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A metabolic network in the evolutionary context: Multiscale structure and modularity

机译:进化背景下的代谢网络:多尺度结构和模块化

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The enormous complexity of biological networks has led to the suggestion that networks are built of modules that perform particular functions and are "reused" in evolution in a manner similar to reusable domains in protein structures or modules of electronic circuits. Analysis of known biological networks has revealed several modules, many of which have transparent biological functions. However, it remains to be shown that identified structural modules constitute evolutionary building blocks, independent and easily interchangeable units. An alternative possibility is that evolutionary modules do not match structural modules. To investigate the structure of evolutionary modules and their relationship to functional ones, we integrated a metabolic network with evolutionary associations between genes inferred from comparative genomics. The resulting metabolic-genomic network places metabolic pathways into evolutionary and genomic context, thereby revealing previously unknown components and modules. We analyzed the integrated metabolic-genomic network on three levels: macro-, meso-, and microscale. The macroscale level demonstrates strong associations between neighboring enzymes and between enzymes that are distant on the network but belong to the same linear pathway. At the mesoscale level, we identified evolutionary metabolic modules and compared them with traditional metabolic pathways. Although, in some cases, there is almost exact correspondence, some pathways are split into independent modules. On the microscale level, we observed high association of enzyme subunits and weak association of isoen-zymes independently catalyzing the same reaction. This study shows that evolutionary modules, rather than pathways, may be thought of as regulatory and functional units in bacterial genomes.
机译:生物网络的巨大复杂性导致人们提出这样的建议:网络由执行特定功能的模块构成,并且在进化中以与蛋白质结构或电子电路模块中的可重用域相似的方式被“重用”。对已知生物网络的分析揭示了几个模块,其中许多模块具有透明的生物学功能。但是,仍然有待证明的是,确定的结构模块构成了进化的构建基块,是独立且易于互换的单元。另一种可能性是,进化模块与结构模块不匹配。为了研究进化模块的结构及其与功能模块的关系,我们将代谢网络与根据比较基因组学推断的基因之间的进化关联进行了整合。产生的代谢基因组网络将代谢途径置于进化和基因组环境中,从而揭示了以前未知的成分和模块。我们在三个层次上分析了整合的代谢基因组网络:宏观,中观和微观。宏观水平证明了相邻酶之间以及网络上相距遥远但属于同一线性途径的酶之间的强关联。在中尺度水平,我们确定了进化代谢模块,并将其与传统代谢途径进行了比较。尽管在某些情况下几乎存在精确的对应关系,但某些途径会分成独立的模块。在微观水平上,我们观察到酶亚基的高缔合和同工酶的弱缔合独立地催化相同的反应。这项研究表明,进化模块而不是途径可以被认为是细菌基因组中的调节和功能单元。

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