National Institutes of Health/National Heart, Lung, and Blood Institute (NIH/NHLBI)
R01HD086634
United States
European Molecular Biology Organization (EMBO)
ALTF 539-2015
Swiss National Science Foundation
310030B_163478
Switzerland
Citation
Journal: Mol Cell / Year: 2020 Title: Gene- and Species-Specific Hox mRNA Translation by Ribosome Expansion Segments. Authors: Kathrin Leppek / Kotaro Fujii / Nick Quade / Teodorus Theo Susanto / Daniel Boehringer / Tea Lenarčič / Shifeng Xue / Naomi R Genuth / Nenad Ban / Maria Barna / Abstract: Ribosomes have been suggested to directly control gene regulation, but regulatory roles for ribosomal RNA (rRNA) remain largely unexplored. Expansion segments (ESs) consist of multitudes of tentacle- ...Ribosomes have been suggested to directly control gene regulation, but regulatory roles for ribosomal RNA (rRNA) remain largely unexplored. Expansion segments (ESs) consist of multitudes of tentacle-like rRNA structures extending from the core ribosome in eukaryotes. ESs are remarkably variable in sequence and size across eukaryotic evolution with largely unknown functions. In characterizing ribosome binding to a regulatory element within a Homeobox (Hox) 5' UTR, we identify a modular stem-loop within this element that binds to a single ES, ES9S. Engineering chimeric, "humanized" yeast ribosomes for ES9S reveals that an evolutionary change in the sequence of ES9S endows species-specific binding of Hoxa9 mRNA to the ribosome. Genome editing to site-specifically disrupt the Hoxa9-ES9S interaction demonstrates the functional importance for such selective mRNA-rRNA binding in translation control. Together, these studies unravel unexpected gene regulation directly mediated by rRNA and how ribosome evolution drives translation of critical developmental regulators.
History
Deposition
Jul 31, 2020
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Header (metadata) release
Dec 2, 2020
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Map release
Dec 2, 2020
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Update
Dec 30, 2020
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Current status
Dec 30, 2020
Processing site: PDBe / Status: Released
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Structure visualization
Movie
Surface view with section colored by density value
Entire : human 40S ribosomal subunit - mouse Hoxa9 IRES like element complex
Entire
Name: human 40S ribosomal subunit - mouse Hoxa9 IRES like element complex
Components
Complex: human 40S ribosomal subunit - mouse Hoxa9 IRES like element complex
Organelle or cellular component: 40S ribosomal subunit
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Supramolecule #1: human 40S ribosomal subunit - mouse Hoxa9 IRES like element complex
Supramolecule
Name: human 40S ribosomal subunit - mouse Hoxa9 IRES like element complex type: complex / ID: 1 / Parent: 0 Details: The map includes the binding site of the mouse Hoxa9 IRES-like element bound to the human 40S ribosomal subunit head. (Mouse Hoxa9 IRES was produced by in vitro transcription)
Source (natural)
Organism: Homo sapiens (human) / Strain: HEK293-6E cells
Model: Quantifoil R2/2 / Material: COPPER / Mesh: 300 / Support film - Material: CARBON / Support film - topology: CONTINUOUS
Vitrification
Cryogen name: ETHANE-PROPANE / Chamber humidity: 100 % / Chamber temperature: 277 K / Instrument: FEI VITROBOT MARK IV
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Electron microscopy
Microscope
TFS KRIOS
Image recording
Film or detector model: FEI FALCON II (4k x 4k) / Detector mode: INTEGRATING / Average electron dose: 40.0 e/Å2
Electron beam
Acceleration voltage: 300 kV / Electron source: FIELD EMISSION GUN
Electron optics
Illumination mode: FLOOD BEAM / Imaging mode: BRIGHT FIELD
Experimental equipment
Model: Titan Krios / Image courtesy: FEI Company
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Image processing
CTF correction
Software - Name: CTFFIND Details: CTF parameters were estimated with with CTFFIND and correction was applied within Relion
Startup model
Type of model: NONE Details: 40S ribosomal subunit structure described in Quade, N., Boehringer, D., Leibundgut, M., van den Heuvel, J., and Ban, N., 2015, Cryo-EM structure of Hepatitis C virus IRES bound to the human ...Details: 40S ribosomal subunit structure described in Quade, N., Boehringer, D., Leibundgut, M., van den Heuvel, J., and Ban, N., 2015, Cryo-EM structure of Hepatitis C virus IRES bound to the human ribosome at 3.9 A resolution. Nat. Commun. 6, 7646:1
Final reconstruction
Resolution.type: BY AUTHOR / Resolution: 3.9 Å / Resolution method: FSC 0.143 CUT-OFF / Software - Name: RELION Details: The final map of the IRES binding site on the 40S ribosomal subunit head was obtained after focused classification following a multi-body refinement. Number images used: 19342
Initial angle assignment
Type: MAXIMUM LIKELIHOOD / Software - Name: RELION
Final angle assignment
Type: MAXIMUM LIKELIHOOD / Software - Name: RELION
Final 3D classification
Software - Name: RELION
FSC plot (resolution estimation)
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