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Identification and Characterization of FGF2-Dependent mRNA: microRNA Networks During Lens Fiber Cell Differentiation

MicroRNAs (miRNAs) and fibroblast growth factor (FGF) signaling regulate a wide range of cellular functions, including cell specification, proliferation, migration, differentiation, and survival. In lens, both these systems control lens fiber cell differentiation; however, a possible link between th...

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Autores principales: Wolf, Louise, Gao, Chun S., Gueta, Karen, Xie, Qing, Chevallier, Tiphaine, Podduturi, Nikhil R., Sun, Jian, Conte, Ivan, Zelenka, Peggy S., Ashery-Padan, Ruth, Zavadil, Jiri, Cvekl, Ales
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Genetics Society of America 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3852386/
https://www.ncbi.nlm.nih.gov/pubmed/24142921
http://dx.doi.org/10.1534/g3.113.008698
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author Wolf, Louise
Gao, Chun S.
Gueta, Karen
Xie, Qing
Chevallier, Tiphaine
Podduturi, Nikhil R.
Sun, Jian
Conte, Ivan
Zelenka, Peggy S.
Ashery-Padan, Ruth
Zavadil, Jiri
Cvekl, Ales
author_facet Wolf, Louise
Gao, Chun S.
Gueta, Karen
Xie, Qing
Chevallier, Tiphaine
Podduturi, Nikhil R.
Sun, Jian
Conte, Ivan
Zelenka, Peggy S.
Ashery-Padan, Ruth
Zavadil, Jiri
Cvekl, Ales
author_sort Wolf, Louise
collection PubMed
description MicroRNAs (miRNAs) and fibroblast growth factor (FGF) signaling regulate a wide range of cellular functions, including cell specification, proliferation, migration, differentiation, and survival. In lens, both these systems control lens fiber cell differentiation; however, a possible link between these processes remains to be examined. Herein, the functional requirement for miRNAs in differentiating lens fiber cells was demonstrated via conditional inactivation of Dicer1 in mouse (Mus musculus) lens. To dissect the miRNA-dependent pathways during lens differentiation, we used a rat (Rattus norvegicus) lens epithelial explant system, induced by FGF2 to differentiate, followed by mRNA and miRNA expression profiling. Transcriptome and miRNome analysis identified extensive FGF2-regulated cellular responses that were both independent and dependent on miRNAs. We identified 131 FGF2-regulated miRNAs. Seventy-six of these miRNAs had at least two in silico predicted and inversely regulated target mRNAs. Genes modulated by the greatest number of FGF-regulated miRNAs include DNA-binding transcription factors Nfib, Nfat5/OREBP, c-Maf, Ets1, and N-Myc. Activated FGF signaling influenced bone morphogenetic factor/transforming growth factor-β, Notch, and Wnt signaling cascades implicated earlier in lens differentiation. Specific miRNA:mRNA interaction networks were predicted for c-Maf, N-Myc, and Nfib (DNA-binding transcription factors); Cnot6, Cpsf6, Dicer1, and Tnrc6b (RNA to miRNA processing); and Ash1l, Med1/PBP, and Kdm5b/Jarid1b/Plu1 (chromatin remodeling). Three miRNAs, including miR-143, miR-155, and miR-301a, down-regulated expression of c-Maf in the 3′-UTR luciferase reporter assays. These present studies demonstrate for the first time global impact of activated FGF signaling in lens cell culture system and predicted novel gene regulatory networks connected by multiple miRNAs that regulate lens differentiation.
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spelling pubmed-38523862013-12-06 Identification and Characterization of FGF2-Dependent mRNA: microRNA Networks During Lens Fiber Cell Differentiation Wolf, Louise Gao, Chun S. Gueta, Karen Xie, Qing Chevallier, Tiphaine Podduturi, Nikhil R. Sun, Jian Conte, Ivan Zelenka, Peggy S. Ashery-Padan, Ruth Zavadil, Jiri Cvekl, Ales G3 (Bethesda) Investigations MicroRNAs (miRNAs) and fibroblast growth factor (FGF) signaling regulate a wide range of cellular functions, including cell specification, proliferation, migration, differentiation, and survival. In lens, both these systems control lens fiber cell differentiation; however, a possible link between these processes remains to be examined. Herein, the functional requirement for miRNAs in differentiating lens fiber cells was demonstrated via conditional inactivation of Dicer1 in mouse (Mus musculus) lens. To dissect the miRNA-dependent pathways during lens differentiation, we used a rat (Rattus norvegicus) lens epithelial explant system, induced by FGF2 to differentiate, followed by mRNA and miRNA expression profiling. Transcriptome and miRNome analysis identified extensive FGF2-regulated cellular responses that were both independent and dependent on miRNAs. We identified 131 FGF2-regulated miRNAs. Seventy-six of these miRNAs had at least two in silico predicted and inversely regulated target mRNAs. Genes modulated by the greatest number of FGF-regulated miRNAs include DNA-binding transcription factors Nfib, Nfat5/OREBP, c-Maf, Ets1, and N-Myc. Activated FGF signaling influenced bone morphogenetic factor/transforming growth factor-β, Notch, and Wnt signaling cascades implicated earlier in lens differentiation. Specific miRNA:mRNA interaction networks were predicted for c-Maf, N-Myc, and Nfib (DNA-binding transcription factors); Cnot6, Cpsf6, Dicer1, and Tnrc6b (RNA to miRNA processing); and Ash1l, Med1/PBP, and Kdm5b/Jarid1b/Plu1 (chromatin remodeling). Three miRNAs, including miR-143, miR-155, and miR-301a, down-regulated expression of c-Maf in the 3′-UTR luciferase reporter assays. These present studies demonstrate for the first time global impact of activated FGF signaling in lens cell culture system and predicted novel gene regulatory networks connected by multiple miRNAs that regulate lens differentiation. Genetics Society of America 2013-10-18 /pmc/articles/PMC3852386/ /pubmed/24142921 http://dx.doi.org/10.1534/g3.113.008698 Text en Copyright © 2013 Wolf et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution Unported License (http://creativecommons.org/licenses/by/3.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Investigations
Wolf, Louise
Gao, Chun S.
Gueta, Karen
Xie, Qing
Chevallier, Tiphaine
Podduturi, Nikhil R.
Sun, Jian
Conte, Ivan
Zelenka, Peggy S.
Ashery-Padan, Ruth
Zavadil, Jiri
Cvekl, Ales
Identification and Characterization of FGF2-Dependent mRNA: microRNA Networks During Lens Fiber Cell Differentiation
title Identification and Characterization of FGF2-Dependent mRNA: microRNA Networks During Lens Fiber Cell Differentiation
title_full Identification and Characterization of FGF2-Dependent mRNA: microRNA Networks During Lens Fiber Cell Differentiation
title_fullStr Identification and Characterization of FGF2-Dependent mRNA: microRNA Networks During Lens Fiber Cell Differentiation
title_full_unstemmed Identification and Characterization of FGF2-Dependent mRNA: microRNA Networks During Lens Fiber Cell Differentiation
title_short Identification and Characterization of FGF2-Dependent mRNA: microRNA Networks During Lens Fiber Cell Differentiation
title_sort identification and characterization of fgf2-dependent mrna: microrna networks during lens fiber cell differentiation
topic Investigations
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3852386/
https://www.ncbi.nlm.nih.gov/pubmed/24142921
http://dx.doi.org/10.1534/g3.113.008698
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