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核酶诱变进化:生存机制。

Ribozyme Mutagenic Evolution: Mechanisms of Survival.

机构信息

Okinawa Institute of Science and Technology Graduate University (OIST), Okinawa Prefecture, Japan.

Yale University, New Haven, CT, USA.

出版信息

Orig Life Evol Biosph. 2021 Dec;51(4):321-339. doi: 10.1007/s11084-021-09617-0. Epub 2022 Jan 7.

Abstract

Primeval populations replicating at high error rates required a mechanism to overcome the accumulation of mutations and information deterioration. Known strategies to overcome mutation pressures include RNA processivity, epistasis, selection, and quasispecies. We investigated the mechanism by which small molecular ribozyme populations can survive under high error rates by propagating several lineages under different mutagen concentrations. We found that every population that evolved without mutagen went extinct, while those subjected to mutagenic evolution survived. To understand how they survived, we characterized the evolved genotypic diversity, the formation of genotype-genotype interaction networks, the fitness of the most common mutants for each enzymatic step, and changes in population size along the course of evolution. We found that the elevated mutation rate was necessary for the populations to survive in the novel environment, in which all the steps of the metabolism worked to promote the survival of even less catalytically efficient ligases. Besides, an increase in population size and the mutational coupling of genotypes in close-knit networks, which helped maintain or recover lost genotypes making their disappearance transient, prevented Muller's ratchet and extinction.

摘要

原始种群以高错误率进行复制,这就需要一种机制来克服突变的积累和信息的恶化。已知的克服突变压力的策略包括 RNA 延续性、上位性、选择和准种。我们通过在不同诱变浓度下繁殖多个谱系,研究了小分子核酶种群如何在高错误率下生存的机制。我们发现,没有诱变进化的每个种群都灭绝了,而经历诱变进化的种群则存活下来。为了了解它们是如何存活的,我们描述了进化产生的基因型多样性、基因型-基因型相互作用网络的形成、每个酶步骤中最常见突变体的适应性以及进化过程中种群大小的变化。我们发现,提高突变率对于种群在新环境中生存是必要的,在这种环境中,新陈代谢的所有步骤都有助于促进即使催化效率较低的连接酶的生存。此外,种群大小的增加和紧密网络中基因型的突变耦合有助于维持或恢复丢失的基因型,使它们的消失暂时化,从而防止了 Muller 的棘轮和灭绝。

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