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Chromosome transplantation as a novel approach for correcting complex genomic disorders

Genomic disorders resulting from large rearrangements of the genome remain an important unsolved issue in gene therapy. Chromosome transplantation, defined as the perfect replacement of an endogenous chromosome with a homologous one, has the potential of curing this kind of disorders. Here we report...

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Autores principales: Paulis, Marianna, Castelli, Alessandra, Susani, Lucia, Lizier, Michela, Lagutina, Irina, Focarelli, Maria Luisa, Recordati, Camilla, Uva, Paolo, Faggioli, Francesca, Neri, Tui, Scanziani, Eugenio, Galli, Cesare, Lucchini, Franco, Villa, Anna, Vezzoni, Paolo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4742100/
https://www.ncbi.nlm.nih.gov/pubmed/26485770
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author Paulis, Marianna
Castelli, Alessandra
Susani, Lucia
Lizier, Michela
Lagutina, Irina
Focarelli, Maria Luisa
Recordati, Camilla
Uva, Paolo
Faggioli, Francesca
Neri, Tui
Scanziani, Eugenio
Galli, Cesare
Lucchini, Franco
Villa, Anna
Vezzoni, Paolo
author_facet Paulis, Marianna
Castelli, Alessandra
Susani, Lucia
Lizier, Michela
Lagutina, Irina
Focarelli, Maria Luisa
Recordati, Camilla
Uva, Paolo
Faggioli, Francesca
Neri, Tui
Scanziani, Eugenio
Galli, Cesare
Lucchini, Franco
Villa, Anna
Vezzoni, Paolo
author_sort Paulis, Marianna
collection PubMed
description Genomic disorders resulting from large rearrangements of the genome remain an important unsolved issue in gene therapy. Chromosome transplantation, defined as the perfect replacement of an endogenous chromosome with a homologous one, has the potential of curing this kind of disorders. Here we report the first successful case of chromosome transplantation by replacement of an endogenous X chromosome carrying a mutation in the Hprt gene with a normal one in mouse embryonic stem cells (ESCs), correcting the genetic defect. The defect was also corrected by replacing the Y chromosome with an X chromosome. Chromosome transplanted clones maintained in vitro and in vivo features of stemness and contributed to chimera formation. Genome integrity was confirmed by cytogenetic and molecular genome analysis. The approach here proposed, with some modifications, might be used to cure various disorders due to other X chromosome aberrations in induced pluripotent stem (iPS) cells derived from affected patients.
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spelling pubmed-47421002016-04-04 Chromosome transplantation as a novel approach for correcting complex genomic disorders Paulis, Marianna Castelli, Alessandra Susani, Lucia Lizier, Michela Lagutina, Irina Focarelli, Maria Luisa Recordati, Camilla Uva, Paolo Faggioli, Francesca Neri, Tui Scanziani, Eugenio Galli, Cesare Lucchini, Franco Villa, Anna Vezzoni, Paolo Oncotarget Priority Research Paper Genomic disorders resulting from large rearrangements of the genome remain an important unsolved issue in gene therapy. Chromosome transplantation, defined as the perfect replacement of an endogenous chromosome with a homologous one, has the potential of curing this kind of disorders. Here we report the first successful case of chromosome transplantation by replacement of an endogenous X chromosome carrying a mutation in the Hprt gene with a normal one in mouse embryonic stem cells (ESCs), correcting the genetic defect. The defect was also corrected by replacing the Y chromosome with an X chromosome. Chromosome transplanted clones maintained in vitro and in vivo features of stemness and contributed to chimera formation. Genome integrity was confirmed by cytogenetic and molecular genome analysis. The approach here proposed, with some modifications, might be used to cure various disorders due to other X chromosome aberrations in induced pluripotent stem (iPS) cells derived from affected patients. Impact Journals LLC 2015-10-17 /pmc/articles/PMC4742100/ /pubmed/26485770 Text en Copyright: © 2015 Paulis et al. http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Priority Research Paper
Paulis, Marianna
Castelli, Alessandra
Susani, Lucia
Lizier, Michela
Lagutina, Irina
Focarelli, Maria Luisa
Recordati, Camilla
Uva, Paolo
Faggioli, Francesca
Neri, Tui
Scanziani, Eugenio
Galli, Cesare
Lucchini, Franco
Villa, Anna
Vezzoni, Paolo
Chromosome transplantation as a novel approach for correcting complex genomic disorders
title Chromosome transplantation as a novel approach for correcting complex genomic disorders
title_full Chromosome transplantation as a novel approach for correcting complex genomic disorders
title_fullStr Chromosome transplantation as a novel approach for correcting complex genomic disorders
title_full_unstemmed Chromosome transplantation as a novel approach for correcting complex genomic disorders
title_short Chromosome transplantation as a novel approach for correcting complex genomic disorders
title_sort chromosome transplantation as a novel approach for correcting complex genomic disorders
topic Priority Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4742100/
https://www.ncbi.nlm.nih.gov/pubmed/26485770
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