生物
细胞生物学
基因沉默
基因表达
基因
RNA沉默
RNA干扰
遗传学
核糖核酸
作者
Luis Daniel Cruz‐Zaragoza,Drishan Dahal,Mats Koschel,Angela Boshnakovska,Aiturgan Zheenbekova,Mehmet Yilmaz,Marcel Morgenstern,Jan-Niklas Dohrke,Julian Bender,Anusha Valpadashi,Kristine A. Henningfeld,Silke Oeljeklaus,Laura S. Kremer,Mirjam Breuer,Oliver Urbach,Sven Dennerlein,Michael Lidschreiber,Stefan Jakobs,Bettina Warscheid,Peter Rehling
出处
期刊:Science
[American Association for the Advancement of Science]
日期:2025-05-22
卷期号:389 (6759): eadr3498-eadr3498
被引量:10
标识
DOI:10.1126/science.adr3498
摘要
Mitochondria fulfill central functions in metabolism and energy supply. They express their own genome, which encodes key subunits of the oxidative phosphorylation system. However, the central mechanisms underlying mitochondrial gene expression remain enigmatic, and a lack of suitable technologies to target mitochondrial protein synthesis in cells has limited experimental access. We silenced the translation of specific mitochondrial mRNAs in living human cells by delivering synthetic peptide-morpholino chimeras. This approach allowed us to perform a comprehensive temporal monitoring of cellular responses. Our study provides insights into mitochondrial translation, its integration into cellular physiology, and provides a strategy to address mitochondrial gene expression in living cells. The approach can potentially be used to analyze mechanisms and pathophysiology of mitochondrial gene expression in a range of cellular model systems.
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