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http://hdl.handle.net/11375/15250
Title: | Role of RanBPM in Drosophila fat body for the remote control of insulin secretion and feeding behavior |
Authors: | Agnihotri, Swati |
Advisor: | Campos, Ana R. Roger Jacobs and Andre Bedard |
Department: | Biology |
Keywords: | Biology;Developmental Biology;Genetics;Biology |
Publication Date: | Oct-2013 |
Abstract: | <p><strong>Abstract</strong></p> <p>RanBPM (Ran-Binding Protein in the Microtubule Organizing Center) is an evolutionarily conserved protein presumed to function as a scaffold in various signal transduction pathways. Null mutations in the <em>Drosophila</em> <em>RanBPM</em> gene cause a pleiotropic effect as seen by the late larval lethality, impaired growth, reduced CNS proliferation and disruption in feeding and response to light behaviours (Scantelbury et al., 2010). We report that<strong> </strong><em>RanBPM</em> mutants display impaired expression and secretion of one of the major <em>Drosophila</em> insulin like peptides, DILP2. Consistent with these findings<strong> </strong><em>RanBPM</em> mutants showed reduced membrane localization of the Phosphatidylinositol (3,4,5)-trisphosphate (PIP3) reporter TGPH (GFP-pleckstrin homology domain (PH) fusion regulated by the Tubulin promoter) and reduced activation of the serine threonine kinase AKT, both read outs of insulin signalling (InS). Ubiquitous overexpression of <em>DILP2</em> partially rescued the reduced larval growth, CNS proliferation and feeding phenotypes caused by <em>RanBPM</em> mutations. Over expression of DILP6 in the glia rescued the reduced CNS proliferation but not the reduced larval growth and feeding behaviour phenotypes. Targeted expression of <em>RanBPM</em> in the fat body suppressed all <em>RanBPM</em> mutant phenotypes except for lethality. In <em>Drosophila</em>, the fat body acts a nutritional sensor involved in coordinating neuroblast proliferation by a TOR- dependent mechanism. Our results present evidence for the role of AKT in the fat body of the <em>RanBPM</em> mutants for the regulation of CNS proliferation, DILP2 secretion, overall growth and feeding</p> |
URI: | http://hdl.handle.net/11375/15250 |
Identifier: | opendissertations/7917 8961 4287753 |
Appears in Collections: | Open Access Dissertations and Theses |
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