Dale Trevor
Cardiff School of Bioscience, Cardiff University, Museum Avenue, Cardiff, CF10 3US.
J Theor Biol. 2006 Jun 7;240(3):337-42. doi: 10.1016/j.jtbi.2005.09.027. Epub 2005 Nov 14.
The ability of RNA to both replicate and carry out enzymic functions has led to the proposal that an 'RNA-world' preceded the emergence of protein function in pre-biotic evolution. This order of function requires a key transition in which replicating RNA-molecules 'breakout' and recruit protein function. Here I propose a mechanism for the co-evolution of protein and nucleic acids as replicating entities from the earliest stages of pre-biotic development. In the model, amyloid protein fibres provide a protective support and compartment for nucleic acids. In turn, replicating nucleic acids stimulate fibre growth at amyloid free ends. Nucleic acid-amyloid fibre combinations are proposed to lengthen and then break through hydrostatic shear, exposing new amyloid free ends. This process would distribute stable replicating complexes throughout the primordial environment. The model provides a route into the RNA-protein world without the need for a distinct 'breakout' transition.
RNA既能进行复制又能执行酶功能,这使得人们提出在生命起源前的进化过程中,在蛋白质功能出现之前存在一个“RNA世界”。这种功能顺序需要一个关键转变,即复制性RNA分子“突破”并招募蛋白质功能。在此,我提出一种从生命起源前发展的最早阶段起,蛋白质和核酸作为复制实体共同进化的机制。在该模型中,淀粉样蛋白纤维为核酸提供保护性支持和分隔空间。反过来,复制性核酸会刺激淀粉样纤维在其自由端生长。核酸 - 淀粉样纤维组合会延长,然后通过流体静力学剪切力断裂,暴露出新的淀粉样自由端。这一过程将在原始环境中分布稳定的复制复合物。该模型提供了一条进入RNA - 蛋白质世界的途径,而无需一个明显的“突破”转变。