IP Library Granted Patent US 9,738,898
Granted Patent B2
US 9,738,898 · App. 12/867,724 · Granted Aug 22, 2017

Yeast cells expressing TAR DNA-binding protein 43 and uses therefor

Inventors: Susan L. Lindquist (Chestnut Hill, MA); Aaron D. Gitler (Philadelphia, PA)
Assignee: Whitehead Institute for Biomedical Research
C12N15/81C12N15/1079G01N33/6872G01N33/6896G01N2500/10
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Quick Facts
Patent No.
US 9,738,898
App. No.
12/867,724
Granted
Aug 22, 2017
Kind
B2
Abstract

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.

Claims (37)

1. A method of inducing toxicity in a yeast cell, the method comprising:

providing a yeast cell comprising an expression construct comprising an inducible 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; and

inducing a level of expression of the nucleic acid in the yeast cell that is toxic to the yeast cell.

2. A method of identifying a compound that prevents or suppresses TDP-43-induced toxicity, the method comprising:

culturing a yeast cell in the presence of a candidate agent and under conditions that allow for expression of the nucleic acid at a level that, in the absence of the candidate agent, is sufficient to induce toxicity in the yeast cell, wherein the yeast cell comprises 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;

measuring cell growth or viability in the presence of the candidate agent; and

comparing cell growth or viability measured in the presence of the candidate agent to cell growth or viability in the absence of the candidate agent,

wherein if cell growth or viability is increased in the presence of the candidate agent as compared to in the absence of the candidate agent, then the candidate agent is identified as a compound that prevents or suppresses TDP-43-induced toxicity.

3. A method of identifying a compound that inhibits the formation or maintenance of cytoplasmic inclusions of TDP-43, the method comprising:

providing a yeast cell comprising an expression construct comprising a nucleic acid encoding a polypeptide comprising a naturally occurring 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;

culturing the yeast cell in the presence of a candidate agent and under conditions that allow for expression of the nucleic acid at a level that, in the absence of the candidate agent, is sufficient to result in the formation or maintenance of cytoplasmic inclusions of the protein;

measuring the formation or maintenance of cytoplasmic inclusions of the protein in the presence of the candidate agent; and

comparing the formation or maintenance of cytoplasmic inclusions of the protein measured in the presence of the candidate agent to the formation or maintenance of cytoplasmic inclusions of the protein in the absence of the candidate agent,

wherein if formation or maintenance of cytoplasmic inclusions of the protein is decreased in the presence of the candidate agent as compared to in the absence of the candidate agent, then the candidate agent is identified as a compound that inhibits the formation or maintenance of cytoplasmic inclusions of TDP-43.

4. The method of claim 2 , wherein expression of the nucleic acid and production of the polypeptide renders the cell non-viable.

5. The method of claim 2 , wherein the expression construct is integrated in the genome of the yeast cell.

6. The method of claim 2 , wherein the expression construct is an integrative plasmid.

7. The method of claim 6 , wherein the integrative plasmid is pRS303, pRS304, pRS305, or pRS306.

8. The method of claim 2 , wherein the promoter is an inducible promoter.

9. The method of claim 8 , wherein the inducible promoter is GAL1-10, GAL1, GALL, GALS, GPD, ADH, TEF, CYC1, MRP7, MET25, TET, VP16, or VP16-ER.

10. The method of claim 2 , wherein the promoter is a constitutively active promoter.

11. The method of claim 2 , wherein the polypeptide comprises SEQ ID NO:1.

12. The method of claim 2 , 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.

13. The method of claim 2 , wherein the polypeptide is a fusion protein comprising a detectable protein.

14. The method of claim 13 , wherein the detectable protein is a fluorescent protein, an enzyme, or an epitope.

15. The method of claim 13 , 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.

16. The method of claim 2 , wherein at least one gene that encodes a protein involved in drug efflux or cell permeability is disrupted.

17. The method of claim 16 , wherein the at least one gene is PDR1, PDR3, PDR5, SNQ2, or ERG6.

18. The method of claim 1 , wherein the inducible promoter is GAL1-10, GAL1, GALL, GALS, GPD, ADH, TEF, CYC1, MRP7, MET25, TET, VP16, or VP16-ER.

19. The method of claim 1 , wherein the naturally occurring TDP-43 protein is at least 95% identical to SEQ ID NO:1.

20. The method of claim 2 , wherein the naturally occurring TDP-43 protein is at least 95% identical to SEQ ID NO:1.

21. The method of claim 3 , wherein the naturally occurring TDP-43 protein is at least 95% identical to SEQ ID NO:1.

22. The method of claim 1 , wherein the polypeptide comprises SEQ ID NO:1.

23. The method of claim 3 , wherein the polypeptide comprises SEQ ID NO:1.

24. The method of claim 1 , wherein the polypeptide comprises amino acid residues 252-414 of SEQ ID NO:1.

25. The method of claim 2 , wherein the polypeptide comprises amino acid residues 252-414 of SEQ ID NO:1.

26. The method of claim 3 , wherein the polypeptide comprises amino acid residues 252-414 of SEQ ID NO:1.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 12, 2017
From: LINDQUIST, SUSAN L.; GITLER, AARON D.
To: WHITEHEAD INSTITUTE FOR BIOMEDICAL RESEARCH
Reel/Frame 040954/0253 →
CONFIRMATORY LICENSE Recorded Feb 8, 2011
From: WHITEHEAD INSTITUTE FOR BIOMEDICAL RES
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 025772/0907 →
Continuity (2)
Provisional Application 61029168 · Feb 15, 2008
Related Publication 20110053857A1 · Mar 3, 2011