Coego Alba, Covelo-Molares Helena, Guallar Diana
Epitranscriptomics and Ageing Group. Center for Research in Molecular Medicine and Chronic Diseases (CiMUS), Universidade de Santiago de Compostela (USC), Santiago de Compostela 15782, Spain.
Biochem Soc Trans. 2023 Apr 26;51(2):783-796. doi: 10.1042/BST20221417.
Ageing is a conserved and unavoidable biological process characterized by progressive decline of physiological functions with time. Despite constituting the greatest risk factor for most human diseases, little is known about the molecular mechanisms driving the ageing process. More than 170 chemical RNA modifications, also known as the epitranscriptome, decorate eukaryotic coding and non-coding RNAs and have emerged as novel regulators of RNA metabolism, modulating RNA stability, translation, splicing or non-coding RNA processing. Studies on short-lived organisms such as yeast or worms connect mutations on RNA modifying enzymes with lifespan changes, and dysregulation of the epitranscriptome has been linked to age-related diseases and ageing hallmarks themselves in mammals. Moreover, transcriptome-wide analyses are starting to reveal changes in messenger RNA modifications in neurodegenerative diseases and in the expression of some RNA modifiers with age. These studies are starting to put the focus on the epitranscriptome as a potential novel regulator of ageing and lifespan, and open new avenues for the identification of targets to treat age-related diseases. In this review, we discuss the connection between RNA modifications and the enzymatic machinery regulating their deposition in coding and non-coding RNAs, and ageing and hypothesize about the potential role of RNA modifications in the regulation of other ncRNAs playing a key role in ageing, such as transposable elements and tRNA fragments. Finally, we reanalyze available datasets of mouse tissues during ageing and report a wide transcriptional dysregulation of proteins involved in the deposition, removal or decoding of several of the best-known RNA modifications.
衰老作为一种保守且不可避免的生物学过程,其特征在于生理功能会随着时间的推移而逐渐衰退。尽管衰老是大多数人类疾病的最大风险因素,但对于驱动衰老过程的分子机制,我们却知之甚少。超过170种化学RNA修饰(也称为表观转录组)修饰真核生物的编码和非编码RNA,并已成为RNA代谢的新型调节因子,可调节RNA稳定性、翻译、剪接或非编码RNA加工。对酵母或蠕虫等短命生物的研究表明,RNA修饰酶的突变与寿命变化有关,并且表观转录组失调与哺乳动物的年龄相关疾病及衰老特征本身有关。此外,全转录组分析开始揭示神经退行性疾病中信使RNA修饰的变化以及某些RNA修饰因子的表达随年龄的变化。这些研究开始将焦点放在表观转录组上,将其视为衰老和寿命的潜在新型调节因子,并为鉴定治疗年龄相关疾病的靶点开辟了新途径。在这篇综述中,我们讨论了RNA修饰与调节它们在编码和非编码RNA中沉积的酶机制之间的联系以及衰老,并推测了RNA修饰在调节其他在衰老中起关键作用的非编码RNA(如转座元件和tRNA片段)中的潜在作用。最后,我们重新分析了衰老过程中小鼠组织的现有数据集,并报告了参与几种最著名RNA修饰的沉积、去除或解码的蛋白质存在广泛的转录失调。