The longterm goal of the proposed research is to determine how genetic regulatory systems are determined by the joint contribution of their developmental and evolutionary histories. The Drosophila glucose dehydrogenase gene (Gld) will be used as a model system to study these determinants of gene regulation because Gld's tissue-specific regulation in the adult reproductive tract is highly variable among a variety of species in the genus Drosophila. The research strategy will be to use a combination of in vitro mutagenesis and gene transformation to critically test hypotheses regarding the role of cis-elements and trans-acting factors responsible for species' differences in developmental expression of GLD.
The specific aims are largely focused on elucidating the regulatory factors underlying GLD expression in the reproductive organs of both males and females, and, in parallel, identifying regulatory differences between species. Since the sex- determination genes tra and tra-2 are required for the unique tissue- specific pattern of GLD expression in D. melanogaster, the Gld regulatory elements that respond to them will be mapped. Misregulation of tra and tra-2 in D. melanogaster leads to ectopic patterns of GLD expression in the reproductive tract that mimic normal patterns seen other Drosophila species. A hypothesis that other species' Gld genes differ in their response to the sex-determination genes will be tested. A newly devised genetic method for identifying genes that encode tissue specific transcription factors will be used to isolate such genes that regulate Gld. Knowledge of gene function alone provides insufficient and sometimes misleading information for understanding why genes are expressed in certain tissues. The proposed research should provide a deeper understanding of how evolution and development affect gene regulation thereby increasing our understanding of how perturbations in genetic regulatory systems can result in human genetic diseases.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
2R01GM034170-09A1
Application #
2177313
Study Section
Mammalian Genetics Study Section (MGN)
Project Start
1984-12-01
Project End
1998-03-31
Budget Start
1994-04-01
Budget End
1995-03-31
Support Year
9
Fiscal Year
1994
Total Cost
Indirect Cost
Name
Vanderbilt University Medical Center
Department
Biochemistry
Type
Schools of Arts and Sciences
DUNS #
004413456
City
Nashville
State
TN
Country
United States
Zip Code
37212
Keplinger, B L; Guo, X; Quine, J et al. (2001) Complex organization of promoter and enhancer elements regulate the tissue- and developmental stage-specific expression of the Drosophila melanogaster Gld gene. Genetics 157:699-716
Olsen, D S; Jordan, B; Chen, D et al. (1998) Isolation of the gene encoding the Drosophila melanogaster homolog of the Saccharomyces cerevisiae GCN2 eIF-2alpha kinase. Genetics 149:1495-509
Keplinger, B L; Rabetoy, A L; Cavener, D R (1996) A somatic reproductive organ enhancer complex activates expression in both the developing and the mature Drosophila reproductive tract. Dev Biol 180:311-23
Gunaratne, P; Ross, J L; Zhang, Q et al. (1994) An evolutionarily conserved palindrome in the Drosophila Gld promoter directs tissue-specific expression. Proc Natl Acad Sci U S A 91:2738-42
Ross, J L; Fong, P P; Cavener, D R (1994) Correlated evolution of the cis-acting regulatory elements and developmental expression of the Drosophila Gld gene in seven species from the subgroup melanogaster. Dev Genet 15:38-50
Quine, J A; Gunaratne, P; Organ, E L et al. (1993) Tissue-specific regulatory elements of the Drosophila Gld gene. Mech Dev 42:3-13
Cavener, D R (1992) GMC oxidoreductases. A newly defined family of homologous proteins with diverse catalytic activities. J Mol Biol 223:811-4
Schiff, N M; Feng, Y; Quine, J A et al. (1992) Evolution of the expression of the Gld gene in the reproductive tract of Drosophila. Mol Biol Evol 9:1029-49
Schonbaum, C P; Organ, E L; Qu, S et al. (1992) The Drosophila melanogaster stranded at second (sas) gene encodes a putative epidermal cell surface receptor required for larval development. Dev Biol 151:431-45
Cavener, D R; Ray, S C (1991) Eukaryotic start and stop translation sites. Nucleic Acids Res 19:3185-92

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