Department of Physical Sciences, Indian Institute of Science Education and Research Kolkata, Mohanpur-741246, India.
Proc Biol Sci. 2021 Nov 24;288(1963):20212098. doi: 10.1098/rspb.2021.2098. Epub 2021 Nov 17.
The encapsulation of genetic material inside compartments together with the creation and sustenance of functionally diverse internal components are likely to have been key steps in the formation of 'live', replicating protocells in an RNA world. Several experiments have shown that RNA encapsulated inside lipid vesicles can lead to vesicular growth and division through physical processes alone. Replication of RNA inside such vesicles can produce a large number of RNA strands. Yet, the impact of such replication processes on the emergence of the first ribozymes inside such protocells and on the subsequent evolution of the protocell population remains an open question. In this paper, we present a model for the evolution of protocells with functionally diverse ribozymes. Distinct ribozymes can be created with small probabilities during the error-prone RNA replication process via the rolling circle mechanism. We identify the conditions that can synergistically enhance the number of different ribozymes inside a protocell and allow functionally diverse protocells containing multiple ribozymes to dominate the population. Our work demonstrates the existence of an effective pathway towards increasing complexity of protocells that might have eventually led to the origin of life in an RNA world.
将遗传物质包裹在隔室中,同时创造和维持功能多样的内部组件,这可能是在 RNA 世界中形成“有生命”、复制原细胞的关键步骤。几项实验表明,包裹在脂质泡中的 RNA 仅通过物理过程就可以导致泡囊的生长和分裂。在这种泡囊中复制 RNA 可以产生大量的 RNA 链。然而,这种复制过程对第一批核酶在原细胞中的出现以及随后原细胞群体的进化的影响仍然是一个悬而未决的问题。在本文中,我们提出了一个具有功能多样核酶的原细胞进化模型。在易错的 RNA 复制过程中,通过滚环机制,可以以小概率产生不同的核酶。我们确定了可以协同增强原细胞内不同核酶数量的条件,并允许含有多个核酶的功能多样的原细胞主导群体。我们的工作证明了一种能够提高原细胞复杂性的有效途径,这种途径可能最终导致了 RNA 世界中生命的起源。