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A high-content RNAi screen reveals multiple roles for long noncoding RNAs in cell division
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...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7160116/ https://www.ncbi.nlm.nih.gov/pubmed/32296040 http://dx.doi.org/10.1038/s41467-020-14978-7 |
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author | Stojic, Lovorka Lun, Aaron T. L. Mascalchi, Patrice Ernst, Christina Redmond, Aisling M. Mangei, Jasmin Barr, Alexis R. Bousgouni, Vicky Bakal, Chris Marioni, John C. Odom, Duncan T. Gergely, Fanni |
author_facet | Stojic, Lovorka Lun, Aaron T. L. Mascalchi, Patrice Ernst, Christina Redmond, Aisling M. Mangei, Jasmin Barr, Alexis R. Bousgouni, Vicky Bakal, Chris Marioni, John C. Odom, Duncan T. Gergely, Fanni |
author_sort | Stojic, Lovorka |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-7160116 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-71601162020-04-22 A high-content RNAi screen reveals multiple roles for long noncoding RNAs in cell division Stojic, Lovorka Lun, Aaron T. L. Mascalchi, Patrice Ernst, Christina Redmond, Aisling M. Mangei, Jasmin Barr, Alexis R. Bousgouni, Vicky Bakal, Chris Marioni, John C. Odom, Duncan T. Gergely, Fanni Nat Commun Article 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. Nature Publishing Group UK 2020-04-15 /pmc/articles/PMC7160116/ /pubmed/32296040 http://dx.doi.org/10.1038/s41467-020-14978-7 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Stojic, Lovorka Lun, Aaron T. L. Mascalchi, Patrice Ernst, Christina Redmond, Aisling M. Mangei, Jasmin Barr, Alexis R. Bousgouni, Vicky Bakal, Chris Marioni, John C. Odom, Duncan T. Gergely, Fanni A high-content RNAi screen reveals multiple roles for long noncoding RNAs in cell division |
title | A high-content RNAi screen reveals multiple roles for long noncoding RNAs in cell division |
title_full | A high-content RNAi screen reveals multiple roles for long noncoding RNAs in cell division |
title_fullStr | A high-content RNAi screen reveals multiple roles for long noncoding RNAs in cell division |
title_full_unstemmed | A high-content RNAi screen reveals multiple roles for long noncoding RNAs in cell division |
title_short | A high-content RNAi screen reveals multiple roles for long noncoding RNAs in cell division |
title_sort | high-content rnai screen reveals multiple roles for long noncoding rnas in cell division |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7160116/ https://www.ncbi.nlm.nih.gov/pubmed/32296040 http://dx.doi.org/10.1038/s41467-020-14978-7 |
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