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Restoration of dystrophin expression using the Sleeping Beauty transposon

The Sleeping beauty (SB) system is a non-viral DNA based vector that has been used to stably integrate therapeutic genes into disease models. Here we report the SB system is capable of stably integrating the ΔR4-R23/CTΔ micro-dystrophin gene into a conditionally immortal dystrophin deficient muscle...

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Detalles Bibliográficos
Autores principales: Muses, Sofia, Morgan, Jennifer E, Wells, Dominic J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3269885/
https://www.ncbi.nlm.nih.gov/pubmed/22318674
http://dx.doi.org/10.1371/currents.RRN1296
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author Muses, Sofia
Morgan, Jennifer E
Wells, Dominic J.
author_facet Muses, Sofia
Morgan, Jennifer E
Wells, Dominic J.
author_sort Muses, Sofia
collection PubMed
description The Sleeping beauty (SB) system is a non-viral DNA based vector that has been used to stably integrate therapeutic genes into disease models. Here we report the SB system is capable of stably integrating the ΔR4-R23/CTΔ micro-dystrophin gene into a conditionally immortal dystrophin deficient muscle cell-line, H2K SF1, a murine cell model for Duchenne muscular dystrophy. Genetically corrected H2K SF1 cells retained their myogenic properties in vitro. Moreover, upon transplantation ΔR4-R23/CTΔ micro-dystrophin expression was detected within mdx nu/nu mice. Our data suggests the SB system is an effective way of stably integrating therapeutic genes into myogenic cells.
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spelling pubmed-32698852012-02-07 Restoration of dystrophin expression using the Sleeping Beauty transposon Muses, Sofia Morgan, Jennifer E Wells, Dominic J. PLoS Curr Muscular Dystrophy The Sleeping beauty (SB) system is a non-viral DNA based vector that has been used to stably integrate therapeutic genes into disease models. Here we report the SB system is capable of stably integrating the ΔR4-R23/CTΔ micro-dystrophin gene into a conditionally immortal dystrophin deficient muscle cell-line, H2K SF1, a murine cell model for Duchenne muscular dystrophy. Genetically corrected H2K SF1 cells retained their myogenic properties in vitro. Moreover, upon transplantation ΔR4-R23/CTΔ micro-dystrophin expression was detected within mdx nu/nu mice. Our data suggests the SB system is an effective way of stably integrating therapeutic genes into myogenic cells. Public Library of Science 2012-02-07 /pmc/articles/PMC3269885/ /pubmed/22318674 http://dx.doi.org/10.1371/currents.RRN1296 Text en http://creativecommons.org/licenses/by/4.0/ 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 properly credited.
spellingShingle Muscular Dystrophy
Muses, Sofia
Morgan, Jennifer E
Wells, Dominic J.
Restoration of dystrophin expression using the Sleeping Beauty transposon
title Restoration of dystrophin expression using the Sleeping Beauty transposon
title_full Restoration of dystrophin expression using the Sleeping Beauty transposon
title_fullStr Restoration of dystrophin expression using the Sleeping Beauty transposon
title_full_unstemmed Restoration of dystrophin expression using the Sleeping Beauty transposon
title_short Restoration of dystrophin expression using the Sleeping Beauty transposon
title_sort restoration of dystrophin expression using the sleeping beauty transposon
topic Muscular Dystrophy
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3269885/
https://www.ncbi.nlm.nih.gov/pubmed/22318674
http://dx.doi.org/10.1371/currents.RRN1296
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