| Literature DB >> 30081189 |
Talita Giacomet de Carvalho1, Roselena Schuh2, Gabriela Pasqualim1, Felipe Matheus Pellenz3, Eduardo Cremonese Filippi-Chiela4, Roberto Giugliani1, Guilherme Baldo1, Ursula Matte5.
Abstract
Mucopolysaccharidosis type I (MPS I) is a lysosomal storage disorder (LSD). It is caused by mutations in the IDUA gene, which lead to the accumulation of the glycosaminoglycans dermatan and heparan sulfate. The CRISPR-Cas9 system is a new and powerful tool that allows gene editing at precise points of the genome, resulting in gene correction through the introduction and genomic integration of a wildtype sequence. In this study, we used the CRISPR-Cas9 genome editing technology to correct in vitro the most common mutation causing MPS I. Human fibroblasts homozygous for p.Trp402* (legacy name W402X) were transfected and analyzed for up to one month after treatment. IDUA activity was significantly increased, lysosomal mass was decreased, and next generation sequencing confirmed that a percentage of cells carried the wildtype sequence. As a proof of concept, this study demonstrates that CRISPR-Cas9 genome editing may be used to correct causative mutations in MPS I. LIST OF ABBREVIATIONS.Entities:
Keywords: CRISPR-Cas9; Gene editing; Hurler syndrome; Mucopolysaccharidosis
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Year: 2018 PMID: 30081189 DOI: 10.1016/j.gene.2018.08.004
Source DB: PubMed Journal: Gene ISSN: 0378-1119 Impact factor: 3.688