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. 2009 May 1;20(9):2438–2450. doi: 10.1091/mbc.E08-10-0987

Table 4.

PRM3 and KAR5 interact genetically

Cross % WT % Kar
WT × prm3Δ 97 3
WT × kar5Δ 89 11
WT × kar5-1162 67 33
prm3Δ × prm3Δ 6 94
kar5Δ × kar5Δ 6 94
kar5-1162 × kar5-1162 4 96
prm3Δ × kar5Δ 72 28
prm3Δ × kar5-1162 28 72
prm3Δ × prm3Δ 3 97
prm3Δ [2μ PRM3] × prm3Δ 53 47
prm3Δ [2μ PRM3] × prm3Δ [2u PRM3] 68 32
prm3Δ [2μ KAR5] × prm3Δ 17 83
prm3Δ [2μ KAR5] × prm3Δ [2u KAR5] 32 68

Matings were performed at 30°C for 2.5 h on nitrocellulose filters on YEPD plates, fixed in 3:1 methanol:acetic acid, and stained with DAPI to visualize the nuclei. Zygotes with one nucleus were counted as WT, whereas zygotes with two nuclei were counted as Kar. Numbers represent the average of at least two independent experiments, with ∼100 zygotes counted in each experiment. The strains used were: prm3 (MS7590 × MS7591), kar5 (MS7673 × MS7674), and kar5-1162 (MS7666 × MS7667). Plasmids used were pMR5757 and pMR5760.