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首页> 外文期刊>BMC Evolutionary Biology >A phylogenetic survey of myotubularin genes of eukaryotes: distribution, protein structure, evolution, and gene expression
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A phylogenetic survey of myotubularin genes of eukaryotes: distribution, protein structure, evolution, and gene expression

机译:真核生物肌管蛋白基因的系统发育调查:分布,蛋白质结构,进化和基因表达

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Background Phosphorylated phosphatidylinositol (PtdIns) lipids, produced and modified by PtdIns kinases and phosphatases, are critical to the regulation of diverse cellular functions. The myotubularin PtdIns-phosphate phosphatases have been well characterized in yeast and especially animals, where multiple isoforms, both catalytically active and inactive, occur. Myotubularin mutations bring about disruption of cellular membrane trafficking, and in humans, disease. Previous studies have suggested that myotubularins are widely distributed amongst eukaryotes, but key evolutionary questions concerning the origin of different myotubularin isoforms remain unanswered, and little is known about the function of these proteins in most organisms. Results We have identified 80 myotubularin homologues amidst the completely sequenced genomes of 30 organisms spanning four eukaryotic supergroups. We have mapped domain architecture, and inferred evolutionary histories. We have documented an expansion in the Amoebozoa of a family of inactive myotubularins with a novel domain architecture, which we dub "IMLRK" (inactive myotubularin/LRR/ROCO/kinase). There is an especially large myotubularin gene family in the pathogen Entamoeba histolytica, the majority of them IMLRK proteins. We have analyzed published patterns of gene expression in this organism which indicate that myotubularins may be important to critical life cycle stage transitions and host infection. Conclusions This study presents an overall framework of eukaryotic myotubularin gene evolution. Inactive myotubularin homologues with distinct domain architectures appear to have arisen on three separate occasions in different eukaryotic lineages. The large and distinctive set of myotubularin genes found in an important pathogen species suggest that in this organism myotubularins might present important new targets for basic research and perhaps novel therapeutic strategies.
机译:背景技术由PtdIns激酶和磷酸酶产生和修饰的磷酸化磷脂酰肌醇(PtdIns)脂质对于调节多种细胞功能至关重要。肌管蛋白PtdIns-磷酸磷酸酶已在酵母中,尤其是动物中得到了很好的表征,在动物中会出现多种具有催化活性和无活性的同工型。肌管蛋白突变引起细胞膜运输的破坏,并在人类中引起疾病​​。先前的研究表明,肌微管蛋白广泛分布于真核生物中,但是关于不同肌微管蛋白同工型起源的关键进化问题仍未得到解答,而且这些蛋白在大多数生物中的功能知之甚少。结果我们在跨越四个真核超群的30种生物的完整测序基因组中鉴定出80个肌微管蛋白同源物。我们已经映射了领域架构,并推断了进化历史。我们已经记录了一种具有新型结构域结构的无活性肌管蛋白家族的变形虫的扩展,我们将其命名为“ IMLRK”(无活性肌管蛋白/ LRR / ROCO /激酶)。在致病性变形杆菌中有一个特别大的肌微管蛋白基因家族,其中大多数是IMMLK蛋白。我们已经分析了这种生物中基因表达的公开模式,这表明肌微管蛋白可能对生命周期的关键阶段转变和宿主感染很重要。结论本研究提供了真核肌微管蛋白基因进化的总体框架。具有不同结构域结构的无活性肌管蛋白同源物似乎在不同的真核细胞谱系中的三种不同情况下出现。在重要病原体物种中发现的大量独特的肌管蛋白基因集表明,在这种生物体中,肌管蛋白可能为基础研究和新的治疗策略提供重要的新靶点。

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