+ Open data
Open data
- Basic information
Basic information
| Entry | Database: PDB / ID: 6eu0 | |||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Title | RNA Polymerase III open pre-initiation complex (OC-PIC) | |||||||||||||||
|  Components | 
 | |||||||||||||||
|  Keywords | TRANSCRIPTION / RNA Pol III / promoter opening | |||||||||||||||
| Function / homology |  Function and homology information RNA polymerase III core binding / TFIIA-class transcription factor complex binding / DNA-templated transcription open complex formation / RNA polymerase III transcription regulatory region sequence-specific DNA binding / RNA polymerase III preinitiation complex assembly / transcription factor TFIIIB complex / TFIIIC-class transcription factor complex binding / RNA polymerase I general transcription initiation factor binding / RNA polymerase III type 3 promoter sequence-specific DNA binding / regulation of transcription by RNA polymerase III ...RNA polymerase III core binding / TFIIA-class transcription factor complex binding / DNA-templated transcription open complex formation / RNA polymerase III transcription regulatory region sequence-specific DNA binding / RNA polymerase III preinitiation complex assembly / transcription factor TFIIIB complex / TFIIIC-class transcription factor complex binding / RNA polymerase I general transcription initiation factor binding / RNA polymerase III type 3 promoter sequence-specific DNA binding / regulation of transcription by RNA polymerase III / RNA polymerase III general transcription initiation factor activity / transcription factor TFIIA complex / RNA polymerase I preinitiation complex assembly / DNA binding, bending / RNA Polymerase I Transcription Initiation / transcription preinitiation complex / Processing of Capped Intron-Containing Pre-mRNA / RNA Polymerase III Transcription Initiation From Type 2 Promoter / RNA Pol II CTD phosphorylation and interaction with CE / Formation of the Early Elongation Complex / mRNA Capping / RNA polymerase II transcribes snRNA genes / TP53 Regulates Transcription of DNA Repair Genes / RNA Polymerase II Promoter Escape / RNA Polymerase II Transcription Pre-Initiation And Promoter Opening / RNA Polymerase II Transcription Initiation / RNA Polymerase II Transcription Initiation And Promoter Clearance / RNA polymerase II general transcription initiation factor activity / termination of RNA polymerase III transcription / transcription factor TFIID complex / RNA Polymerase II Pre-transcription Events / RNA-templated transcription / Formation of TC-NER Pre-Incision Complex / transcription initiation at RNA polymerase III promoter / RNA Polymerase I Promoter Escape / termination of RNA polymerase I transcription / nucleolar large rRNA transcription by RNA polymerase I / Gap-filling DNA repair synthesis and ligation in TC-NER / transcription initiation at RNA polymerase I promoter / Estrogen-dependent gene expression / transcription by RNA polymerase III / Dual incision in TC-NER / RNA polymerase I complex / transcription elongation by RNA polymerase I / RNA polymerase III complex / RNA polymerase II core promoter sequence-specific DNA binding / RNA polymerase II, core complex / tRNA transcription by RNA polymerase III / RNA polymerase II preinitiation complex assembly / transcription by RNA polymerase I / nucleotidyltransferase activity / TBP-class protein binding / transcription initiation at RNA polymerase II promoter / transcription elongation by RNA polymerase II / DNA-templated transcription initiation / ribonucleoside binding / DNA-directed RNA polymerase / disordered domain specific binding / DNA-directed RNA polymerase activity / peroxisome / ribosome biogenesis / single-stranded DNA binding / transcription regulator complex / DNA-binding transcription factor binding / nucleic acid binding / RNA polymerase II-specific DNA-binding transcription factor binding / transcription by RNA polymerase II / protein dimerization activity / nucleotide binding / negative regulation of DNA-templated transcription / chromatin binding / regulation of DNA-templated transcription / nucleolus / positive regulation of transcription by RNA polymerase II / protein-containing complex / mitochondrion / DNA binding / zinc ion binding / nucleoplasm / metal ion binding / nucleus / cytoplasm / cytosol Similarity search - Function | |||||||||||||||
