Long Term Objective: To understand how the immune system of Drosophila melanogaster protects the fly from bacterial disease. Background: The blood of normal Drosophila contains no factors that kill bacteria, but the blood of flies inoculated with bacteria contains a newly synthesized set of polypeptides, the Antibacterial immune Response polypeptides (ARs), some of which (AntiBacterial polypeptides, ABs) kill bacteria. The overall problem is to determine how the fly recognizes the invading bacteria; how regulatory mechanisms result in the appearance of the immune polypeptides; and how the antibacterial proteins eliminate the bacterial invasion.
Specific Aims : 1) To determine the molecular organization of Drosophila's antibacterial immune response genes; 2) To understand the mechanisms of induction of the immune response using a genetic approach. Methodology: Immune response genes will be cloned, and their structure analyzed. Mutations will be induced in immune response genes to identify their functions. Mutations that block the induction of immunity will be sought and their cellular and molecular phenotypes investigated to understand mechanisms that induce immunity. Potential Significance: 1) Progress in understanding basic molecular mechanisms regulating tissue-specific and environmentally induced gene expression. 2) Development of novel methodologies for controlling populations of insect vectors of human disease by blocking insect immunity.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Project (R01)
Project #
5R01AI026734-02
Application #
3140631
Study Section
Genetics Study Section (GEN)
Project Start
1988-07-01
Project End
1993-06-30
Budget Start
1989-07-01
Budget End
1990-06-30
Support Year
2
Fiscal Year
1989
Total Cost
Indirect Cost
Name
University of Oregon
Department
Type
Schools of Arts and Sciences
DUNS #
948117312
City
Eugene
State
OR
Country
United States
Zip Code
97403
Schier, A F; Neuhauss, S C; Helde, K A et al. (1997) The one-eyed pinhead gene functions in mesoderm and endoderm formation in zebrafish and interacts with no tail. Development 124:327-42
Halpern, M E; Hatta, K; Amacher, S L et al. (1997) Genetic interactions in zebrafish midline development. Dev Biol 187:154-70
Johnson, S L; Gates, M A; Johnson, M et al. (1996) Centromere-linkage analysis and consolidation of the zebrafish genetic map. Genetics 142:1277-88
Halpern, M E; Thisse, C; Ho, R K et al. (1995) Cell-autonomous shift from axial to paraxial mesodermal development in zebrafish floating head mutants. Development 121:4257-64
Thisse, C; Thisse, B; Halpern, M E et al. (1994) Goosecoid expression in neurectoderm and mesendoderm is disrupted in zebrafish cyclops gastrulas. Dev Biol 164:420-9
Postlethwait, J H; Johnson, S L; Midson, C N et al. (1994) A genetic linkage map for the zebrafish. Science 264:699-703
Johnson, S L; Midson, C N; Ballinger, E W et al. (1994) Identification of RAPD primers that reveal extensive polymorphisms between laboratory strains of zebrafish. Genomics 19:152-6
Thisse, C; Thisse, B; Schilling, T F et al. (1993) Structure of the zebrafish snail1 gene and its expression in wild-type, spadetail and no tail mutant embryos. Development 119:1203-15
Yan, Y L (1990) A simple and inexpensive method for drying high-percentage polyacrylamide gradient gels. Biotechniques 8:381-2