A Peptide Nucleic Acid (PNA) Masking the miR-145-5p Binding Site of the 3′UTR of the Cystic Fibrosis Transmembrane Conductance Regulator (<i>CFTR</i>) mRNA Enhances CFTR Expression in Calu-3 Cells
Shaiq Sultan,
Andrea Rozzi,
Jessica Gasparello,
Alex Manicardi,
Roberto Corradini,
Chiara Papi,
Alessia Finotti,
Ilaria Lampronti,
Eva Reali,
Giulio Cabrini,
Roberto Gambari,
Monica Borgatti
Affiliations
Shaiq Sultan
Department of Life Sciences and Biotechnology, University of Ferrara, 44121 Ferrara, Italy
Andrea Rozzi
Department of Chemistry, Life Sciences and Environmental Sustainability, University of Parma, 43124 Parma, Italy
Jessica Gasparello
Department of Life Sciences and Biotechnology, University of Ferrara, 44121 Ferrara, Italy
Alex Manicardi
Department of Chemistry, Life Sciences and Environmental Sustainability, University of Parma, 43124 Parma, Italy
Roberto Corradini
Department of Chemistry, Life Sciences and Environmental Sustainability, University of Parma, 43124 Parma, Italy
Chiara Papi
Department of Life Sciences and Biotechnology, University of Ferrara, 44121 Ferrara, Italy
Alessia Finotti
Department of Life Sciences and Biotechnology, University of Ferrara, 44121 Ferrara, Italy
Ilaria Lampronti
Department of Life Sciences and Biotechnology, University of Ferrara, 44121 Ferrara, Italy
Peptide nucleic acids (PNAs) have been demonstrated to be very useful tools for gene regulation at different levels and with different mechanisms of action. In the last few years the use of PNAs for targeting microRNAs (anti-miRNA PNAs) has provided impressive advancements. In particular, targeting of microRNAs involved in the repression of the expression of the cystic fibrosis transmembrane conductance regulator (CFTR) gene, which is defective in cystic fibrosis (CF), is a key step in the development of new types of treatment protocols. In addition to the anti-miRNA therapeutic strategy, inhibition of miRNA functions can be reached by masking the miRNA binding sites present within the 3′UTR region of the target mRNAs. The objective of this study was to design a PNA masking the binding site of the microRNA miR-145-5p present within the 3′UTR of the CFTR mRNA and to determine its activity in inhibiting miR-145-5p function, with particular focus on the expression of both CFTR mRNA and CFTR protein in Calu-3 cells. The results obtained support the concept that the PNA masking the miR-145-5p binding site of the CFTR mRNA is able to interfere with miR-145-5p biological functions, leading to both an increase of CFTR mRNA and CFTR protein content.