| Biological species |   Saccharomyces cerevisiae (brewer's yeast)   Saccharomyces cerevisiae S288c (yeast) | |||||||||||||||
| Method | ELECTRON MICROSCOPY / single particle reconstruction / cryo EM / Resolution: 4 Å | |||||||||||||||
|  Authors | Abascal-Palacios, G. / Ramsay, E.P. / Beuron, F. / Morris, E. / Vannini, A. | |||||||||||||||
| Funding support |  United Kingdom, 4items 
 | |||||||||||||||
|  Citation |  Journal: Nature / Year: 2018 Title: Structural basis of RNA polymerase III transcription initiation. Authors: Guillermo Abascal-Palacios / Ewan Phillip Ramsay / Fabienne Beuron / Edward Morris / Alessandro Vannini /  Abstract: RNA polymerase (Pol) III transcribes essential non-coding RNAs, including the entire pool of transfer RNAs, the 5S ribosomal RNA and the U6 spliceosomal RNA, and is often deregulated in cancer cells. ...RNA polymerase (Pol) III transcribes essential non-coding RNAs, including the entire pool of transfer RNAs, the 5S ribosomal RNA and the U6 spliceosomal RNA, and is often deregulated in cancer cells. The initiation of gene transcription by Pol III requires the activity of the transcription factor TFIIIB to form a transcriptionally active Pol III preinitiation complex (PIC). Here we present electron microscopy reconstructions of Pol III PICs at 3.4-4.0 Å and a reconstruction of unbound apo-Pol III at 3.1 Å. TFIIIB fully encircles the DNA and restructures Pol III. In particular, binding of the TFIIIB subunit Bdp1 rearranges the Pol III-specific subunits C37 and C34, thereby promoting DNA opening. The unwound DNA directly contacts both sides of the Pol III cleft. Topologically, the Pol III PIC resembles the Pol II PIC, whereas the Pol I PIC is more divergent. The structures presented unravel the molecular mechanisms underlying the first steps of Pol III transcription and also the general conserved mechanisms of gene transcription initiation. | |||||||||||||||
| History | 
 | 
- Structure visualization
Structure visualization
| Movie | 
 
  Movie viewer | 
|---|---|
| Structure viewer | Molecule:  Molmil  Jmol/JSmol | 
- Downloads & links
Downloads & links
- Download
Download
| PDBx/mmCIF format |  6eu0.cif.gz | 1.1 MB | Display |  PDBx/mmCIF format | 
|---|---|---|---|---|
| PDB format |  pdb6eu0.ent.gz | 891.5 KB | Display |  PDB format | 
| PDBx/mmJSON format |  6eu0.json.gz | Tree view |  PDBx/mmJSON format | |
| Others |  Other downloads | 
-Validation report
| Summary document |  6eu0_validation.pdf.gz | 976.1 KB | Display |  wwPDB validaton report | 
|---|---|---|---|---|
| Full document |  6eu0_full_validation.pdf.gz | 1 MB | Display | |
| Data in XML |  6eu0_validation.xml.gz | 160.1 KB | Display | |
| Data in CIF |  6eu0_validation.cif.gz | 245.3 KB | Display | |
| Arichive directory |  https://data.pdbj.org/pub/pdb/validation_reports/eu/6eu0  ftp://data.pdbj.org/pub/pdb/validation_reports/eu/6eu0 | HTTPS FTP | 
-Related structure data
| Related structure data |  3955MC  3956C  3957C  3958C  3959C  6eu1C  6eu2C  6eu3C M: map data used to model this data C: citing same article ( | 
|---|---|
| Similar structure data | 
- Links
Links
- Assembly
Assembly
| Deposited unit |  
 | 
|---|---|
| 1 | 
 | 
- Components
Components
-DNA-directed RNA polymerase III subunit  ... , 10 types, 10 molecules ABDGIMNOPQ         
| #1: Protein | Mass: 162517.812 Da / Num. of mol.: 1 / Source method: isolated from a natural source Source: (natural)   Saccharomyces cerevisiae (strain ATCC 204508 / S288c) (yeast) Strain: ATCC 204508 / S288c / References: UniProt: P04051, DNA-directed RNA polymerase | 
