Luo Yufan, Liang Minglun, Yu Chunwu, Ma Wentao
Hubei Key Laboratory of Cell Homeostasis, College of Life Sciences, Wuhan University, Wuhan, China.
College of Computer Sciences, Wuhan University, Wuhan, China.
RNA Biol. 2024 Jan;21(1):17-31. doi: 10.1080/15476286.2024.2380130. Epub 2024 Jul 17.
It is likely that an RNA world existed in early life, when RNA played both the roles of the genome and functional molecules, thereby undergoing Darwinian evolution. However, even with only one type of polymer, it seems quite necessary to introduce a labour division concerning these two roles because folding is required for functional molecules (ribozymes) but unfavourable for the genome (as a template in replication). Notably, while ribozymes tend to have adopted a linear form for folding without constraints, a circular form, which might have been topologically hindered in folding, seems more suitable for an RNA template. Another advantage of involving a circular genome could have been to resist RNA's end-degradation. Here, we explore the scenario of a circular RNA genome plus linear ribozyme(s) at the precellular stage of the RNA world through computer modelling. The results suggest that a one-gene scene could have been 'maintained', albeit with rather a low efficiency for the circular genome to produce the ribozyme, which required precise chain-break or chain-synthesis. This strict requirement may have been relieved by introducing a 'noncoding' sequence into the genome, which had the potential to derive a second gene through mutation. A two-gene scene may have 'run well' with the two corresponding ribozymes promoting the replication of the circular genome from different respects. Circular genomes with more genes might have arisen later in RNA-based protocells. Therefore, circular genomes, which are common in the modern living world, may have had their 'root' at the very beginning of life.
在生命早期可能存在一个RNA世界,当时RNA同时扮演基因组和功能分子的角色,从而经历达尔文式进化。然而,即使只有一种聚合物,由于功能分子(核酶)的折叠是必需的,但对基因组(作为复制模板)却是不利的,因此在这两种角色之间引入分工似乎是非常必要的。值得注意的是,虽然核酶倾向于采用无限制折叠的线性形式,但一种在折叠时可能受到拓扑阻碍的环状形式似乎更适合作为RNA模板。引入环状基因组的另一个好处可能是抵抗RNA的末端降解。在这里,我们通过计算机建模探索RNA世界细胞前阶段环状RNA基因组加线性核酶的情况。结果表明,单基因情况可能得以“维持”,尽管环状基因组产生核酶的效率相当低,这需要精确的链断裂或链合成。通过在基因组中引入一个“非编码”序列,这种严格要求可能得到缓解,该序列有可能通过突变衍生出第二个基因。双基因情况可能会“良好运行”,两个相应的核酶从不同方面促进环状基因组的复制。具有更多基因的环状基因组可能在基于RNA的原始细胞后期出现。因此,在现代生物界很常见的环状基因组可能在生命最初就有其“根源”。