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. 2008 Jul 14;182(1):77–88. doi: 10.1083/jcb.200804062

Figure 5.

Figure 5.

Rescue experiments reveal that the head and tail of Myo10 mediate different aspects of Myo10 function in mitosis. (a) Schematic diagram of the constructs used in Myo10 morphant rescue experiments. (b) Low-magnification images of α-tubulin staining in rescue experiment embryos. For these experiments, embryos were microinjected with water or Myo10 MO along with RNA encoding each of the Myo10 constructs shown in panel a. (c) Quantification of bipolar and multipolar spindles in rescue experiment embryos. n = 18, 47, 22, 16, and 12 embryos for water, MO, MO + GFP-Myo10, MO + GFP-Myo10-HMM, and MO + GFP-Myo10-IQT, respectively. Error bars represent the standard error of the mean. (d) Box and whisker plots of spindle length measurements in rescue experiment samples. Spindle length was calculated as a percentage of total cell length to allow for variation in cell size. n = 109, 141, 136, 115, and 87 spindles for water, MO, MO + GFP-Myo10, MO + GFP-Myo10-HMM, and MO + GFP-Myo10-IQT, respectively. For significance testing, unpaired Student's t tests were performed: *, P < 0.05; **, P < 0.01; ***, P < 0.001; ****, P < 0.0001.