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Table 6 Activity of the PHO84, SPL2 and CYC1 promoter determined by flow cytometry using GFP reporters

From: Lack of 14-3-3 proteins in Saccharomyces cerevisiae results in cell-to-cell heterogeneity in the expression of Pho4-regulated genes SPL2 and PHO84

 

GFP fluorescence (arbitrary units) (± SD; n = 3)

Strain

50 mM

0 mM

Experiments PHO84

 BY4741 PPHO84– GFP–TPHO84

30 ± 1

58 ± 2

 BY4741 PCYC1 – GFP–TCYC1

198 ± 29

179 ± 8

 bmh1Δ PPHO84– GFP–TPHO84

13 ± 2a

37 ± 3

 bmh1Δ PCYC1 – GFP–TCYC1

204 ± 12

146 ± 54

Experiments SPL2

 BY4741 PSPL2– GFP–TSPl2

3.7 ± 1.6

7.1 ± 2.8

 BY4741 PCYC1 – GFP–TCYC1

204 ± 12

219 ± 30

 bmh1Δ PSPL2– GFP–TSPL2

0.8 ± 0.3b

2.7 ± 0.5

 bmh1Δ PCYC1 – GFP–TCYC1

131 ± 5

139 ± 24

  1. aStudent’s t-test indicated a significant difference between bmh1Δ and BY4741 at 50 mM KCl (P < 0.001)
  2. bStudent’s t-test indicated a significant difference between bmh1Δ and BY4741 at 50 mM KCl (P = 0.03)