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Fig. 4. The mitotic arrest induced in Cdc16RNAi and Cdc27RNAi cells is morphologically distinct. (A) A graph showing the mitotic index of mock-, Cdc16RNAi-, Cdc27RNAi- or Cdc16RNAi- + Cdc27RNAi-treated S2 cells. This was calculated by counting the percentage of cells in mitosis as judged by phospho-histone H3 staining. Error bars represent the standard deviation. Results were pooled from four different experiments. (B) A low magnification view of Cdc16RNAi- (top panel) or Cdc27RNAi- (bottom panel) treated cells stained to reveal the distribution of DNA (red), phosphohistone H3 (blue) and microtubules (green). Note how most of the mitotic Cdc16RNAi cells have their chromosomes roughly aligned at the equator of a metaphase-like spindle, whereas most of the mitotic Cdc27RNAi cells have elongated spindles that are in a much more disorganised state. Bar, 10 µm. (C) A graph showing the proportions of mitotic cells in different states of mitosis. Typical examples of each mitotic state are shown underneath each graph; the colours are the same as in B: chromosomes aligned on a metaphase-like spindle (panel 1); chromosomes spread throughout an elongated spindle (panel 2); condensed and decondensed chromatin (which appears red, as it is not stained by the anti-phosphohistone H3 antibody) in the same cell (panel 3); a telophase-like cell (panel 4). Error bars represent the standard deviation. Bar, 5 µm.





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