+Open data
-Basic information
Entry | Database: EMDB / ID: EMD-20859 | |||||||||
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Title | Cryo-EM map of human CPSF73-CPSF100-Symplekin complex | |||||||||
Map data | Cryo-EM map of human CPSF73-CPSF100-Symplekin complex | |||||||||
Sample |
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Biological species | Homo sapiens (human) | |||||||||
Method | single particle reconstruction / cryo EM / Resolution: 7.4 Å | |||||||||
Authors | Sun Y / Zhang Y / Walz T / Tong L | |||||||||
Funding support | United States, 1 items
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Citation | Journal: Mol Cell / Year: 2020 Title: Structural Insights into the Human Pre-mRNA 3'-End Processing Machinery. Authors: Yixiao Zhang / Yadong Sun / Yongsheng Shi / Thomas Walz / Liang Tong / Abstract: The mammalian pre-mRNA 3'-end-processing machinery consists of cleavage and polyadenylation specificity factor (CPSF), cleavage stimulation factor (CstF), and other proteins, but the overall ...The mammalian pre-mRNA 3'-end-processing machinery consists of cleavage and polyadenylation specificity factor (CPSF), cleavage stimulation factor (CstF), and other proteins, but the overall architecture of this machinery remains unclear. CPSF contains two functionally distinct modules: a cleavage factor (mCF) and a polyadenylation specificity factor (mPSF). Here, we have produced recombinant human CPSF and CstF and examined these factors by electron microscopy (EM). We find that mPSF is the organizational core of the machinery, while the conformations of mCF and CstF and the position of mCF relative to mPSF are highly variable. We have identified by cryo-EM a segment in CPSF100 that tethers mCF to mPSF, and we have named it the PSF interaction motif (PIM). Mutations in the PIM can abolish CPSF formation, indicating that it is a crucial contact in CPSF. We have also obtained reconstructions of mCF and CstF77 by cryo-EM, assembled around the mPSF core. | |||||||||
History |
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-Structure visualization
Movie |
Movie viewer |
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Structure viewer | EM map: SurfViewMolmilJmol/JSmol |
Supplemental images |
-Downloads & links
-EMDB archive
Map data | emd_20859.map.gz | 59.8 MB | EMDB map data format | |
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Header (meta data) | emd-20859-v30.xml emd-20859.xml | 15 KB 15 KB | Display Display | EMDB header |
Images | emd_20859.png | 92.1 KB | ||
Archive directory | http://ftp.pdbj.org/pub/emdb/structures/EMD-20859 ftp://ftp.pdbj.org/pub/emdb/structures/EMD-20859 | HTTPS FTP |
-Validation report
Summary document | emd_20859_validation.pdf.gz | 78.9 KB | Display | EMDB validaton report |
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Full document | emd_20859_full_validation.pdf.gz | 78 KB | Display | |
Data in XML | emd_20859_validation.xml.gz | 495 B | Display | |
Arichive directory | https://ftp.pdbj.org/pub/emdb/validation_reports/EMD-20859 ftp://ftp.pdbj.org/pub/emdb/validation_reports/EMD-20859 | HTTPS FTP |
-Related structure data
-Links
EMDB pages | EMDB (EBI/PDBe) / EMDataResource |
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-Map
File | Download / File: emd_20859.map.gz / Format: CCP4 / Size: 64 MB / Type: IMAGE STORED AS FLOATING POINT NUMBER (4 BYTES) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Annotation | Cryo-EM map of human CPSF73-CPSF100-Symplekin complex | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Projections & slices | Image control
