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Article Dans Une Revue International Journal of Molecular Sciences Année : 2019

Dysregulation of Circular RNAs in Myotonic Dystrophy Type 1

Laura Valentina Renna
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Simona Baghai Sain
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Carlo Gaetano
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Germana Falcone

Résumé

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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hal-02142017 , version 1 (28-05-2019)

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Laura Valentina Renna, Simona Baghai Sain, Christine Voellenkle, Alessandra Perfetti, Matteo Carrara, et al.. Dysregulation of Circular RNAs in Myotonic Dystrophy Type 1. International Journal of Molecular Sciences, 2019, 20 (8), pp.1938. ⟨10.3390/ijms20081938⟩. ⟨hal-02142017⟩
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