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模拟前生物网络中的突变和致死性。

Mutations and lethality in simulated prebiotic networks.

机构信息

Department of Molecular Genetics and the Crown Human Genome Center, Weizmann Institute of Science, Rehovot, 76100, Israel.

出版信息

J Mol Evol. 2009 Nov;69(5):568-78. doi: 10.1007/s00239-009-9281-y. Epub 2009 Sep 29.

Abstract

The Graded Autocatalysis Replication Domain (GARD) model describes an origin of life scenario which involves non-covalent compositional assemblies, made of monomeric mutually catalytic molecules. GARD constitutes an alternative to informational biopolymers as a mechanism of primordial inheritance. In the present work, we examined the effect of mutations, one of the most fundamental mechanisms for evolution, in the context of the networks of mutual interaction within GARD prebiotic assemblies. We performed a systematic analysis analogous to single and double gene deletions within GARD. While most deletions have only a small effect on both growth rate and molecular composition of the assemblies, ~10% of the deletions caused lethality, or sometimes showed enhanced fitness. Analysis of 14 different network properties on 2,000 different GARD networks indicated that lethality usually takes place when the deleted node has a high molecular count, or when it is a catalyst for such node. A correlation was also found between lethality and node degree centrality, similar to what is seen in real biological networks. Addressing double knockout mutations, our results demonstrate the occurrence of both synthetic lethality and extragenic suppression within GARD networks, and convey an attempt to correlate synthetic lethality to network node-pair properties. The analyses presented help establish GARD as a workable alternative prebiotic scenario, suggesting that life may have begun with large molecular networks of low fidelity, that later underwent evolutionary compaction and fidelity augmentation.

摘要

分级自催化复制域 (GARD) 模型描述了一种生命起源场景,其中涉及非共价组成的组装体,由单体相互催化的分子组成。GARD 作为原始遗传的一种机制,构成了信息生物聚合物的替代方案。在本工作中,我们研究了突变的影响,突变是进化最基本的机制之一,在 GARD 前生物组装体的相互作用网络中进行了检查。我们进行了类似于 GARD 内单基因和双基因缺失的系统分析。虽然大多数缺失对组装体的生长速度和分子组成只有很小的影响,但约 10%的缺失会导致致死性,或者有时表现出增强的适应性。对 2000 个不同 GARD 网络的 14 种不同网络特性进行分析表明,当删除的节点具有高分子计数或它是该节点的催化剂时,通常会发生致死性。还发现致死性与节点度数中心度之间存在相关性,类似于真实生物网络中看到的情况。在处理双敲除突变时,我们的结果表明 GARD 网络中存在合成致死性和基因外抑制,试图将合成致死性与网络节点对特性相关联。所提出的分析有助于确立 GARD 作为可行的前生物场景替代方案,表明生命可能始于低保真度的大型分子网络,后来经历了进化的压缩和保真度的提高。

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