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. 2007 Sep 5;104(37):14688–14693. doi: 10.1073/pnas.0702906104

Fig. 2.

Fig. 2.

Expression of cdc25+ and spo6+ during meiosis and effects of mei4+ overexpression or mutation. (A) Cells of the indicated genotypes (WT, HM1307; mei4, HM2163; mik1 wee1, HM605; mei4 mik1 wee1, HM1959; and mei4+-OP, HM4582) were subjected to synchronous induction of meiosis as described in Fig. 1. Samples were collected at the indicated times thereafter and subjected to Northern blot analysis of cdc25+ and spo6+ mRNA. Transcripts of cdc2+ were analyzed as a loading control. (B) Cells expressing GFP-tagged Cdc25p (WT cdc25+-GFP, HM4732; mei4 cdc25+-GFP, HM4833; and mei4+-OP cdc25+-GFP, HM4735) were treated as in A and subjected to immunoblot analysis with antibodies to GFP and to α-tubulin (loading control). (C) Cells of the indicated genotypes were induced to undergo meiosis as in Fig. 1. After incubation for 24 h at 34°C, the cells were examined with staining with iodine.