Genome Editing and the Problem of Tetraploidy in Cell Modeling of the Genetic Form of Parkinsonism
- Авторлар: Simonova V.1, Vetchinova A.1, Novosadova E.2, Khaspekov L.1, Illarioshkin S.1
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Мекемелер:
- Research Center of Neurology
- Institute of Molecular Genetics
- Шығарылым: Том 83, № 9 (2018)
- Беттер: 1040-1045
- Бөлім: Mini-Review
- URL: https://journals.rcsi.science/0006-2979/article/view/151711
- DOI: https://doi.org/10.1134/S0006297918090055
- ID: 151711
Дәйексөз келтіру
Аннотация
The prevalent form of familial parkinsonism is caused by mutations in the LRRK2 gene encoding for the mitochondrial protein kinase. In the review, we discuss possible causes of appearance of tetraploid cells in neuronal precursors obtained from induced pluripotent stem cells from patients with the LRRK2-associated form of parkinsonism after genome editing procedure. As LRRK2 protein participates in cell proliferation and maintenance of the nuclear envelope, spindle fibers, and cytoskeleton, mutations in the LRRK2 gene can affect protein functions and lead, via various mechanisms, to the mitotic machinery disintegration and chromosomal aberration. These abnormalities can appear at different stages of fibroblast reprogramming; therefore, editing of the LRRK2 nucleotide sequence should be done during or before the reprogramming stage.
Негізгі сөздер
Авторлар туралы
V. Simonova
Research Center of Neurology
Email: snillario@gmail.com
Ресей, Moscow, 125367
A. Vetchinova
Research Center of Neurology
Email: snillario@gmail.com
Ресей, Moscow, 125367
E. Novosadova
Institute of Molecular Genetics
Email: snillario@gmail.com
Ресей, Moscow, 123182
L. Khaspekov
Research Center of Neurology
Email: snillario@gmail.com
Ресей, Moscow, 125367
S. Illarioshkin
Research Center of Neurology
Хат алмасуға жауапты Автор.
Email: snillario@gmail.com
Ресей, Moscow, 125367