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. 2015 Mar 30;4:e06029. doi: 10.7554/eLife.06029

Figure 8. KIF1C's N-terminal Rab6A binding site is required for the maintenance of Golgi morphology.

(A) Golgi morphology (p115) of HeLa cells transfected with control siRNA or KIF1C siRNA and the indicated rescue plasmid. Scale bar, 10 µm. (B) Golgi ribbon rescue, defined as the mean fraction of Golgi staining present as large objects (>4.11 µm²), normalized by KIF1C intensity, quantified from cells such as those shown in A (bars = SE, >90 cells/condition). KIF1C wild-type rescue cells were statistically different from KIF1C depleted and loop mutant rescue cells but not those rescued with KIF1C K103A (p < 0.001).

DOI: http://dx.doi.org/10.7554/eLife.06029.016

Figure 8.

Figure 8—figure supplement 1. siRNA rescue shows that KIF1C's N-terminal Rab6A binding site is required for the maintenance of Golgi morphology.

Figure 8—figure supplement 1.

Golgi morphology (p115) of HeLa cells transfected with control siRNA or KIF1C siRNA and the indicated rescue plasmid. Scale bar, 10 µm. One cell of each type is also shown in Figure 8.
Figure 8—figure supplement 2. Full-length KIF1C mutant protein localization.

Figure 8—figure supplement 2.

Vero cells transfected with the indicated CFP-tagged full-length KIF1C construct were MeOH fixed and imaged by fluorescence microscopy. Scale bar is 20 µm.
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