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Characterization of insulin-like peptides (ILPs) in the sea urchin Strongylocentrotus purpuratus: Insights on the evolution of the insulin family

机译:海胆Strongylocentrotus purpuratusus中胰岛素样肽(ILPs)的表征:对胰岛素家族进化的见解

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The evolutionary history of the insulin-like peptides (ILPs), members of the insulin family, is still a matter of debate. Although ILPs structure and expression have been described in different metazoans, little is known about these molecules in non-chordate deuterostomes, such as the echinoderms. In order to fill this gap in the current literature, we have characterized two members of the insulin family found in the sea urchin Strongylocentrotus purpuratus genome (SpIgf1 and SpIgf2 that, after our analysis, we suggest to rename SpILP1 and SpILP2, respectively) together with their putative receptor (Spinsr). We found that SpILP1 gene structure is more similar to the cephalochordate amphioxus ILP, while the SpILP2 gene shows a completely different organization. In addition, we have revealed that SpILP1 and SpILP2 transcripts are expressed in different compartments during embryo/larva development and that the SpILP1 protein mature form differs in the egg and the larva, suggesting different biological roles. Finally, we have analyzed SpILP1 transcript and protein expression in response to different feeding regimes through real-time quantitative PCR, Western blot and immunohistochemistry methodologies, and found that its expression and localization are feeding-dependent. We discuss our findings in a comparative evolutionary perspective including data available in other animal models and provide new insights into the evolution of the insulin family molecules. In the model we put forward, the last common ancestor of all deuterostomes presented an ILP composed of the B-C-A-D-E domains, and successive lineage specific independent gene duplication events resulted in the presence of several ILPs in vertebrates and in echinoderms. (C) 2014 Elsevier Inc. All rights reserved.
机译:作为胰岛素家族成员的胰岛素样肽(ILPs)的进化历史仍是一个有争议的问题。尽管已在不同的后生动物中描述了ILPs的结构和表达,但对这些非无齿氘化吻合器(如棘皮动物)中的这些分子知之甚少。为了填补当前文献中的空白,我们对海胆Strongylocentrotus purpuratus基因组中发现的胰岛素家族的两个成员(SpIgf1和SpIgf2)进行了特征分析,在我们进行分析后,我们建议将SpILP1和SpILP2重命名为他们的推定受体(Spinsr)。我们发现SpILP1基因的结构与头孢双歧头ILP更相似,而SpILP2基因显示出完全不同的组织。此外,我们已经揭示了在胚胎/幼虫发育过程中,SpILP1和SpILP2转录本在不同的区室中表达,并且在卵和幼虫中,SpILP1蛋白的成熟形式有所不同,表明它们的生物学作用不同。最后,我们通过实时定量PCR,Western印迹和免疫组织化学方法分析了SpILP1转录本和蛋白质表达对不同饲喂方式的反应,发现其表达和定位均依赖于饲喂。我们以比较进化的观点讨论我们的发现,包括其他动物模型中可获得的数据,并提供有关胰岛素家族分子进化的新见解。在我们提出的模型中,所有氘核体的最后一个共同祖先提出了一个由B-C-A-D-E结构域组成的ILP,连续的谱系特异性独立基因复制事件导致脊椎动物和棘皮动物中存在多个ILP。 (C)2014 Elsevier Inc.保留所有权利。

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