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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...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2015
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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. |
format | Online Article Text |
id | pubmed-4742100 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
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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