Fluorescent mouse model
The present invention relates to compositions and methods useful for detecting and/or measuring, e.g., intracellular signaling in vivo. More particularly, compositions and methods are provided, which include transgenic animals, that are useful in mapping and examining, e.g., calcium fluctuations in vivo between and within populations of cells in real time. Methods for screening for candidate compounds that effect, e.g., intracellular calcium signaling are also provided.
1. A transgenic mouse comprising in its genome:
(a) a first polynucleotide encoding a G-CaMP sensor linked to an inducible regulatory element comprising at least one tetracycline resistant operon (tetO) sequence; and
(b) a second polynucleotide encoding a tetracycline transactivator operably linked to a tissue specific regulatory element comprising a tissue specific promoter,
wherein the transgenic mouse expresses the G-CaMP sensor in a tissue specific manner and expression of the G-CaMP sensor is detectable in vivo.
2. The transgenic mouse according to claim 1 , wherein the G-CaMP sensor is a G-CaMP2 sensor.
3. The transgenic mouse according to claim 1 , wherein the tissue specific regulatory element is an olfactory marker protein (OMP) promoter.
4. A method for identifying a candidate compound that modulates intracellular calcium signaling comprising:
(a) providing a candidate compound;
(b) providing a transgenic mouse according to claim 1 ;
(c) inducing expression of the G-CaMP sensor in the brain of the transgenic mouse
(d) administering the candidate compound to the transgenic mouse; and
(e) evaluating an effect, if any, of the candidate compound on intracellular calcium signaling in the transgenic mouse by detecting an alteration in fluorescence intensity of the G-CaMP sensor.
5. The method according to claim 4 , wherein the evaluating step is performed non-invasively through a tissue of the mouse.
6. A method for identifying a candidate compound that modulates intracellular calcium signaling in the brain comprising:
(a) providing a candidate compound;
(b) providing a transgenic mouse comprising in its genome:
(i) a first polynucleotide encoding a G-CaMP sensor linked to an inducible regulatory element comprising at least one tetO sequence and
(ii) a second polynucleotide encoding a tetracycline transactivator operably linked to a brain-specific regulatory element comprising a brain-specific promoter;
(c) inducing expression of the G-CaMP sensor in the brain;
(d) administering the candidate compound to the brain of the transgenic mouse; and
(e) evaluating an effect, if any, of the candidate compound on brain intracellular calcium signaling in the transgenic mouse by detecting an alteration in fluorescence intensity of the G-CaMP sensor in the brain.
7. The method according to claim 6 , wherein the evaluating step is performed non-invasively through the skull of the mouse.
8. The method according to claim 6 , wherein the evaluating step comprises thinning at least a portion of the mouse skull covering an area of interest.
9. The method according to claim 8 , wherein the thinning comprises shaving the bone down to about 50 micron thickness.
10. The method according to claim 6 , wherein the candidate compound is administered to the mouse through olfaction.
11. A method for identifying a candidate compound that modulates intracellular calcium signaling in the brain comprising:
(a) providing a candidate compound;
(b) providing a brain slice from a transgenic mouse comprising in its genome:
(i) a first polynucleotide encoding a G-CaMP sensor linked to an inducible regulatory element comprising at least one tetO sequence and
(ii) a second polynucleotide encoding a tetracycline transactivator operably linked to a brain-specific regulatory element comprising a brain-specific promoter,
wherein the transgenic mouse expresses the G-CaMP sensor in the brain;
(c) administering the candidate compound to the brain slice of the transgenic mouse; and
(d) evaluating an effect, if any, of the candidate compound on brain intracellular calcium signaling in the transgenic mouse by detecting an alteration in fluorescence intensity of the G-CaMP sensor in the brain slice.