Microarray and deep sequencing cross-platform analysis of the mirRNome and isomiR variation in response to epidermal growth factor
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- dc.contributor.author Llorens, Francca
- dc.contributor.author Hummel, Manuelaca
- dc.contributor.author Pantano Rubiño, Lorena, 1982-ca
- dc.contributor.author Pastor, Xavierca
- dc.contributor.author Vivancos Prellezo, Anaca
- dc.contributor.author Castillo Andreo, Estherca
- dc.contributor.author Mattlin, Heidica
- dc.contributor.author Ferrer Admetlla, Annaca
- dc.contributor.author Ingham, Matthewca
- dc.contributor.author Noguera, Marcca
- dc.contributor.author Kofler, Robertca
- dc.contributor.author Dohm, Juliane C.ca
- dc.contributor.author Pluvinet, Raquelca
- dc.contributor.author Bayés, Mònicaca
- dc.contributor.author Himmelbauer, Heinzca
- dc.contributor.author del Río, José Antonioca
- dc.contributor.author Martí, Eulàliaca
- dc.contributor.author Sumoy Van Dyck, Lauroca
- dc.date.accessioned 2015-03-17T08:18:02Z
- dc.date.available 2015-03-17T08:18:02Z
- dc.date.issued 2013ca
- dc.description.abstract Background: Epidermal Growth Factor (EGF) plays an important function in the regulation of cell growth, proliferation, and differentiation by binding to its receptor (EGFR) and providing cancer cells with increased survival responsiveness. Signal transduction carried out by EGF has been extensively studied at both transcriptional and post-transcriptional levels. Little is known about the involvement of microRNAs (miRNAs) in the EGF signaling pathway. miRNAs have emerged as major players in the complex networks of gene regulation, and cancer miRNA expression studies have evidenced a direct involvement of miRNAs in cancer progression. Results: In this study, we have used an integrative high content analysis approach to identify the specific miRNAs implicated in EGF signaling in HeLa cells as potential mediators of cancer mediated functions. We have used microarray and deep-sequencing technologies in order to obtain a global view of the EGF miRNA transcriptome with a robust experimental cross-validation. By applying a procedure based on Rankprod tests, we have delimited a solid set of EGF-regulated miRNAs. After validating regulated miRNAs by reverse transcription quantitative PCR, we have derived protein networks and biological functions from the predicted targets of the regulated miRNAs to gain insight into the potential role of miRNAs in EGF-treated cells. In addition, we have analyzed sequence heterogeneity due to editing relative to the reference sequence (isomiRs) among regulated miRNAs. Conclusions: We propose that the use of global genomic miRNA cross-validation derived from high throughput technologies can be used to generate more reliable datasets inferring more robust networks of co-regulated predicted miRNA target genes.en
- dc.description.sponsorship This work was supported by grants from Ministerio de Ciencia e Innovación [MICINN; BFU2012-32617] to JADR and FL, Generalitat de Catalunya [SGR2009-366] to JADR and FL, and the EU-FP7 PRIORITY to JADR. Start up funds from the Institute for Predictive and Personalized Medicine of Cancer and the Center for Genomic Regulation to LS; by the Spanish Ministry of Science and Technology [SAF2004-06976] to LS, Juan de la Cierva researcher contract to FL, and by excellence in research team recognitions by the Catalan government, Departament de Innovació, Universitats i Ensenyament, Generalitat de Catalunya [SGR2005-404] to LS, and by the Instituto de Salud Carlos III Fondo de Investigaciones Sanitarias to JADR and to LS [PI10/01154]en
- dc.format.mimetype application/pdfca
- dc.identifier.citation Llorens F, Hummel M, Pantano L, Pastor X, Vivancos A, Castillo E, Mattlin H, Ferrer A, Ingham M, Noguera M, Kofler R, Dohm JC, Pluvinet R, Bayés M, Himmelbauer H, del Rio JA, Martí E, Sumoy L. Microarray and deep sequencing cross-platform analysis of the mirRNome and isomiR variation in response to epidermal growth factor. BMC Genomics. 2013; 14: 371. DOI 10.1186/1471-2164-14-371ca
- dc.identifier.doi http://dx.doi.org/10.1186/1471-2164-14-371
- dc.identifier.issn 1471-2164ca
- dc.identifier.uri http://hdl.handle.net/10230/23196
- dc.language.iso engca
- dc.publisher BioMed Centralca
- dc.relation.ispartof BMC Genomics. 2013; 14: 371
- dc.relation.projectID info:eu-repo/grantAgreement/ES/3PN/BFU2012-32617
- dc.relation.projectID info:eu-repo/grantAgreement/ES/3PN/SAF2004-06976
- dc.rights © 2013 Llorens et al.; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.ca
- dc.rights.accessRights info:eu-repo/semantics/openAccessca
- dc.rights.uri http://creativecommons.org/licenses/by/2.0
- dc.subject.other RNA no missatgersca
- dc.subject.other Genètica molecular humanaca
- dc.title Microarray and deep sequencing cross-platform analysis of the mirRNome and isomiR variation in response to epidermal growth factorca
- dc.type info:eu-repo/semantics/articleca
- dc.type.version info:eu-repo/semantics/publishedVersionca