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. 1997 Dec;8(12):2519–2537. doi: 10.1091/mbc.8.12.2519

Table 3.

Effect of checkpoint mutations on dna2-22 viability and G2/M arrest

Strain Viability
% Large Budded
24°C 37°C 30°C 37°C
WT 97.5 ± .94 96.4 ± 2.3 30.0 ± 5.6 24.0 ± 3.6
mec1 92.3 ± 1.1 77.4 ± 5.8 29.0 ± 2.65 27.3 ± 2.52
rad9 94.6 ± .49 94.8 ± 1.9 25.7 ± 1.53 23.3 ± 2.31
dna2-22 94.6 ± 1.7 2.77 ± 1.6 26.7 ± 3.79 86.3 ± 5.13
dna2-22 mec1-1 89.3 ± 2.0 3.48 ± 1.4 27.3 ± 0.58 4.50 ± 2.65
dna2-22 rad9 93.7 ± 1.3 6.53 ± 2.4 26.3 ± 3.21 40.7 ± 0.58
cdc2 92.7 ± .45 7.7 ± 1.5 ND ND
cdc2 rad9 43.6 ± .38 .09 ± .02 ND ND
cdc13 92.7 ± .86 40.7 ± 2.9 ND ND
cdc13 rad9 70.6 ± 4.0 2.2 ± 1.9 ND ND
cdc9 91.2 ± 1.1 7.4 ± .50 ND ND
cdc9 rad9 92.1 ± .66 28.1 ± 2.7 ND ND

Indicated strains were incubated in YPD at 24° to OD = .02 (approx. 8 × 106 cells/ml). Cultures were split and incubated at 24° or 37° for 4 hr. Cells were sonicated, visualized for large budded morphology, and plated on YPD at 24° for 16 hr before assaying for viability microscopically. Yeast giving rise to colonies containing >30 cells after 16 hr were considered viable. A minimum of 250 colonies was counted for each strain. Numbers represent the averages and standard deviations from 3 independent experiments.