Weiss Joshua L, Decker J C, Bolano Ariadna, Krahn Natalie
Department of Biochemistry and Molecular Biology, University of Georgia, Athens, GA, United States.
Front Genet. 2024 Jun 25;15:1436860. doi: 10.3389/fgene.2024.1436860. eCollection 2024.
Transfer RNAs have been extensively explored as the molecules that translate the genetic code into proteins. At this interface of genetics and biochemistry, tRNAs direct the efficiency of every major step of translation by interacting with a multitude of binding partners. However, due to the variability of tRNA sequences and the abundance of diverse post-transcriptional modifications, a guidebook linking tRNA sequences to specific translational outcomes has yet to be elucidated. Here, we review substantial efforts that have collectively uncovered tRNA engineering principles that can be used as a guide for the tuning of translation fidelity. These principles have allowed for the development of basic research, expansion of the genetic code with non-canonical amino acids, and tRNA therapeutics.
转运RNA作为将遗传密码翻译成蛋白质的分子已得到广泛研究。在遗传学和生物化学的这一交叉领域,转运RNA通过与众多结合伴侣相互作用,指导翻译每个主要步骤的效率。然而,由于转运RNA序列的可变性以及转录后修饰的多样性,将转运RNA序列与特定翻译结果联系起来的指南尚未阐明。在此,我们回顾了一系列重要研究成果,这些成果共同揭示了可用于指导调整翻译保真度的转运RNA工程原理。这些原理推动了基础研究的发展、利用非规范氨基酸扩展遗传密码以及开展转运RNA疗法。