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Translation termination efficiency can be regulated in Saccharomyces cerevisiae by environmental stress through a prion-mediated mechanism
[PSI + ] is a protein‐based heritable phenotype of the yeast Saccharomyces cerevisiae which reflects the prion‐like behaviour of the endogenous Sup35p protein release factor. [PSI + ] strains exhibit a marked decrease in translation termination efficiency, which permits decoding of translation termi...
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Published in: | The EMBO journal 1999-04, Vol.18 (7), p.1974-1981 |
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Main Authors: | , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that cite this one |
Online Access: | Get full text |
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Summary: | [PSI
+
]
is a protein‐based heritable phenotype of the yeast
Saccharomyces cerevisiae
which reflects the prion‐like behaviour of the endogenous Sup35p protein release factor.
[PSI
+
]
strains exhibit a marked decrease in translation termination efficiency, which permits decoding of translation termination signals and, presumably, the production of abnormally extended polypeptides. We have examined whether the
[PSI
+
]‐
induced expression of such an altered proteome might confer some selective growth advantage over
[psi
−
]
strains. Although otherwise isogenic
[PSI
+
]
and
[psi
−
]
strains show no difference in growth rates under normal laboratory conditions, we demonstrate that
[PSI
+
]
strains do exhibit enhanced tolerance to heat and chemical stress, compared with
[psi
−
]
strains. Moreover, we also show that the prion‐like determinant
[PSI
+
]
is able to regulate translation termination efficiency in response to environmental stress, since growth in the presence of ethanol results in a transient increase in the efficiency of translation termination and a loss of the
[PSI
+
]
phenotype. We present a model to describe the prion‐mediated regulation of translation termination efficiency and discuss its implications in relation to the potential physiological role of prions in
S.cerevisiae
and other fungi. |
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ISSN: | 0261-4189 1460-2075 1460-2075 |
DOI: | 10.1093/emboj/18.7.1974 |