Publication: GENYOi004-A: An induced pluripotent stem cells (iPSCs) line generated from a patient with autism-related ADNP syndrome carrying a pTyr719* mutation.
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Date
2019-04-22
Authors
Montes, Rosa
Mollinedo, Pilar
Perales, Sonia
Gonzalez-Lamuño, Domingo
Ramos-Mejía, Veronica
Fernandez-Luna, Jose L
Real, Pedro J
Advisors
Journal Title
Journal ISSN
Volume Title
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Abstract
ADNP syndrome is an intellectual disability associated with Autism spectrum disorder caused by mutations in ADNP. We generated an iPSC line from an ADNP syndrome pediatric patient harboring the mutation p.Trp719* (GENYOi004-A). Peripheral blood mononuclear cells were reprogrammed using a non-transmissible form of Sendai viruses expressing the four Yamanaka factors (Oct3/4, SOX2, KLF4 and c-MYC). Characterization of GENYOi004-A included mutation analysis of ADNP by allele-specific PCR, genetic identity by Short Tandem Repeats polymorphism profiling, alkaline phosphatase enzymatic activity, expression of pluripotency-associated factors and pluripotency studies in vivo. GENYOi004-A will be useful to evaluate ADNP syndrome alterations at early developmental stages.
Description
MeSH Terms
Animals
Autism Spectrum Disorder
Cell Differentiation
Cells, Cultured
Cellular Reprogramming
Child
Female
Homeodomain Proteins
Humans
Induced Pluripotent Stem Cells
Kruppel-Like Factor 4
Leukocytes, Mononuclear
Mice
Mice, Inbred NOD
Mice, SCID
Mutation
Nerve Tissue Proteins
Phenotype
Teratoma
Autism Spectrum Disorder
Cell Differentiation
Cells, Cultured
Cellular Reprogramming
Child
Female
Homeodomain Proteins
Humans
Induced Pluripotent Stem Cells
Kruppel-Like Factor 4
Leukocytes, Mononuclear
Mice
Mice, Inbred NOD
Mice, SCID
Mutation
Nerve Tissue Proteins
Phenotype
Teratoma