Noda-García Lianet, Barona-Gómez Francisco
Evolution of Metabolic Diversity Laboratory; Laboratorio Nacional de Genómica para la Biodiversidad (Langebio); Cinvestav-IPN; Irapuato, México.
Mob Genet Elements. 2013 Sep 1;3(5):e26439. doi: 10.4161/mge.26439. Epub 2013 Oct 2.
Understanding the evolution of enzyme function after gene duplication has been a major goal of molecular biologists, biochemists and evolutionary biologists alike, for almost half a century. In contrast, the impact that horizontal gene transfer (HGT) has had on the evolution of enzyme specialization and the assembly of metabolic networks has just started to being investigated. Traditionally, evolutionary studies of enzymes have been limited to either the function of enzymes in vitro, or to sequence variability at the population level, where in almost all cases the starting conceptual framework embraces gene duplication as the mechanism responsible for the appearance of genetic redundancy. Very recently, we merged comparative phylogenomics, detection of selection signals, enzyme kinetics, X-ray crystallography and computational molecular dynamics, to characterize the sub-functionalization process of an amino acid biosynthetic enzyme prompted by an episode of HGT in bacteria. Some of the evolutionary implications of these functional studies, including a proposed model of enzyme specialization independent of gene duplication, are developed in this commentary.
近半个世纪以来,了解基因复制后酶功能的进化一直是分子生物学家、生物化学家和进化生物学家的主要目标。相比之下,水平基因转移(HGT)对酶特化进化和代谢网络组装的影响才刚刚开始被研究。传统上,酶的进化研究要么局限于酶在体外的功能,要么局限于群体水平的序列变异性,在几乎所有情况下,最初的概念框架都将基因复制视为导致遗传冗余出现的机制。最近,我们结合了比较系统发育基因组学、选择信号检测、酶动力学、X射线晶体学和计算分子动力学,来表征细菌中一次HGT事件引发的氨基酸生物合成酶的亚功能化过程。本评论阐述了这些功能研究的一些进化意义,包括一个独立于基因复制的酶特化模型。