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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...

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Autores principales: 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
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2007
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.
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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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