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Transcriptional silencing of long noncoding RNA GNG12-AS1 uncouples its transcriptional and product-related functions
Long noncoding RNAs (lncRNAs) regulate gene expression via their RNA product or through transcriptional interference, yet a strategy to differentiate these two processes is lacking. To address this, we used multiple small interfering RNAs (siRNAs) to silence GNG12-AS1, a nuclear lncRNA transcribed i...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4740813/ https://www.ncbi.nlm.nih.gov/pubmed/26832224 http://dx.doi.org/10.1038/ncomms10406 |
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author | Stojic, Lovorka Niemczyk, Malwina Orjalo, Arturo Ito, Yoko Ruijter, Anna Elisabeth Maria Uribe-Lewis, Santiago Joseph, Nimesh Weston, Stephen Menon, Suraj Odom, Duncan T. Rinn, John Gergely, Fanni Murrell, Adele |
author_facet | Stojic, Lovorka Niemczyk, Malwina Orjalo, Arturo Ito, Yoko Ruijter, Anna Elisabeth Maria Uribe-Lewis, Santiago Joseph, Nimesh Weston, Stephen Menon, Suraj Odom, Duncan T. Rinn, John Gergely, Fanni Murrell, Adele |
author_sort | Stojic, Lovorka |
collection | PubMed |
description | Long noncoding RNAs (lncRNAs) regulate gene expression via their RNA product or through transcriptional interference, yet a strategy to differentiate these two processes is lacking. To address this, we used multiple small interfering RNAs (siRNAs) to silence GNG12-AS1, a nuclear lncRNA transcribed in an antisense orientation to the tumour-suppressor DIRAS3. Here we show that while most siRNAs silence GNG12-AS1 post-transcriptionally, siRNA complementary to exon 1 of GNG12-AS1 suppresses its transcription by recruiting Argonaute 2 and inhibiting RNA polymerase II binding. Transcriptional, but not post-transcriptional, silencing of GNG12-AS1 causes concomitant upregulation of DIRAS3, indicating a function in transcriptional interference. This change in DIRAS3 expression is sufficient to impair cell cycle progression. In addition, the reduction in GNG12-AS1 transcripts alters MET signalling and cell migration, but these are independent of DIRAS3. Thus, differential siRNA targeting of a lncRNA allows dissection of the functions related to the process and products of its transcription. |
format | Online Article Text |
id | pubmed-4740813 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-47408132016-03-04 Transcriptional silencing of long noncoding RNA GNG12-AS1 uncouples its transcriptional and product-related functions Stojic, Lovorka Niemczyk, Malwina Orjalo, Arturo Ito, Yoko Ruijter, Anna Elisabeth Maria Uribe-Lewis, Santiago Joseph, Nimesh Weston, Stephen Menon, Suraj Odom, Duncan T. Rinn, John Gergely, Fanni Murrell, Adele Nat Commun Article Long noncoding RNAs (lncRNAs) regulate gene expression via their RNA product or through transcriptional interference, yet a strategy to differentiate these two processes is lacking. To address this, we used multiple small interfering RNAs (siRNAs) to silence GNG12-AS1, a nuclear lncRNA transcribed in an antisense orientation to the tumour-suppressor DIRAS3. Here we show that while most siRNAs silence GNG12-AS1 post-transcriptionally, siRNA complementary to exon 1 of GNG12-AS1 suppresses its transcription by recruiting Argonaute 2 and inhibiting RNA polymerase II binding. Transcriptional, but not post-transcriptional, silencing of GNG12-AS1 causes concomitant upregulation of DIRAS3, indicating a function in transcriptional interference. This change in DIRAS3 expression is sufficient to impair cell cycle progression. In addition, the reduction in GNG12-AS1 transcripts alters MET signalling and cell migration, but these are independent of DIRAS3. Thus, differential siRNA targeting of a lncRNA allows dissection of the functions related to the process and products of its transcription. Nature Publishing Group 2016-02-02 /pmc/articles/PMC4740813/ /pubmed/26832224 http://dx.doi.org/10.1038/ncomms10406 Text en Copyright © 2016, Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved. http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Stojic, Lovorka Niemczyk, Malwina Orjalo, Arturo Ito, Yoko Ruijter, Anna Elisabeth Maria Uribe-Lewis, Santiago Joseph, Nimesh Weston, Stephen Menon, Suraj Odom, Duncan T. Rinn, John Gergely, Fanni Murrell, Adele Transcriptional silencing of long noncoding RNA GNG12-AS1 uncouples its transcriptional and product-related functions |
title | Transcriptional silencing of long noncoding RNA GNG12-AS1 uncouples its transcriptional and product-related functions |
title_full | Transcriptional silencing of long noncoding RNA GNG12-AS1 uncouples its transcriptional and product-related functions |
title_fullStr | Transcriptional silencing of long noncoding RNA GNG12-AS1 uncouples its transcriptional and product-related functions |
title_full_unstemmed | Transcriptional silencing of long noncoding RNA GNG12-AS1 uncouples its transcriptional and product-related functions |
title_short | Transcriptional silencing of long noncoding RNA GNG12-AS1 uncouples its transcriptional and product-related functions |
title_sort | transcriptional silencing of long noncoding rna gng12-as1 uncouples its transcriptional and product-related functions |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4740813/ https://www.ncbi.nlm.nih.gov/pubmed/26832224 http://dx.doi.org/10.1038/ncomms10406 |
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