Skip to main content
. 2003 May 12;92(2):165–170. doi: 10.1016/S0168-1702(03)00042-X

Table 2.

Frameshifting efficiencies of wild type and mutant RNA signals from CYDV-RPV or MMTV in E. coli and yeast S. cerevisiae

E. coli
S. cerevisiae
Construct Luciferase activity (RLU×10−5) FS efficiency (%) Luciferase activity (RLU×10−3) FS efficiency (%)
CYDV: 0 7530±200 (100) 8030±250 (100)
Wild type 150±30 2.0±0.5 120±20 1.5±0.3
Stem 1 140±20 1.9±0.4 30±3 0.4±0.1
Stem 2 155±20 2.1±0.3 29±3 0.4±0.1
Del enhancer 170±30 2.3±0.4 15±1 0.2±0.05
Shift site 6±3 0.08±0.02 4±0.5 0.05±0.02
Spacer (−3) 120±5 1.6±0.1 10±2 0.1±0.03
Spacer (−6) 110±4 1.5±0.1 8±2 0.1±0.03
Spacer (+6) 110±5 1.5±0.1 9±3 0.1±0.04
MMTV: 0 7600±300 (100) 8100±300 (100)
MMTV: −1 530±70 7±1 490±50 6±1
U13C 520±60 7±1 480±50 6±1
APK 520±60 7±1 160±30 2±0.6
ΔA14U13C 450±50 6±1 80±3 1±0.5

Cells were normalized and frameshifting (FS) efficiencies were calculated as the ratio of luciferase activity between the zero frame construct and the −1 frame construct. Data shown here are averages of eight independent measurements.