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Single copy shRNA configuration for ubiquitous gene knockdown in mice

RNA interference through the expression of small hairpin RNA (shRNA) molecules has become a very promising tool in reverse mouse genetics as it may allow inexpensive and rapid gene function analysis in vivo. However, the prerequisites for ubiquitous and reproducible shRNA expression are not well def...

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Autores principales: Seibler, Jost, Küter-Luks, Birgit, Kern, Heidrun, Streu, Sandra, Plum, Leona, Mauer, Jan, Kühn, Ralf, Brüning, Jens C., Schwenk, Frieder
Formato: Texto
Lenguaje:English
Publicado: Oxford University Press 2005
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1079974/
https://www.ncbi.nlm.nih.gov/pubmed/15831785
http://dx.doi.org/10.1093/nar/gni065
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author Seibler, Jost
Küter-Luks, Birgit
Kern, Heidrun
Streu, Sandra
Plum, Leona
Mauer, Jan
Kühn, Ralf
Brüning, Jens C.
Schwenk, Frieder
author_facet Seibler, Jost
Küter-Luks, Birgit
Kern, Heidrun
Streu, Sandra
Plum, Leona
Mauer, Jan
Kühn, Ralf
Brüning, Jens C.
Schwenk, Frieder
author_sort Seibler, Jost
collection PubMed
description RNA interference through the expression of small hairpin RNA (shRNA) molecules has become a very promising tool in reverse mouse genetics as it may allow inexpensive and rapid gene function analysis in vivo. However, the prerequisites for ubiquitous and reproducible shRNA expression are not well defined. Here we show that a single copy shRNA-transgene can mediate body-wide gene silencing in mice when inserted in a defined locus of the genome. The most commonly used promoters for shRNA expression, H1 and U6, showed a comparably broad activity in this configuration. Taken together, the results define a novel approach for efficient interference with expression of defined genes in vivo. Moreover, we provide a rapid strategy for the production of gene knockdown mice combining recombinase mediated cassette exchange and tetraploid blastocyst complementation approaches.
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spelling pubmed-10799742005-04-14 Single copy shRNA configuration for ubiquitous gene knockdown in mice Seibler, Jost Küter-Luks, Birgit Kern, Heidrun Streu, Sandra Plum, Leona Mauer, Jan Kühn, Ralf Brüning, Jens C. Schwenk, Frieder Nucleic Acids Res Methods Online RNA interference through the expression of small hairpin RNA (shRNA) molecules has become a very promising tool in reverse mouse genetics as it may allow inexpensive and rapid gene function analysis in vivo. However, the prerequisites for ubiquitous and reproducible shRNA expression are not well defined. Here we show that a single copy shRNA-transgene can mediate body-wide gene silencing in mice when inserted in a defined locus of the genome. The most commonly used promoters for shRNA expression, H1 and U6, showed a comparably broad activity in this configuration. Taken together, the results define a novel approach for efficient interference with expression of defined genes in vivo. Moreover, we provide a rapid strategy for the production of gene knockdown mice combining recombinase mediated cassette exchange and tetraploid blastocyst complementation approaches. Oxford University Press 2005 2005-04-14 /pmc/articles/PMC1079974/ /pubmed/15831785 http://dx.doi.org/10.1093/nar/gni065 Text en © The Author 2005. Published by Oxford University Press. All rights reserved
spellingShingle Methods Online
Seibler, Jost
Küter-Luks, Birgit
Kern, Heidrun
Streu, Sandra
Plum, Leona
Mauer, Jan
Kühn, Ralf
Brüning, Jens C.
Schwenk, Frieder
Single copy shRNA configuration for ubiquitous gene knockdown in mice
title Single copy shRNA configuration for ubiquitous gene knockdown in mice
title_full Single copy shRNA configuration for ubiquitous gene knockdown in mice
title_fullStr Single copy shRNA configuration for ubiquitous gene knockdown in mice
title_full_unstemmed Single copy shRNA configuration for ubiquitous gene knockdown in mice
title_short Single copy shRNA configuration for ubiquitous gene knockdown in mice
title_sort single copy shrna configuration for ubiquitous gene knockdown in mice
topic Methods Online
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1079974/
https://www.ncbi.nlm.nih.gov/pubmed/15831785
http://dx.doi.org/10.1093/nar/gni065
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