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. 2010 Aug 17;19(21):4253–4264. doi: 10.1093/hmg/ddq348

Table 2.

Neuronal defects observed in kismet MARCM mutants

Neuron Gal4-line n Defects observed % P-value
γ neurons, MB 201Y
 control (pupal) 8 Unpruned axons 0%
kis mutant (pupal) 10 Unpruned axons 40% <0.05
α, β, γ neurons, MB OK107
 Control (adult) 9 Lobe structure 0%
Cell migration 0%
Axon migration 11%
kis mutant (adult) 11 Lobe structure 55% <0.05
Cell migration 36% <0.05
Axon migration 55% <0.05
DCNs Atonal
 Control (larval) 9 Cell position 0%
Axon migration 0%
Cells out of cluster 0%
 Control (adult) 6 Axon extension (13.5 axons in medulla) 0%
kis mutant (larval) 19 Cell position 53% <0.001
Axon migration 32% <0.05
Cells out of cluster 32% <0.05
kis mutant (adult) 6 Axon extension (5.5 axons in medulla) 100% <0.001

Quantification of defects observed in different kismet mutant neurons. MB, mushroom body. Unpruned axons refers to the number of clones with unpruned γ axons extending into the α lobe at 18–20 h APF. Lobe structure indicates missing or altered lobe morphology in α, β or γ lobes. Cell position indicates the number of soma that appear lateral to their appropriate locations by the developmental time indicated. Axon migration indicates either axons crossing the midline for adult Kenyon cells or commissural axons failing to cross the midline or failing to migrate to their proper contralateral targets in larval DCNs. Axon extension indicates the presence of axons failing to extend from lobulla into the medulla in adult brains. P-values are indicated from a two-tailed Student's t-test comparing kis mutant with control.