcite sclerites. However, the carbonic anhydrase CruCA4 is present in the skeletons of both polymorphs. Phylogenetic analysis highlighted several possible instances of protein co-option in octocorals. These include acidic proteins and scleritin, which appear to have been secondarily recruited for calcification and likely derive from proteins playing different functions. Similarities between octocorals and scleractinians included presence of a galaxin-related protein, carbonic anhydrases, and one hephaestin-like protein. Although the first two appear to have been independently recruited, the third appear to share a common origin. This work represents the first attempt to identify and compare proteins associated with coral skeleton polymorph diversity, providing several new research targets and enabling both future functional and evolutionary studies aimed at elucidating the origin and evolution of coral biomineralization.
机译:珊瑚是珊瑚礁的生态系统工程师,是最多的生物多样性海洋生态系统之一。珊瑚形成珊瑚礁的能力取决于生物对照下碳酸钙(CaCO3)的沉淀。然而,珊瑚生物矿化的几种机制仍然是难以捉摸的,例如,珊瑚是否采用不同的分子机械沉积不同的CaCO 3多晶型物(即,化身或方解石)。在这里,我们使用串联质谱(MS / MS)将蛋白质与三个八封型和一种硬溶液物种的骨架中堵塞:Tubipora Musica和Sinularia CF. Cruciata(Calcite Sclerites),蓝珊瑚Heliopora coerulea(金属神经内骨架)和巩膜外神经内氏菌Montipora digitata。互易爆炸分析显示在基石和钙质物种之间的极低重叠,而核心蛋白在八陶瓷生产方解石硬质矿之间共用。然而,碳酸酐酶CRUCA4存在于两种多晶型物的骨架中。系统发育分析突出了八封装中的几种可能的蛋白质共选项实例。这些包括酸性蛋白质和硬质素,其似乎已经归因于钙化并且可能导致蛋白质发挥不同功能的蛋白质。八陶瓷和巩膜外肌肉之间的相似性包括Galaxin相关蛋白质,碳酸酐酶和一种胃蛋白样蛋白质的存在。虽然前两个似乎已被独立招募,但第三个似乎共享了共同的起源。这项工作代表了第一次试图识别和比较与珊瑚骨架多型多型多型多型多种多数相关的蛋白质,提供了几种新的研究目标,并实现了旨在阐明珊瑚生物矿化的起源和演变的未来功能和进化研究。

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