Our research goal is to understand the molecular events that result in female reproductive development and egg formation. Our studies will take advantage of the biological fact that male worms are necessary to stimulate females to complete reproductive development and to maintain reproductive activity. The significance of the research is that egg production, the end product of reproductive activity, is responsible for the pathogenesis of schistosomiasis. The obtained information should identify potential modes for drug therapy and vaccine development. To accomplish the goal we will: 1) Identify and characterize genes that are expressed during the development and function of the female reproductive system. As the male worm controls female reproduction by stimulating vitelline gland development, the focus will be on vitellaria-specific genes such as phenol oxidase. 2) Once identified, the biological function the gene products during reproductive development and activity will be elucidated. Determination of when (temporal) and where (tissue, cell) the female-specific gene and gene product are expressed will be made. To study eggshell formation, recombinant gene products representing two putative eggshell proteins will be mixed in vitro with phenol oxidase. 3) To understand how the genes that control female development and egg production are regulated, the 5' flanking regions of the genes which usually contain DNA elements responsible for sex-, tissue- and temporal-specific expression will be studied. A Drosophila surrogate system will be employed while attempts to develop a schistosome transfection model are made. A well characterized eggshell gene will serve as a model. 4) Once the DNA elements that control gene expression are identified, attempts to identify the regulatory factors and the genes that encode them will be made.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Unknown (R22)
Project #
1R22AI027219-01A1
Application #
3565524
Study Section
Tropical Medicine and Parasitology Study Section (TMP)
Project Start
1989-08-01
Project End
1992-07-31
Budget Start
1989-08-01
Budget End
1990-07-31
Support Year
1
Fiscal Year
1989
Total Cost
Indirect Cost
Name
State University New York Stony Brook
Department
Type
DUNS #
804878247
City
Stony Brook
State
NY
Country
United States
Zip Code
11794
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Freebern, W J; Osman, A; Niles, E G et al. (1999) Identification of a cDNA encoding a retinoid X receptor homologue from Schistosoma mansoni. Evidence for a role in female-specific gene expression. J Biol Chem 274:4577-85
Osman, A; Niles, E G; LoVerde, P T (1999) Characterization of the Ras homologue of Schistosoma mansoni. Mol Biochem Parasitol 100:27-41
Davis, R E; Parra, A; LoVerde, P T et al. (1999) Transient expression of DNA and RNA in parasitic helminths by using particle bombardment. Proc Natl Acad Sci U S A 96:8687-92
Kiang, D; Karim, A M; LoVerde, P T (1996) Cloning the gene encoding Schistosoma mansoni p50, an immunophilin. Gene 170:137-40
Hirai, H; LoVerde, P T (1996) Identification of the telomeres on Schistosoma mansoni chromosomes by FISH. J Parasitol 82:511-2
Osman, A; Kiang, D; Lo Verde, P T et al. (1995) Schistosoma mansoni: characterization of p50, an immunophilin. Exp Parasitol 80:550-9
Hirai, H; Tanaka, M; LoVerde, P T (1993) Schistosoma mansoni: chromosomal localization of female-specific genes and a female-specific DNA element. Exp Parasitol 76:175-81