Department of Medical Sciences, Institute of Biomedicine (iBiMED), University of Aveiro, 3810 Aveiro, Portugal.
Int J Mol Sci. 2018 Nov 24;19(12):3738. doi: 10.3390/ijms19123738.
Transfer RNAs (tRNAs) are key players of protein synthesis, as they decode the genetic information organized in mRNA codons, translating them into the code of 20 amino acids. To be fully active, tRNAs undergo extensive post-transcriptional modifications, catalyzed by different tRNA-modifying enzymes. Lack of these modifications increases the level of missense errors and affects codon decoding rate, contributing to protein aggregation with deleterious consequences to the cell. Recent works show that tRNA hypomodification and tRNA-modifying-enzyme deregulation occur in several diseases where proteostasis is affected, namely, neurodegenerative and metabolic diseases. In this review, we discuss the recent findings that correlate aberrant tRNA modification with proteostasis imbalances, in particular in neurological and metabolic disorders, and highlight the association between tRNAs, their modifying enzymes, translational decoding, and disease onset.
转移 RNA(tRNA)是蛋白质合成的关键参与者,因为它们可以解码 mRNA 密码子中组织的遗传信息,将其翻译成 20 种氨基酸的密码。为了充分发挥活性,tRNA 经历广泛的转录后修饰,由不同的 tRNA 修饰酶催化。缺乏这些修饰会增加错义错误的水平,并影响密码子解码率,导致蛋白质聚集,对细胞产生有害影响。最近的研究表明,tRNA 修饰不足和 tRNA 修饰酶失调发生在几种蛋白质稳态受到影响的疾病中,即神经退行性疾病和代谢疾病。在这篇综述中,我们讨论了最近的发现,即异常的 tRNA 修饰与蛋白质稳态失衡相关,特别是在神经和代谢疾病中,并强调了 tRNA、其修饰酶、翻译解码和疾病发病之间的关联。