Heritable and stable gene knockdown in rats

Proc Natl Acad Sci U S A. 2006 Jul 25;103(30):11246-51. doi: 10.1073/pnas.0604657103. Epub 2006 Jul 14.

Abstract

The rat has served as an excellent model for studies on animal physiology and as a model for human diseases such as diabetes and alcoholism; however, genetic studies have been limited because of the inability to knock out genes. Our goal was to produce heritable deficiencies in specific gene function in the rat using RNA interference to knock down gene expression in vivo. Lentiviral-mediated transgenesis was used to produce rats expressing a short hairpin RNA targeting Dazl, a gene expressed in germ cells and required for fertility in mice. Germ-line transmission of the transgene occurred, and its expression correlated with significant reductions in DAZL protein levels and male sterility, and the knockdown was stable over multiple generations (F(1)-F(3)). This study demonstrates an efficient system by which directed reverse genetic analysis can now be performed in the rat.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Animals, Genetically Modified
  • Base Sequence
  • Female
  • Genetic Techniques*
  • Lentivirus / genetics
  • Male
  • Models, Genetic
  • Molecular Sequence Data
  • RNA Interference*
  • RNA-Binding Proteins / genetics
  • RNA-Binding Proteins / physiology*
  • Rats
  • Rats, Sprague-Dawley
  • Transgenes

Substances

  • DAZL protein, rat
  • RNA-Binding Proteins