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


Cite item

Full Text

Open Access Open Access
Restricted Access Access granted
Restricted Access Subscription Access

Abstract

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.

About the authors

E. V. Novosadova

Institute of Molecular Genetics, Russian Academy of Sciences

Email: snillario@gmail.com
Russian Federation, Moscow

E. S. Manuilova

Institute of Molecular Genetics, Russian Academy of Sciences

Email: snillario@gmail.com
Russian Federation, Moscow

V. V. Nenasheva

Institute of Molecular Genetics, Russian Academy of Sciences

Email: snillario@gmail.com
Russian Federation, Moscow

V. Z. Tarantul

Institute of Molecular Genetics, Russian Academy of Sciences

Email: snillario@gmail.com
Russian Federation, Moscow

I. A. Grivennikov

Institute of Molecular Genetics, Russian Academy of Sciences

Email: snillario@gmail.com
Russian Federation, Moscow

L. G. Khaspekov

Research Center of Neurology

Email: snillario@gmail.com
Russian Federation, Moscow

S. N. Illarioshkin

Research Center of Neurology

Author for correspondence.
Email: snillario@gmail.com
Russian Federation, Moscow

A. S. Vetchinova

Research Center of Neurology

Email: snillario@gmail.com
Russian Federation, Moscow

V. V. Simonova

Research Center of Neurology

Email: snillario@gmail.com
Russian Federation, Moscow


Copyright (c) 2018 Springer Science+Business Media, LLC, part of Springer Nature

This website uses cookies

You consent to our cookies if you continue to use our website.

About Cookies