Skip to main content
. 2005 Aug;4(8):1434–1445. doi: 10.1128/EC.4.8.1434-1445.2005

TABLE 5.

Phenotypic regulation of gene expression assessed by Northern blot analysis reflects promoter activity assessed in cells transformed with promoter-luciferase fusions

Gene Northern blotting result RLUC sp act (104 RLUC units/30 s/μg protein)a
RLUC result Fold difference of RLUC comparison
Strain 40F1 (a)
Strain 12F1 (α)
Wh DB Wh DB Comparison MTLa MTLα
PMP3 DB > Wh 2.8 ± 1.6 21.1 ± 7.9 1.1 ± 0.5 4.8 ± 1.8 DB > Wh DB/Wh 7.5 4.3
TAR1 DB > Wh 1.6 ± 0.8 18.6 ± 8.2 1.3 ± 0.8 12.4 ± 5.9 DB > Wh DB/Wh 11.6 9.5
ECM17 DB > Wh 1.2 ± 0.6 6.9 ± 2.6 1.2 ± 0.6 6.5 ± 2.8 DB > Wh DB/Wh 5.7 6.1
HSP104 DB > Wh 1.9 ± 0.9 17.0 ± 8.4 1.2 ± 0.7 7.3 ± 4.6 DB > Wh DB/Wh 8.9 6.1
APC9 Wh > DB 13.1 ± 5.1 2.2 ± 1.1 14.0 ± 6.3 2.3 ± 1.5 Wh > DB Wh/DB 5.9 6.1
SUT1 Wh ≅ DB 4.3 ± 2.4 3.5 ± 2.0 2.6 ± 1.7 2.9 ± 1.8 Wh ≅ DB Wh/DB 1.2 0.9
TEF4 Wh ≅ DB 1.9 ± 1.1 1.5 ± 0.8 1.5 ± 0.5 1.9 ± 0.9 Wh ≅ DB Wh/DB 1.3 0.8
a

The basal RLUC activity of strains harboring the promoterless vector pH12.7 targeted to the HO gene ranged between 5.9 × 103 and 6.2 × 103 units. This was subtracted from all RLUC activities obtained with promoter-containing constructs. Each measurement shown is the mean (± standard deviation) of six measurements of relative luminescence, three from each of two independent transformants.