The yeast prions [PSI+] and [URE3] are molecular degenerative diseases

被引:0
|
作者
Wickner, Reed B. [1 ]
Edskes, Herman K. [1 ]
Bateman, David [1 ]
Kelly, Amy C. [1 ]
Gorkovskiy, Anton [1 ]
机构
[1] NIDDK, Lab Biochem & Genet, NIH, Bethesda, MD 20892 USA
关键词
URE3; PSI+; prion; Sup35p; Ure2p; TERMINATION FACTOR ERF3; 2-MU-M CIRCLE PLASMID; SACCHAROMYCES-CEREVISIAE; MESSENGER-RNA; SEXUAL TRANSMISSION; PROTEIN; GENE; INCOMPATIBILITY; CONSERVATION; MAINTENANCE;
D O I
10.4161/pri.5.4.17748
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页码:258 / 262
页数:5
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