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dc.contributor.authorStojic, L
dc.contributor.authorLun, ATL
dc.contributor.authorMascalchi, P
dc.contributor.authorErnst, C
dc.contributor.authorRedmond, AM
dc.contributor.authorMangei, J
dc.contributor.authorBarr, AR
dc.contributor.authorBousgouni, V
dc.contributor.authorBakal, C
dc.contributor.authorMarioni, JC
dc.contributor.authorOdom, DT
dc.contributor.authorGergely, F
dc.date.accessioned2020-05-26T11:16:19Z
dc.date.issued2020-04-15
dc.identifier.citationNature communications, 2020, 11 (1), pp. 1851 - ?
dc.identifier.issn2041-1723
dc.identifier.urihttps://repository.icr.ac.uk/handle/internal/3634
dc.identifier.eissn2041-1723
dc.identifier.doi10.1038/s41467-020-14978-7
dc.description.abstractGenome stability relies on proper coordination of mitosis and cytokinesis, where dynamic microtubules capture and faithfully segregate chromosomes into daughter cells. With a high-content RNAi imaging screen targeting more than 2,000 human lncRNAs, we identify numerous lncRNAs involved in key steps of cell division such as chromosome segregation, mitotic duration and cytokinesis. Here, we provide evidence that the chromatin-associated lncRNA, linc00899, leads to robust mitotic delay upon its depletion in multiple cell types. We perform transcriptome analysis of linc00899-depleted cells and identify the neuronal microtubule-binding protein, TPPP/p25, as a target of linc00899. We further show that linc00899 binds TPPP/p25 and suppresses its transcription. In cells depleted of linc00899, upregulation of TPPP/p25 alters microtubule dynamics and delays mitosis. Overall, our comprehensive screen uncovers several lncRNAs involved in genome stability and reveals a lncRNA that controls microtubule behaviour with functional implications beyond cell division.
dc.formatElectronic
dc.format.extent1851 - ?
dc.languageeng
dc.language.isoeng
dc.publisherNATURE PUBLISHING GROUP
dc.rights.urihttps://creativecommons.org/licenses/by/4.0
dc.subjectHela Cells
dc.subjectHumans
dc.subjectProteins
dc.subjectCell Division
dc.subjectMitosis
dc.subjectRNA Interference
dc.subjectHigh-Throughput Screening Assays
dc.subjectRNA, Long Noncoding
dc.titleA high-content RNAi screen reveals multiple roles for long noncoding RNAs in cell division.
dc.typeJournal Article
dcterms.dateAccepted2020-02-09
rioxxterms.versionofrecord10.1038/s41467-020-14978-7
rioxxterms.licenseref.urihttps://creativecommons.org/licenses/by/4.0
rioxxterms.licenseref.startdate2020-04-15
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/Cancer Biology
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Cancer Biology/Dynamical Cell Systems
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/Cancer Biology
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Cancer Biology/Dynamical Cell Systems
pubs.publication-statusPublished
pubs.volume11
pubs.embargo.termsNot known
icr.researchteamDynamical Cell Systems
dc.contributor.icrauthorBousgouni, Paraskevi
dc.contributor.icrauthorBakal, Christopher


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