The expression of glucose dehydrogenase (GO) is either monophasic or biphasic in various species within the genus Drosophila. The majority of species exhibit a single peak of GO activity (monophasic) during the pupal stage. Four subgroups within the melanogaster species group exhibit two peaks of GO activity: one peak during the pupal stages and one peak which is limited to the ejaculatory duct of males. The expression of male limited GO is correlated with a distinct ejaculatory duct morphology. GO has been shown to be required for the process of eclosion and is transferred from males to females during copulation in Drosophila melanogaster (one of the biphasic species). The primary objective of the proposed research is to elucidate the evolution of GO regulation in a few representative species within the genus Drosophila. Two monophasic species (D. pseudoobscura and D. takahashii) and two biphasic species (D. melanogaster and D. eugracilis) have been chosen for investigation. Three experimental methods will be used to examine GO regulation at various levels of control: DNA sequence analysis, gene transformation, and imaginal disc transplantation. Interspecific gene transformation and imaginal disc transplantation experiments will allow us to explore the GO regulatory differences in vivo. The combination of these two methods offers a novel approach to investigate the evolution of regulatory systems. In addition, the proposed research should add to our knowledge of how tissue and developmental specific factors control gene expression.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM034170-02
Application #
3284716
Study Section
Genetics Study Section (GEN)
Project Start
1984-12-01
Project End
1987-11-30
Budget Start
1985-12-01
Budget End
1986-11-30
Support Year
2
Fiscal Year
1986
Total Cost
Indirect Cost
Name
Vanderbilt University Medical Center
Department
Type
Schools of Arts and Sciences
DUNS #
004413456
City
Nashville
State
TN
Country
United States
Zip Code
37203
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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