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Dysregulation of Circular RNAs in Myotonic Dystrophy Type 1

Articolo
Data di Pubblicazione:
2019
Abstract:
Circular RNAs (circRNAs) constitute a recently re-discovered class of non-coding RNAs functioning as sponges for miRNAs and proteins, aecting RNA splicing and regulating transcription. CircRNAs are generated by "back-splicing", which is the linking covalently of 30- and 50-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 aected 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 dierentiated myogenic cell lines derived from DM1 patients. In conclusion, this pilot study identified circRNA dysregulation in DM1 patients.
Tipologia CRIS:
01.01 Articolo in rivista
Keywords:
circular RNA; alternative splicing; muscular dystrophies
Elenco autori:
Falcone, Germana
Autori di Ateneo:
FALCONE GERMANA
Link alla scheda completa:
https://iris.cnr.it/handle/20.500.14243/392428
Pubblicato in:
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES (ONLINE)
Journal
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URL

https://www.mdpi.com/1422-0067/20/8/1938
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