Schiller Martin R
Nevada Institute of Personalized Medicine and School of Life Sciences, University of Nevada, Las Vegas, Nevada, USA.
J Transl Sci. 2016;2(5):289-296. doi: 10.15761/JTS.1000154. Epub 2016 Jul 19.
Several theories for the origin of life have gained widespread acceptance, led by primordial soup, chemical evolution, metabolism first, and the RNA world. However, while new and existing theories often address a key step, there is less focus on a comprehensive abiogenic continuum leading to the last universal common ancestor. Herein, I present the "minimotif synthesis" hypothesis unifying select origin of life theories with new and revised steps. The hypothesis is based on first principles, on the concept of selection over long time scales, and on a stepwise progression toward complexity. The major steps are the thermodynamically-driven origination of extant molecular specificity emerging from primordial soup leading to the rise of peptide catalysts, and a cyclic feed-forward catalytic diversification of compound and peptides in the primordial soup. This is followed by degenerate, semi-partially conservative peptide replication to pass on catalytic knowledge to progeny protocells. At some point during this progression, the emergence of RNA and selection could drive the separation of catalytic and genetic functions, allowing peptides and proteins to permeate the catalytic space, and RNA to encode higher fidelity information transfer. Translation may have emerged from RNA template driven organization and successive ligation of activated amino acids as a predecessor to translation.
几种关于生命起源的理论已得到广泛认可,其中以原始汤、化学进化、新陈代谢优先以及RNA世界为主导。然而,尽管新理论和现有理论常常涉及关键步骤,但对于通向最后共同祖先的全面非生物连续过程的关注较少。在此,我提出“最小基序合成”假说,将选定的生命起源理论与新的及修订的步骤统一起来。该假说基于第一原理、长期选择的概念以及向复杂性的逐步演进。主要步骤包括从原始汤中通过热力学驱动产生现存分子特异性从而导致肽催化剂的出现,以及原始汤中化合物和肽的循环前馈催化多样化。随后是简并的、半部分保守的肽复制,以将催化知识传递给后代原始细胞。在这一进程中的某个时刻,RNA的出现和选择可能推动催化功能与遗传功能的分离,使肽和蛋白质能够渗透到催化空间,而RNA能够编码更高保真度的信息传递。翻译可能源于RNA模板驱动的活化氨基酸的组织和连续连接,作为翻译的前身。