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MicroRNA miR-301a is a novel cardiac regulator of Cofilin-2

Calsarcin-1 deficient mice develop dilated cardiomyopathy (DCM) phenotype in pure C57BL/6 genetic background (Cs1-ko) despite severe contractile dysfunction and robust activation of fetal gene program. Here we performed a microRNA microarray to identify the molecular causes of this cardiac phenotype...

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Autores principales: Rangrez, Ashraf Yusuf, Hoppe, Phillip, Kuhn, Christian, Zille, Elisa, Frank, Johanne, Frey, Norbert, Frank, Derk
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5590826/
https://www.ncbi.nlm.nih.gov/pubmed/28886070
http://dx.doi.org/10.1371/journal.pone.0183901
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author Rangrez, Ashraf Yusuf
Hoppe, Phillip
Kuhn, Christian
Zille, Elisa
Frank, Johanne
Frey, Norbert
Frank, Derk
author_facet Rangrez, Ashraf Yusuf
Hoppe, Phillip
Kuhn, Christian
Zille, Elisa
Frank, Johanne
Frey, Norbert
Frank, Derk
author_sort Rangrez, Ashraf Yusuf
collection PubMed
description Calsarcin-1 deficient mice develop dilated cardiomyopathy (DCM) phenotype in pure C57BL/6 genetic background (Cs1-ko) despite severe contractile dysfunction and robust activation of fetal gene program. Here we performed a microRNA microarray to identify the molecular causes of this cardiac phenotype that revealed the dysregulation of several microRNAs including miR-301a, which was highly downregulated in Cs1-ko mice compared to the wild-type littermates. Cofilin-2 (Cfl2) was identified as one of the potential targets of miR-301a using prediction databases, which we validated by luciferase assay and mutation of predicted binding sites. Furthermore, expression of miR-301a contrastingly regulated Cfl2 expression levels in neonatal rat ventricular cardiomyocytes (NRVCM). Along these lines, Cfl2 was significantly upregulated in Cs1-ko mice, indicating the physiological association between miR-301a and Cfl2 in vivo. Mechanistically, we found that Cfl2 activated serum response factor response element (SRF-RE) driven luciferase activity in neonatal rat cardiomyocytes and in C2C12 cells. Similarly, knockdown of miR301a activated, whereas, its overexpression inhibited the SRF-RE driven luciferase activity, further strengthening physiological interaction between miR-301a and Cfl2. Interestingly, the expression of SRF and its target genes was strikingly increased in Cs1-ko suggesting a possible in vivo correlation between expression levels of Cfl2/miR-301a and SRF activation, which needs to be independently validated. In summary, our data demonstrates that miR-301a regulates Cofilin-2 in vitro in NRVCM, and in vivo in Cs1-ko mice. Our findings provide an additional and important layer of Cfl2 regulation, which we believe has an extended role in cardiac signal transduction and dilated cardiomyopathy presumably due to the reported involvement of Cfl2 in these mechanisms.
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spelling pubmed-55908262017-09-15 MicroRNA miR-301a is a novel cardiac regulator of Cofilin-2 Rangrez, Ashraf Yusuf Hoppe, Phillip Kuhn, Christian Zille, Elisa Frank, Johanne Frey, Norbert Frank, Derk PLoS One Research Article Calsarcin-1 deficient mice develop dilated cardiomyopathy (DCM) phenotype in pure C57BL/6 genetic background (Cs1-ko) despite severe contractile dysfunction and robust activation of fetal gene program. Here we performed a microRNA microarray to identify the molecular causes of this cardiac phenotype that revealed the dysregulation of several microRNAs including miR-301a, which was highly downregulated in Cs1-ko mice compared to the wild-type littermates. Cofilin-2 (Cfl2) was identified as one of the potential targets of miR-301a using prediction databases, which we validated by luciferase assay and mutation of predicted binding sites. Furthermore, expression of miR-301a contrastingly regulated Cfl2 expression levels in neonatal rat ventricular cardiomyocytes (NRVCM). Along these lines, Cfl2 was significantly upregulated in Cs1-ko mice, indicating the physiological association between miR-301a and Cfl2 in vivo. Mechanistically, we found that Cfl2 activated serum response factor response element (SRF-RE) driven luciferase activity in neonatal rat cardiomyocytes and in C2C12 cells. Similarly, knockdown of miR301a activated, whereas, its overexpression inhibited the SRF-RE driven luciferase activity, further strengthening physiological interaction between miR-301a and Cfl2. Interestingly, the expression of SRF and its target genes was strikingly increased in Cs1-ko suggesting a possible in vivo correlation between expression levels of Cfl2/miR-301a and SRF activation, which needs to be independently validated. In summary, our data demonstrates that miR-301a regulates Cofilin-2 in vitro in NRVCM, and in vivo in Cs1-ko mice. Our findings provide an additional and important layer of Cfl2 regulation, which we believe has an extended role in cardiac signal transduction and dilated cardiomyopathy presumably due to the reported involvement of Cfl2 in these mechanisms. Public Library of Science 2017-09-08 /pmc/articles/PMC5590826/ /pubmed/28886070 http://dx.doi.org/10.1371/journal.pone.0183901 Text en © 2017 Rangrez et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Rangrez, Ashraf Yusuf
Hoppe, Phillip
Kuhn, Christian
Zille, Elisa
Frank, Johanne
Frey, Norbert
Frank, Derk
MicroRNA miR-301a is a novel cardiac regulator of Cofilin-2
title MicroRNA miR-301a is a novel cardiac regulator of Cofilin-2
title_full MicroRNA miR-301a is a novel cardiac regulator of Cofilin-2
title_fullStr MicroRNA miR-301a is a novel cardiac regulator of Cofilin-2
title_full_unstemmed MicroRNA miR-301a is a novel cardiac regulator of Cofilin-2
title_short MicroRNA miR-301a is a novel cardiac regulator of Cofilin-2
title_sort microrna mir-301a is a novel cardiac regulator of cofilin-2
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5590826/
https://www.ncbi.nlm.nih.gov/pubmed/28886070
http://dx.doi.org/10.1371/journal.pone.0183901
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