J-Protein Regulation of Yeast Prion Propagation

Lafayette College, Easton PA

Investigators

Linked publications, trials & patents

Abstract

A critical barrier to advancing the understanding of chaperone function in prion biology is that the fundamental chaperone interactions for most yeast prions remain unidentified. Existing knowledge is disjointed due to a lack of systematic evaluation that controls for variation in yeast strain background and prion structure. The continued existence of this barrier is an important problem because, until it is overcome, an understanding of how protein sequences give rise to amyloids with distinct patterns of chaperone interaction cannot be fully realized. The long- term goal is to utilize the highly tractable budding yeast, S. cerevisiae, to systematically decipher the complex relationships between amyloid-forming yeast prions and molecular chaperone proteins with a goal of better un- derstanding J-domain protein (JDP) function and prion behavior. The objective of this particular application is to utilize genetic systems and biochemical assays to determine the functional elements involved in specific prion- chaperone interactions. The central hypothesis is that differences in amyloid structure, arising primarily from amino acid composition, create distinct challenges for prion transmission which are overcome by specific JDP functions that buffer prions against loss during mitosis. The hypothesis has been formulated on the basis of data produced in the applicant’s laboratory. The rationale for the proposed research is that unambiguous determina- tions of JDP functional requirements are a necessary step toward understanding the mechanisms of chaperone function in amyloid biology. Using a distinct set of chimeric prions, our own collection of well-studied, naturally occurring prions, and the yeast cytosol as model systems, this hypothesis will be tested by pursuing two specific aims: 1) Identify elements of J-domain proteins that allow for amyloid conformer-specific propagation and prion elimination, and 2) Determine the impact of individual amino acid identities, and Q vs. N-richness, on prion- chaperone interactions. Proven yeast genetic manipulations, which have been established as feasible in the applicant’s laboratory, will be the primary methods used to accomplish these aims. The approach is innovative because it represents a substantive departure from the status quo by placing emphasis on the ability to draw distinctions and make comparisons among multiple JDPs and yeast prions as a way to broadly understand chaperone function. The contribution of the proposed research is expected to be the elucidation of the roles of distinct chaperones in prion propagation and prion elimination. This contribution is significant because it is the next step in a continuum of research which is expected to contribute to the understanding of the biochemical basis of amyloid-chaperone interactions. A molecular understanding of amyloid-chaperone interactions has the potential to inform the development of interventions for protein misfolding disorders, including the increasing prevalent neurodegenerative disorders Alzheimer’s and Parkinson’s.