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Variability of Inducible Expression across the Hematopoietic System of Tetracycline Transactivator Transgenic Mice

The tetracycline (tet)-regulated expression system allows for the inducible overexpression of protein-coding genes, or inducible gene knockdown based on expression of short hairpin RNAs (shRNAs). The system is widely used in mice, however it requires robust expression of a tet transactivator protein...

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Autores principales: Takiguchi, Megumi, Dow, Lukas E., Prier, Julia E., Carmichael, Catherine L., Kile, Benjamin T., Turner, Stephen J., Lowe, Scott W., Huang, David C. S., Dickins, Ross A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3543435/
https://www.ncbi.nlm.nih.gov/pubmed/23326559
http://dx.doi.org/10.1371/journal.pone.0054009
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author Takiguchi, Megumi
Dow, Lukas E.
Prier, Julia E.
Carmichael, Catherine L.
Kile, Benjamin T.
Turner, Stephen J.
Lowe, Scott W.
Huang, David C. S.
Dickins, Ross A.
author_facet Takiguchi, Megumi
Dow, Lukas E.
Prier, Julia E.
Carmichael, Catherine L.
Kile, Benjamin T.
Turner, Stephen J.
Lowe, Scott W.
Huang, David C. S.
Dickins, Ross A.
author_sort Takiguchi, Megumi
collection PubMed
description The tetracycline (tet)-regulated expression system allows for the inducible overexpression of protein-coding genes, or inducible gene knockdown based on expression of short hairpin RNAs (shRNAs). The system is widely used in mice, however it requires robust expression of a tet transactivator protein (tTA or rtTA) in the cell type of interest. Here we used an in vivo tet-regulated fluorescent reporter approach to characterise inducible gene/shRNA expression across a range of hematopoietic cell types of several commonly used transgenic tet transactivator mouse strains. We find that even in strains where the tet transactivator is expressed from a nominally ubiquitous promoter, the efficiency of tet-regulated expression can be highly variable between hematopoietic lineages and between differentiation stages within a lineage. In some cases tet-regulated reporter expression differs markedly between cells within a discrete, immunophenotypically defined population, suggesting mosaic transactivator expression. A recently developed CAG-rtTA3 transgenic mouse displays intense and efficient reporter expression in most blood cell types, establishing this strain as a highly effective tool for probing hematopoietic development and disease. These findings have important implications for interpreting tet-regulated hematopoietic phenotypes in mice, and identify mouse strains that provide optimal tet-regulated expression in particular hematopoietic progenitor cell types and mature blood lineages.
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spelling pubmed-35434352013-01-16 Variability of Inducible Expression across the Hematopoietic System of Tetracycline Transactivator Transgenic Mice Takiguchi, Megumi Dow, Lukas E. Prier, Julia E. Carmichael, Catherine L. Kile, Benjamin T. Turner, Stephen J. Lowe, Scott W. Huang, David C. S. Dickins, Ross A. PLoS One Research Article The tetracycline (tet)-regulated expression system allows for the inducible overexpression of protein-coding genes, or inducible gene knockdown based on expression of short hairpin RNAs (shRNAs). The system is widely used in mice, however it requires robust expression of a tet transactivator protein (tTA or rtTA) in the cell type of interest. Here we used an in vivo tet-regulated fluorescent reporter approach to characterise inducible gene/shRNA expression across a range of hematopoietic cell types of several commonly used transgenic tet transactivator mouse strains. We find that even in strains where the tet transactivator is expressed from a nominally ubiquitous promoter, the efficiency of tet-regulated expression can be highly variable between hematopoietic lineages and between differentiation stages within a lineage. In some cases tet-regulated reporter expression differs markedly between cells within a discrete, immunophenotypically defined population, suggesting mosaic transactivator expression. A recently developed CAG-rtTA3 transgenic mouse displays intense and efficient reporter expression in most blood cell types, establishing this strain as a highly effective tool for probing hematopoietic development and disease. These findings have important implications for interpreting tet-regulated hematopoietic phenotypes in mice, and identify mouse strains that provide optimal tet-regulated expression in particular hematopoietic progenitor cell types and mature blood lineages. Public Library of Science 2013-01-11 /pmc/articles/PMC3543435/ /pubmed/23326559 http://dx.doi.org/10.1371/journal.pone.0054009 Text en © 2013 Takiguchi 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
Takiguchi, Megumi
Dow, Lukas E.
Prier, Julia E.
Carmichael, Catherine L.
Kile, Benjamin T.
Turner, Stephen J.
Lowe, Scott W.
Huang, David C. S.
Dickins, Ross A.
Variability of Inducible Expression across the Hematopoietic System of Tetracycline Transactivator Transgenic Mice
title Variability of Inducible Expression across the Hematopoietic System of Tetracycline Transactivator Transgenic Mice
title_full Variability of Inducible Expression across the Hematopoietic System of Tetracycline Transactivator Transgenic Mice
title_fullStr Variability of Inducible Expression across the Hematopoietic System of Tetracycline Transactivator Transgenic Mice
title_full_unstemmed Variability of Inducible Expression across the Hematopoietic System of Tetracycline Transactivator Transgenic Mice
title_short Variability of Inducible Expression across the Hematopoietic System of Tetracycline Transactivator Transgenic Mice
title_sort variability of inducible expression across the hematopoietic system of tetracycline transactivator transgenic mice
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3543435/
https://www.ncbi.nlm.nih.gov/pubmed/23326559
http://dx.doi.org/10.1371/journal.pone.0054009
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