Methods of identifying compounds that target tRNA splicing endonuclease and uses of said compounds as anti-proliferative agents
View Patent ↗The present invention relates to a method for screening and identifying compounds that modulate the activity tRNA splicing endonuclease. In particular, the invention provides assays for the identification of compounds that inhibit animalia tRNA splicing endonuclease. The methods of the present invention provide a simple, sensitive assay for high-throughput screening of libraries of compounds to identify pharmaceutical leads useful for treating and/or preventing cancer.
1. A method for identifying a compound that modulates the ability of animalia tRNA splicing endonuclease to produce mature tRNA, the method comprising:
(a) contacting a compound or a compound from a library of compounds with an animalia cell that contains the animalia tRNA splicing endonuclease and expresses a full-length protein encoded by the coding region of a reporter gene of a nucleic acid substrate, wherein the nucleic acid substrate comprises the coding region of a reporter gene and a tRNA intron in a mature domain of a precursor tRNA, and wherein the tRNA intron is contained within the nucleic acid substrate such that the transcribed mRNA from the coding region of the reporter gene is out of frame; and
(b) detecting the amount of full-length protein expressed, wherein an alteration in the amount of the full-length protein expressed in the presence of the compound or the compound from the library of compounds relative to the amount of the full-length protein expressed in the absence of the compound or the compound from a library of compounds, or in the presence of a negative control indicates that the compound or the compound from the library of compounds modulates the ability of animalia tRNA splicing endonuclease to produce mature tRNA.
2. The method of claim 1 , wherein a decrease in the amount of the full-length protein expressed in the presence of the compound or the compound from the library of compounds relative to the amount of the full-length protein expressed in the absence of the compound or the compound from the library of compounds, or the presence of a negative control indicates that the compound or the compound from the library of compounds reduces the ability of animalia tRNA splicing endonuclease to produce mature tRNA.
3. The method of claim 1 , wherein an increase in the amount of the full-length protein expressed in the presence of the compound or the compound from the library of compounds relative to the amount of the full-length protein expressed in the absence of the compound or the compound from the library of compounds, or the presence of a negative control indicates that the compound or the compound from the library of compounds increases the ability of animalia tRNA splicing endonuclease to produce mature tRNA.
4. The method of claim 1 , 2 or 3 , wherein the coding region of the reporter gene encodes at least one or more coding regions of the reporter genes from the group consisting of firefly luciferase, renilla luciferase, click beetle luciferase, green fluorescent protein, yellow fluorescent protein, red fluorescent protein, cyan fluorescent protein, blue fluorescent protein, beta-galactosidase, beta-glucoronidase, beta-lactamase, chloramphenicol acetyltransferase, and alkaline phosphatase.
5. The method of claim 1 , 2 or 3 , wherein the animalia cell is a human cell.
6. The method of claim 4 , wherein the animalia cell is a human cell.
7. The method of claim 1 , 2 or 3 , wherein the animalia tRNA splicing endonuclease is a human tRNA splicing endonuclease.
8. The method of claim 4 , wherein the animalia tRNA splicing endonuclease is a human tRNA splicing endonuclease.
9. The method of claim 5 , wherein the animalia tRNA splicing endonuclease is a human tRNA splicing endonuclease.
10. The method of claim 1 , 2 or 3 , wherein the tRNA intron is in the coding region of the reporter gene.
11. The method of claim 4 , wherein the tRNA intron is in the coding region of the reporter gene.
12. The method of claim 5 , wherein the tRNA intron is in the coding region of the reporter gene.