[PSI+]:: An epigenetic modulator of translation termination efficiency

被引:88
作者
Serio, TR [1 ]
Lindquist, SL
机构
[1] Univ Chicago, Dept Mol Genet & Cell Biol, Chicago, IL 60637 USA
[2] Univ Chicago, Howard Hughes Med Inst, Chicago, IL 60637 USA
关键词
amyloid; prion; Sup35; nonsense suppression; epigenetic;
D O I
10.1146/annurev.cellbio.15.1.661
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The [PSI+] factor of the yeast Saccharomyces cerevisiae is an epigenetic regulator of translation termination. More than three decades ago, genetic analysis of the transmission of [PSI+].revealed a complex and often contradictory series of observations. However, many of these discrepancies may now be reconciled by a revolutionary hypothesis: protein conformation-based inheritance (the prion hypothesis). This model predicts that a single protein can stably exist in at least two distinct physical states, each associated with a different phenotype. Propagation of one of these traits is achieved by a self-perpetuating change in the protein from one form to the other. Mounting genetic and biochemical evidence suggests that the determinant of [PSI+] is the nuclear encoded Sup35p, a component of the translation termination complex. Here we review the series of experiments supporting the yeast prion hypothesis and provide another look at the 30 years of work preceding this theory in light of our current state of knowledge.
引用
收藏
页码:661 / 703
页数:43
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