Peregrín-Alvarez José M, Sanford Chris, Parkinson John
Program in Molecular Structure and Function, Hospital for Sick Children, College Street, Toronto, ON M5G1L7, Canada.
Genome Biol. 2009;10(6):R63. doi: 10.1186/gb-2009-10-6-r63. Epub 2009 Jun 12.
Cellular metabolism is a fundamental biological system consisting of myriads of enzymatic reactions that together fulfill the basic requirements of life. The recent availability of vast amounts of sequence data from diverse sets of organisms provides an opportunity to systematically examine metabolism from a comparative perspective. Here we supplement existing genome and protein resources with partial genome datasets derived from 193 eukaryotes to present a comprehensive survey of the conservation of metabolism across 26 taxa representing the three domains of life.
In general, metabolic enzymes are highly conserved. However, organizing these enzymes within the context of functional pathways revealed a spectrum of conservation from those that are highly conserved (for example, carbohydrate, energy, amino acid and nucleotide metabolism enzymes) to those specific to individual taxa (for example, those involved in glycan metabolism and secondary metabolite pathways). Applying a novel co-conservation analysis, KEGG defined pathways did not generally display evolutionary coherence. Instead, such modularity appears restricted to smaller subsets of enzymes. Expanding analyses to a global metabolic network revealed a highly conserved, but nonetheless flexible, 'core' of enzymes largely involved in multiple reactions across different pathways. Enzymes and pathways associated with the periphery of this network were less well conserved and associated with taxon-specific innovations.
These findings point to an emerging picture in which a core of enzyme activities involving amino acid, energy, carbohydrate and lipid metabolism have evolved to provide the basic functions required for life. However, the precise complement of enzymes associated within this core for each species is flexible.
细胞代谢是一个基本的生物系统,由无数的酶促反应组成,这些反应共同满足生命的基本需求。最近从各种生物体中获得的大量序列数据,为从比较的角度系统地研究代谢提供了机会。在这里,我们用来自193种真核生物的部分基因组数据集补充现有的基因组和蛋白质资源,以全面调查代表生命三个域的26个分类群中的代谢保守性。
一般来说,代谢酶高度保守。然而,在功能途径的背景下组织这些酶,揭示了从高度保守的酶(例如,碳水化合物、能量、氨基酸和核苷酸代谢酶)到特定于单个分类群的酶(例如,参与聚糖代谢和次生代谢物途径的酶)的一系列保守性。应用一种新的共保守分析,KEGG定义的途径一般不显示进化连贯性。相反,这种模块化似乎仅限于较小的酶子集。将分析扩展到全球代谢网络,揭示了一个高度保守但仍具灵活性的酶“核心”,其主要参与不同途径的多种反应。与该网络外围相关的酶和途径保守性较差,且与分类群特异性创新相关。
这些发现指向了一个新出现的图景,即涉及氨基酸、能量、碳水化合物和脂质代谢的酶活性核心已经进化,以提供生命所需的基本功能。然而,每个物种在这个核心内相关酶的确切组成是灵活的。