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dc.contributor.authorLee, E-Chiang
dc.date.accessioned2018-07-12T18:51:50Z
dc.date.available2018-07-12T18:51:50Z
dc.date.issued1997
dc.identifier.citationSource: Dissertation Abstracts International, Volume: 58-05, Section: B, page: 2247.;Advisors: Nicholas E. Baker.
dc.identifier.urihttps://yulib002.mc.yu.edu/login?url=http://gateway.proquest.com/openurl?url_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:dissertation&res_dat=xri:pqm&rft_dat=xri:pqdiss:9733871
dc.identifier.urihttps://hdl.handle.net/20.500.12202/3736
dc.description.abstractCell-cell interactions mediated by Notch signaling are implicated in a wide variety of cell fate decisions during development of invertebrates and vertebrates. In Drosophila, the Notch (N) gene encodes a surface receptor with two known ligands, Delta (Dl) and Serrate (Ser). It has been suggested that the scabrous (sca) gene might be a another Notch ligand acting in the peripheral nervous system because the sca gene sequence predicts a secreted protein and sca interacts genetically with N and Dl. Alternatively Sca could bind to other receptors and work parallel to Notch signaling.;Using expression in Drosophila Schnieder cells, I showed that sca encodes a secreted, homodimeric glycoprotein and this protein is similar to protein detected in embryos. To determine whether sca encodes a N ligand, the secreted Sca was purified and a cell line expressing 18,000 N molecules per cell surface was used to test sca binding by cell adhesion assays and cell binding with labeled Sca. No interaction was detected between Sca and N or Dl, suggesting that Sca is not a high affinity Notch ligand.;The sca gene sequence predicts two domains, one being amino-terminal coiled-coil domain and the other the carboxy-terminal fibrinogen-related domain (FReD). To identify the receptor-binding domain, and help clone the Sca receptor in the future, these two domains were respectively expressed in flies using the GAL4/UAS expression system. The coiled-coil domain rescued the sca mutant extrabristle phenotype, whereas the FReD enhanced it, suggesting that both domains are potentially involved in protein-protein interactions and the coiled-coil domain contains a potential receptor-binding site.;N signaling is required to organize the dorsal-ventral axis in the developing wing margin. Ectopic expression of full length or coiled-coil domain of Sca in decapentaplegic-expressing region leads to notches of the wing margin. I provide evidence that ectopic expression of Sca blocks expression of N-downstream genes including vestigial, wingless, cut, and Enhancer of split-m 8. Moreover, ectopic Sca suppresses ectopic Cut expression induced by Dl, and affects the ectopic Cut expression pattern induced by Ser. This effect caused by Sca is through downregulation of N activity, because loss of N activity causes similar results and increasing N activity suppresses Sca-induced wing notches. I propose that ectopic Sca antagonizes N signaling through downregulation of N activity to lead to a wing-notch phenotype.
dc.publisherProQuest Dissertations & Theses
dc.subjectGenetics.
dc.subjectMolecular biology.
dc.subjectNeurosciences.
dc.titleStructure and function of scabrous, a secreted glycoprotein in Drosophila neurogenesis
dc.typeDissertation


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