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Yorodumi- EMDB-15340: MCM C-tier local refinement. Human replisome bound by pol alpha, ... -
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Open data
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Basic information
| Entry | ![]() | |||||||||
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| Title | MCM C-tier local refinement. Human replisome bound by pol alpha, engaged on fork DNA with 60 nt lagging strand. | |||||||||
Map data | MCM C-tier local refinement. Human replisome - pol alpha complex. Engaged with fork DNA substrate with 60 nt lagging strand. Sharp | |||||||||
Sample |
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Keywords | Replication / helicase / polymerase / pol alpha / priming | |||||||||
| Biological species | ![]() | |||||||||
| Method | single particle reconstruction / cryo EM / Resolution: 3.7 Å | |||||||||
Authors | Jones ML / Yeeles JTP | |||||||||
| Funding support | United Kingdom, 1 items
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Citation | Journal: Mol Cell / Year: 2023Title: How Pol α-primase is targeted to replisomes to prime eukaryotic DNA replication. Authors: Morgan L Jones / Valentina Aria / Yasemin Baris / Joseph T P Yeeles / ![]() Abstract: During eukaryotic DNA replication, Pol α-primase generates primers at replication origins to start leading-strand synthesis and every few hundred nucleotides during discontinuous lagging-strand ...During eukaryotic DNA replication, Pol α-primase generates primers at replication origins to start leading-strand synthesis and every few hundred nucleotides during discontinuous lagging-strand replication. How Pol α-primase is targeted to replication forks to prime DNA synthesis is not fully understood. Here, by determining cryoelectron microscopy (cryo-EM) structures of budding yeast and human replisomes containing Pol α-primase, we reveal a conserved mechanism for the coordination of priming by the replisome. Pol α-primase binds directly to the leading edge of the CMG (CDC45-MCM-GINS) replicative helicase via a complex interaction network. The non-catalytic PRIM2/Pri2 subunit forms two interfaces with CMG that are critical for in vitro DNA replication and yeast cell growth. These interactions position the primase catalytic subunit PRIM1/Pri1 directly above the exit channel for lagging-strand template single-stranded DNA (ssDNA), revealing why priming occurs efficiently only on the lagging-strand template and elucidating a mechanism for Pol α-primase to overcome competition from RPA to initiate primer synthesis. | |||||||||
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Structure visualization
| Supplemental images |
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Downloads & links
-EMDB archive
| Map data | emd_15340.map.gz | 116.8 MB | EMDB map data format | |
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| Header (meta data) | emd-15340-v30.xml emd-15340.xml | 16.2 KB 16.2 KB | Display Display | EMDB header |
| FSC (resolution estimation) | emd_15340_fsc.xml | 10.5 KB | Display | FSC data file |
| Images | emd_15340.png | 148.4 KB | ||
| Others | emd_15340_additional_1.map.gz emd_15340_additional_2.map.gz emd_15340_half_map_1.map.gz emd_15340_half_map_2.map.gz | 118 MB 60.4 MB 116.1 MB 116.1 MB | ||
| Archive directory | http://ftp.pdbj.org/pub/emdb/structures/EMD-15340 ftp://ftp.pdbj.org/pub/emdb/structures/EMD-15340 | HTTPS FTP |
-Validation report
| Summary document | emd_15340_validation.pdf.gz | 965 KB | Display | EMDB validaton report |
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| Full document | emd_15340_full_validation.pdf.gz | 964.5 KB | Display | |
| Data in XML | emd_15340_validation.xml.gz | 18.6 KB | Display | |
| Data in CIF | emd_15340_validation.cif.gz | 24 KB | Display | |
| Arichive directory | https://ftp.pdbj.org/pub/emdb/validation_reports/EMD-15340 ftp://ftp.pdbj.org/pub/emdb/validation_reports/EMD-15340 | HTTPS FTP |
-Related structure data
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Links
| EMDB pages | EMDB (EBI/PDBe) / EMDataResource |
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Map
| File | Download / File: emd_15340.map.gz / Format: CCP4 / Size: 125 MB / Type: IMAGE STORED AS FLOATING POINT NUMBER (4 BYTES) | ||||||||||||||||||||||||||||||||||||
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| Annotation | MCM C-tier local refinement. Human replisome - pol alpha complex. Engaged with fork DNA substrate with 60 nt lagging strand. Sharp | ||||||||||||||||||||||||||||||||||||
| Projections & slices | Image control
Images are generated by Spider. | ||||||||||||||||||||||||||||||||||||
| Voxel size | X=Y=Z: 1.2363 Å | ||||||||||||||||||||||||||||||||||||
| Density |
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| Symmetry | Space group: 1 | ||||||||||||||||||||||||||||||||||||
| Details | EMDB XML:
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-Supplemental data
-Additional map: MCM C-tier local refinement. Human replisome - pol...
| File | emd_15340_additional_1.map | ||||||||||||
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| Annotation | MCM C-tier local refinement. Human replisome - pol alpha complex. Engaged with fork DNA substrate with 60 nt lagging strand. Sharp | ||||||||||||
| Projections & Slices |
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| Density Histograms |
-Additional map: MCM C-tier local refinement. Human replisome - pol...
| File | emd_15340_additional_2.map | ||||||||||||
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| Annotation | MCM C-tier local refinement. Human replisome - pol alpha complex. Engaged with fork DNA substrate with 60 nt lagging strand. Unsharp | ||||||||||||
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| Density Histograms |
-Half map: Half map B
| File | emd_15340_half_map_1.map | ||||||||||||
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| Annotation | Half map B | ||||||||||||
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| Density Histograms |
-Half map: Half map A
| File | emd_15340_half_map_2.map | ||||||||||||
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| Annotation | Half map A | ||||||||||||
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| Density Histograms |
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Sample components
-Entire : Replisome - pol alpha complex
| Entire | Name: Replisome - pol alpha complex |
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| Components |
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-Supramolecule #1: Replisome - pol alpha complex
| Supramolecule | Name: Replisome - pol alpha complex / type: complex / ID: 1 / Parent: 0 Details: S. cerevisiae pol alpha bound to the core replisome engaged with a fork DNA substrate containing a 60 nucleotide lagging strand. |
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| Source (natural) | Organism: ![]() |
-Experimental details
-Structure determination
| Method | cryo EM |
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Processing | single particle reconstruction |
| Aggregation state | particle |
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Sample preparation
| Buffer | pH: 7.6 |
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| Vitrification | Cryogen name: ETHANE |
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Electron microscopy
| Microscope | FEI TITAN KRIOS |
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| Image recording | Film or detector model: GATAN K3 (6k x 4k) / Average electron dose: 40.184 e/Å2 |
| Electron beam | Acceleration voltage: 300 kV / Electron source: FIELD EMISSION GUN |
| Electron optics | Illumination mode: FLOOD BEAM / Imaging mode: BRIGHT FIELD / Nominal defocus max: 3.5 µm / Nominal defocus min: 1.5 µm |
| Experimental equipment | ![]() Model: Titan Krios / Image courtesy: FEI Company |
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Keywords
Authors
United Kingdom, 1 items
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Processing
FIELD EMISSION GUN

