Cell-autonomous defect in <i>FASN</i> mutant FB cells.

<p>(A-L) Phalloidin staining of FB from feeding L3 larvae containing MARCM clones labeled with GFP. At the top right corner of each image, the genotype of the clonal cells and the percentage of sucrose supplementation are shown in green and yellow, respectively. <i>FASN</i>^{<i>Δ24-23</i>} (<i>Δ24-23</i>), <i>PFK1-RNAi</i> (<i>PFK1-Ri</i>), <i>PK-RNAi</i> (<i>PK-Ri</i>), <i>glo1-RNAi</i> (<i>glo1-Ri</i>) and <i>UAS-glo1</i> (+<i>glo1</i>). Scale bars: 20μm. (M-P) Size ratio between at least ten clonal cells and the neighbouring control cells, as shown in A, B, C, D (M), E, F, G, H (N), I, J, K (O) and L (P). For each condition, at least 10 larvae were dissected; whilst searching for <i>FASN</i>^{<i>Δ24-23</i>} clones expressing <i>glo1-RNAi</i> in larvae fed a 20%-SSD at least 40 animals were dissected.