First Author | Siira SJ | Year | 2017 |
Journal | Nat Commun | Volume | 8 |
Issue | 1 | Pages | 1532 |
PubMed ID | 29146908 | Mgi Jnum | J:257215 |
Mgi Id | MGI:6106161 | Doi | 10.1038/s41467-017-01221-z |
Citation | Siira SJ, et al. (2017) LRPPRC-mediated folding of the mitochondrial transcriptome. Nat Commun 8(1):1532 |
abstractText | The expression of the compact mammalian mitochondrial genome requires transcription, RNA processing, translation and RNA decay, much like the more complex chromosomal systems, and here we use it as a model system to understand the fundamental aspects of gene expression. Here we combine RNase footprinting with PAR-CLIP at unprecedented depth to reveal the importance of RNA-protein interactions in dictating RNA folding within the mitochondrial transcriptome. We show that LRPPRC, in complex with its protein partner SLIRP, binds throughout the mitochondrial transcriptome, with a preference for mRNAs, and its loss affects the entire secondary structure and stability of the transcriptome. We demonstrate that the LRPPRC-SLIRP complex is a global RNA chaperone that stabilizes RNA structures to expose the required sites for translation, stabilization, and polyadenylation. Our findings reveal a general mechanism where extensive RNA-protein interactions ensure that RNA is accessible for its biological functions. |