Literature DB >> 30081189

CRISPR-Cas9-mediated gene editing in human MPS I fibroblasts.

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.
Copyright © 2018 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  CRISPR-Cas9; Gene editing; Hurler syndrome; Mucopolysaccharidosis

Mesh:

Substances:

Year:  2018        PMID: 30081189     DOI: 10.1016/j.gene.2018.08.004

Source DB:  PubMed          Journal:  Gene        ISSN: 0378-1119            Impact factor:   3.688


  8 in total

1.  Efficient CRISPR/Cas9 nickase-mediated genome editing in an in vitro model of mucopolysaccharidosis IVA.

Authors:  Andrés Felipe Leal; Carlos Javier Alméciga-Díaz
Journal:  Gene Ther       Date:  2022-05-18       Impact factor: 5.250

Review 2.  Cell and Gene Therapies for Mucopolysaccharidoses: Base Editing and Therapeutic Delivery to the CNS.

Authors:  Chloe L Christensen; Rhea E Ashmead; Francis Y M Choy
Journal:  Diseases       Date:  2019-06-26

Review 3.  Genome Editing for Mucopolysaccharidoses.

Authors:  Edina Poletto; Guilherme Baldo; Natalia Gomez-Ospina
Journal:  Int J Mol Sci       Date:  2020-01-13       Impact factor: 5.923

4.  DDIEM: drug database for inborn errors of metabolism.

Authors:  Marwa Abdelhakim; Eunice McMurray; Ali Raza Syed; Senay Kafkas; Allan Anthony Kamau; Paul N Schofield; Robert Hoehndorf
Journal:  Orphanet J Rare Dis       Date:  2020-06-11       Impact factor: 4.123

5.  In silico analysis of potential off-target sites to gene editing for Mucopolysaccharidosis type I using the CRISPR/Cas9 system: Implications for population-specific treatments.

Authors:  Paola Carneiro; Martiela Vaz de Freitas; Ursula Matte
Journal:  PLoS One       Date:  2022-01-24       Impact factor: 3.240

6.  Delivery and assessment of a CRISPR/nCas9-based genome editing system on in vitro models of mucopolysaccharidoses IVA assisted by magnetite-based nanoparticles.

Authors:  Andrés Felipe Leal; Javier Cifuentes; Carlos Emilio Torres; Diego Suárez; Valentina Quezada; Saúl Camilo Gómez; Juan C Cruz; Luis H Reyes; Angela Johana Espejo-Mojica; Carlos Javier Alméciga-Díaz
Journal:  Sci Rep       Date:  2022-09-03       Impact factor: 4.996

Review 7.  Novel Gene-Correction-Based Therapeutic Modalities for Monogenic Liver Disorders.

Authors:  Mahsa Ghasemzad; Mahdieh Hashemi; Zohre Miri Lavasani; Nikoo Hossein-Khannazer; Haleh Bakhshandeh; Roberto Gramignoli; Hani Keshavarz Alikhani; Mustapha Najimi; Saman Nikeghbalian; Massoud Vosough
Journal:  Bioengineering (Basel)       Date:  2022-08-15

Review 8.  Delivering gene therapy for mucopolysaccharide diseases.

Authors:  Shaun R Wood; Brian W Bigger
Journal:  Front Mol Biosci       Date:  2022-09-12
  8 in total

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