Generation of two induced pluripotent stem cell lines and the corresponding isogenic controls from Parkinson’s disease patients carrying the heterozygous mutations c.815G > A (p.R272Q) or c.1348C > T (p.R450C) in the RHOT1 gene encoding Miro1

Fibroblasts from two Parkinson’s disease (PD) patients carrying either the heterozygous mutation c.815G > A (Miro1 p.R272Q) or c.1348C > T (Miro1 p.R450C) in the RHOT1 gene, were converted into induced pluripotent stem cells (iPSCs) using RNA-based and episomal reprogramming, respectively. The...

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Main Authors: Axel Chemla, Giuseppe Arena, Gizem Onal, Jonas Walter, Clara Berenguer-Escuder, Dajana Grossmann, Anne Grünewald, Jens C. Schwamborn, Rejko Krüger
Format: Article
Language:English
Published: Elsevier 2023-09-01
Series:Stem Cell Research
Online Access:http://www.sciencedirect.com/science/article/pii/S1873506123001319
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author Axel Chemla
Giuseppe Arena
Gizem Onal
Jonas Walter
Clara Berenguer-Escuder
Dajana Grossmann
Anne Grünewald
Jens C. Schwamborn
Rejko Krüger
author_facet Axel Chemla
Giuseppe Arena
Gizem Onal
Jonas Walter
Clara Berenguer-Escuder
Dajana Grossmann
Anne Grünewald
Jens C. Schwamborn
Rejko Krüger
author_sort Axel Chemla
collection DOAJ
description Fibroblasts from two Parkinson’s disease (PD) patients carrying either the heterozygous mutation c.815G > A (Miro1 p.R272Q) or c.1348C > T (Miro1 p.R450C) in the RHOT1 gene, were converted into induced pluripotent stem cells (iPSCs) using RNA-based and episomal reprogramming, respectively. The corresponding isogenic gene-corrected lines have been generated using CRISPR/Cas9 technology. These two isogenic pairs will be used to study Miro1-related molecular mechanisms underlying neurodegeneration in relevant iPSC-derived neuronal models (e.g., midbrain dopaminergic neurons and astrocytes).
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spelling doaj.art-4a91b68674934c279644a2bb4ca1375a2023-09-06T04:50:45ZengElsevierStem Cell Research1873-50612023-09-0171103145Generation of two induced pluripotent stem cell lines and the corresponding isogenic controls from Parkinson’s disease patients carrying the heterozygous mutations c.815G > A (p.R272Q) or c.1348C > T (p.R450C) in the RHOT1 gene encoding Miro1Axel Chemla0Giuseppe Arena1Gizem Onal2Jonas Walter3Clara Berenguer-Escuder4Dajana Grossmann5Anne Grünewald6Jens C. Schwamborn7Rejko Krüger8Translational Neuroscience, Luxembourg Centre for Systems Biomedicine (LCSB), University of Luxembourg, LuxembourgTranslational Neuroscience, Luxembourg Centre for Systems Biomedicine (LCSB), University of Luxembourg, Luxembourg; Corresponding authors at: Translational Neuroscience team, Luxembourg Centre for Systems Biomedicine (LCSB), University of Luxembourg, Campus Belval, 6 Avenue du Swing, L-4367 Esch-sur-Alzette, Luxembourg.Department of Physiology, Anatomy and Genetics, University of Oxford, UK; Kavli Institute for Nanoscience Discovery, University of Oxford, UK; Department of Medical Biology, Faculty of Medicine, Balikesir University, TurkeyDevelopmental and Cellular Biology, Luxembourg Centre for Systems Biomedicine (LCSB), University of Luxembourg, LuxembourgTranslational Neuroscience, Luxembourg Centre for Systems Biomedicine (LCSB), University of Luxembourg, LuxembourgTranslational Neuroscience, Luxembourg Centre for Systems Biomedicine (LCSB), University of Luxembourg, Luxembourg; Translational Neurodegeneration Section “Albrecht-Kossel”, Department of