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Genome editing in mucopolysaccharidoses and mucolipidoses
- Source :
- Progress in Molecular Biology and Translational Science ISBN: 9780323853019
- Publication Year :
- 2021
- Publisher :
- Elsevier, 2021.
-
Abstract
- Mucopolysaccharidoses (MPS) and mucolipidoses (ML) are disorders that alter lysosome function. While MPS are caused by mutation in enzymes that degrade glycosaminoglycans, the ML are disorders characterized by reduced function in the phosphotransferase enzyme. Multiple clinical features are associated with these diseases and the exact mechanisms that could explain such different clinical manifestations in patients are still unknown. Furthermore, there are no curative treatment for any of MPS and ML conditions so far. Gene editing holds promise as a tool for the creation of cell and animal models to help explain disease pathogenesis, as well as a platform for gene therapy. In this chapter, we discuss the main studies involving genome editing for MPS and the prospect applications for ML.
- Subjects :
- 0301 basic medicine
congenital, hereditary, and neonatal diseases and abnormalities
Mutation
Genetic enhancement
Mucolipidoses
Computational biology
Biology
medicine.disease_cause
Phosphotransferase
03 medical and health sciences
030104 developmental biology
0302 clinical medicine
medicine.anatomical_structure
Genome editing
030220 oncology & carcinogenesis
Lysosome
medicine
In patient
Function (biology)
Subjects
Details
- ISBN :
- 978-0-323-85301-9
- ISBNs :
- 9780323853019
- Database :
- OpenAIRE
- Journal :
- Progress in Molecular Biology and Translational Science ISBN: 9780323853019
- Accession number :
- edsair.doi...........d0f98e6985b0ef7fd3a135511fc48eb2
- Full Text :
- https://doi.org/10.1016/bs.pmbts.2021.01.026