Abstract
Based on the RNAi technique, we have developed a new approach that generates transgenic animals capable of mimicking human genetic diseases. The new system is a combination of siRNA with Cre-loxP and tetracycline-on. It has the characteristics of being stable, inheritable, and inducible, with the siRNA able to be transcribed tissue specifically. To support the ability of this new method to generate a model for a disease, we created an ABCA1-deficient mouse line that mimics Tangier disease under controlled conditions. Thus, it should now be possible to rapidly establish human genetic diseases as a whole animal model without the use of embryonic stem cell and gene targeting. This system also provides a tool for pathological and pharmacological studies of aspects peculiar to particular human genetic diseases.
Original language | English |
---|---|
Pages (from-to) | 1535-1541 |
Number of pages | 7 |
Journal | American Journal of Pathology |
Volume | 165 |
Issue number | 5 |
Publication status | Published - Nov 2004 |
Externally published | Yes |
ASJC Scopus subject areas
- Pathology and Forensic Medicine