|---|---|
| #2: Protein | Mass: 129629.383 Da / Num. of mol.: 1 / Source method: isolated from a natural source Source: (natural)   Saccharomyces cerevisiae (strain ATCC 204508 / S288c) (yeast) Strain: ATCC 204508 / S288c / References: UniProt: P22276, DNA-directed RNA polymerase | 
| #4: Protein | Mass: 18623.123 Da / Num. of mol.: 1 / Source method: isolated from a natural source Source: (natural)   Saccharomyces cerevisiae (strain ATCC 204508 / S288c) (yeast) Strain: ATCC 204508 / S288c / References: UniProt: P47076 | 
| #7: Protein | Mass: 24349.770 Da / Num. of mol.: 1 / Source method: isolated from a natural source Source: (natural)   Saccharomyces cerevisiae (strain ATCC 204508 / S288c) (yeast) Strain: ATCC 204508 / S288c / References: UniProt: P35718 | 
| #9: Protein | Mass: 12525.109 Da / Num. of mol.: 1 / Source method: isolated from a natural source Source: (natural)   Saccharomyces cerevisiae (strain ATCC 204508 / S288c) (yeast) Strain: ATCC 204508 / S288c / References: UniProt: Q04307 | 
| #13: Protein | Mass: 32178.115 Da / Num. of mol.: 1 / Source method: isolated from a natural source Source: (natural)   Saccharomyces cerevisiae (strain ATCC 204508 / S288c) (yeast) Strain: ATCC 204508 / S288c / References: UniProt: P36121 | 
| #14: Protein | Mass: 46751.469 Da / Num. of mol.: 1 / Source method: isolated from a natural source Source: (natural)   Saccharomyces cerevisiae (strain ATCC 204508 / S288c) (yeast) Strain: ATCC 204508 / S288c / References: UniProt: P25441 | 
| #15: Protein | Mass: 74112.820 Da / Num. of mol.: 1 / Source method: isolated from a natural source Source: (natural)   Saccharomyces cerevisiae (strain ATCC 204508 / S288c) (yeast) Strain: ATCC 204508 / S288c / References: UniProt: P32349 | 
| #16: Protein | Mass: 36174.160 Da / Num. of mol.: 1 / Source method: isolated from a natural source Source: (natural)   Saccharomyces cerevisiae (strain ATCC 204508 / S288c) (yeast) Strain: ATCC 204508 / S288c / References: UniProt: P32910 | 
| #17: Protein | Mass: 27752.971 Da / Num. of mol.: 1 / Source method: isolated from a natural source Source: (natural)   Saccharomyces cerevisiae (strain ATCC 204508 / S288c) (yeast) Strain: ATCC 204508 / S288c / References: UniProt: P17890 | 
-DNA-directed RNA polymerases I and III subunit  ... , 2 types, 2 molecules CK 
| #3: Protein | Mass: 37732.613 Da / Num. of mol.: 1 / Source method: isolated from a natural source Source: (natural)   Saccharomyces cerevisiae (strain ATCC 204508 / S288c) (yeast) Strain: ATCC 204508 / S288c / References: UniProt: P07703 | 
|---|---|
| #11: Protein | Mass: 16167.860 Da / Num. of mol.: 1 / Source method: isolated from a natural source Source: (natural)   Saccharomyces cerevisiae (strain ATCC 204508 / S288c) (yeast) Strain: ATCC 204508 / S288c / References: UniProt: P28000 | 
-DNA-directed RNA polymerases I, II, and III subunit  ... , 5 types, 5 molecules EFHJL    
| #5: Protein | Mass: 25117.094 Da / Num. of mol.: 1 / Source method: isolated from a natural source Source: (natural)   Saccharomyces cerevisiae (strain ATCC 204508 / S288c) (yeast) Strain: ATCC 204508 / S288c / References: UniProt: P20434 | 
|---|---|
| #6: Protein | Mass: 17931.834 Da / Num. of mol.: 1 / Source method: isolated from a natural source Source: (natural)   Saccharomyces cerevisiae (strain ATCC 204508 / S288c) (yeast) Strain: ATCC 204508 / S288c / References: UniProt: P20435 | 
| #8: Protein | Mass: 16525.363 Da / Num. of mol.: 1 / Source method: isolated from a natural source Source: (natural)   Saccharomyces cerevisiae (strain ATCC 204508 / S288c) (yeast) Strain: ATCC 204508 / S288c / References: UniProt: P20436 | 
| #10: Protein | Mass: 8290.732 Da / Num. of mol.: 1 / Source method: isolated from a natural source Source: (natural)   Saccharomyces cerevisiae (strain ATCC 204508 / S288c) (yeast) Strain: ATCC 204508 / S288c / References: UniProt: P22139 | 
