Back to Search Start Over

Dysregulation of circular RNAs in myotonic dystrophy type 1

Authors :
Carlo Gaetano
Ivano Legnini
Marialucia Longo
Alessandra Perfetti
Gabriella Silvestri
Rea Valaperta
Christine Voellenkle
Laura Valentina Renna
Giovanni Meola
Paola Fuschi
Germana Falcone
Matteo Carrara
Denis Furling
Fabio Martelli
Irene Bozzoni
Rosanna Cardani
Publication Year :
2018
Publisher :
Cold Spring Harbor Laboratory, 2018.

Abstract

Circular RNAs (circRNAs) constitute a recently re-discovered class of non-coding RNAs functioning as sponge for miRNAs and proteins, affecting RNA splicing and regulating transcription. CircRNAs are generated by “back-splicing”, linking covalently 3’- and 5’-ends of exons. Thus, circRNA levels might be deregulated in conditions associated to altered RNA-splicing. Indeed, increasing 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, resulting 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 9 tested, 4 transcripts showed an increased circular fraction: CDYL, HIPK3, RTN4_03 and ZNF609. The circular fraction values correlated positively with skeletal muscle strength and Receiver-Operating-Characteristics curves showed that these four circRNAs allow to distinguish DM1 patients from controls. The identified circRNAs were also detectable in peripheral-blood-mononuclear-cells (PBMCs) and plasma of DM1 patients, but they were not regulated significantly, indicating a tissue-selectivity of the identified modulations. Finally, increased circular fractions of RTN4_03 and ZNF609 were also observed in differentiated myogenic cell lines derived from DM1 patients. In conclusion, this proof-of-principle study identified circRNA dysregulation in DM1 patients.

Details

Database :
OpenAIRE
Accession number :
edsair.doi.dedup.....0e0caa1ab28f58c9f368ec1ba78d45d1
Full Text :
https://doi.org/10.1101/452391