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. 2003 Aug 15;22(16):4304–4313. doi: 10.1093/emboj/cdg406

graphic file with name cdg406f7.jpg

Fig. 7. elg1Δ mutants are defective in recovery from MMS-induced replication fork stalling. (A) S phase progression in the presence of MMS. Wild-type or elg1Δ cells were arrested in G1 (t = 0) and released synchronously into medium containing 0.035% (v/v) MMS. Samples were removed at the indicated times and analyzed by flow cytometry. The shaded histograms represent the cell cycle distribution of the asynchronous cultures before the G1 arrest. Overlaid histograms represent the cell cycle distribution at the indicated times after release from the G1 arrest. (B) Checkpoint activation of Rad53 during recovery from MMS damage. Cells were arrested in G1, released into MMS for 1 h, and then transferred to medium lacking MMS (t = 0). At the indicated times, samples were withdrawn and Rad53 activation was analyzed by immunoblotting.