Derivation of Induced Pluripotent Stem Cells Line (RCPCMi009-A-1) with Knockout of the UBE2A Gene Using CRISPR/Cas9 Genome Editing

The deletions and mutations in the UBE2A gene cause X-linked mental retardation syndrome of the Nascimento type first described in 2006 (Nascimento et al., 2006). At the moment, approximately two dozen missense and nonsense mutations in the UBE2A gene associated with Nascimento-type mental retardati...

Full description

Saved in:
Bibliographic Details
Published in:Russian journal of developmental biology 2023-12, Vol.54 (6), p.365-373
Main Authors: Khomyakova, E. A., Fedorenko, A. V., Surdina, A. V., Volovikov, E. A., Belikova, L. D., Zerkalenkova, E. A., Lagarkova, M. A., Bogomazova, A. N.
Format: Article
Language:English
Subjects:
Animal Anatomy
Biomedical and Life Sciences
Collection of Pluripotent Stem Cell Lines
CRISPR
Cytology
Developmental Biology
Genomes
Histology
Intellectual disabilities
Karyotypes
Life Sciences
Morphology
Mutation
Pluripotency
Stem cells
Western blotting
Citations: Items that this one cites
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:The deletions and mutations in the UBE2A gene cause X-linked mental retardation syndrome of the Nascimento type first described in 2006 (Nascimento et al., 2006). At the moment, approximately two dozen missense and nonsense mutations in the UBE2A gene associated with Nascimento-type mental retardation syndrome are known (Cordeddu et al., 2020). To study the role of the UBE2A gene in neurodevelopment, the authors generated a human iPSC line with knockout of the UBE2A gene (RCPCMi009-A-1) using genome editing CRISPR/Cas9 technology. The knockout of the UBE2A gene was confirmed by Western blotting. The pluripotent state of the RCPCMi009-A-1 iPSC line was confirmed by typical stem cell morphology, normal male karyotype (46,XY) maintenance, expression of pluripotency markers, and the ability to differentiate into the derivatives of three germ layers.
ISSN:1062-3604
1608-3326
DOI:10.1134/S1062360423060048