Cytogenetic Analysis of the Results of Genome Editing on the Cell Model of Parkinson’s Disease


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Resumo

We performed a cytogenetic analysis of the results of CRISPR/Cas9-correction of G2019S mutation in LRRK2 gene associated with Parkinson’s disease. Genome editing was performed on induced pluripotent stem cells derived from fibroblasts of a patient carrying this mutation. A mosaic variant of tetraploidy 92 XXYY/46,XY (24-43% cells from various clones) was found in neuronal precursors differentiated from the induced pluripotent stem cells after gene editing procedure. Solitary cases of translocations and chromosome breaks were observed. These data confirm the importance of the development of new approaches ensuring genome stability in CRISPR/Cas9-edited cultures.

Sobre autores

E. Novosadova

Institute of Molecular Genetics, Russian Academy of Sciences

Email: snillario@gmail.com
Rússia, Moscow

E. Manuilova

Institute of Molecular Genetics, Russian Academy of Sciences

Email: snillario@gmail.com
Rússia, Moscow

V. Nenasheva

Institute of Molecular Genetics, Russian Academy of Sciences

Email: snillario@gmail.com
Rússia, Moscow

V. Tarantul

Institute of Molecular Genetics, Russian Academy of Sciences

Email: snillario@gmail.com
Rússia, Moscow

I. Grivennikov

Institute of Molecular Genetics, Russian Academy of Sciences

Email: snillario@gmail.com
Rússia, Moscow

L. Khaspekov

Research Center of Neurology

Email: snillario@gmail.com
Rússia, Moscow

S. Illarioshkin

Research Center of Neurology

Autor responsável pela correspondência
Email: snillario@gmail.com
Rússia, Moscow

A. Vetchinova

Research Center of Neurology

Email: snillario@gmail.com
Rússia, Moscow

V. Simonova

Research Center of Neurology

Email: snillario@gmail.com
Rússia, Moscow


Declaração de direitos autorais © Springer Science+Business Media, LLC, part of Springer Nature, 2018

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