Seibler Jost, Küter-Luks Birgit, Kern Heidrun, Streu Sandra, Plum Leona, Mauer Jan, Kühn Ralf, Brüning Jens C, Schwenk Frieder
Artemis Pharmaceuticals GmbH Neurather Ring 1, 51063 Cologne, Germany.
Nucleic Acids Res. 2005 Apr 14;33(7):e67. doi: 10.1093/nar/gni065.
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.
通过表达小发夹RNA(shRNA)分子进行RNA干扰已成为反向小鼠遗传学中一种非常有前景的工具,因为它可能允许在体内进行低成本且快速的基因功能分析。然而,普遍存在且可重复的shRNA表达的先决条件尚未明确界定。在此,我们表明,当插入基因组的特定位点时,单拷贝的shRNA转基因可介导小鼠全身的基因沉默。在这种配置下,最常用于shRNA表达的启动子H1和U6表现出相当广泛的活性。综上所述,这些结果定义了一种在体内有效干扰特定基因表达的新方法。此外,我们提供了一种快速策略,用于结合重组酶介导的盒式交换和四倍体囊胚互补方法来生产基因敲低小鼠。