Role of the C Terminus of Mec1 Checkpoint Kinase in Its Localization to Sites of DNA Damage
Mol. Biol. Cell Nakada et al.
16: 5227
Supplemental Figures
This article contains the following supporting material:
Figure S1
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Effect of mec1-85 mutation on cell viability after MMS treatment. Viability was determined after treatment of various concentrations of MMS for 30 min. Strains used were wild-type (KSC1560), mec1Δ (KSC1561), and mec1-85 (KSC1641) cells.
Figure S2
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Degradation of the HO-induced DSB ends. Wild-type (KSC1560) and mec1-85 (KSC1641) cells carrying YCpA-GAL-HO were grown in sucrose and treated with nocodazole. After arrest at G2/M, the culture was incubated with galactose to induce HO expression. Purified DNAs were fixed to a membrane and hybridized with oligonucleotide probes, each complementary to 5’ to 3’- or 3’ to 5’-degrading strand.