From the Department of Chemistry and Biochemistry, Center for RNA Biology, and Center for Retroviral Research, The Ohio State University, Columbus, Ohio 43210
J Biol Chem. 2019 Apr 5;294(14):5292-5293. doi: 10.1074/jbc.REV119.007721. Epub 2019 Feb 24.
Aminoacyl-tRNA synthetases (ARSs) catalyze the attachment of specific amino acids to cognate tRNAs for use in protein synthesis. This historical function of ARSs and tRNAs is fairly well understood. However, ARSs and tRNAs also perform noncanonical functions that are continuing to be unveiled at a rapid pace. The expanded functions of these essential molecules of life range from roles in retroviral replication to stimulation of mammalian target of rapamycin (mTOR) activity; DNA repair, splicing, and transcriptional and translational regulation; and other aspects of cellular homeostasis. Furthermore, mutations in tRNAs and synthetases are known to drive human maladies, such as the neurodegenerative disorder Charcot-Marie-Tooth disease along with other central nervous system dysfunctions and cancer. This series of reviews focuses on the diseases that result from natural variations in human cytoplasmic tRNAs, as well as from mutations in mitochondrial tRNAs and ARSs. Ultimately, the exciting work in this rapidly emerging area may lead to new therapies for microbial and parasitic infections, cancer, and neurodegenerative diseases.
氨酰-tRNA 合成酶(ARSs)催化特定氨基酸与相应 tRNA 的连接,用于蛋白质合成。ARSs 和 tRNA 的这一历史功能已被相当好地理解。然而,ARSs 和 tRNA 还具有非典型的功能,这些功能正在迅速被揭示。这些生命基本分子的扩展功能从逆转录病毒复制到刺激哺乳动物雷帕霉素靶蛋白(mTOR)活性;DNA 修复、剪接以及转录和翻译调控;以及细胞内稳态的其他方面。此外,tRNA 和合成酶的突变已知会导致人类疾病,如神经退行性疾病——遗传性运动感觉神经病,以及其他中枢神经系统功能障碍和癌症。这一系列综述重点介绍了人类细胞质 tRNA 的自然变异以及线粒体 tRNA 和 ARSs 突变所导致的疾病。最终,这一快速发展领域令人兴奋的工作可能为微生物和寄生虫感染、癌症和神经退行性疾病带来新的治疗方法。