GENYOi004-A: An induced pluripotent stem cells (iPSCs) line generated from a patient with autism-related ADNP syndrome carrying a pTyr719* mutation

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-transmi...

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Main Authors: Rosa Montes, Pilar Mollinedo, Sonia Perales, Domingo Gonzalez-Lamuño, Veronica Ramos-Mejía, Jose L. Fernandez-Luna, Pedro J. Real
Format: Article
Language:English
Published: Elsevier 2019-05-01
Series:Stem Cell Research
Online Access:http://www.sciencedirect.com/science/article/pii/S1873506119300765
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spelling doaj-6ab74d7d8ea946f68cd05b3aae56ba6e2020-11-24T23:55:26ZengElsevierStem Cell Research1873-50612019-05-0137GENYOi004-A: An induced pluripotent stem cells (iPSCs) line generated from a patient with autism-related ADNP syndrome carrying a pTyr719* mutationRosa Montes0Pilar Mollinedo1Sonia Perales2Domingo Gonzalez-Lamuño3Veronica Ramos-Mejía4Jose L. Fernandez-Luna5Pedro J. Real6Gene Regulation, Stem Cells and Development Group, Department of Genomic Oncology, GENYO: Centre for Genomics and Oncological Research-Pfizer, University of Granada, Junta de Andalucía, PTS, 18016 Granada, SpainGenetics Unit, Hospital Valdecilla, 39008 Santander, Spain; Instituto de Investigación Valdecilla (IDIVAL), 39012 Santander, SpainGene Regulation, Stem Cells and Development Group, Department of Genomic Oncology, GENYO: Centre for Genomics and Oncological Research-Pfizer, University of Granada, Junta de Andalucía, PTS, 18016 Granada, Spain; Department of Biochemistry and Molecular Biology I, Faculty of Science, University of Granada, 18016 Granada, SpainInstituto de Investigación Valdecilla (IDIVAL), 39012 Santander, Spain; Pediatrics Service, Hospital Valdecilla, 39008 Santander, SpainGene Regulation, Stem Cells and Development Group, Department of Genomic Oncology, GENYO: Centre for Genomics and Oncological Research-Pfizer, University of Granada, Junta de Andalucía, PTS, 18016 Granada, SpainGenetics Unit, Hospital Valdecilla, 39008 Santander, Spain; Instituto de Investigación Valdecilla (IDIVAL), 39012 Santander, Spain; Correspondence to: J. L. Fernandez-Luna, Genetics Unit, Hospital Valdecilla, 39008 Santander, Spain.Gene Regulation, Stem Cells and Development Group, Department of Genomic Oncology, GENYO: Centre for Genomics and Oncological Research-Pfizer, University of Granada, Junta de Andalucía, PTS, 18016 Granada, Spain; Department of Biochemistry and Molecular Biology I, Faculty of Science, University of Granada, 18016 Granada, Spain; Correspondence to: Pedro J. Real, Gene Regulation, Stem Cells and Development Group, Department of Genomic Oncology, GENYO: Centre for Genomics and Oncological Research-Pfizer, University of Granada, Junta de Andalucía, PTS, 18016 Granada, Spain.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.http://www.sciencedirect.com/science/article/pii/S1873506119300765
collection DOAJ
language English
format Article
sources DOAJ
author Rosa Montes
Pilar Mollinedo
Sonia Perales
Domingo Gonzalez-Lamuño
Veronica Ramos-Mejía
Jose L. Fernandez-Luna
Pedro J. Real
spellingShingle Rosa Montes
Pilar Mollinedo
Sonia Perales
Domingo Gonzalez-Lamuño
Veronica Ramos-Mejía
Jose L. Fernandez-Luna
Pedro J. Real
GENYOi004-A: An induced pluripotent stem cells (iPSCs) line generated from a patient with autism-related ADNP syndrome carrying a pTyr719* mutation
Stem Cell Research
author_facet Rosa Montes
Pilar Mollinedo
Sonia Perales
Domingo Gonzalez-Lamuño
Veronica Ramos-Mejía
Jose L. Fernandez-Luna
Pedro J. Real
author_sort Rosa Montes
title GENYOi004-A: An induced pluripotent stem cells (iPSCs) line generated from a patient with autism-related ADNP syndrome carrying a pTyr719* mutation
title_short GENYOi004-A: An induced pluripotent stem cells (iPSCs) line generated from a patient with autism-related ADNP syndrome carrying a pTyr719* mutation
title_full GENYOi004-A: An induced pluripotent stem cells (iPSCs) line generated from a patient with autism-related ADNP syndrome carrying a pTyr719* mutation
title_fullStr GENYOi004-A: An induced pluripotent stem cells (iPSCs) line generated from a patient with autism-related ADNP syndrome carrying a pTyr719* mutation
title_full_unstemmed GENYOi004-A: An induced pluripotent stem cells (iPSCs) line generated from a patient with autism-related ADNP syndrome carrying a pTyr719* mutation
title_sort genyoi004-a: an induced pluripotent stem cells (ipscs) line generated from a patient with autism-related adnp syndrome carrying a ptyr719* mutation
publisher Elsevier
series Stem Cell Research
issn 1873-5061
publishDate 2019-05-01
description 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.
url http://www.sciencedirect.com/science/article/pii/S1873506119300765
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