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. 2005 Oct 6;102(42):15230–15235. doi: 10.1073/pnas.0507393102

Fig. 5.

Fig. 5.

Requirement of the UPS pathway and quantitation of mutant phenotypes in C4da neurons during dendrite degradation. (A and B) Live confocal images of ppk-Gal4 driving expression of both UAS-mCD8::GFP and UAS-UBP2 in C4da neurons at 20 h APF. Arrows point to the V′ neuron in A and the D neuron in B, showing attached larval dendritic branches. (C and D) Live confocal images of Uba1 and Mov34 C4da MARCM clones at 20 h APF. Anterior is up and dorsal is right in all images. (E) Number of 1° and 2° larval dendrites attached to soma in WT and mutant C4da neurons during metamorphosis. Number of samples (n) in the group is above each bar. *, P < 0.05; **, P < 0.001, Wilcoxon two-sample test. Error bars represent SEM. (F) Regulation of large-scale dendritic pruning in C4da neurons during metamorphosis. (Scale bars: 100 μm.)