Long-Term Objectives: Transposable genetic elements are ubiquitous in eukaryotic genomes. The goal is to understand how such elements are able to insert into new genomic positions, excise from old ones, and regulate these activities.
Specific Aims : Transposition: Some transposable elements transpose by replicating themselves in new positions, whereas others jump """"""""conservatively"""""""", with the donor site being deleted in the process. Proposed experiments will determine the mechanism of mobility for the P family of transposable elements in Drosophila melanogaster. Regulation: Some P elements are known to produce a gene product that regulates their own mobility. Experiments will determine the genetic requirements for this regulation and its relationship to the element's gene expression. Health Relatedness: Transposable element insertions are thought to be a major source of spontaneous mutations. These experiments will provide the basic data on how P elements function, and thus contribute to the understanding of the rate and control of harmful mutations. In addition, P elements are widely used as genetic vectors for studying general questions of gene function. Results of the proposed experiments can be used to enhance these techniques. Finally, it is thought that insect transposable elements will eventually prove useful in fighting insect pests. An understanding of their basic biology, as will be obtained from these experiments, will be essential for any such effort. Methods: A combination of standard genetic and molecular techniques will be employed. Drosophila will be cultured in the laboratory and screened by phenotype for the genetic variations of interest. Molecular techniques include DNA sequencing and polymerase chain reaction for amplification of specific DNA se-

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM030948-10
Application #
3278837
Study Section
Genetics Study Section (GEN)
Project Start
1982-07-01
Project End
1994-11-30
Budget Start
1991-12-01
Budget End
1992-11-30
Support Year
10
Fiscal Year
1992
Total Cost
Indirect Cost
Name
University of Wisconsin Madison
Department
Type
Schools of Medicine
DUNS #
161202122
City
Madison
State
WI
Country
United States
Zip Code
53715
Engels, William R (2009) Exact tests for Hardy-Weinberg proportions. Genetics 183:1431-41
Johnson-Schlitz, Dena M; Flores, Carlos; Engels, William R (2007) Multiple-pathway analysis of double-strand break repair mutations in Drosophila. PLoS Genet 3:e50
Preston, Christine R; Flores, Carlos C; Engels, William R (2006) Differential usage of alternative pathways of double-strand break repair in Drosophila. Genetics 172:1055-68
Preston, Christine R; Flores, Carlos; Engels, William R (2006) Age-dependent usage of double-strand-break repair pathways. Curr Biol 16:2009-15
Johnson-Schlitz, Dena M; Engels, William R (2006) The effect of gap length on double-strand break repair in Drosophila. Genetics 173:2033-8
Johnson-Schlitz, Dena; Engels, William R (2006) Template disruptions and failure of double Holliday junction dissolution during double-strand break repair in Drosophila BLM mutants. Proc Natl Acad Sci U S A 103:16840-5
Ciapponi, Laura; Cenci, Giovanni; Ducau, Judith et al. (2004) The Drosophila Mre11/Rad50 complex is required to prevent both telomeric fusion and chromosome breakage. Curr Biol 14:1360-6
Preston, Christine R; Engels, William; Flores, Carlos (2002) Efficient repair of DNA breaks in Drosophila: evidence for single-strand annealing and competition with other repair pathways. Genetics 161:711-20
Kusano, K; Johnson-Schlitz, D M; Engels, W R (2001) Sterility of Drosophila with mutations in the Bloom syndrome gene--complementation by Ku70. Science 291:2600-2
Flores, C; Engels, W (1999) Microsatellite instability in Drosophila spellchecker1 (MutS homolog) mutants. Proc Natl Acad Sci U S A 96:2964-9

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