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  Tetracycline-controlled transgene activation using the ROSA26-iM2-GFP knock-in mouse strain permits GFP monitoring of DOX-regulated transgene-expression

Wortge, S., Eshkind, L., Cabezas-Wallscheid, N., Lakaye, B., Kim, J.-H., Heck, R., et al. (2010). Tetracycline-controlled transgene activation using the ROSA26-iM2-GFP knock-in mouse strain permits GFP monitoring of DOX-regulated transgene-expression. BMC Developmental Biology, 10: 95, pp. 1-13. doi:10.1186/1471-213X-10-95.

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Genre: Zeitschriftenartikel
Alternativer Titel : Tetracycline-controlled transgene activation using the ROSA26-iM2-GFP knock-in mouse strain permits GFP monitoring of DOX-regulated transgene-expression

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 Urheber:
Wortge, Simone1, Autor
Eshkind, Leonid1, Autor
Cabezas-Wallscheid, Nina2, Autor           
Lakaye, Bernard1, Autor
Kim, Jin-Hyun1, Autor
Heck, Rosario1, Autor
Abassi, Yasmin1, Autor
Diken, Mustafa1, Autor
Sprengel, Rolf3, Autor           
Bockamp, Ernesto1, Autor
Affiliations:
1External Organizations, ou_persistent22              
2Department of Cellular and Molecular Immunology, Max Planck Institute of Immunobiology and Epigenetics, ou_2243641              
3Department of Molecular Neurobiology, Max Planck Institute for Medical Research, Max Planck Society, ou_1497704              

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 Zusammenfassung: Conditional gene activation is an efficient strategy for studying gene function in genetically modified animals. Among the presently available gene switches, the tetracycline-regulated system has attracted considerable interest because of its unique potential for reversible and adjustable gene regulation.
RESULTS:

To investigate whether the ubiquitously expressed Gt(ROSA)26Sor locus enables uniform DOX-controlled gene expression, we inserted the improved tetracycline-regulated transcription activator iM2 together with an iM2 dependent GFP gene into the Gt(ROSA)26Sor locus, using gene targeting to generate ROSA26-iM2-GFP (R26t1Δ) mice. Despite the presence of ROSA26 promoter driven iM2, R26t1Δ mice showed very sparse DOX-activated expression of different iM2-responsive reporter genes in the brain, mosaic expression in peripheral tissues and more prominent expression in erythroid, myeloid and lymphoid lineages, in hematopoietic stem and progenitor cells and in olfactory neurons.
CONCLUSIONS:

The finding that gene regulation by the DOX-activated transcriptional factor iM2 in the Gt(ROSA)26Sor locus has its limitations is of importance for future experimental strategies involving transgene activation from the endogenous ROSA26 promoter. Furthermore, our ROSA26-iM2 knock-in mouse model (R26t1Δ) represents a useful tool for implementing gene function in vivo especially under circumstances requiring the side-by-side comparison of gene manipulated and wild type cells. Since the ROSA26-iM2 mouse allows mosaic gene activation in peripheral tissues and haematopoietic cells, this model will be very useful for uncovering previously unknown or unsuspected phenotypes.

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Sprache(n): eng - English
 Datum: 2010-02-052010-09-032010-09-03
 Publikationsstatus: Erschienen
 Seiten: 13
 Ort, Verlag, Ausgabe: -
 Inhaltsverzeichnis: -
 Art der Begutachtung: Expertenbegutachtung
 Identifikatoren: eDoc: 664580
DOI: 10.1186/1471-213X-10-95
URI: https://www.ncbi.nlm.nih.gov/pubmed/20815887
Anderer: 7606
 Art des Abschluß: -

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Titel: BMC Developmental Biology
Genre der Quelle: Zeitschrift
 Urheber:
Affiliations:
Ort, Verlag, Ausgabe: BioMed Central
Seiten: - Band / Heft: 10 Artikelnummer: 95 Start- / Endseite: 1 - 13 Identifikator: ISSN: 1471-213X
CoNE: https://pure.mpg.de/cone/journals/resource/111000136905004