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EnglishFabry disease is a rare X-linked lysosomal storage disorder caused by deficiency of the α-galactosidase A (α-Gal A) enzyme, which is encoded by the GLA gene. GLA transcription in humans produces a major mRNA encoding α-Gal A and a minor mRNA of unknown function, which retains a 57-nucleotide-long cryptic exon between exons 4 and 5, bearing a premature termination codon. NM_000169.2:c.639+861C>T and NM_000169.2:c.639+919G>A GLA deep intronic mutations have been described to cause Fabry disease by inducing overexpression of the alternatively spliced mRNA, along with a dramatic decrease in the major one. Here, we built a wild-type GLA minigene and two minigenes that carry mutations c.639+861C>T and c.639+919G>A. Once transfected into cells, the minigenes recapitulate the molecular patterns observed in patients, at the mRNA, protein, and enzymatic level. We constructed a set of specific double-target U1asRNAs to correct c.639+861C>T and c.639+919G>A GLA mutations. Efficacy of U1asRNAs in inducing the skipping of the cryptic exon was evaluated upon their transient co-transfection with the minigenes in COS-1 cells, by real-time polymerase chain reaction (PCR), western blot analysis, and α-Gal A enzyme assay. We identified a set of U1asRNAs that efficiently restored α-Gal A enzyme activity and the correct splicing pathways in reporter minigenes. We also identified a unique U1asRNA correcting both mutations as efficently as the mutation-specific U1asRNAs. Our study proves that an exon skipping-based approach recovering α-Gal A activity in the c.639+861C>T and c.639+919G>A GLA mutations is active.
Double-target Antisense U1snRNAs Correct Mis-splicing Due to c.639+861C>T and c.639+919G>A GLA Deep Intronic Mutations / Ferri, Lorenzo; Covello, Giuseppina; Caciotti, Anna; Guerrini, Renzo; Denti, Michela Alessandra; Morrone, Amelia. - In: MOLECULAR THERAPY NUCLEIC ACIDS. - ISSN 2162-2531. - ELETTRONICO. - 5:10(2016), pp. 380-391. [10.1038/mtna.2016.88]
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| Titolo: | Double-target Antisense U1snRNAs Correct Mis-splicing Due to c.639+861C>T and c.639+919G>A GLA Deep Intronic Mutations | |
| Autori: | Ferri, Lorenzo; Covello, Giuseppina; Caciotti, Anna; Guerrini, Renzo; Denti, Michela Alessandra; Morrone, Amelia | |
| Autori Unitn: | ||
| Titolo del periodico: | MOLECULAR THERAPY NUCLEIC ACIDS | |
| Anno di pubblicazione: | 2016 | |
| Numero e parte del fascicolo: | 10 | |
| Codice identificativo Scopus: | 2-s2.0-85015187198 | |
| Codice identificativo Pubmed: | 27779620 | |
| Codice identificativo WOS: | WOS:000395781700001 | |
| Digital Object Identifier (DOI): | http://dx.doi.org/10.1038/mtna.2016.88 | |
| Handle: | http://hdl.handle.net/11572/175312 | |
| Citazione: | Double-target Antisense U1snRNAs Correct Mis-splicing Due to c.639+861C>T and c.639+919G>A GLA Deep Intronic Mutations / Ferri, Lorenzo; Covello, Giuseppina; Caciotti, Anna; Guerrini, Renzo; Denti, Michela Alessandra; Morrone, Amelia. - In: MOLECULAR THERAPY NUCLEIC ACIDS. - ISSN 2162-2531. - ELETTRONICO. - 5:10(2016), pp. 380-391. [10.1038/mtna.2016.88] | |
| Appare nelle tipologie: | 03.1 Articolo su rivista (Journal article) |
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| Ferri_et_al_MolTherNuclAcids_2016.pdf | Ferri_et_al_MolTherNuclAcids_2016 | Versione editoriale (Publisher’s layout) |  | Open Access Visualizza/Apri |
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