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Utrophin Up-Regulation by an Artificial Transcription Factor in Transgenic Mice
Duchenne Muscular Dystrophy (DMD) is a severe muscle degenerative disease, due to absence of dystrophin. There is currently no effective treatment for DMD. Our aim is to up-regulate the expression level of the dystrophin related gene utrophin in DMD, complementing in this way the lack of dystrophin...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Public Library of Science
2007
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1942121/ https://www.ncbi.nlm.nih.gov/pubmed/17712422 http://dx.doi.org/10.1371/journal.pone.0000774 |
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author | Mattei, Elisabetta Corbi, Nicoletta Di Certo, Maria Grazia Strimpakos, Georgios Severini, Cinzia Onori, Annalisa Desantis, Agata Libri, Valentina Buontempo, Serena Floridi, Aristide Fanciulli, Maurizio Baban, Dilair Davies, Kay E. Passananti, Claudio |
author_facet | Mattei, Elisabetta Corbi, Nicoletta Di Certo, Maria Grazia Strimpakos, Georgios Severini, Cinzia Onori, Annalisa Desantis, Agata Libri, Valentina Buontempo, Serena Floridi, Aristide Fanciulli, Maurizio Baban, Dilair Davies, Kay E. Passananti, Claudio |
author_sort | Mattei, Elisabetta |
collection | PubMed |
description | Duchenne Muscular Dystrophy (DMD) is a severe muscle degenerative disease, due to absence of dystrophin. There is currently no effective treatment for DMD. Our aim is to up-regulate the expression level of the dystrophin related gene utrophin in DMD, complementing in this way the lack of dystrophin functions. To this end we designed and engineered several synthetic zinc finger based transcription factors. In particular, we have previously shown that the artificial three zinc finger protein named Jazz, fused with the appropriate effector domain, is able to drive the transcription of a test gene from the utrophin promoter “A”. Here we report on the characterization of Vp16-Jazz-transgenic mice that specifically over-express the utrophin gene at the muscular level. A Chromatin Immunoprecipitation assay (ChIP) demonstrated the effective access/binding of the Jazz protein to active chromatin in mouse muscle and Vp16-Jazz was shown to be able to up-regulate endogenous utrophin gene expression by immunohistochemistry, western blot analyses and real-time PCR. To our knowledge, this is the first example of a transgenic mouse expressing an artificial gene coding for a zinc finger based transcription factor. The achievement of Vp16-Jazz transgenic mice validates the strategy of transcriptional targeting of endogenous genes and could represent an exclusive animal model for use in drug discovery and therapeutics. |
format | Text |
id | pubmed-1942121 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2007 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-19421212007-08-22 Utrophin Up-Regulation by an Artificial Transcription Factor in Transgenic Mice Mattei, Elisabetta Corbi, Nicoletta Di Certo, Maria Grazia Strimpakos, Georgios Severini, Cinzia Onori, Annalisa Desantis, Agata Libri, Valentina Buontempo, Serena Floridi, Aristide Fanciulli, Maurizio Baban, Dilair Davies, Kay E. Passananti, Claudio PLoS One Research Article Duchenne Muscular Dystrophy (DMD) is a severe muscle degenerative disease, due to absence of dystrophin. There is currently no effective treatment for DMD. Our aim is to up-regulate the expression level of the dystrophin related gene utrophin in DMD, complementing in this way the lack of dystrophin functions. To this end we designed and engineered several synthetic zinc finger based transcription factors. In particular, we have previously shown that the artificial three zinc finger protein named Jazz, fused with the appropriate effector domain, is able to drive the transcription of a test gene from the utrophin promoter “A”. Here we report on the characterization of Vp16-Jazz-transgenic mice that specifically over-express the utrophin gene at the muscular level. A Chromatin Immunoprecipitation assay (ChIP) demonstrated the effective access/binding of the Jazz protein to active chromatin in mouse muscle and Vp16-Jazz was shown to be able to up-regulate endogenous utrophin gene expression by immunohistochemistry, western blot analyses and real-time PCR. To our knowledge, this is the first example of a transgenic mouse expressing an artificial gene coding for a zinc finger based transcription factor. The achievement of Vp16-Jazz transgenic mice validates the strategy of transcriptional targeting of endogenous genes and could represent an exclusive animal model for use in drug discovery and therapeutics. Public Library of Science 2007-08-22 /pmc/articles/PMC1942121/ /pubmed/17712422 http://dx.doi.org/10.1371/journal.pone.0000774 Text en Mattei et al. 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 | Research Article Mattei, Elisabetta Corbi, Nicoletta Di Certo, Maria Grazia Strimpakos, Georgios Severini, Cinzia Onori, Annalisa Desantis, Agata Libri, Valentina Buontempo, Serena Floridi, Aristide Fanciulli, Maurizio Baban, Dilair Davies, Kay E. Passananti, Claudio Utrophin Up-Regulation by an Artificial Transcription Factor in Transgenic Mice |
title | Utrophin Up-Regulation by an Artificial Transcription Factor in Transgenic Mice |
title_full | Utrophin Up-Regulation by an Artificial Transcription Factor in Transgenic Mice |
title_fullStr | Utrophin Up-Regulation by an Artificial Transcription Factor in Transgenic Mice |
title_full_unstemmed | Utrophin Up-Regulation by an Artificial Transcription Factor in Transgenic Mice |
title_short | Utrophin Up-Regulation by an Artificial Transcription Factor in Transgenic Mice |
title_sort | utrophin up-regulation by an artificial transcription factor in transgenic mice |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1942121/ https://www.ncbi.nlm.nih.gov/pubmed/17712422 http://dx.doi.org/10.1371/journal.pone.0000774 |
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