Institute for Organic Chemistry and Chemical Biology, Center for Biomolecular Magnetic Resonance (BMRZ), Johann Wolfgang Goethe University, Max-von-Laue-Str. 7, 60438, Frankfurt/Main, Germany.
Chembiochem. 2022 Apr 5;23(7):e202200022. doi: 10.1002/cbic.202200022. Epub 2022 Feb 15.
During evolution of an RNA world, the development of enzymatic function was essential. Such enzymatic function was linked to RNA sequences capable of adopting specific RNA folds that possess catalytic pockets to promote catalysis. Within this primordial RNA world, initially evolved self-replicating ribozymes presumably mutated to ribozymes with new functions. Schultes and Bartel (Science 2000, 289, 448-452) investigated such conversion from one ribozyme to a new ribozyme with distinctly different catalytic functions. Within a neutral network that linked these two prototype ribozymes, a single RNA chain could be identified that exhibited both enzymatic functions. As commented by Schultes and Bartel, this system possessing one sequence with two enzymatic functions serves as a paradigm for an evolutionary system that allows neutral drifts by stepwise mutation from one ribozyme into a different ribozyme without loss of intermittent function. Here, we investigated this complex functional diversification of ancestral ribozymes by analyzing several RNA sequences within this neutral network between two ribozymes with class III ligase activity and with self-cleavage reactivity. We utilized rapid RNA sample preparation for NMR spectroscopic studies together with SHAPE analysis and in-line probing to characterize secondary structure changes within the neutral network. Our investigations allowed delineation of the secondary structure space and by comparison with the previously determined catalytic function allowed correlation of the structure-function relation of ribozyme function in this neutral network.
在 RNA 世界的进化过程中,酶功能的发展是必不可少的。这种酶功能与能够采用特定 RNA 折叠的 RNA 序列相关联,这些折叠具有催化口袋以促进催化。在这个原始的 RNA 世界中,最初进化的自我复制核酶可能突变为具有新功能的核酶。Schultes 和 Bartel(Science 2000, 289, 448-452)研究了从一种核酶到具有明显不同催化功能的新核酶的这种转换。在连接这两种原型核酶的中性网络中,可以鉴定出一条具有两种酶功能的单一 RNA 链。正如 Schultes 和 Bartel 所评论的那样,这个具有一个序列两种酶功能的系统为进化系统提供了一个范例,允许通过逐步突变从一种核酶到另一种核酶而不会失去间歇功能的中性漂移。在这里,我们通过分析具有 III 类连接酶活性和自我切割反应性的两种核酶之间的中性网络中的几个 RNA 序列,研究了祖先核酶的这种复杂功能多样化。我们利用快速 RNA 样品制备进行 NMR 光谱研究,以及 SHAPE 分析和在线探测,以表征中性网络内的二级结构变化。我们的研究允许描绘二级结构空间,并通过与先前确定的催化功能进行比较,允许在这个中性网络中关联核酶功能的结构-功能关系。