NSF/NASA Center for Chemical Evolution, Georgia Institute of Technology, Atlanta, Georgia, United States of America.
PLoS One. 2012;7(4):e34166. doi: 10.1371/journal.pone.0034166. Epub 2012 Apr 6.
Many models for the origin of life have focused on understanding how evolution can drive the refinement of a preexisting enzyme, such as the evolution of efficient replicase activity. Here we present a model for what was, arguably, an even earlier stage of chemical evolution, when polymer sequence diversity was generated and sustained before, and during, the onset of functional selection. The model includes regular environmental cycles (e.g. hydration-dehydration cycles) that drive polymers between times of replication and functional activity, which coincide with times of different monomer and polymer diffusivity. Template-directed replication of informational polymers, which takes place during the dehydration stage of each cycle, is considered to be sequence-independent. New sequences are generated by spontaneous polymer formation, and all sequences compete for a finite monomer resource that is recycled via reversible polymerization. Kinetic Monte Carlo simulations demonstrate that this proposed prebiotic scenario provides a robust mechanism for the exploration of sequence space. Introduction of a polymer sequence with monomer synthetase activity illustrates that functional sequences can become established in a preexisting pool of otherwise non-functional sequences. Functional selection does not dominate system dynamics and sequence diversity remains high, permitting the emergence and spread of more than one functional sequence. It is also observed that polymers spontaneously form clusters in simulations where polymers diffuse more slowly than monomers, a feature that is reminiscent of a previous proposal that the earliest stages of life could have been defined by the collective evolution of a system-wide cooperation of polymer aggregates. Overall, the results presented demonstrate the merits of considering plausible prebiotic polymer chemistries and environments that would have allowed for the rapid turnover of monomer resources and for regularly varying monomer/polymer diffusivities.
许多生命起源模型都集中于理解进化如何能够改进预先存在的酶,例如提高复制酶的效率。在这里,我们提出了一个模型,用于解释化学进化更早的阶段,即功能选择之前和期间聚合物序列多样性的产生和维持。该模型包括周期性的环境变化(例如水合-去水合循环),这些变化促使聚合物在复制和功能活动之间转换,与单体和聚合物扩散率不同的时期相吻合。模板指导的信息聚合物复制发生在每个循环的去水合阶段,被认为是序列无关的。新序列通过聚合物的自发形成产生,所有序列竞争有限的单体资源,该资源通过可逆聚合进行回收。动力学蒙特卡罗模拟表明,这种拟议的前生物情景为探索序列空间提供了一个稳健的机制。引入具有单体合成酶活性的聚合物序列说明了功能序列可以在预先存在的非功能序列池中建立。功能选择并不主导系统动态,序列多样性仍然很高,允许一个以上的功能序列出现和传播。还观察到,在聚合物扩散速度比单体慢的模拟中,聚合物会自发形成团簇,这一特征让人联想到先前的一个提议,即生命的最早阶段可以通过聚合物聚集体的系统级合作的集体进化来定义。总的来说,所呈现的结果表明,考虑合理的前生物聚合物化学和环境是值得的,这些环境可以允许单体资源的快速转换,以及单体/聚合物扩散率的定期变化。