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Characterizing isomiR variants within the microRNA‐34/449 family
miR‐34/449 microRNAs are conserved regulators of multiciliated cell differentiation. Here, we evidence and characterize expression of two isomiR variant sequences from the miR‐34/449 family in human airway epithelial cells. These isomiRs differ from their canonical counterparts miR‐34b and miR‐449c...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5363356/ https://www.ncbi.nlm.nih.gov/pubmed/28192603 http://dx.doi.org/10.1002/1873-3468.12595 |
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author | Mercey, Olivier Popa, Alexandra Cavard, Amélie Paquet, Agnès Chevalier, Benoît Pons, Nicolas Magnone, Virginie Zangari, Joséphine Brest, Patrick Zaragosi, Laure‐Emmanuelle Ponzio, Gilles Lebrigand, Kevin Barbry, Pascal Marcet, Brice |
author_facet | Mercey, Olivier Popa, Alexandra Cavard, Amélie Paquet, Agnès Chevalier, Benoît Pons, Nicolas Magnone, Virginie Zangari, Joséphine Brest, Patrick Zaragosi, Laure‐Emmanuelle Ponzio, Gilles Lebrigand, Kevin Barbry, Pascal Marcet, Brice |
author_sort | Mercey, Olivier |
collection | PubMed |
description | miR‐34/449 microRNAs are conserved regulators of multiciliated cell differentiation. Here, we evidence and characterize expression of two isomiR variant sequences from the miR‐34/449 family in human airway epithelial cells. These isomiRs differ from their canonical counterparts miR‐34b and miR‐449c by one supplemental uridine at their 5′‐end, leading to a one‐base shift in their seed region. Overexpression of canonical miR‐34/449 or 5′‐isomiR‐34/449 induces distinct gene expression profiles and biological effects. However, some target transcripts and functional activities are shared by both canonical microRNAs and isomiRs. Indeed, both repress important targets that result in cell cycle blockage and Notch pathway inhibition. Our findings suggest that 5′‐isomiR‐34/449 may represent additional mechanisms by which miR‐34/449 family finely controls several pathways to drive multiciliogenesis. |
format | Online Article Text |
id | pubmed-5363356 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-53633562017-04-06 Characterizing isomiR variants within the microRNA‐34/449 family Mercey, Olivier Popa, Alexandra Cavard, Amélie Paquet, Agnès Chevalier, Benoît Pons, Nicolas Magnone, Virginie Zangari, Joséphine Brest, Patrick Zaragosi, Laure‐Emmanuelle Ponzio, Gilles Lebrigand, Kevin Barbry, Pascal Marcet, Brice FEBS Lett Research Letters miR‐34/449 microRNAs are conserved regulators of multiciliated cell differentiation. Here, we evidence and characterize expression of two isomiR variant sequences from the miR‐34/449 family in human airway epithelial cells. These isomiRs differ from their canonical counterparts miR‐34b and miR‐449c by one supplemental uridine at their 5′‐end, leading to a one‐base shift in their seed region. Overexpression of canonical miR‐34/449 or 5′‐isomiR‐34/449 induces distinct gene expression profiles and biological effects. However, some target transcripts and functional activities are shared by both canonical microRNAs and isomiRs. Indeed, both repress important targets that result in cell cycle blockage and Notch pathway inhibition. Our findings suggest that 5′‐isomiR‐34/449 may represent additional mechanisms by which miR‐34/449 family finely controls several pathways to drive multiciliogenesis. John Wiley and Sons Inc. 2017-02-28 2017-03 /pmc/articles/PMC5363356/ /pubmed/28192603 http://dx.doi.org/10.1002/1873-3468.12595 Text en © 2017 The Authors. FEBS Letters published by John Wiley & Sons Ltd on behalf of Federation of European Biochemical Societies. This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Letters Mercey, Olivier Popa, Alexandra Cavard, Amélie Paquet, Agnès Chevalier, Benoît Pons, Nicolas Magnone, Virginie Zangari, Joséphine Brest, Patrick Zaragosi, Laure‐Emmanuelle Ponzio, Gilles Lebrigand, Kevin Barbry, Pascal Marcet, Brice Characterizing isomiR variants within the microRNA‐34/449 family |
title | Characterizing isomiR variants within the microRNA‐34/449 family |
title_full | Characterizing isomiR variants within the microRNA‐34/449 family |
title_fullStr | Characterizing isomiR variants within the microRNA‐34/449 family |
title_full_unstemmed | Characterizing isomiR variants within the microRNA‐34/449 family |
title_short | Characterizing isomiR variants within the microRNA‐34/449 family |
title_sort | characterizing isomir variants within the microrna‐34/449 family |
topic | Research Letters |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5363356/ https://www.ncbi.nlm.nih.gov/pubmed/28192603 http://dx.doi.org/10.1002/1873-3468.12595 |
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