Images are generated by Spider. | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Voxel size | X=Y=Z: 1.07 Å | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Density |
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Symmetry | Space group: 1 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Details | EMDB XML:
CCP4 map header:
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-Supplemental data
-Sample components
-Entire : The complex of human CPSF73-CPSF100-Symplekin
Entire | Name: The complex of human CPSF73-CPSF100-Symplekin |
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Components |
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-Supramolecule #1: The complex of human CPSF73-CPSF100-Symplekin
Supramolecule | Name: The complex of human CPSF73-CPSF100-Symplekin / type: complex / ID: 1 / Parent: 0 / Macromolecule list: all |
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Source (natural) | Organism: Homo sapiens (human) |
Recombinant expression | Organism: Trichoplusia ni (cabbage looper) |
-Macromolecule #1: CPSF73
Macromolecule | Name: CPSF73 / type: protein_or_peptide / ID: 1 / Enantiomer: LEVO |
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Source (natural) | Organism: Homo sapiens (human) |
Recombinant expression | Organism: Trichoplusia ni (cabbage looper) |
Sequence | String: MSAIPAEESD QLLIRPLGAG QEVGRSCIIL EFKGRKIMLD CGIHPGLEGM DALPYIDLID PAEIDLLLIS HFHLDHCGAL PWFLQKTSFK GRTFMTHATK AIYRWLLSDY VKVSNISADD MLYTETDLEE SMDKIETINF HEVKEVAGIK FWCYHAGHVL GAAMFMIEIA ...String: MSAIPAEESD QLLIRPLGAG QEVGRSCIIL EFKGRKIMLD CGIHPGLEGM DALPYIDLID PAEIDLLLIS HFHLDHCGAL PWFLQKTSFK GRTFMTHATK AIYRWLLSDY VKVSNISADD MLYTETDLEE SMDKIETINF HEVKEVAGIK FWCYHAGHVL GAAMFMIEIA GVKLLYTGDF SRQEDRHLMA AEIPNIKPDI LIIESTYGTH IHEKREEREA RFCNTVHDIV NRGGRGLIPV FALGRAQELL LILDEYWQNH PELHDIPIYY ASSLAKKCMA VYQTYVNAMN DKIRKQININ NPFVFKHISN LKSMDHFDDI GPSVVMASPG MMQSGLSREL FESWCTDKRN GVIIAGYCVE GTLAKHIMSE PEEITTMSGQ KLPLKMSVDY ISFSAHTDYQ QTSEFIRALK PPHVILVHGE QNEMARLKAA LIREYEDNDE VHIEVHNPRN TEAVTLNFRG EKLAKVMGFL ADKKPEQGQR VSGILVKRN FNYHILSPCD LSNYTDLAMS TVKQTQAIPY TGPFNLLCYQ LQKLTGDVEE LEIQEKPALK VFKNITVIQE PGMVVLEWLA NPSNDMYADT VTTVILEVQS NPKIRKGAVQ KVSKKLEMHV YSKRLEIMLQ DIFGEDCVSV KDDSILSVTV DGKTANLNLE TRTVECEEGS EDDESLREMV ELAAQRLYEA LTPVH |
-Macromolecule #2: CPSF100
Macromolecule | Name: CPSF100 / type: protein_or_peptide / ID: 2 / Enantiomer: LEVO |
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Source (natural) | Organism: Homo sapiens (human) |
Recombinant expression | Organism: Trichoplusia ni (cabbage looper) |
Sequence | String: MTSIIKLTTL SGVQEESALC YLLQVDEFRF LLDCGWDEHF SMDIIDSLRK HVHQIDAVLL SHPDPLHLGA LPYAVGKLGL NCAIYATIPV YKMGQMFMYD LYQSRHNTED FTLFTLDDVD AAFDKIQQLK FSQIVNLKGK GHGLSITPLP AGHMIGGTIW KIVKDGEEEI ...String: MTSIIKLTTL SGVQEESALC YLLQVDEFRF LLDCGWDEHF SMDIIDSLRK HVHQIDAVLL SHPDPLHLGA LPYAVGKLGL NCAIYATIPV YKMGQMFMYD LYQSRHNTED FTLFTLDDVD AAFDKIQQLK FSQIVNLKGK GHGLSITPLP AGHMIGGTIW KIVKDGEEEI VYAVDFNHKR EIHLNGCSLE MLSRPSLLIT DSFNATYVQP RRKQRDEQLL TNVLETLRGD GNVLIAVDTA GRVLELAQLL DQIWRTKDAG LGVYSLALLN NVSYNVVEFS KSQVEWMSDK LMRCFEDKRN NPFQFRHLSL CHGLSDLARV PSPKVVLASQ PDLECGFSRD LFIQWCQDPK NSIILTYRTT PGTLARFLID NPSEKITEIE LRKRVKLEGK ELEEYLEKEK LKKEAAKKLE QSKEADIDSS DESDIEEDID QPSAHKTKHD LMMKGEGSRK GSFFKQAKKS YPMFPAPEER IKWDEYGEII KPEDFLVPEL QATEEEKSKL ESGLTNGDEP MDQDLSDVPT KCISTTESIE IKARVTYIDY EGRSDGDSIK KIINQMKPRQ LIIVHGPPEA SQDLAECCRA FGGKDIKVYM PKLHETVDAT SETHIYQVRL KDSLVSSLQF CKAKAELAWI DGVLDMRVSK VDTGVILEEG ELKDDGEDSE MQVEAPSDSS VIAQQKAMKS LFGDDEKETG EESEIIPTLE PLPPHEVPGH QSVFMNEPRL SDFKQVLLRE GIQAEFVGGV LVCNNQVAVR RTETGRIGLE GCLCQDFYRI RDLLYEQYAI V |
