Abstract

We characterized the establishment of an Epidermal Growth Factor Receptor (EGFR) organizing center (EOC) during leg development in Drosophila melanogaster. Initial EGFR activation occurs in the center of leg discs by expression of the EGFR ligand Vn and the EGFR ligand-processing protease Rho, each through single enhancers, vnE and rhoE, that integrate inputs from Wg, Dpp, Dll and Sp1. Deletion of vnE and rhoE eliminates vn and rho expression in the center of the leg imaginal discs, respectively. Animals with deletions of both vnE and rhoE (but not individually) show distal but not medial leg truncations, suggesting that the distal source of EGFR ligands acts at short-range to only specify distal-most fates, and that multiple additional ‘ring’ enhancers are responsible for medial fates. Further, based on the cis-regulatory logic of vnE and rhoE we identified many additional leg enhancers, suggesting that this logic is broadly used by many genes during Drosophila limb development.

Highlights

  • We explored the integration of inputs from the Wnt- and TGF-beta signaling pathways and the leg-specifying transcription factors Distal-less and Sp1 at enhancer elements of Epidermal Growth Factor Receptor (EGFR) ligands

  • Our findings suggest that activation of the EGFR pathway during fly leg development occurs through the activation of multiple EGFR ligand enhancers that are active at different positions along the proximo-distal axis

  • August 24, 2018 cis-regulation of EGFR activation in Drosophila melanogaster leg Society grant 5250-12 awarded to RV

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Summary

Methods

The following mutant alleles and enhancer trap alleles were used in this study: arr, btdXA, cicQ474X, cicP[PZ]08482, dacp7d23 (dac-Gal4), DllSA1, Dllem212 (Dll-Gal4), Egfrtsla, Egfrf, grkΔFRT, Krn27-7-B, Mad, pntΔ88, rho7M43, ru, ruinga, Sp1HR (shared ahead of publication, [47]), spiSC1, spiDf(2L)Exel8041, vnL6, vnGAL4. Transgenic alleles used for in vivo clonal ectopic expression of genes were: UAS-armΔN, UAS-tkvQD, UAS-Dll. To perform RNAi knockdown of vein and spitz the following strains were used: UAS-vnRNAi (TRiP.HMC04390)/CyO, Dfd:EYFP; UAS-spiRNAi (TRiP.HMS01120) crossed to either Dll-GAL4 (Dllem212), spiDf(2L)Exel8041/ CyO, Dfd-EYFP; vnL6/TM6B, or spiDf(2L)Exel8041/CyO, Dfd-EYFP; vnGAL4/TM6B (vnGAL4 is a null allele [48]). For assessment of larval phenotypes, crosses remained at 25 ̊C until fixation and dissection as wandering larvae. For assessment of adult leg phenotypes, crosses were returned to 18 ̊C after 24h until eclosion

Results
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