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dc.contributor.authorRamsay, EP
dc.contributor.authorAbascal-Palacios, G
dc.contributor.authorDaiß, JL
dc.contributor.authorKing, H
dc.contributor.authorGouge, J
dc.contributor.authorPilsl, M
dc.contributor.authorBeuron, F
dc.contributor.authorMorris, E
dc.contributor.authorGunkel, P
dc.contributor.authorEngel, C
dc.contributor.authorVannini, A
dc.date.accessioned2021-01-11T11:06:45Z
dc.date.issued2020-12-17
dc.identifier.citationNature communications, 2020, 11 (1), pp. 6409 - ?
dc.identifier.issn2041-1723
dc.identifier.urihttps://repository.icr.ac.uk/handle/internal/4272
dc.identifier.eissn2041-1723
dc.identifier.doi10.1038/s41467-020-20262-5
dc.description.abstractIn eukaryotes, RNA Polymerase (Pol) III is specialized for the transcription of tRNAs and other short, untranslated RNAs. Pol III is a determinant of cellular growth and lifespan across eukaryotes. Upregulation of Pol III transcription is observed in cancer and causative Pol III mutations have been described in neurodevelopmental disorders and hypersensitivity to viral infection. Here, we report a cryo-EM reconstruction at 4.0 Å of human Pol III, allowing mapping and rationalization of reported genetic mutations. Mutations causing neurodevelopmental defects cluster in hotspots affecting Pol III stability and/or biogenesis, whereas mutations affecting viral sensing are located in proximity to DNA binding regions, suggesting an impairment of Pol III cytosolic viral DNA-sensing. Integrating x-ray crystallography and SAXS, we also describe the structure of the higher eukaryote specific RPC5 C-terminal extension. Surprisingly, experiments in living cells highlight a role for this module in the assembly and stability of human Pol III.
dc.formatElectronic
dc.format.extent6409 - ?
dc.languageeng
dc.language.isoeng
dc.publisherNATURE RESEARCH
dc.rights.urihttps://creativecommons.org/licenses/by/4.0
dc.subjectHela Cells
dc.subjectHumans
dc.subjectDNA-Directed RNA Polymerases
dc.subjectRNA Polymerase III
dc.subjectProtein Subunits
dc.subjectCryoelectron Microscopy
dc.subjectX-Ray Diffraction
dc.subjectEnzyme Stability
dc.subjectProtein Conformation
dc.subjectMutation
dc.subjectModels, Molecular
dc.subjectScattering, Small Angle
dc.titleStructure of human RNA polymerase III.
dc.typeJournal Article
dcterms.dateAccepted2020-11-20
rioxxterms.versionofrecord10.1038/s41467-020-20262-5
rioxxterms.licenseref.urihttps://creativecommons.org/licenses/by/4.0
rioxxterms.licenseref.startdate2020-12-17
rioxxterms.typeJournal Article/Review
dc.relation.isPartOfNature communications
pubs.issue1
pubs.notesNot known
pubs.organisational-group/ICR
pubs.organisational-group/ICR/Primary Group
pubs.organisational-group/ICR/Primary Group/ICR Divisions
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Structural Biology
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Structural Biology/Structural Electron Microscopy
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Structural Biology/Vannini Group
pubs.organisational-group/ICR
pubs.organisational-group/ICR/Primary Group
pubs.organisational-group/ICR/Primary Group/ICR Divisions
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Structural Biology
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Structural Biology/Structural Electron Microscopy
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Structural Biology/Vannini Group
pubs.publication-statusPublished
pubs.volume11
pubs.embargo.termsNot known
icr.researchteamStructural Electron Microscopy
icr.researchteamVannini Group
dc.contributor.icrauthorAbascal Palacios, Guillermo
dc.contributor.icrauthorBeuron, Fabienne
dc.contributor.icrauthorMorris, Edward
dc.contributor.icrauthorVannini, Alessandro


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