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Investigating the epi-miRNome: identification of epi-miRNAs using transfection experiments.
Reale, Elisa; Taverna, Daniela; Cantini, Laura; Martignetti, Loredana; Osella, Matteo; De Pittà, Cristiano; Virga, Federico; Orso, Francesca; Caselle, Michele.
Afiliación
  • Reale E; Department of Physics & INFN, University of Torino, 10125, Torino, Italy.
  • Taverna D; Molecular Biotechnology Center (MBC), 10126, Torino, Italy.
  • Cantini L; Department of Molecular Biotechnology & Health Sciences, 10126, Torino, Italy.
  • Martignetti L; Center for Complex Systems in Molecular Biology & Medicine, University of Torino, 10123, Torino, Italy.
  • Osella M; Institut Curie, PSL Research University, INSERM U900, Paris, France.
  • De Pittà C; Computational Systems Biology Team, Institut de Biologie de l'Ecole Normale Supérieure, CNRS UMR8197, INSERM U1024, Ecole Normale Supérieure, Paris Sciences et Lettres Research University, 75005 Paris, France.
  • Virga F; Institut Curie, PSL Research University, INSERM U900, Paris, France.
  • Orso F; Department of Physics & INFN, University of Torino, 10125, Torino, Italy.
  • Caselle M; Department of Biology, University of Padova, 3522, Padova, Italy.
Epigenomics ; 11(14): 1581-1599, 2019 11.
Article en En | MEDLINE | ID: mdl-31693439
ABSTRACT

Aim:

Growing evidence shows a strong interplay between post-transcriptional regulation, mediated by miRNAs (miRs) and epigenetic regulation. Nevertheless, the number of experimentally validated miRs (called epi-miRs) involved in these regulatory circuitries is still very small. Material &

methods:

We propose a pipeline to prioritize candidate epi-miRs and to identify potential epigenetic interactors of any given miR starting from miR transfection experiment datasets. Results &

conclusion:

We identified 34 candidate epi-miRs 19 of them are known epi-miRs, while 15 are new. Moreover, using an in-house generated gene expression dataset, we experimentally proved that a component of the polycomb-repressive complex 2, the histone methyltransferase enhancer of zeste homolog 2 (EZH2), interacts with miR-214, a well-known prometastatic miR in melanoma and breast cancer, highlighting a miR-214-EZH2 regulatory axis potentially relevant in tumor progression.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: MicroARNs / Epigénesis Genética Tipo de estudio: Diagnostic_studies Límite: Female / Humans Idioma: En Revista: Epigenomics Año: 2019 Tipo del documento: Article País de afiliación: Italia

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: MicroARNs / Epigénesis Genética Tipo de estudio: Diagnostic_studies Límite: Female / Humans Idioma: En Revista: Epigenomics Año: 2019 Tipo del documento: Article País de afiliación: Italia