Lambert Camille N, Opuu Vaitea, Calvanese Francesco, Pavlinova Polina, Zamponi Francesco, Hayden Eric J, Weigt Martin, Smerlak Matteo, Nghe Philippe
Laboratoire de Biophysique et Evolution, UMR CNRS-ESPCI 8231 Chimie Biologie Innovation, ESPCI Paris, Université PSL, Paris, France.
Max Planck Institute for Mathematics in the Sciences, Leipzig, Germany.
Nat Commun. 2025 Aug 22;16(1):7836. doi: 10.1038/s41467-025-63151-5.
Estimating the plausibility of RNA self-reproduction is central to origin-of-life scenarios. However, this property has been shown in only a handful of catalytic RNAs. Here, we compare models for their generative power in diversifying a reference ribozyme, based on statistical covariation and secondary structure prediction, and experimentally test model predictions using high-throughput sequencing. Leveraging statistical physics methods, we compute the number of ribozymes capable of autocatalytic self-reproduction from oligonucleotide fragments to be over 10, with sequences found up to 65 mutations from the original sequence and 99 mutations away from each other, far beyond the 10 mutations achieved by deep mutational scanning. The findings demonstrate an efficient method for exploring RNA sequence space, and provide quantitative data on self-reproducing RNA that further illuminates the potential pathways to abiogenesis.
评估RNA自我复制的合理性是生命起源假说的核心。然而,只有少数催化RNA具备这种特性。在此,我们基于统计协变和二级结构预测,比较了用于使参考核酶多样化的生成能力模型,并使用高通量测序对模型预测进行了实验验证。利用统计物理方法,我们计算出能够从寡核苷酸片段进行自催化自我复制的核酶数量超过10个,其序列与原始序列的差异多达65个突变,彼此之间的差异多达99个突变,远远超过深度突变扫描所达到的10个突变。这些发现展示了一种探索RNA序列空间的有效方法,并提供了关于自我复制RNA的定量数据,进一步阐明了无生源说的潜在途径。