Active RNA interference in mitochondria

• Published in: Cell research Vol. 31; no. 2; pp. 219 - 228
• Main Authors: Gao, Kuanxing, Cheng, Man, Zuo, Xinxin, Lin, Jinzhong, Hoogewijs, Kurt, Murphy, Michael P., Fu, Xiang-Dong, Zhang, Xiaorong
• Format: Journal Article
• Language: English
• Published: Singapore Springer Singapore 01.02.2021; Nature Publishing Group
• Subjects: 13/31; 13/89; 14/1; 14/34; 45/29; 45/77; 631/337/505; 631/80/642/333; Animals; Argonaute 2 protein; Argonaute Proteins - genetics; Argonaute Proteins - metabolism; Biomedical and Life Sciences; Cell Biology; Cell lines; Crosstalk; DNA, Mitochondrial - genetics; DNA, Mitochondrial - metabolism; Electron transport; Fibroblasts - metabolism; Gene expression; Genomes; HEK293 Cells; HeLa Cells; Homology; Humans; Interference; Life Sciences; Membrane Potential, Mitochondrial - genetics; Mice; miRNA; Mitochondria; Mitochondria - genetics; Mitochondria - metabolism; Mitochondrial DNA; Myocytes, Cardiac - metabolism; Oxygen - metabolism; Prokaryotes; Retrotransposition; Ribonucleic acid; RNA; RNA Interference; RNA, Messenger - genetics; RNA, Messenger - metabolism; RNA, Small Interfering - genetics; RNA, Small Interfering - metabolism; RNA-mediated interference; siRNA; Transfection
• ISSN: 1001-0602; 1748-7838; 1748-7838
• DOI: 10.1038/s41422-020-00394-5

RNA interference (RNAi) has been thought to be a gene-silencing pathway present in most eukaryotic cells to safeguard the genome against retrotransposition. Small interfering RNAs (siRNAs) have also become a powerful tool for studying gene functions. Given the endosymbiotic hypothesis that mitochondria originated from prokaryotes, mitochondria have been generally assumed to lack active RNAi; however, certain bacteria have Argonaute homologs and various reports suggest the presence of specific microRNAs and nuclear genome (nDNA)-encoded Ago2 in the mitochondria. Here we report that transfected siRNAs are not only able to enter the matrix of mitochondria, but also function there to specifically silence targeted mitochondrial transcripts. The mitoRNAi effect is readily detectable at the mRNA level, but only recordable on relatively unstable proteins, such as the mtDNA-encoded complex IV subunits. We also apply mitoRNAi to directly determine the postulated crosstalk between individual respiratory chain complexes, and our result suggests that the controversial observations previously made in patient-derived cells might result from differential adaptation in different cell lines. Our findings bring a new tool to study mitochondrial biology.