Rison Stuart C G, Thornton Janet M
Department of Biochemistry and Molecular Biology, University College London, Darwin Building, Gower Street, London WC1E 6BT, UK.
Curr Opin Struct Biol. 2002 Jun;12(3):374-82. doi: 10.1016/s0959-440x(02)00331-7.
Small-molecule metabolism forms the core of the metabolic processes of all living organisms. As early as 1945, possible mechanisms for the evolution of such a complex metabolic system were considered. The problem is to explain the appearance and development of a highly regulated complex network of interacting proteins and substrates from a limited structural and functional repertoire. By permitting the co-analysis of phylogeny and metabolism, the combined exploitation of pathway and structural databases, as well as the use of multiple-sequence alignment search algorithms, sheds light on this problem. Much of the current research suggests a chemistry-driven 'patchwork' model of pathway evolution, but other mechanisms may play a role. In the future, as metabolic structure and sequence space are further explored, it should become easier to trace the finer details of pathway development and understand how complexity has evolved.
小分子代谢构成了所有生物体代谢过程的核心。早在1945年,人们就开始思考这种复杂代谢系统的进化可能机制。问题在于如何从有限的结构和功能组成中解释一个由相互作用的蛋白质和底物构成的高度调控的复杂网络的出现和发展。通过允许对系统发育和代谢进行联合分析,综合利用途径和结构数据库,以及使用多序列比对搜索算法,为这个问题提供了线索。当前的许多研究表明了一种由化学驱动的途径进化“拼凑”模型,但其他机制可能也发挥了作用。未来,随着代谢结构和序列空间的进一步探索,追踪途径发展的更细微细节以及理解复杂性是如何进化的应该会变得更容易。