The reasons organisms encode multiple Hsp70s are that it provides broader capacity to regulate abundance of Hsp70 in accordance with needs, or that having different Hsp70s provides similar, but distinct functions important for carrying out specific tasks either within cells in general or in specific types of cells. Earlier we constructed a yeast system to evaluate functions of Hsp70 from any source. We are using it to investigate how Hsp70s from both within and across species perform with regard to providing essential activities for cell growth and for propagation of different prions. This very sensitive system gives us the unique ability to distinguish exquisite functional differences among nearly identical Hsp70 isoforms and provides a means to approach the problem of uncovering the underlying mechanisms. Previously we showed the four S. cerevisiae Hsp70s Ssa1 - Ssa4 have distinct functions that affect the propagation of different prions in different ways. These differences in the ways the prions depend on subtle distinctions in Hsp70 activities provide a sensitive way to monitor functional distinctions among the Hsp70s. For example, we identified a specific residue in the ATPase domain of the 98% identical Ssa1 and Ssa2 (A83 or G83, respectively) as solely responsible for a functional distinction between Ssa1p and Ssa2p that is critical for a vacuolar import protein degradation pathway. Our findings show that exquisitely fine differences in structure can underlie distinctions in function of nearly identical Hsp70s and that regulation of Hsp70 substrate interactions, rather than substrate binding per se, is the important parameter that determines functional distinctions. In the cell these subtle differences can lead to large-scale effects on cellular processes and might be all that is needed to direct different Hsp70s to specialized tasks. Our continued work focuses on determining if differences in functions of various Hsp70s are mediated by differences in the way they cooperate with other components of the cellular """"""""protein quality control"""""""" machinery, such as co-chaperones or other major chaperones. We are also interested in learning whether such differences in Hsp70 function contribute to protection from amyloid toxicity that we see in some of our strains, and the extent to which human Hsp70s might possess such protective functions. Elevating Hsp70 can moderate pathology in models of protein folding disorders, while in the same models reducing Hsp70 activity can exacerbate, or alone even cause, pathology. Hsp70 is therefore a promising therapeutic candidate for amyloid and other protein folding disorders and it is being studied intensively as a drug target. Our work can help guide decisions about which Hsp70-family members would be most useful for such applications.

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17
Fiscal Year
2014
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U.S. National Inst Diabetes/Digst/Kidney
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Reidy, Michael; Kumar, Shailesh; Anderson, D Eric et al. (2018) Dual Roles for Yeast Sti1/Hop in Regulating the Hsp90 Chaperone Cycle. Genetics 209:1139-1154
Xue, You-Lin; Wang, Hao; Riedy, Michael et al. (2018) Molecular dynamics simulations of Hsp40 J-domain mutants identifies disruption of the critical HPD-motif as the key factor for impaired curing in vivo of the yeast prion [URE3]. J Biomol Struct Dyn 36:1764-1775
Kravats, Andrea N; Hoskins, Joel R; Reidy, Michael et al. (2018) Functional and physical interaction between yeast Hsp90 and Hsp70. Proc Natl Acad Sci U S A 115:E2210-E2219
Zuehlke, Abbey D; Reidy, Michael; Lin, Coney et al. (2017) An Hsp90 co-chaperone protein in yeast is functionally replaced by site-specific posttranslational modification in humans. Nat Commun 8:15328
Masison, Daniel C; Reidy, Michael (2015) Yeast prions are useful for studying protein chaperones and protein quality control. Prion 9:174-83
Reidy, Michael; Masison, Daniel C (2014) Yeast prions help identify and define chaperone interaction networks. Curr Pharm Biotechnol 15:1008-18
Reidy, Michael; Sharma, Ruchika; Masison, Daniel C (2013) Schizosaccharomyces pombe disaggregation machinery chaperones support Saccharomyces cerevisiae growth and prion propagation. Eukaryot Cell 12:739-45
Sharma, Deepak; Masison, Daniel C (2011) Single methyl group determines prion propagation and protein degradation activities of yeast heat shock protein (Hsp)-70 chaperones Ssa1p and Ssa2p. Proc Natl Acad Sci U S A 108:13665-70
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
Sharma, Deepak; Masison, Daniel C (2009) Hsp70 structure, function, regulation and influence on yeast prions. Protein Pept Lett 16:571-81

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