Please use this identifier to cite or link to this item: http://hdl.handle.net/2445/66803
Title: Therapeutic strategies based on modified U1 snRNAs and chaperones for Sanfilippo C splicing mutations
Author: Matos, Liliana
Canals Montferrer, Isaac
Dridi, Larbi
Choi, Yoo
Prata, Maria Joao
Jordan, Peter
Desviat, Lourdes R.
Pérez, Belén
Pshezhetsky, Alexey V.
Grinberg Vaisman, Daniel Raúl
Alves, Sandra
Vilageliu i Arqués, Lluïsa
Keywords: Mutació (Biologia)
Lisosomes
Mutation (Biology)
Lysosomes
Issue Date: 24-Dec-2014
Publisher: BioMed Central
Abstract: Mutations affecting RNA splicing represent more than 20% of the mutant alleles in Sanfilippo syndrome type C, a rare lysosomal storage disorder that causes severe neurodegeneration. Many of these mutations are localized in the conserved donor or acceptor splice sites, while few are found in the nearby nucleotides. In this study we tested several therapeutic approaches specifically designed for different splicing mutations depending on how the mutations affect mRNA processing. For three mutations that affect the donor site (c.234 + 1G > A, c.633 + 1G > A and c.1542 + 4dupA), different modified U1 snRNAs recognizing the mutated donor sites, have been developed in an attempt to rescue the normal splicing process. For another mutation that affects an acceptor splice site (c.372-2A > G) and gives rise to a protein lacking four amino acids, a competitive inhibitor of the HGSNAT protein, glucosamine, was tested as a pharmacological chaperone to correct the aberrant folding and to restore the normal trafficking of the protein to the lysosome. Partial correction of c.234 + 1G > A mutation was achieved with a modified U1 snRNA that completely matches the splice donor site suggesting that these molecules may have a therapeutic potential for some splicing mutations. Furthermore, the importance of the splice site sequence context is highlighted as a key factor in the success of this type of therapy. Additionally, glucosamine treatment resulted in an increase in the enzymatic activity, indicating a partial recovery of the correct folding. We have assayed two therapeutic strategies for different splicing mutations with promising results for the future applications.
Note: Reproducció del document publicat a: http://dx.doi.org/10.1186/s13023-014-0180-y
It is part of: Orphanet Journal of Rare Diseases, 2014, vol. 9, num. 180
Related resource: http://dx.doi.org/10.1186/s13023-014-0180-y
URI: http://hdl.handle.net/2445/66803
ISSN: 1750-1172
Appears in Collections:Articles publicats en revistes (Genètica, Microbiologia i Estadística)

Files in This Item:
File Description SizeFormat 
647725.pdf1.38 MBAdobe PDFView/Open


This item is licensed under a Creative Commons License Creative Commons