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...

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Bibliographic Details
Published in:	Russian journal of developmental biology Vol. 54; no. 6; pp. 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:	Journal Article
Language:	English
Published:	Moscow Pleiades Publishing 01-12-2023 Springer Nature B.V
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 gene knockout induced pluripotent stem cells Nascimento type X-linked mental retardation gene
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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