Sup35p is a Saccharomyces cerevisiae protein with an essential function in promoting translation termination. In a state referred to as [PSI], Sup35p adopts an altered conformation causing it to aggregate. [PSI] is believed to be propagated as an altered form of Sup35p in a manner consistent with the prion model. [PSI] is maintained cytoplasmically and is inherited infallibly during mitosis and meiosis. By an unknown mechanism, [PSI] is eliminated from yeast cells during growth in the presence of millimolar levels of guanidine-hydrochloride (GuHCl). Our goal is to elucidate the underlying mechanisms involved in prion metabolism using [PSI] as our model system. Our approach is to isolate mutant strains displaying aberrant [PSI] behavior, identify the genes involved, and determine the mechanisms behind the effects. We have discovered that expression of proteins involved in response to environmental stress are aberrantly expressed in a mutant strain in which [PSI] has become mitotically unstable. For two among four additional mutant strains in which [PSI] has become weakened or unstable, the wild type alleles have been identified. To date, attempts at isolating the wild type allele of a mutation allowing maintenance of [PSI] despite the presence of GuHCl in the growth medium has resulted in isolation of an unlinked suppressor. We have found a known mutant to be strikingly hypersensitive to the curative effects of GuHCl. I have also discovered that certain combinations of known mutations lead to instability of [PSI] during meiosis. This has been found to reside in defects during the process of meiosis rather than in the products of it. I have also identified mutants in which [PSI] is progressively eliminated from spores as they age. In the course of the [PSI] studies I have discovered that a previously known mutation causes significant read-through of translation termination independently of [PSI]. Such an effect for this mutant has yet to be described. This project is not a major goal of the laboratory but will be pursued until the results are published. - Prion, [PSI], Sup35, Yeast

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Intramural Research (Z01)
Project #
1Z01DK024946-02
Application #
6289732
Study Section
Special Emphasis Panel (LBG)
Project Start
Project End
Budget Start
Budget End
Support Year
2
Fiscal Year
1999
Total Cost
Indirect Cost
City
State
Country
United States
Zip Code
Sharma, Deepak; Martineau, Celine N; Le Dall, Marie-Therese et al. (2009) Function of SSA subfamily of Hsp70 within and across species varies widely in complementing Saccharomyces cerevisiae cell growth and prion propagation. PLoS One 4:e6644
Masison, Daniel C; Kirkland, P Aaron; Sharma, Deepak (2009) Influence of Hsp70s and their regulators on yeast prion propagation. Prion 3:65-73
Needham, Patrick G; Masison, Daniel C (2008) Prion-impairing mutations in Hsp70 chaperone Ssa1: effects on ATPase and chaperone activities. Arch Biochem Biophys 478:167-74
Shewmaker, Frank; Mull, Lori; Nakayashiki, Toru et al. (2007) Ure2p function is enhanced by its prion domain in Saccharomyces cerevisiae. Genetics 176:1557-65
Hung, Guo-Chiuan; Masison, Daniel C (2006) N-terminal domain of yeast Hsp104 chaperone is dispensable for thermotolerance and prion propagation but necessary for curing prions by Hsp104 overexpression. Genetics 173:611-20
Wu, Yue-Xuan; Masison, Daniel C; Eisenberg, Evan et al. (2006) Application of photobleaching for measuring diffusion of prion proteins in cytosol of yeast cells. Methods 39:43-9
Song, Youtao; Masison, Daniel C (2005) Independent regulation of Hsp70 and Hsp90 chaperones by Hsp70/Hsp90-organizing protein Sti1 (Hop1). J Biol Chem 280:34178-85
Song, Youtao; Wu, Yue-Xuan; Jung, Giman et al. (2005) Role for Hsp70 chaperone in Saccharomyces cerevisiae prion seed replication. Eukaryot Cell 4:289-97
Wu, Yue-Xuan; Greene, Lois E; Masison, Daniel C et al. (2005) Curing of yeast [PSI+] prion by guanidine inactivation of Hsp104 does not require cell division. Proc Natl Acad Sci U S A 102:12789-94
Jones, Gary; Song, Youtao; Chung, Seyung et al. (2004) Propagation of Saccharomyces cerevisiae [PSI+] prion is impaired by factors that regulate Hsp70 substrate binding. Mol Cell Biol 24:3928-37

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