Transgenic Mouse with Prostate-Specific, Constitutively Active mTOR
Washington University in St. Louis
posted on 03/07/2007
The current invention describes a novel transgenic mouse in the FVB/n strain background that expresses constitutively active mTOR under the prostate-specific probasin promoter. Mice develop constitutive phosphorylation of the ribosomal protein S6, which can be easily detected and quantified by immunofluorescence.
Suggested Uses
- Screening for novel prostate cancer therapeutics associated with inhibiting the PI3K pathway.
- Evaluation of potential therapeutic compounds that specifically inhibit mTOR or S6K.
- Research involving the PI3K pathway and its downstream targets, mTOR and S6K.
Advantages
Detection of mTOR activity and the S6 protein is easily detected and quantified by immunofluorescence.
Detailed Description
Background:
The mammalian target of rapamycin (mTOR) regulates cell growth and proliferation as a downstream target of phosphatidylinositol-3-kinase (PI3K) and protein kinase B (Akt). mTOR is a key regulator of protein translation that, when activated, allows mRNA recruitment to the ribosome and phosphorylates the 70 kD ribosomal protein, S6K, to further enhance ribosome efficiency. In this pathway, the tumor suppressors tuberous sclerosis complex 1 (TSC1) and TSC2 negatively regulate mTOR activity to inhibit protein translation. Dysregulation of mTOR and other proteins in its signaling pathway has been implicated in various cancer types.
Technology Description:
The current invention describes a novel transgenic mouse in the FVB/n strain background that expresses constitutively active mTOR under the prostate-specific probasin promoter. Mice develop constitutive phosphorylation of the ribosomal protein S6, which can be easily detected and quantified by immunofluorescence.
File Number: CU0687
This innovation currently is not available for online licensing. Please contact Erin Brosnahan at Washington University in St. Louis for more information.
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