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Files in this Data Supplement:
Fig. S1. The M/+ to M+ transformation in the esg-M+ experiment affects all imaginal discs. (A) CNS and imaginal discs of a M(3)67C ubi-GFP /+ larva stained for GFP and topro-3 (red). All the structures express GFP and topro-3. (B) CNS and imaginal discs of an esg-Gal4; M(3)67C ubi-GFP FRT2A/mwh jv FRT2A larva stained in the same way as in A. All the imaginal discs (and part of the larval brains) have lost the GFP label and are therefore M+.
Fig. S2. Apoptosis does not play a role in controlling final size in esg-M+ discs. (A) A prepupal wing disc stained for wg (blue) and caspase 3 (red) showing the normal low levels of apoptosis. (B) Adult esg-M+ wing showing a normal pattern, except for the radius incompletus phenotype caused by the ri mutation in cis in the mwh jv chromosome. (C) Prepupal esg-M+ p35 wing disc showing high levels of P35 (red). (D) Adult wing of the same phenotype showing normal size. There is an exacerbation of the ri phenotype due to P35.
Fig. S3. Apoptosis levels. Apoptosis levels were determined in M/+ (A), ci-M+ (B) and en-M+ (C) discs. Staining for TUNEL (red) or anti-caspase 3 (blue) reveals no significant increase in apoptotic levels in any of these genotypes. (D) Late third instar en-M+ p35 disc showing groups of cells with strong GFP expression. We believe they are M/M cells that are maintained alive by p35 throughout larval development, even though they do not divide. (E) Wing of the same genotype as D, showing a normal size and pattern except for the shortening of vein 5, a distinctive feature caused by P35.
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