1. cis-regulatory architecture of a short-range EGFR organizing center in theDrosophila melanogasterleg
- Author
-
Richard S. Mann, Roumen Voutev, Rebecca K. Delker, Aurélie Jory, Susan Elizabeth Newcomb, and Matthew Slattery
- Subjects
0301 basic medicine ,Cancer Research ,Cell signaling ,Gene Expression ,Signal transduction ,QH426-470 ,0302 clinical medicine ,Transforming Growth Factor beta ,Gene expression ,Medicine and Health Sciences ,Morphogenesis ,Drosophila Proteins ,Epidermal growth factor receptor ,Musculoskeletal System ,Genetics (clinical) ,Neuregulins ,Regulation of gene expression ,0303 health sciences ,biology ,Drosophila Melanogaster ,Eukaryota ,Gene Expression Regulation, Developmental ,Genomics ,Animal Models ,Cell biology ,Insects ,ErbB Receptors ,Imaginal disc ,Enhancer Elements, Genetic ,Imaginal Discs ,Experimental Organism Systems ,Legs ,Drosophila ,Gene Cloning ,Anatomy ,Drosophila melanogaster ,EGFR signaling ,Transcriptome Analysis ,Research Article ,Growth factors--Receptors ,Arthropoda ,Sp1 Transcription Factor ,Egfr ligand ,Wnt1 Protein ,Research and Analysis Methods ,03 medical and health sciences ,Model Organisms ,Genetics ,Animals ,Limb development ,Molecular Biology Techniques ,Receptors, Invertebrate Peptide ,Enhancer ,Biology ,Molecular Biology ,Gene ,Ecology, Evolution, Behavior and Systematics ,Alleles ,030304 developmental biology ,Homeodomain Proteins ,Limbs (Anatomy) ,Organizers, Embryonic ,Organisms ,Biology and Life Sciences ,Computational Biology ,Extremities ,Drosophila melanogaster--Genetics ,Genome Analysis ,biology.organism_classification ,Invertebrates ,030104 developmental biology ,biology.protein ,Genome Expression Analysis ,Developmental biology ,Gene Deletion ,030217 neurology & neurosurgery ,Cloning ,Developmental Biology ,Transcription Factors - 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., Author summary The EGFR signaling pathway plays a major role in innumerable developmental processes in all animals and its deregulation leads to different types of cancer, as well as many other developmental diseases in humans. Here 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 EGFR ligands. These enhancers trigger a specific EGFR-dependent developmental output in the fly leg that is limited to specifying distal-most fates. 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. Similar enhancer elements are likely to control EGFR activation in humans as well. Such DNA elements might be ‘hot spots’ that cause formation of EGFR-dependent tumors if mutations in them occur. Thus, understanding the molecular characteristics of such DNA elements could facilitate the detection and treatment of cancer.
- Published
- 2018
- Full Text
- View/download PDF