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. 1999 Sep 6;146(5):1019–1032. doi: 10.1083/jcb.146.5.1019

Figure 1.

F-actin is not required for maintenance of spindle orientation. Wild-type cells (DLY5) were grown in YEPD at 30°C, synchronized by addition of 200 mM hydroxyurea for 3 h, harvested, and resuspended in fresh YEPD supplemented with 0 or 100 μM Lat-A. At various times after release from hydroxyurea arrest, the cells were fixed and processed to visualize F-actin, tubulin, and DNA. A, Tubulin (left) and rhodamine-phalloidin (right) staining of cells 30 min after release from hydroxyurea arrest. Bar, 10 μm. B, Kinetics of anaphase. Percent of nuclear division was scored in DAPI-stained cells. C, Spindle orientation was scored as described in Materials and Methods, and reflects counts on both preanaphase and postanaphase spindles. n = 200 for each sample.

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