Radakovic Aleksandar, Todisco Marco, Mishra Anmol, Szostak Jack W
Howard Hughes Medical Institute, Department of Chemistry, University of Chicago, Chicago IL 60637, USA.
Sci Adv. 2025 Apr 4;11(14):eadu3693. doi: 10.1126/sciadv.adu3693. Epub 2025 Apr 2.
Autocatalytic reactions driving the self-assembly of biological polymers are important for the origin of life, yet few experimental examples of such reactions exist. Here we report an autocatalytic assembly pathway that generates a chimeric, amino acid-bridged aminoacyl-RNA synthetase ribozyme. The noncovalent complex of ribozyme fragments initiates low-level aminoacylation of one of the fragments, which, after loop-closing ligation, generates a highly active covalently linked chimeric ribozyme. The generation of this ribozyme is increasingly efficient over time due to the autocatalytic assembly cycle that sustains the ribozyme over indefinite cycles of serial dilution. Because of its trans activity, this ribozyme also assembles ribozymes distinct from itself, such as the hammerhead, suggesting that RNA aminoacylation, coupled with nonenzymatic ligation, could have facilitated the emergence and propagation of ribozymes.
驱动生物聚合物自组装的自催化反应对生命起源至关重要,但此类反应的实验实例却很少。在此,我们报告了一条自催化组装途径,该途径产生了一种嵌合的、氨基酸桥连的氨酰 - RNA合成酶核酶。核酶片段的非共价复合物引发其中一个片段的低水平氨酰化,在环化连接后,产生一种高活性的共价连接的嵌合核酶。由于自催化组装循环能在无限次连续稀释循环中维持核酶,随着时间推移,这种核酶的产生效率越来越高。由于其转活性,这种核酶还能组装与其自身不同的核酶,比如锤头状核酶,这表明RNA氨酰化与非酶促连接相结合,可能促进了核酶的出现和传播。