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. 2006 Feb;17(2):658–666. doi: 10.1091/mbc.E05-04-0336

Figure 4.

Figure 4.

(A) Benomyl sensitivity and epistasis. (A) cdc55Δ mutant in combination with deletions of the checkpoint genes MAD2 and BUB2. Stationary phase cultures were normalized to equal densities (1 × 107 cells/ml) and spotted in a 10-fold serial dilution series on YPD (rich medium) or YPD plus 12 μg/ml benomyl. Plates were incubated at 25°C. Strains were wild-type (8058-4-4), mad2Δ (8426-9-4), bub2Δ (8862-10-2), cdc55Δ (8615-1-4), mad2Δ cdc55Δ (8667-2-3), and bub2Δ cdc55Δ (8818-9-3). (B) Deletion of LTE1 in combination with cdc55Δ. Strains were wild type (8058-4-4), cdc55Δ (8615-1-4), lte1Δ (8505-12-4), and cdc55Δ lte1Δ (8665-17-3). (C) Deletion of the FEAR components SLK19 and SPO12 in combination with cdc55Δ. Strains were wild-type (8058-4-4), cdc55Δ (8615-1-4), spo12Δ slk19Δ (8933-1-3), and cdc55Δ spo12Δ slk19Δ (8933-5-4).