Structural basis of LRPPRC–SLIRP-dependent translation by the mitoribosome

In mammalian mitochondria, mRNAs are cotranscriptionally stabilized by the protein factor LRPPRC (leucine-rich pentatricopeptide repeat-containing protein). Here, we characterize LRPPRC as an mRNA delivery factor and report its cryo-electron microscopy structure in complex with SLIRP (SRA stem-loop-interacting RNA-binding protein), mRNA and the mitoribosome. The structure shows that LRPPRC associates with the mitoribosomal proteins mS39 and the N terminus of mS31 through recognition of the LRPPRC helical repeats. Together, the proteins form a corridor for handoff of the mRNA. The mRNA is directly bound to SLIRP, which also has a stabilizing function for LRPPRC. To delineate the effect of LRPPRC on individual mitochondrial transcripts, we used RNA sequencing, metabolic labeling and mitoribosome profiling, which showed a transcript-specific influence on mRNA translation efficiency, with cytochrome c oxidase subunit 1 and 2 translation being the most affected. Our data suggest that LRPPRC-SLIRP acts in recruitment of mitochondrial mRNAs to modulate their translation. Collectively, the data define LRPPRC-SLIRP as a regulator of the mitochondrial gene expression system.

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Publication Details

Journal
Nature Structural & Molecular Biology
Published
2024-08-12
DOI
https://doi.org/10.1038/s41594-024-01365-9
Citations
29
Primary Topic
Mitochondrial Function and Pathology
Type
article
Field-Weighted Citation Impact
6.78
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article

Structural basis of LRPPRC–SLIRP-dependent translation by the mitoribosome

Mary Couvillion, J. Conor Moran, Vivek Singh, Yuzuru Itoh et al.
29 citations
Nature Structural & Molecular Biology
Mitochondrial Function and Pathology
6.78
article

Structural basis of LRPPRC–SLIRP-dependent translation by the mitoribosome

Mary Couvillion, J. Conor Moran, Vivek Singh, Yuzuru Itoh, Iliana C. Soto, Antoni Barrientos, Martijn A. Huynen, L. Stirling Churchman, Alexey Amunts, Flavia Fontanesi
article en
29 citations

Abstract

In mammalian mitochondria, mRNAs are cotranscriptionally stabilized by the protein factor LRPPRC (leucine-rich pentatricopeptide repeat-containing protein). Here, we characterize LRPPRC as an mRNA delivery factor and report its cryo-electron microscopy structure in complex with SLIRP (SRA stem-loop-interacting RNA-binding protein), mRNA and the mitoribosome. The structure shows that LRPPRC associates with the mitoribosomal proteins mS39 and the N terminus of mS31 through recognition of the LRPPRC helical repeats. Together, the proteins form a corridor for handoff of the mRNA. The mRNA is directly bound to SLIRP, which also has a stabilizing function for LRPPRC. To delineate the effect of LRPPRC on individual mitochondrial transcripts, we used RNA sequencing, metabolic labeling and mitoribosome profiling, which showed a transcript-specific influence on mRNA translation efficiency, with cytochrome c oxidase subunit 1 and 2 translation being the most affected. Our data suggest that LRPPRC-SLIRP acts in recruitment of mitochondrial mRNAs to modulate their translation. Collectively, the data define LRPPRC-SLIRP as a regulator of the mitochondrial gene expression system.

Nature Structural & Molecular BiologyVol. 31(12)
Harvard University (US), University of Miami (US), Radboud University Nijmegen (NL), Tokyo University of Science (JP), Stockholm University (SE), Science for Life Laboratory (SE), Radboud University Medical Center (NL), Westlake University (CN), Center for Human Genetics (US), Boston VA Research Institute (US), The University of Tokyo (JP)
Openalex Percentile: Top 2%
Mitochondrial Function and Pathology
6.78
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