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Gene targets of mouse miR-709: regulation of distinct pools

MicroRNA (miRNA) are short non-coding RNA molecules that regulate multiple cellular processes, including development, cell differentiation, proliferation and death. Nevertheless, little is known on whether miRNA control the same gene networks in different tissues. miR-709 is an abundant miRNA expres...

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Autores principales: Surendran, Sneha, Jideonwo, Victoria N., Merchun, Chris, Ahn, Miwon, Murray, John, Ryan, Jennifer, Dunn, Kenneth W., Kota, Janaiah, Morral, Núria
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4705522/
https://www.ncbi.nlm.nih.gov/pubmed/26743462
http://dx.doi.org/10.1038/srep18958
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author Surendran, Sneha
Jideonwo, Victoria N.
Merchun, Chris
Ahn, Miwon
Murray, John
Ryan, Jennifer
Dunn, Kenneth W.
Kota, Janaiah
Morral, Núria
author_facet Surendran, Sneha
Jideonwo, Victoria N.
Merchun, Chris
Ahn, Miwon
Murray, John
Ryan, Jennifer
Dunn, Kenneth W.
Kota, Janaiah
Morral, Núria
author_sort Surendran, Sneha
collection PubMed
description MicroRNA (miRNA) are short non-coding RNA molecules that regulate multiple cellular processes, including development, cell differentiation, proliferation and death. Nevertheless, little is known on whether miRNA control the same gene networks in different tissues. miR-709 is an abundant miRNA expressed ubiquitously. Through transcriptome analysis, we have identified targets of miR-709 in hepatocytes. miR-709 represses genes implicated in cytoskeleton organization, extracellular matrix attachment, and fatty acid metabolism. Remarkably, none of the previously identified targets in non-hepatic tissues are silenced by miR-709 in hepatocytes, even though several of these genes are abundantly expressed in liver. In addition, miR-709 is upregulated in hepatocellular carcinoma, suggesting it participates in the genetic reprogramming that takes place during cell division, when cytoskeleton remodeling requires substantial changes in gene expression. In summary, the present study shows that miR-709 does not repress the same pool of genes in separate cell types. These results underscore the need for validating gene targets in every tissue a miRNA is expressed.
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spelling pubmed-47055222016-01-19 Gene targets of mouse miR-709: regulation of distinct pools Surendran, Sneha Jideonwo, Victoria N. Merchun, Chris Ahn, Miwon Murray, John Ryan, Jennifer Dunn, Kenneth W. Kota, Janaiah Morral, Núria Sci Rep Article MicroRNA (miRNA) are short non-coding RNA molecules that regulate multiple cellular processes, including development, cell differentiation, proliferation and death. Nevertheless, little is known on whether miRNA control the same gene networks in different tissues. miR-709 is an abundant miRNA expressed ubiquitously. Through transcriptome analysis, we have identified targets of miR-709 in hepatocytes. miR-709 represses genes implicated in cytoskeleton organization, extracellular matrix attachment, and fatty acid metabolism. Remarkably, none of the previously identified targets in non-hepatic tissues are silenced by miR-709 in hepatocytes, even though several of these genes are abundantly expressed in liver. In addition, miR-709 is upregulated in hepatocellular carcinoma, suggesting it participates in the genetic reprogramming that takes place during cell division, when cytoskeleton remodeling requires substantial changes in gene expression. In summary, the present study shows that miR-709 does not repress the same pool of genes in separate cell types. These results underscore the need for validating gene targets in every tissue a miRNA is expressed. Nature Publishing Group 2016-01-08 /pmc/articles/PMC4705522/ /pubmed/26743462 http://dx.doi.org/10.1038/srep18958 Text en Copyright © 2016, Macmillan Publishers Limited 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
Surendran, Sneha
Jideonwo, Victoria N.
Merchun, Chris
Ahn, Miwon
Murray, John
Ryan, Jennifer
Dunn, Kenneth W.
Kota, Janaiah
Morral, Núria
Gene targets of mouse miR-709: regulation of distinct pools
title Gene targets of mouse miR-709: regulation of distinct pools
title_full Gene targets of mouse miR-709: regulation of distinct pools
title_fullStr Gene targets of mouse miR-709: regulation of distinct pools
title_full_unstemmed Gene targets of mouse miR-709: regulation of distinct pools
title_short Gene targets of mouse miR-709: regulation of distinct pools
title_sort gene targets of mouse mir-709: regulation of distinct pools
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4705522/
https://www.ncbi.nlm.nih.gov/pubmed/26743462
http://dx.doi.org/10.1038/srep18958
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