J Clin Invest. 2022 May 2;132(9). doi: 10.1172/JCI158449.
The mechanisms that explain mitochondrial dysfunction in aging and healthspan continue to be studied, but one element has been unexplored: microproteins. Small open reading frames in circular mitochondria DNA can encode multiple microproteins, called mitochondria-derived peptides (MDPs). Currently, eight MDPs have been published: humanin, MOTS-c, and SHLPs 1-6. This Review describes recent advances in microprotein discovery with a focus on MDPs. It discusses what is currently known about MDPs in aging and how this new understanding could add to the way we understand age-related diseases including type 2 diabetes, cancer, and neurodegenerative diseases at the genomic, proteomic, and drug-development levels.
解释衰老和健康寿命中线粒体功能障碍的机制仍在研究中,但有一个因素尚未得到探索:微蛋白。圆形线粒体 DNA 中的小开放阅读框可以编码多种微蛋白,称为线粒体衍生肽(MDPs)。目前,已经发表了八种 MDP:神经调节蛋白、MOTS-c 和 SHLPs1-6。这篇综述描述了微蛋白发现的最新进展,重点是 MDPs。它讨论了目前已知的 MDPs 在衰老中的作用,以及这种新的理解如何在基因组、蛋白质组和药物开发水平上增加我们对包括 2 型糖尿病、癌症和神经退行性疾病在内的与年龄相关疾病的理解。