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Dysregulation of Circular RNAs in Myotonic Dystrophy Type 1.
Voellenkle, Christine; Perfetti, Alessandra; Carrara, Matteo; Fuschi, Paola; Renna, Laura Valentina; Longo, Marialucia; Sain, Simona Baghai; Cardani, Rosanna; Valaperta, Rea; Silvestri, Gabriella; Legnini, Ivano; Bozzoni, Irene; Furling, Denis; Gaetano, Carlo; Falcone, Germana; Meola, Giovanni; Martelli, Fabio.
Afiliação
  • Voellenkle C; Molecular Cardiology Laboratory, IRCCS Policlinico San Donato, San Donato Milanese, 20097 Milan, Italy. christine.voellenkle@grupposandonato.it.
  • Perfetti A; Molecular Cardiology Laboratory, IRCCS Policlinico San Donato, San Donato Milanese, 20097 Milan, Italy. alessandra.perfetti@grupposandonato.it.
  • Carrara M; Molecular Cardiology Laboratory, IRCCS Policlinico San Donato, San Donato Milanese, 20097 Milan, Italy. carrara.matt@gmail.com.
  • Fuschi P; Molecular Cardiology Laboratory, IRCCS Policlinico San Donato, San Donato Milanese, 20097 Milan, Italy. paola.fuschi@grupposandonato.it.
  • Renna LV; Laboratory of Muscle Histopathology and Molecular Biology, IRCCS Policlinico San Donato, San Donato Milanese, 20097 Milan, Italy. lauravalentina.renna@grupposandonato.it.
  • Longo M; Molecular Cardiology Laboratory, IRCCS Policlinico San Donato, San Donato Milanese, 20097 Milan, Italy. marialucia.longo@grupposandonato.it.
  • Sain SB; Center for Translational Genomics and Bioinformatics, IRCCS San Raffaele Scientific Institute, 20132 Milan, Italy. baghaisain.simona@hsr.it.
  • Cardani R; Laboratory of Muscle Histopathology and Molecular Biology, IRCCS Policlinico San Donato, San Donato Milanese, 20097 Milan, Italy. rosanna.cardani@grupposandonato.it.
  • Valaperta R; Research Laboratories, IRCCS Policlinico San Donato, San Donato Milanese, 20097 Milan, Italy. rea.valaperta@grupposandonato.it.
  • Silvestri G; Department of Geriatrics, Orthopaedic and Neuroscience, Institute of Neurology, Catholic University of Sacred Heart, Fondazione Policlinico Gemelli, 00168 Rome, Italy. Gabriella.Silvestri@unicatt.it.
  • Legnini I; Department of Biology and Biotechnology "Charles Darwin", Sapienza University of Rome, 00185 Rome, Italy. Ivano.Legnini@mdc-berlin.de.
  • Bozzoni I; Department of Biology and Biotechnology "Charles Darwin", Sapienza University of Rome, 00185 Rome, Italy. irene.bozzoni@uniroma1.it.
  • Furling D; Sorbonne Université, INSERM, Association Institut de Myologie, Centre de Recherche en Myologie, F-75013 Paris, France. denis.furling@upmc.fr.
  • Gaetano C; Laboratory of Epigenetics, Istituti Clinici Scientifici Maugeri, 27100 Pavia, Italy. carlo.gaetano@icsmaugeri.it.
  • Falcone G; Institute of Cell Biology and Neurobiology, National Research Council, Monterotondo, 00015 Rome, Italy. germana.falcone@cnr.it.
  • Meola G; Laboratory of Muscle Histopathology and Molecular Biology, IRCCS Policlinico San Donato, San Donato Milanese, 20097 Milan, Italy. giovanni.meola@unimi.it.
  • Martelli F; Department of Neurology, IRCCS Policlinico San Donato, San Donato Milanese, 20097 Milan, Italy. giovanni.meola@unimi.it.
Int J Mol Sci ; 20(8)2019 Apr 19.
Article em En | MEDLINE | ID: mdl-31010208
ABSTRACT
Circular RNAs (circRNAs) constitute a recently re-discovered class of non-coding RNAs functioning as sponges for miRNAs and proteins, affecting RNA splicing and regulating transcription. CircRNAs are generated by "back-splicing", which is the linking covalently of 3'- and 5'-ends of exons. Thus, circRNA levels might be deregulated in conditions associated with altered RNA-splicing. Significantly, growing evidence indicates their role in human diseases. Specifically, myotonic dystrophy type 1 (DM1) is a multisystemic disorder caused by expanded CTG repeats in the DMPK gene which results in abnormal mRNA-splicing. In this investigation, circRNAs expressed in DM1 skeletal muscles were identified by analyzing RNA-sequencing data-sets followed by qPCR validation. In muscle biopsies, out of nine tested, four transcripts showed an increased circular fraction CDYL, HIPK3, RTN4_03, and ZNF609. Their circular fraction values correlated with skeletal muscle strength and with splicing biomarkers of disease severity, and displayed higher values in more severely affected patients. Moreover, Receiver-Operating-Characteristics curves of these four circRNAs discriminated DM1 patients from controls. The identified circRNAs were also detectable in peripheral-blood-mononuclear-cells (PBMCs) and the plasma of DM1 patients, but they were not regulated significantly. Finally, increased circular fractions of RTN4_03 and ZNF609 were also observed in differentiated myogenic cell lines derived from DM1 patients. In conclusion, this pilot study identified circRNA dysregulation in DM1 patients.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: RNA / Regulação da Expressão Gênica / Distrofia Miotônica Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Female / Humans / Male Idioma: En Revista: Int J Mol Sci Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: RNA / Regulação da Expressão Gênica / Distrofia Miotônica Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Female / Humans / Male Idioma: En Revista: Int J Mol Sci Ano de publicação: 2019 Tipo de documento: Article