Yeast cells expressing TAR DNA-binding protein 43 and uses therefor
View Patent ↗Disclosed are yeast cells expressing TAR DNA-binding protein 43 (TDP-43) and methods of screening yeast cells to identify compounds that prevent or suppress TDP-43-induced toxicity, compounds that inhibit the formation or maintenance of cytoplasmic inclusions of TDP-43, genetic suppressors or enhancers of TDP-43-induced toxicity, and genetic suppressors or enhancers of the formation or maintenance of cytoplasmic inclusions of TDP-43. Compounds identified by such screens can be used to treat or prevent TDP-43 proteinopathies such as frontotemporal lobar degeneration or amyotrophic lateral sclerosis.
1. A method of identifying a genetic suppressor or enhancer of TDP-43-induced toxicity, the method comprising:
providing a yeast cell comprising an expression construct comprising a promoter operably linked to a nucleic acid encoding a polypeptide comprising a naturally-occurring TAR DNA-binding protein 43 (TDP-43) protein, wherein the naturally-occurring TDP-43 protein comprises an amino acid sequence that is at least 95% identical to amino acid residues 252-414 of SEQ ID NO:1, wherein expression of the nucleic acid and production of the polypeptide results in a decrease in growth or viability of the cell, wherein the yeast cell has been genetically modified to overexpress a gene;
culturing the yeast cell under conditions that allow for expression of the polypeptide at a level that, in the absence of overexpression of the gene, is sufficient to induce toxicity in the yeast cell;
measuring cell growth or viability in the presence of overexpression of the gene; and
comparing cell growth or viability measured in the presence of overexpression of the gene to cell growth or viability in the absence of overexpression of the gene,
wherein (i) if cell growth or viability is increased in the presence of overexpression of the gene as compared to in the absence of overexpression of the gene, then the gene is identified as a genetic suppressor of TDP-43-induced toxicity, and (ii) if cell growth or viability is decreased in the presence of overexpression of the gene as compared to in the absence of overexpression of the gene, then the gene is identified as a genetic enhancer of TDP-43-induced toxicity.
2. A method of identifying a genetic suppressor or enhancer of TDP-43-induced toxicity, the method comprising:
providing a yeast cell comprising an expression construct comprising a promoter operably linked to a nucleic acid encoding a polypeptide comprising a naturally-occurring TAR DNA-binding protein 43 (TDP-43) protein, wherein the naturally-occurring TDP-43 protein comprises an amino acid sequence that is at least 95% identical to amino acid residues 252-414 of SEQ ID NO:1, wherein expression of the nucleic acid and production of the polypeptide results in a decrease in growth or viability of the cell, wherein an endogenous gene of the yeast cell has been disrupted;
culturing the yeast cell under conditions that allow for expression of the polypeptide at a level that, in the absence of disruption of the endogenous gene, is sufficient to induce toxicity in the yeast cell;
measuring cell growth or viability in the presence of disruption of the endogenous gene; and
comparing cell growth or viability measured in the presence of disruption of the endogenous gene to cell growth or viability in the absence of disruption of the endogenous gene,
wherein (i) if cell growth or viability is increased in the presence of disruption of the endogenous gene as compared to in the absence of disruption of the endogenous gene, then the gene is identified as a genetic enhancer of TDP-43-induced toxicity, and (ii) if cell growth or viability is decreased in the presence of disruption of the endogenous gene as compared to in the absence of disruption of the endogenous gene, then the gene is identified as a genetic suppressor of TDP-43-induced toxicity.
3. The method of claim 1 , wherein expression of the nucleic acid and production of the polypeptide renders the cell non-viable.
4. The method of claim 1 , wherein the expression construct is integrated in the genome of the yeast cell.
5. The method of claim 1 , wherein the expression construct is an integrative plasmid.
6. The method of claim 5 , wherein the integrative plasmid is pRS303, pRS304, pRS305, or pRS306.
7. The method of claim 1 , wherein the promoter is an inducible promoter.
8. The method of claim 7 , wherein the inducible promoter is GAL1-10, GAL1, GALL, GALS, GPD, ADH, TEF, CYC1, MRP7, MET25, TET, VP16, or VP16-ER.
9. The method of claim 1 , wherein the promoter is a constitutively active promoter.
10. The method of claim 1 , wherein the yeast is Saccharomyces cerevisiae, Saccharomyces uvae, Saccharomyces kluyveri, Schizosaccharomyces pombe, Kluyveromyces lactis, Hansenula polymorpha, Pichia pastoris, Pichia methanolica, Pichia kluyveri, Yarrowia lipolytica, Candida sp., Candida utilis, Candida cacaoi, Geotrichum sp., or Geotrichum fermentans.
11. The method of claim 1 , wherein the polypeptide is a fusion protein comprising a detectable protein.
12. The method of claim 11 , wherein the detectable protein is a fluorescent protein, an enzyme, or an epitope.
13. The method of claim 11 , wherein the detectable protein is a fluorescent protein selected from the group consisting of a red fluorescent protein, green fluorescent protein, blue fluorescent protein, yellow fluorescent protein, and cyan fluorescent protein.
14. The method of claim 1 , wherein the yeast cell comprises a disruption of at least one gene that encodes a protein involved in drug efflux or cell permeability.
15. The method of claim 14 , wherein the at least one gene is PDR1, PDR3, PDR5, SNQ2, or ERG6.
16. The method of claim 1 , wherein the naturally occurring TDP-43 protein is at least 95% identical to SEQ ID NO:1 .
17. The method of claim 1 , wherein the polypeptide comprises amino acid residues 252-414 of SEQ ID NO:1.
18. The method of claim 1 , wherein the polypeptide comprises SEQ ID NO:1.