Boza Gergely, Szilágyi András, Kun Ádám, Santos Mauro, Szathmáry Eörs
Department of Plant Systematics, Ecology and Theoretical Biology, Institute of Biology, Eötvös Loránd University, Budapest, Hungary; MTA-ELTE-MTMT Ecology Research Group, Budapest, Hungary.
Department of Plant Systematics, Ecology and Theoretical Biology, Institute of Biology, Eötvös Loránd University, Budapest, Hungary; Parmenides Center for the Conceptual Foundations of Science, Pullach, Germany; MTA-ELTE Research Group in Theoretical Biology and Evolutionary Ecology, Budapest, Hungary.
PLoS Comput Biol. 2014 Dec 4;10(12):e1003936. doi: 10.1371/journal.pcbi.1003936. eCollection 2014 Dec.
The RNA world is a very likely interim stage of the evolution after the first replicators and before the advent of the genetic code and translated proteins. Ribozymes are known to be able to catalyze many reaction types, including cofactor-aided metabolic transformations. In a metabolically complex RNA world, early division of labor between genes and enzymes could have evolved, where the ribozymes would have been transcribed from the genes more often than the other way round, benefiting the encapsulating cells through this dosage effect. Here we show, by computer simulations of protocells harboring unlinked RNA replicators, that the origin of replicational asymmetry producing more ribozymes from a gene template than gene strands from a ribozyme template is feasible and robust. Enzymatic activities of the two modeled ribozymes are in trade-off with their replication rates, and the relative replication rates compared to those of complementary strands are evolvable traits of the ribozymes. The degree of trade-off is shown to have the strongest effect in favor of the division of labor. Although some asymmetry between gene and enzymatic strands could have evolved even in earlier, surface-bound systems, the shown mechanism in protocells seems inevitable and under strong positive selection. This could have preadapted the genetic system for transcription after the subsequent origin of chromosomes and DNA.
RNA世界很可能是第一个复制子出现之后、遗传密码和翻译蛋白质出现之前进化过程中的一个过渡阶段。已知核酶能够催化多种反应类型,包括辅因子辅助的代谢转化。在一个代谢复杂的RNA世界中,基因和酶之间早期的分工可能已经进化,其中核酶从基因转录而来的频率可能比相反的情况更高,通过这种剂量效应使包封细胞受益。在这里,我们通过对含有未连接RNA复制子的原始细胞进行计算机模拟表明,从基因模板产生比从核酶模板产生更多核酶的复制不对称性的起源是可行且稳健的。所模拟的两种核酶的酶活性与其复制速率相互权衡,与互补链相比的相对复制速率是核酶的可进化特征。权衡程度显示出对分工最为有利。尽管即使在更早的表面结合系统中,基因链和酶链之间也可能进化出一些不对称性,但原始细胞中所示的机制似乎是不可避免的,并且处于强烈的正选择之下。这可能为染色体和DNA随后出现后的转录遗传系统做好了预先适应。