| #12: Protein | Mass: 7729.969 Da / Num. of mol.: 1 / Source method: isolated from a natural source Source: (natural)   Saccharomyces cerevisiae (strain ATCC 204508 / S288c) (yeast) Strain: ATCC 204508 / S288c / References: UniProt: P40422 | 
-DNA chain , 2 types, 2 molecules RS 
| #18: DNA chain | Mass: 21445.754 Da / Num. of mol.: 1 / Source method: obtained synthetically / Source: (synth.)    Saccharomyces cerevisiae S288c (yeast) | 
|---|---|
| #19: DNA chain | Mass: 21708.973 Da / Num. of mol.: 1 / Source method: obtained synthetically / Source: (synth.)    Saccharomyces cerevisiae S288c (yeast) | 
-Transcription factor  ... , 2 types, 2 molecules VZ 
| #20: Protein | Mass: 67801.906 Da / Num. of mol.: 1 Source method: isolated from a genetically manipulated source Source: (gene. exp.)   Saccharomyces cerevisiae (strain ATCC 204508 / S288c) (yeast) Strain: ATCC 204508 / S288c / Gene: BDP1, TFC5, YNL039W, N2682 / Production host:   Escherichia coli (E. coli) / References: UniProt: P46678 | 
|---|---|
| #22: Protein | Mass: 67011.477 Da / Num. of mol.: 1 Source method: isolated from a genetically manipulated source Source: (gene. exp.)   Saccharomyces cerevisiae (strain ATCC 204508 / S288c) (yeast) Strain: ATCC 204508 / S288c / Gene: BRF1, PCF4, TDS4, YGR246C / Production host:   Escherichia coli (E. coli) / References: UniProt: P29056 | 
-Protein , 1 types, 1 molecules Y
| #21: Protein | Mass: 27042.275 Da / Num. of mol.: 1 Source method: isolated from a genetically manipulated source Source: (gene. exp.)   Saccharomyces cerevisiae (strain ATCC 204508 / S288c) (yeast) Strain: ATCC 204508 / S288c / Gene: SPT15, BTF1, TBP1, YER148W / Production host:   Escherichia coli (E. coli) / References: UniProt: P13393 | 
|---|
-Non-polymers , 2 types, 8 molecules 


| #23: Chemical | ChemComp-ZN / #24: Chemical | ChemComp-MG / |  | 
|---|
-Experimental details
-Experiment
| Experiment | Method: ELECTRON MICROSCOPY | 
|---|---|
| EM experiment | Aggregation state: PARTICLE / 3D reconstruction method: single particle reconstruction | 
- Sample preparation
Sample preparation
| Component | 
 | ||||||||||||||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Molecular weight | Experimental value: NO | ||||||||||||||||||||||||||||||
| Source (natural) | 
 | ||||||||||||||||||||||||||||||
| Source (recombinant) | 
 | ||||||||||||||||||||||||||||||
| Buffer solution | pH: 8 | ||||||||||||||||||||||||||||||
| Specimen | Conc.: 0.1 mg/ml / Embedding applied: NO / Shadowing applied: NO / Staining applied: NO / Vitrification applied: YES | ||||||||||||||||||||||||||||||
| Specimen support | Grid material: COPPER / Grid type: Quantifoil R1.2/1.3 | ||||||||||||||||||||||||||||||
| Vitrification | Cryogen name: ETHANE / Humidity: 100 % | 
- Electron microscopy imaging
Electron microscopy imaging
| Experimental equipment |  Model: Titan Krios / Image courtesy: FEI Company | 
|---|---|
| Microscopy | Model: FEI TITAN KRIOS | 
| Electron gun | Electron source:  FIELD EMISSION GUN / Accelerating voltage: 300 kV / Illumination mode: FLOOD BEAM | 
| Electron lens | Mode: BRIGHT FIELD | 
| Image recording | Electron dose: 39 e/Å2 / Detector mode: COUNTING / Film or detector model: GATAN K2 SUMMIT (4k x 4k) | 
- Processing
Processing
| Software | Name: PHENIX / Version: 1.12_2829: / Classification: refinement | ||||||||||||||||||||||||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| EM software | 
 | ||||||||||||||||||||||||||||||||||||||||
| CTF correction | Type: PHASE FLIPPING AND AMPLITUDE CORRECTION | ||||||||||||||||||||||||||||||||||||||||
| Symmetry | Point symmetry: C1 (asymmetric) | ||||||||||||||||||||||||||||||||||||||||
| 3D reconstruction | Resolution: 4 Å / Resolution method: FSC 0.143 CUT-OFF / Num. of particles: 40847 / Symmetry type: POINT | ||||||||||||||||||||||||||||||||||||||||
| Refine LS restraints | 
 | 
 Movie
Movie Controller
Controller













 PDBj
PDBj











































