Regulation of the Hsp104 middle domain activity is critical for yeast prion propagation.

PLoS One

Department of Cell Biology and Physiology, Washington University School of Medicine, St. Louis, Missouri, United States of America.

Published: September 2014

AI Article Synopsis

  • Molecular chaperones, specifically Hsp104 in yeast, help prevent protein misfolding and are essential for propagating prion proteins, which can have functional roles in yeast biology.
  • The study focused on the M-domain of Hsp104, finding that mutations affecting its conformation can inhibit general chaperone activity and influence ATP hydrolysis and disaggregation processes.
  • Variable effects of M-domain changes on different prion variants highlight its role in prion propagation, indicating that understanding this domain is crucial for grasping how Hsp104 supports the spread of prions.

Article Abstract

Molecular chaperones play a significant role in preventing protein misfolding and aggregation. Indeed, some protein conformational disorders have been linked to changes in the chaperone network. Curiously, in yeast, chaperones also play a role in promoting prion maintenance and propagation. While many amyloidogenic proteins are associated with disease in mammals, yeast prion proteins, and their ability to undergo conformational conversion into a prion state, are proposed to play a functional role in yeast biology. The chaperone Hsp104, a AAA+ ATPase, is essential for yeast prion propagation. Hsp104 fragments large prion aggregates to generate a population of smaller oligomers that can more readily convert soluble monomer and be transmitted to daughter cells. Here, we show that the middle (M) domain of Hsp104, and its mobility, plays an integral part in prion propagation. We generated and characterized mutations in the M-domain of Hsp104 that are predicted to stabilize either a repressed or de-repressed conformation of the M-domain (by analogy to ClpB in bacteria). We show that the predicted stabilization of the repressed conformation inhibits general chaperone activity. Mutation to the de-repressed conformation, however, has differential effects on ATP hydrolysis and disaggregation, suggesting that the M-domain is involved in coupling these two activities. Interestingly, we show that changes in the M-domain differentially affect the propagation of different variants of the [PSI+] and [RNQ+] prions, which indicates that some prion variants are more sensitive to changes in the M-domain mobility than others. Thus, we provide evidence that regulation of the M-domain of Hsp104 is critical for efficient prion propagation. This shows the importance of elucidating the function of the M-domain in order to understand the role of Hsp104 in the propagation of different prions and prion variants.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3900729PMC
http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0087521PLOS

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