Skip to main content
. 2011 Feb 1;6:5. doi: 10.1186/1749-8104-6-5

Figure 5.

Figure 5

Other BRM complex component mutants do not exhibit the same phenotypes as Bap55 mutants. (A) Dendrites of brm-/- DL1 PNs mistarget to non-stereotyped areas of the antennal lobe. (B, C) brm-/- anterodorsal (B) and lateral (C) neuroblast clone PNs exhibit perturbed cell morphology, weak labeling, and dendrite mistargeting, with small meandering projections to incorrect glomeruli. (D) brm-/- ventral neuroblast clone PNs exhibit perturbed cell morphology, weak labeling, and a lack of innervation throughout the antennal lobe. (E) Dendrites of Snr1-/- DL1 PNs mistarget to non-stereotyped areas of the antennal lobe. (F, G) Snr1-/- anterodorsal (F) and lateral (G) neuroblast clone PNs exhibit perturbed cell morphology, weak labeling, and dendrite mistargeting, with small meandering projections to incorrect glomeruli. (H) Snr1-/- ventral neuroblast clone PNs exhibit perturbed cell morphology, weak labeling, and a lack of innervation throughout the antennal lobe. Green marks mCD8-GFP-labeled PNs generated by MARCM and labeled using GH146-GAL4. All panels show full confocal stacks; magenta is the presynaptic marker nc82; symbols are as in Figure 2. Scale bar: 20 μm in (A) (for A-H).