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. Author manuscript; available in PMC: 2008 Feb 1.
Published in final edited form as: Biochim Biophys Acta. 2006 Oct 26;1773(2):232–242. doi: 10.1016/j.bbamcr.2006.10.011

Figure 7.

Figure 7

UPR induction in Δerj5 cells measured by the GFP-fluorescence of a UPR reporter. W303 yeast cells bearing pRS314-UPRE-GFP were grown in minimal medium without tryptophane to mid-log phase. GFP-fluorescence was quantified as described in Materials and Methods from cells incubated for 90 min in the absence or presence of 5 mM DTT. The mean fluorescence of wild-type (WT) and Δerj5 (erj5) cells were normalized to the fluorescence values of the WT in absence of DTT treatment. The mean fold induction was calculated from five experiments and the standard deviation is represented as error bars.