Abstract
The yeast prions [URE3] and [PSI] are not found in wild strains, suggesting they are not an advantage. Prion-forming ability is not conserved, even within Saccharomyces, suggesting it is a disease. Prion domains have non-prion functions, explaining some conservation of sequence. However, in spite of the sequence being constrained in evolution by these non-prion functions, the prion domains vary more rapidly than the remainder of the molecule, and these changes produce a transmission barrier, suggesting that these changes were selected to block prion infection. Yeast prions [PSI] and [URE3] induce a cellular stress response (Hsp104 and Hsp70 induction), suggesting the cells are not happy about being infected. Recently, we showed that the array of [PSI] and [URE3] prions includes a majority of lethal or very toxic variants, a result not expected if either prion were an adaptive cellular response to stress.
Cite
CITATION STYLE
Wickner, R. B., Edskes, H. K., Bateman, D., Kelly, A. C., & Gorkovskiy, A. (2011). The yeast prions [PSI+] and [URE3] are molecular degenerative diseases. Prion, 5(4), 258–262. https://doi.org/10.4161/pri.17748
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