-Macromolecule #3: Symplekin
Macromolecule | Name: Symplekin / type: protein_or_peptide / ID: 3 / Enantiomer: LEVO |
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Source (natural) | Organism: Homo sapiens (human) |
Recombinant expression | Organism: Trichoplusia ni (cabbage looper) |
Sequence | String: SDSTLKKMKL EPNLGEDDED KDLEPGPSGT SKASAQISGQ SDTDITAEFL QPLLTPDNVA NLVLISMVYL PEAMPASFQA IYTPVESAGT EAQIKHLARL MATQMTAAGL GPGVEQTKQC KEEPKEEKVV KTESVLIKRR LSAQGQAISV VGSLSSMSPL EEEAPQAKRR ...String: SDSTLKKMKL EPNLGEDDED KDLEPGPSGT SKASAQISGQ SDTDITAEFL QPLLTPDNVA NLVLISMVYL PEAMPASFQA IYTPVESAGT EAQIKHLARL MATQMTAAGL GPGVEQTKQC KEEPKEEKVV KTESVLIKRR LSAQGQAISV VGSLSSMSPL EEEAPQAKRR PEPIIPVTQP RLAGAGGRKK IFRLSDVLKP LTDAQVEAMK LGAVKRILRA EKAVACSGAA QVRIKILASL VTQFNSGLKA EVLSFILEDV RARLDLAFAW LYQEYNAYLA AGASGSLDKY EDCLIRLLSG LQEKPDQKDG IFTKVVLEAP LITESALEVV RKYCEDESRT YLGMSTLRDL IFKRPSRQFQ YLHVLLDLSS HEKDKVRSQA LLFIKRMYEK EQLREYVEKF ALNYLQLLVH PNPPSVLFGA DKDTEVAAPW TEETVKQCLY LYLALLPQNH KLIHELAAVY TEAIADIKRT VLRVIEQPIR GMGMNSPELL LLVENCPKGA ETLVTRCLHS LTDKVPPSPE LVKRVRDLYH KRLPDVRFLI PVLNGLEKKE VIQALPKLIK LNPIVVKEVF NRLLGTQHGE GNSALSPLNP GELLIALHNI DSVKCDMKSI IKATNLCFAE RNVYTSEVLA VVMQQLMEQS PLPMLLMRTV IQSLTMYPRL GGFVMNILSR LIMKQVWKYP KVWEGFIKCC QRTKPQSFQV ILQLPPQQLG AVFDKCPELR EPLLAHVRSF TPHQQAHIPN SIMTILEASG KQEPEAKE |
-Experimental details
-Structure determination
Method | cryo EM |
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Processing | single particle reconstruction |
Aggregation state | particle |
-Sample preparation
Concentration | 0.25 mg/mL |
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Buffer | pH: 8 / Component - Concentration: 150.0 mM / Component - Formula: NaCl / Component - Name: sodium chloride / Details: 25 mM Tris-HCl, pH 8.0, 150 mM NaCl, 5 mM DTT |
Grid | Support film - Material: CARBON / Support film - topology: HOLEY / Details: unspecified |
Vitrification | Cryogen name: ETHANE / Chamber humidity: 100 % / Chamber temperature: 277 K / Instrument: FEI VITROBOT MARK IV |
-Electron microscopy
Microscope | FEI TITAN KRIOS |
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Image recording | Film or detector model: GATAN K2 SUMMIT (4k x 4k) / Detector mode: COUNTING / Average exposure time: 10.0 sec. / Average electron dose: 70.0 e/Å2 |
Electron beam | Acceleration voltage: 300 kV / Electron source: FIELD EMISSION GUN |
Electron optics | C2 aperture diameter: 100.0 µm / Calibrated defocus max: 2.8 µm / Calibrated defocus min: 0.9 µm / Calibrated magnification: 46729 / Illumination mode: FLOOD BEAM / Imaging mode: BRIGHT FIELD / Cs: 2.7 mm / Nominal defocus max: 2.5 µm / Nominal defocus min: 1.2 µm / Nominal magnification: 225000 |
Sample stage | Specimen holder model: FEI TITAN KRIOS AUTOGRID HOLDER / Cooling holder cryogen: NITROGEN |
Experimental equipment | Model: Titan Krios / Image courtesy: FEI Company |
-Image processing
CTF correction | Software - Name: CTFFIND |
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Final reconstruction | Resolution.type: BY AUTHOR / Resolution: 7.4 Å / Resolution method: FSC 0.143 CUT-OFF / Software - Name: RELION / Number images used: 35040 |
Initial angle assignment | Type: PROJECTION MATCHING |
Final angle assignment | Type: PROJECTION MATCHING |