A high-content RNAi screen reveals multiple roles for long noncoding RNAs in cell division.

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Date
2020-04-15Author
Stojic, L
Lun, ATL
Mascalchi, P
Ernst, C
Redmond, AM
Mangei, J
Barr, AR
Bousgouni, V
Bakal, C
Marioni, JC
Odom, DT
Gergely, F
Type
Journal Article
Metadata
Show full item recordAbstract
Genome 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.
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Subject
Hela Cells
Humans
Proteins
Cell Division
Mitosis
RNA Interference
High-Throughput Screening Assays
RNA, Long Noncoding
Research team
Dynamical Cell Systems
Language
eng
Date accepted
2020-02-09
License start date
2020-04-15
Citation
Nature communications, 2020, 11 (1), pp. 1851 - ?
Publisher
NATURE PUBLISHING GROUP