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Open data
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Basic information
Entry | ![]() | |||||||||
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Title | Untethered Cytoplasmic Fission Yeast Ribosome | |||||||||
![]() | Untethered Cytosolic Ribosome of S. pombe generated by M | |||||||||
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![]() | Hibernating / Yeast / In Situ / RACK1 / cytosolic / RIBOSOME / untethered | |||||||||
Biological species | ![]() ![]() | |||||||||
Method | subtomogram averaging / cryo EM / Resolution: 14.64 Å | |||||||||
![]() | Rosa H / Gemin O / Gluc M / Mattei S / Jomaa A | |||||||||
Funding support | 1 items
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![]() | ![]() Title: Ribosomes hibernate on mitochondria during cellular stress. Authors: Olivier Gemin / Maciej Gluc / Higor Rosa / Michael Purdy / Moritz Niemann / Yelena Peskova / Simone Mattei / Ahmad Jomaa / ![]() ![]() Abstract: Cell survival under nutrient-deprived conditions relies on cells' ability to adapt their organelles and rewire their metabolic pathways. In yeast, glucose depletion induces a stress response mediated ...Cell survival under nutrient-deprived conditions relies on cells' ability to adapt their organelles and rewire their metabolic pathways. In yeast, glucose depletion induces a stress response mediated by mitochondrial fragmentation and sequestration of cytosolic ribosomes on mitochondria. This cellular adaptation promotes survival under harsh environmental conditions; however, the underlying mechanism of this response remains unknown. Here, we demonstrate that upon glucose depletion protein synthesis is halted. Cryo-electron microscopy structure of the ribosomes show that they are devoid of both tRNA and mRNA, and a subset of the particles depicted a conformational change in rRNA H69 that could prevent tRNA binding. Our in situ structural analyses reveal that the hibernating ribosomes tether to fragmented mitochondria and establish eukaryotic-specific, higher-order storage structures by assembling into oligomeric arrays on the mitochondrial surface. Notably, we show that hibernating ribosomes exclusively bind to the outer mitochondrial membrane via the small ribosomal subunit during cellular stress. We identify the ribosomal protein Cpc2/RACK1 as the molecule mediating ribosomal tethering to mitochondria. This study unveils the molecular mechanism connecting mitochondrial stress with the shutdown of protein synthesis and broadens our understanding of cellular responses to nutrient scarcity and cell quiescence. | |||||||||
History |
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Structure visualization
Supplemental images |
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Downloads & links
-EMDB archive
Map data | ![]() | 13 MB | ![]() | |
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Header (meta data) | ![]() ![]() | 13.7 KB 13.7 KB | Display Display | ![]() |
FSC (resolution estimation) | ![]() ![]() | 5.7 KB 5.4 KB | Display Display | ![]() |
Images | ![]() | 92.7 KB | ||
Filedesc metadata | ![]() | 4.2 KB | ||
Others | ![]() ![]() | 7.1 MB 7.1 MB | ||
Archive directory | ![]() ![]() | HTTPS FTP |
-Validation report
Summary document | ![]() | 754.2 KB | Display | ![]() |
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Full document | ![]() | 753.8 KB | Display | |
Data in XML | ![]() | 10.5 KB | Display | |
Data in CIF | ![]() | 14.9 KB | Display | |
Arichive directory | ![]() ![]() | HTTPS FTP |
-Related structure data
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Links
EMDB pages | ![]() ![]() |
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Map
File | ![]() | ||||||||||||||||||||||||||||||||||||
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Annotation | Untethered Cytosolic Ribosome of S. pombe generated by M | ||||||||||||||||||||||||||||||||||||
Projections & slices | Image control
Images are generated by Spider. | ||||||||||||||||||||||||||||||||||||
Voxel size | X=Y=Z: 4.15 Å | ||||||||||||||||||||||||||||||||||||
Density |
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Symmetry | Space group: 1 | ||||||||||||||||||||||||||||||||||||
Details | EMDB XML:
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-Supplemental data
-Half map: Untethered Cytosolic Ribosome of S. pombe Half-Map 2 generated by M
File | emd_51002_half_map_1.map | ||||||||||||
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Annotation | Untethered Cytosolic Ribosome of S. pombe Half-Map 2 generated by M | ||||||||||||
Projections & Slices |
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Density Histograms |
-Half map: Untethered Cytosolic Ribosome of S. pombe Half-Map 1 generated by M
File | emd_51002_half_map_2.map | ||||||||||||
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Annotation | Untethered Cytosolic Ribosome of S. pombe Half-Map 1 generated by M | ||||||||||||
Projections & Slices |
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Density Histograms |
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Sample components
-Entire : Cytoplasmic Ribosome Untethered to the Outer Mitochondrial Membrane
Entire | Name: Cytoplasmic Ribosome Untethered to the Outer Mitochondrial Membrane |
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Components |
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-Supramolecule #1: Cytoplasmic Ribosome Untethered to the Outer Mitochondrial Membrane
Supramolecule | Name: Cytoplasmic Ribosome Untethered to the Outer Mitochondrial Membrane type: complex / ID: 1 / Parent: 0 |
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Source (natural) | Organism: ![]() ![]() |
-Experimental details
-Structure determination
Method | cryo EM |
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![]() | subtomogram averaging |
Aggregation state | cell |
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Sample preparation
Buffer | pH: 5.5 |
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Vitrification | Cryogen name: ETHANE / Chamber humidity: 100 % / Chamber temperature: 300 K / Instrument: LEICA EM GP |
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Electron microscopy
Microscope | FEI TITAN KRIOS |
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Specialist optics | Energy filter - Name: GIF Bioquantum / Energy filter - Slit width: 30 eV |
Image recording | Film or detector model: GATAN K3 BIOQUANTUM (6k x 4k) / Average electron dose: 2.23 e/Å2 |
Electron beam | Acceleration voltage: 300 kV / Electron source: ![]() |
Electron optics | C2 aperture diameter: 50.0 µm / Illumination mode: FLOOD BEAM / Imaging mode: BRIGHT FIELD / Cs: 2.7 mm / Nominal defocus max: 4.0 µm / Nominal defocus min: 2.0 µm / Nominal magnification: 42000 |
Sample stage | Specimen holder model: FEI TITAN KRIOS AUTOGRID HOLDER / Cooling holder cryogen: NITROGEN |
Experimental equipment | ![]() Model: Titan Krios / Image courtesy: FEI Company |