Germ-line recombination activity of the widely used hGFAP-Cre and nestin-Cre transgenes.

Herein we demonstrate with PCR, immunodetection and reporter gene approaches that the widely used human Glial Fibrillary Acidic Protein (hGFAP)-Cre transgene exhibits spontaneous germ-line recombination activity in leading to deletion in brain, heart and tail tissue with high frequency. The ectopic...

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Main Authors: Jiong Zhang, Pavel Dublin, Stephanie Griemsmann, Alexandra Klein, Ralph Brehm, Peter Bedner, Bernd K Fleischmann, Christian Steinhäuser, Martin Theis
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2013-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3857304?pdf=render
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spelling doaj-2155fe001cfc497b98c178e24ea912b62020-11-25T00:47:15ZengPublic Library of Science (PLoS)PLoS ONE1932-62032013-01-01812e8281810.1371/journal.pone.0082818Germ-line recombination activity of the widely used hGFAP-Cre and nestin-Cre transgenes.Jiong ZhangPavel DublinStephanie GriemsmannAlexandra KleinRalph BrehmPeter BednerBernd K FleischmannChristian SteinhäuserMartin TheisHerein we demonstrate with PCR, immunodetection and reporter gene approaches that the widely used human Glial Fibrillary Acidic Protein (hGFAP)-Cre transgene exhibits spontaneous germ-line recombination activity in leading to deletion in brain, heart and tail tissue with high frequency. The ectopic activity of hGFAP-Cre requires a rigorous control. We likewise observed that a second widely used nestin-Cre transgene shows germ-line deletion. Here we describe procedures to identify mice with germ-line recombination mediated by the hGFAP-Cre and nestin-Cre transgenes. Such control is essential to avoid pleiotropic effects due to germ-line deletion of loxP-flanked target genes and to maintain the CNS-restricted deletion status in transgenic mouse colonies.http://europepmc.org/articles/PMC3857304?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Jiong Zhang
Pavel Dublin
Stephanie Griemsmann
Alexandra Klein
Ralph Brehm
Peter Bedner
Bernd K Fleischmann
Christian Steinhäuser
Martin Theis
spellingShingle Jiong Zhang
Pavel Dublin
Stephanie Griemsmann
Alexandra Klein
Ralph Brehm
Peter Bedner
Bernd K Fleischmann
Christian Steinhäuser
Martin Theis
Germ-line recombination activity of the widely used hGFAP-Cre and nestin-Cre transgenes.
PLoS ONE
author_facet Jiong Zhang
Pavel Dublin
Stephanie Griemsmann
Alexandra Klein
Ralph Brehm
Peter Bedner
Bernd K Fleischmann
Christian Steinhäuser
Martin Theis
author_sort Jiong Zhang
title Germ-line recombination activity of the widely used hGFAP-Cre and nestin-Cre transgenes.
title_short Germ-line recombination activity of the widely used hGFAP-Cre and nestin-Cre transgenes.
title_full Germ-line recombination activity of the widely used hGFAP-Cre and nestin-Cre transgenes.
title_fullStr Germ-line recombination activity of the widely used hGFAP-Cre and nestin-Cre transgenes.
title_full_unstemmed Germ-line recombination activity of the widely used hGFAP-Cre and nestin-Cre transgenes.
title_sort germ-line recombination activity of the widely used hgfap-cre and nestin-cre transgenes.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2013-01-01
description Herein we demonstrate with PCR, immunodetection and reporter gene approaches that the widely used human Glial Fibrillary Acidic Protein (hGFAP)-Cre transgene exhibits spontaneous germ-line recombination activity in leading to deletion in brain, heart and tail tissue with high frequency. The ectopic activity of hGFAP-Cre requires a rigorous control. We likewise observed that a second widely used nestin-Cre transgene shows germ-line deletion. Here we describe procedures to identify mice with germ-line recombination mediated by the hGFAP-Cre and nestin-Cre transgenes. Such control is essential to avoid pleiotropic effects due to germ-line deletion of loxP-flanked target genes and to maintain the CNS-restricted deletion status in transgenic mouse colonies.
url http://europepmc.org/articles/PMC3857304?pdf=render
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