Transgenic mammals introduced a Period 1 promoter that confers rhythmical expression
View Patent ↗The present invention relates to an isolated Period 1 (Per1) promoter DNA inducing rhythmical expression of a gene operably linked thereto. This invention also provides a DNA comprising a Period 1 promoter DNA and a gene operably linked thereto, the gene being under the regulation of the promoter DNA. The present invention further provides transformants and transgenic mammals into which the DNA has been introduced. The transformants and transgenic mammals are useful in the screening of pharmaceutical drugs against diseases and disorders pertaining to the circadian rhythm.
1. An isolated Period 1 promoter DNA that induces rhythmical expression of a gene operably linked thereto in a mammal, wherein said Period 1 promoter DNA is selected from the group consisting of:
(a) a nucleic acid comprising the nucleotide sequence from positions 23 to 6787 of SEQ ID NO: 1; and
(b) a nucleic acid comprising the nucleotide sequence of SEQ ID NO: 2.
2. The isolated Period 1 promoter DNA of claim 1 , wherein said Period 1 promoter DNA is a nucleic acid comprising the nucleotide sequence of SEQ ID NO: 2.
3. A recombinant DNA comprising the Period 1 promoter DNA according to claim 2 and a gene operably linked to said promoter, wherein said gene is rhythmically expressed under the control of said promoter in a mammal.
4. The recombinant DNA according to claim 3 , wherein said gene is a luciferase gene, a green fluorescent protein (GFP) gene or a chloramphenicol acetyltransferase (CAT) gene.
5. The recombinant DNA according to claim 3 , wherein said gene is a reporter gene.
6. An isolated cell comprising the recombinant DNA according to claim 3 .
7. An isolated cell comprising the recombinant DNA according to claim 5 .
8. A transgenic mouse or whose genome comprises a recombinant DNA comprising a Period 1 promoter DNA operably linked to a reporter gene, wherein said promoter induces rhythmical expression of a reporter gene operably linked thereto and wherein said Period 1 promoter DNA is a nucleic acid comprising the nucleotide sequence of SEQ ID NO: 2.
9. The transgenic mouse or rat according to claim 8 , wherein said reporter gene is a luciferase gene, a green fluorescent protein (GFP) gene or a chloramphenicol acetyltransferase (CAT) gene.
10. A progeny of the transgenic mouse or rat according to claim 8 , wherein the genome of said progeny comprises the recombinant DNA.
11. An isolated cell isolated from the transgenic mouse or rat according to claim 8 , wherein said cell comprises the recombinant DNA.
12. An isolated tissue isolated from the transgenic mouse or rat of claim 8 , wherein said tissue comprises the recombinant DNA.
13. A method of testing or screening a compound that has an activity to modify the expression of the transgene in the cell according to claim 6 , comprising:
(a) treating said cell with said compound;
(b) measuring the expression of said transgene in the treated cell;
(c) comparing the transgene expression after administration of the compound with that prior to the administration; and
(d) selecting a compound that modifies the transgene expression.
14. A method of testing or screening for a pharmaceutical drug useful for treating a circadian rhythm sleep disorder, comprising:
(a) treating the cell according to claim 7 with the pharmaceutical drug;
(b) measuring the expression of the reporter gene in the cell;
(c) comparing the reporter gene expression rhythm after administration of the compound with that prior to the administration; and
(d) selecting a compound that modifies the phase, period or amplitude of the reporter gene expression rhythm following the treatment in (a), whereupon said compound is useful for treating a circadian rhythm sleep disorder.
15. A method of testing or screening a compound that has an activity to modify the expression of the transgene in the mouse or rat according to claim 8 , comprising:
(a) treating said mouse or rat with said compound;
(b) measuring the expression of said transgene in the treated mouse or rat;
(c) comparing the transgene expression rhythm after administration of the compound with that prior to the administration; and
(d) selecting a compound that modifies the transgene expression.
16. A method of testing or screening for a pharmaceutical drug useful for treating a circadian rhythm sleep disorder, comprising:
(a) treating the transgenic mouse or rat according to claim 8 with the pharmaceutical drug;
(b) measuring the expression of the reporter gene in the treated transgenic mouse or rat;
(c) comparing the reporter gene expression rhythm after administration of the compound with that prior to the administration; and
(d) selecting a compound that modifies the phase, period or amplitude of the reporter gene expression rhythm following the treatment in (a), whereupon said compound is useful for treating a circadian rhythm sleep disorder.
17. A method of screening for a putative factor that regulates Period 1 expression, comprising the steps of:
(a) administering a compound to a transgenic mouse or rat according to claim 8 , whose circadian rhythm has already been determined;
(b) periodically detecting expression level of the reporter gene in the transgenic mouse or rat and verifying the expression rhythm;
(c) comparing the reporter gene expression rhythm after administration of the compound with that prior to the administration; and,
(d) selecting a compound that modifies the phase, period or amplitude of the reporter gene expression rhythm, whereupon said factor regulates Period 1 expression.
18. A method of screening for a pharmaceutical drug useful for treating a circadian rhythm sleep disorder, comprising:
(a) culturing the cell according to claim 11 or 12 ;
(b) treating the cell with a compound for an appropriate period of time, and then continuing culturing;
(c) periodically detecting reporter gene expression level; and
(d) selecting a compound that modifies the phase, period or amplitude of the reporter gene expression rhythm following the treatment in (b), whereupon said compound is useful for treating a circadian rhythm sleep disorder.
19. A method of screening for a pharmaceutical drug useful for treating a circadian rhythm sleep disorder, comprising:
(a) culturing the tissue according to claim 12 ;
(b) treating the tissues with a compound for an appropriate period of time, and then continuing culturing;
(c) periodically detecting reporter gene expression level; and
(d) selecting a compound that modifies the phase, period or amplitude of the reporter gene expression rhythm following the treatment in (b), whereupon said compound is useful for treating a circadian rhythm sleep disorder.