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All Human EF1α Promoters Are Not Equal: Markedly Affect Gene Expression in Constructs from Different Sources

The promoter is a major element in the expression cassette of gene therapy vectors. Optimal promoter selection can enhance target specificity and gene expression. Recently, we evaluated three different human elongation factor 1 alpha (EF1α) promoters. The three promoters were put into the same expre...

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Detalles Bibliográficos
Autores principales: Zheng, Changyu, Baum, Bruce J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Ivyspring International Publisher 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3970091/
https://www.ncbi.nlm.nih.gov/pubmed/24688302
http://dx.doi.org/10.7150/ijms.8033
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author Zheng, Changyu
Baum, Bruce J.
author_facet Zheng, Changyu
Baum, Bruce J.
author_sort Zheng, Changyu
collection PubMed
description The promoter is a major element in the expression cassette of gene therapy vectors. Optimal promoter selection can enhance target specificity and gene expression. Recently, we evaluated three different human elongation factor 1 alpha (EF1α) promoters. The three promoters were put into the same expression vector, pAC-luc, driving expression of the luciferase cDNA. The activity from one EF1α promoter (termed EF1α -3), obtained in a commercial vector, was markedly lower when tested in vitro (from 50 - 500 x) in four cell lines and in vivo in rat submandibular glands (~250 x). Sequence differences in the EF1α -3 promoter likely account for the activity differences seen. Investigators need to recognize that all promoters of the same name may not be equivalent in driving transgene expression.
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spelling pubmed-39700912014-03-31 All Human EF1α Promoters Are Not Equal: Markedly Affect Gene Expression in Constructs from Different Sources Zheng, Changyu Baum, Bruce J. Int J Med Sci Short Research Communication The promoter is a major element in the expression cassette of gene therapy vectors. Optimal promoter selection can enhance target specificity and gene expression. Recently, we evaluated three different human elongation factor 1 alpha (EF1α) promoters. The three promoters were put into the same expression vector, pAC-luc, driving expression of the luciferase cDNA. The activity from one EF1α promoter (termed EF1α -3), obtained in a commercial vector, was markedly lower when tested in vitro (from 50 - 500 x) in four cell lines and in vivo in rat submandibular glands (~250 x). Sequence differences in the EF1α -3 promoter likely account for the activity differences seen. Investigators need to recognize that all promoters of the same name may not be equivalent in driving transgene expression. Ivyspring International Publisher 2014-03-07 /pmc/articles/PMC3970091/ /pubmed/24688302 http://dx.doi.org/10.7150/ijms.8033 Text en © Ivyspring International Publisher. This is an open-access article distributed under the terms of the Creative Commons License (http://creativecommons.org/licenses/by-nc-nd/3.0/). Reproduction is permitted for personal, noncommercial use, provided that the article is in whole, unmodified, and properly cited.
spellingShingle Short Research Communication
Zheng, Changyu
Baum, Bruce J.
All Human EF1α Promoters Are Not Equal: Markedly Affect Gene Expression in Constructs from Different Sources
title All Human EF1α Promoters Are Not Equal: Markedly Affect Gene Expression in Constructs from Different Sources
title_full All Human EF1α Promoters Are Not Equal: Markedly Affect Gene Expression in Constructs from Different Sources
title_fullStr All Human EF1α Promoters Are Not Equal: Markedly Affect Gene Expression in Constructs from Different Sources
title_full_unstemmed All Human EF1α Promoters Are Not Equal: Markedly Affect Gene Expression in Constructs from Different Sources
title_short All Human EF1α Promoters Are Not Equal: Markedly Affect Gene Expression in Constructs from Different Sources
title_sort all human ef1α promoters are not equal: markedly affect gene expression in constructs from different sources
topic Short Research Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3970091/
https://www.ncbi.nlm.nih.gov/pubmed/24688302
http://dx.doi.org/10.7150/ijms.8033
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