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LncRNA OIP5-AS1/cyrano suppresses GAK expression to control mitosis

Some long noncoding RNAs (lncRNAs) can regulate gene expression programs, in turn affecting specific cellular processes. We sought to identify the mechanism through which the lncRNA OIP5-AS1, which is abundant in the cytoplasm, suppressed cell proliferation. Silencing of OIP5-AS1 in human cervical c...

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Autores principales: Kim, Jiyoung, Noh, Ji Heon, Lee, Seung-Kyu, Munk, Rachel, Sharov, Alexei, Lehrmann, Elin, Zhang, Yongqing, Wang, Weidong, Abdelmohsen, Kotb, Gorospe, Myriam
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5564778/
https://www.ncbi.nlm.nih.gov/pubmed/28472763
http://dx.doi.org/10.18632/oncotarget.17219
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author Kim, Jiyoung
Noh, Ji Heon
Lee, Seung-Kyu
Munk, Rachel
Sharov, Alexei
Lehrmann, Elin
Zhang, Yongqing
Wang, Weidong
Abdelmohsen, Kotb
Gorospe, Myriam
author_facet Kim, Jiyoung
Noh, Ji Heon
Lee, Seung-Kyu
Munk, Rachel
Sharov, Alexei
Lehrmann, Elin
Zhang, Yongqing
Wang, Weidong
Abdelmohsen, Kotb
Gorospe, Myriam
author_sort Kim, Jiyoung
collection PubMed
description Some long noncoding RNAs (lncRNAs) can regulate gene expression programs, in turn affecting specific cellular processes. We sought to identify the mechanism through which the lncRNA OIP5-AS1, which is abundant in the cytoplasm, suppressed cell proliferation. Silencing of OIP5-AS1 in human cervical carcinoma HeLa cells triggered the appearance of many aberrant (monopolar, multipolar, misaligned) mitotic spindles. Through a combination of approaches to pull down mRNAs bound to OIP5-AS1 and identify proteins differentially expressed when OIP5-AS1 was silenced, we identified a subset of human cell cycle regulatory proteins encoded by mRNAs that interacted with OIP5-AS1 in HeLa cells. Further analysis revealed that GAK mRNA, which encodes a cyclin G-associated kinase important for mitotic progression, associated prominently with OIP5-AS1. The interaction between these two transcripts led to a reduction in GAK mRNA stability and GAK protein abundance, as determined in cells in which OIP5-AS1 levels were increased or decreased. Importantly, the aberrant mitotic cell division seen after silencing OIP5-AS1 was partly rescued if GAK was simultaneously silenced. These findings indicate that the abnormal mitoses seen after silencing OIP5-AS1 were caused by an untimely rise in GAK levels and suggest that OIP5-AS1 suppresses cell proliferation at least in part by reducing GAK levels.
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spelling pubmed-55647782017-08-23 LncRNA OIP5-AS1/cyrano suppresses GAK expression to control mitosis Kim, Jiyoung Noh, Ji Heon Lee, Seung-Kyu Munk, Rachel Sharov, Alexei Lehrmann, Elin Zhang, Yongqing Wang, Weidong Abdelmohsen, Kotb Gorospe, Myriam Oncotarget Research Paper Some long noncoding RNAs (lncRNAs) can regulate gene expression programs, in turn affecting specific cellular processes. We sought to identify the mechanism through which the lncRNA OIP5-AS1, which is abundant in the cytoplasm, suppressed cell proliferation. Silencing of OIP5-AS1 in human cervical carcinoma HeLa cells triggered the appearance of many aberrant (monopolar, multipolar, misaligned) mitotic spindles. Through a combination of approaches to pull down mRNAs bound to OIP5-AS1 and identify proteins differentially expressed when OIP5-AS1 was silenced, we identified a subset of human cell cycle regulatory proteins encoded by mRNAs that interacted with OIP5-AS1 in HeLa cells. Further analysis revealed that GAK mRNA, which encodes a cyclin G-associated kinase important for mitotic progression, associated prominently with OIP5-AS1. The interaction between these two transcripts led to a reduction in GAK mRNA stability and GAK protein abundance, as determined in cells in which OIP5-AS1 levels were increased or decreased. Importantly, the aberrant mitotic cell division seen after silencing OIP5-AS1 was partly rescued if GAK was simultaneously silenced. These findings indicate that the abnormal mitoses seen after silencing OIP5-AS1 were caused by an untimely rise in GAK levels and suggest that OIP5-AS1 suppresses cell proliferation at least in part by reducing GAK levels. Impact Journals LLC 2017-04-19 /pmc/articles/PMC5564778/ /pubmed/28472763 http://dx.doi.org/10.18632/oncotarget.17219 Text en Copyright: © 2017 Kim et al. http://creativecommons.org/licenses/by/3.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) (CC-BY), which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Research Paper
Kim, Jiyoung
Noh, Ji Heon
Lee, Seung-Kyu
Munk, Rachel
Sharov, Alexei
Lehrmann, Elin
Zhang, Yongqing
Wang, Weidong
Abdelmohsen, Kotb
Gorospe, Myriam
LncRNA OIP5-AS1/cyrano suppresses GAK expression to control mitosis
title LncRNA OIP5-AS1/cyrano suppresses GAK expression to control mitosis
title_full LncRNA OIP5-AS1/cyrano suppresses GAK expression to control mitosis
title_fullStr LncRNA OIP5-AS1/cyrano suppresses GAK expression to control mitosis
title_full_unstemmed LncRNA OIP5-AS1/cyrano suppresses GAK expression to control mitosis
title_short LncRNA OIP5-AS1/cyrano suppresses GAK expression to control mitosis
title_sort lncrna oip5-as1/cyrano suppresses gak expression to control mitosis
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5564778/
https://www.ncbi.nlm.nih.gov/pubmed/28472763
http://dx.doi.org/10.18632/oncotarget.17219
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