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非生物自我复制。

Abiotic self-replication.

机构信息

Institute for Cellular and Molecular Biology, University of Texas at Austin, Austin, Texas 78712, USA.

出版信息

Acc Chem Res. 2012 Dec 18;45(12):2097-105. doi: 10.1021/ar200325v. Epub 2012 Aug 15.

Abstract

The key to the origins of life is the replication of information. Linear polymers such as nucleic acids that both carry information and can be replicated are currently what we consider to be the basis of living systems. However, these two properties are not necessarily coupled. The ability to mutate in a discrete or quantized way, without frequent reversion, may be an additional requirement for Darwinian evolution, in which case the notion that Darwinian evolution defines life may be less of a tautology than previously thought. In this Account, we examine a variety of in vitro systems of increasing complexity, from simple chemical replicators up to complex systems based on in vitro transcription and translation. Comparing and contrasting these systems provides an interesting window onto the molecular origins of life. For nucleic acids, the story likely begins with simple chemical replication, perhaps of the form A + B → T, in which T serves as a template for the joining of A and B. Molecular variants capable of faster replication would come to dominate a population, and the development of cycles in which templates could foster one another's replication would have led to increasingly complex replicators and from thence to the initial genomes. The initial genomes may have been propagated by RNA replicases, ribozymes capable of joining oligonucleotides and eventually polymerizing mononucleotide substrates. As ribozymes were added to the genome to fill gaps in the chemistry necessary for replication, the backbone of a putative RNA world would have emerged. It is likely that such replicators would have been plagued by molecular parasites, which would have been passively replicated by the RNA world machinery without contributing to it. These molecular parasites would have been a major driver for the development of compartmentalization/cellularization, as more robust compartments could have outcompeted parasite-ridden compartments. The eventual outsourcing of metabolic functions (including the replication of nucleic acids) to more competent protein enzymes would complete the journey from an abiotic world to the molecular biology we see today.

摘要

生命起源的关键是信息的复制。线性聚合物,如既携带信息又可复制的核酸,目前被认为是生命系统的基础。然而,这两个特性不一定是耦合的。以离散或量子化的方式突变,而不是频繁回复的能力,可能是达尔文进化的另一个要求,在这种情况下,达尔文进化定义生命的概念可能比以前认为的不那么自相矛盾。在本报告中,我们检查了各种越来越复杂的体外系统,从简单的化学复制子到基于体外转录和翻译的复杂系统。比较和对比这些系统为生命的分子起源提供了一个有趣的视角。对于核酸,这个故事可能始于简单的化学复制,也许是 A + B → T 的形式,其中 T 作为 A 和 B 连接的模板。能够更快复制的分子变体将在种群中占据主导地位,而模板可以促进彼此复制的循环的发展将导致越来越复杂的复制子,并由此产生最初的基因组。最初的基因组可能是由 RNA 复制酶传播的,RNA 复制酶能够连接寡核苷酸并最终聚合单核苷酸底物。随着核酶被添加到基因组中以填补复制所需的化学物质的空白,假设的 RNA 世界的骨架就会出现。这样的复制子很可能会受到分子寄生虫的困扰,这些寄生虫会被 RNA 世界的机器被动复制,而不会对其做出贡献。这些分子寄生虫将是分隔/细胞化发展的主要驱动力,因为更强大的隔室可以竞争过寄生虫丛生的隔室。最终将代谢功能(包括核酸的复制)外包给更有能力的蛋白质酶,将完成从无生命世界到我们今天看到的分子生物学的旅程。

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