Department of Biology, University of Massachusetts Dartmouth, North Dartmouth, Massachusetts 02747, USA.
J Eukaryot Microbiol. 2010 Jan-Feb;57(1):11-8. doi: 10.1111/j.1550-7408.2009.00458.x. Epub 2009 Dec 18.
Horizontal gene transfer (HGT) and common descent interact in space and time. Because events of HGT co-occur with phylogenetic evolution, it is difficult to depict evolutionary patterns graphically. Tree-like representations of life's diversification are useful, but they ignore the significance of HGT in evolutionary history, particularly of unicellular organisms, ancestors of multicellular life. Here we integrate the reticulated-tree model, ring of life, symbiogenesis whole-organism model, and eliminative pattern pluralism to represent evolution. Using Entamoeba histolytica alcohol dehydrogenase 2 (EhADH2), a bifunctional enzyme in the glycolytic pathway of amoeba, we illustrate how EhADH2 could be the product of both horizontally acquired features from ancestral prokaryotes (i.e. aldehyde dehydrogenase [ALDH] and alcohol dehydrogenase [ADH]), and subsequent functional integration of these enzymes into EhADH2, which is now inherited by amoeba via common descent. Natural selection has driven the evolution of EhADH2 active sites, which require specific amino acids (cysteine 252 in the ALDH domain; histidine 754 in the ADH domain), iron- and NAD(+) as cofactors, and the substrates acetyl-CoA for ALDH and acetaldehyde for ADH. Alternative views invoking "common design" (i.e. the non-naturalistic emergence of major taxa independent from ancestry) to explain the interaction between horizontal and vertical evolution are unfounded.
水平基因转移(HGT)和共同祖先在时间和空间上相互作用。由于 HGT 事件与系统发育进化同时发生,因此很难以图形方式描绘进化模式。生命多样化的树状表示形式很有用,但它们忽略了 HGT 在进化历史中的重要性,特别是在单细胞生物中,这些单细胞生物是多细胞生命的祖先。在这里,我们整合了网状树模型、生命之环、共生整体生物模型和消除模式多元论来表示进化。我们使用溶组织内阿米巴醇脱氢酶 2(EhADH2),即阿米巴糖酵解途径中的双功能酶,来说明 EhADH2 如何可能是来自祖先原核生物的水平获得特征(即醛脱氢酶[ALDH]和醇脱氢酶[ADH])的产物,以及随后这些酶在 EhADH2 中的功能整合,EhADH2 现在通过共同祖先遗传给阿米巴。自然选择驱动了 EhADH2 活性位点的进化,这些活性位点需要特定的氨基酸(ALDH 结构域中的半胱氨酸 252;ADH 结构域中的组氨酸 754)、铁和 NAD(+)作为辅因子,以及 ALDH 的乙酰辅酶 A 和 ADH 的乙醛作为底物。援引“共同设计”(即主要分类群的非自然出现独立于祖先)来解释水平和垂直进化之间相互作用的替代观点是没有根据的。