Neurology, University Medical Center Rostock, University of Rostock, Rostock, GermanyMolecular and Functional Neurobiology, Luxembourg Centre for Systems Biomedicine (LCSB), University of Luxembourg, Luxembourg; Institute of Neurogenetics, University of Lübeck, Lübeck, GermanyDevelopmental and Cellular Biology, Luxembourg Centre for Systems Biomedicine (LCSB), University of Luxembourg, LuxembourgTranslational Neuroscience, Luxembourg Centre for Systems Biomedicine (LCSB), University of Luxembourg, Luxembourg; Centre Hospitalier de Luxembourg, Luxembourg; Transversal Translational Medicine, Luxembourg Institute of Health (LIH), Luxembourg; Corresponding authors at: Translational Neuroscience team, Luxembourg Centre for Systems Biomedicine (LCSB), University of Luxembourg, Campus Belval, 6 Avenue du Swing, L-4367 Esch-sur-Alzette, Luxembourg.Fibroblasts from two Parkinson’s disease (PD) patients carrying either the heterozygous mutation c.815G > A (Miro1 p.R272Q) or c.1348C > T (Miro1 p.R450C) in the RHOT1 gene, were converted into induced pluripotent stem cells (iPSCs) using RNA-based and episomal reprogramming, respectively. The corresponding isogenic gene-corrected lines have been generated using CRISPR/Cas9 technology. These two isogenic pairs will be used to study Miro1-related molecular mechanisms underlying neurodegeneration in relevant iPSC-derived neuronal models (e.g., midbrain dopaminergic neurons and astrocytes).http://www.sciencedirect.com/science/article/pii/S1873506123001319
spellingShingle Axel Chemla
Giuseppe Arena
Gizem Onal
Jonas Walter
Clara Berenguer-Escuder
Dajana Grossmann
Anne Grünewald
Jens C. Schwamborn
Rejko Krüger
Generation of two induced pluripotent stem cell lines and the corresponding isogenic controls from Parkinson’s disease patients carrying the heterozygous mutations c.815G > A (p.R272Q) or c.1348C > T (p.R450C) in the RHOT1 gene encoding Miro1
Stem Cell Research
title Generation of two induced pluripotent stem cell lines and the corresponding isogenic controls from Parkinson’s disease patients carrying the heterozygous mutations c.815G > A (p.R272Q) or c.1348C > T (p.R450C) in the RHOT1 gene encoding Miro1
title_full Generation of two induced pluripotent stem cell lines and the corresponding isogenic controls from Parkinson’s disease patients carrying the heterozygous mutations c.815G > A (p.R272Q) or c.1348C > T (p.R450C) in the RHOT1 gene encoding Miro1
title_fullStr Generation of two induced pluripotent stem cell lines and the corresponding isogenic controls from Parkinson’s disease patients carrying the heterozygous mutations c.815G > A (p.R272Q) or c.1348C > T (p.R450C) in the RHOT1 gene encoding Miro1
title_full_unstemmed Generation of two induced pluripotent stem cell lines and the corresponding isogenic controls from Parkinson’s disease patients carrying the heterozygous mutations c.815G > A (p.R272Q) or c.1348C > T (p.R450C) in the RHOT1 gene encoding Miro1
title_short Generation of two induced pluripotent stem cell lines and the corresponding isogenic controls from Parkinson’s disease patients carrying the heterozygous mutations c.815G > A (p.R272Q) or c.1348C > T (p.R450C) in the RHOT1 gene encoding Miro1
title_sort generation of two induced pluripotent stem cell lines and the corresponding isogenic controls from parkinson s disease patients carrying the heterozygous mutations c 815g a p r272q or c 1348c t p r450c in the rhot1 gene encoding miro1
url http://www.sciencedirect.com/science/article/pii/S1873506123001319
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