[PSI] and [URE3] as yeast prions

被引:131
作者
Wickner, RB
Masison, DC
Edskes, HK
机构
[1] Section on Genetics of Simple Eukaryotes, National Institute of Diabetes, NIH, Bethesda, Maryland, 20892-0830, Bldg. 8
关键词
nitrogen repression; translation termination; suppressor; non-Mendelian; ureidosuccinate uptake;
D O I
10.1002/yea.320111609
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
[URE3] is a non-Mendelian genetic element that mimics recessive mutations in the chromosomal URE2 gene making cells derepressed for nitrogen catabolic enzymes. [PSI] is a non-Mendelian enhancer of readthrough of translational termination similar in its effects to some mutations in the chromosomal SUP35 gene. Three Lines of evidence led to the proposal(75) that both [URES] and [PSI] are prions, infectious proteins analogous to the scrapie agent mediating transmissible spongiform encephalopathies of mammals. 1) Both [PSI] and [URE3] are reversibly curable. 2) [PSI] propagation requires SUP35 and [URE3] propagation requires URE2 with recessive chromosomal mutants having the same phenotypes as the presence of the respective dominant non-Mendelian element. 3) Overproduction of Sup35p and Ure2p increases the frequency of cells acquiring [PSI] or [URE3], respectively.
引用
收藏
页码:1671 / 1685
页数:15
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