
Open Access

Subscription Access
Transcriptional profiling of iPSC-derived neurons with reciprocal monogenic CNV in 3p26.3 region
https://doi.org/10.25557/2073-7998.2020.03.10-11
Abstract
The gene expression analysis of iPSC-derived neurons, obtained from patients with idiopathic intellectual disability and reciprocal microdeletion and microduplication in 3p26.3 region affecting the single CNTN6 gene was performed. The global gene expression dysregulation was demonstrated for cells with CNTN6 copy number variation. Gene expression in neurons with CNTN6 copy number changes was downregulated for genes, whose products are involved in the central nervous system development.
About the Authors
M. E. Lopatkina
Research Institute of Medical Genetics, Tomsk National Research Medical Center RAS
Russian Federation
V. S. Fishman
Federal Research Center Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences
Russian Federation
M. M. Gridina
Federal Research Center Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences
Russian Federation
N. A. Skryabin
Research Institute of Medical Genetics, Tomsk National Research Medical Center RAS
Russian Federation
T. V. Nikitina
Research Institute of Medical Genetics, Tomsk National Research Medical Center RAS
Russian Federation
A. A. Kashevarova
Research Institute of Medical Genetics, Tomsk National Research Medical Center RAS
Russian Federation
L. P. Nazarenko
Research Institute of Medical Genetics, Tomsk National Research Medical Center RAS
Russian Federation
O. L. Serov
Federal Research Center Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences
Russian Federation
I. N. Lebedev
Research Institute of Medical Genetics, Tomsk National Research Medical Center RAS
Russian Federation
For citations:
Lopatkina M.E.,
Fishman V.S.,
Gridina M.M.,
Skryabin N.A.,
Nikitina T.V.,
Kashevarova A.A.,
Nazarenko L.P.,
Serov O.L.,
Lebedev I.N.
Transcriptional profiling of iPSC-derived neurons with reciprocal monogenic CNV in 3p26.3 region. Medical Genetics. 2020;19(3):10-11.
(In Russ.)
https://doi.org/10.25557/2073-7998.2020.03.10-11
Views:
532