Early in their development, ovarian follicles enter a vitellogenic phase that entails the deposition in the oocyte of a yolk mass embedded in an RNA-rich cytoplasm. There is evidence that control of this important phase of development entails the setting of homeostatic levels of cytoplasmic free Ca2+ and cAMP, two widely recognized internal regulators of cellular processes. This proposal is for a physiological and biochemical analysis of how the levels of Ca2+ and cAMP are set, with how they change during the onset and termination of vitellogenesis, and with how they in turn affect two major aspects of oocyte function--vitellogenin uptake from the hemolymph and the relegation of all egg RNA synthesis to the nurse cells. In many dipteran and hemipteran disease vectors the vitellogenic phase of development is triggered by the blood meal that nourishes egg formation. In Hyalophora cecropia it occurs spontaneously as a part of metamorphosis, but the large size and number of follicles make their biochemistry and physiology much more accessible to analysis. Vitellogenin uptake, the suppression of transcription in the oocyte, and the point of insertion of these two processes into the sequence of other events entailed in egg formation are virtually identical among these insects. Studying intracytoplasmic regulation by Ca2+ and cAMP in Hyalophora follicles would therefore yield insights that will be applicable to all insects with nurse cells.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM032909-12
Application #
2176784
Study Section
Tropical Medicine and Parasitology Study Section (TMP)
Project Start
1983-12-01
Project End
1996-11-30
Budget Start
1994-12-01
Budget End
1995-11-30
Support Year
12
Fiscal Year
1995
Total Cost
Indirect Cost
Name
University of Pennsylvania
Department
Biology
Type
Schools of Arts and Sciences
DUNS #
042250712
City
Philadelphia
State
PA
Country
United States
Zip Code
19104
Wang, Y; Telfer, W H (2000) Cyclic nucleotide-dependent protein phosphorylation in vitellogenic follicles of Hyalophora cecropia. Insect Biochem Mol Biol 30:29-34
Pan, M L; Telfer, W H (1999) Equivalence of riboflavin-binding hexamerin and arylphorin as reserves for adult development in two saturniid moths. Arch Insect Biochem Physiol 42:138-46
Woodruff, R I; Tilney, L G (1998) Intercellular bridges between epithelial cells in the Drosophila ovarian follicle: a possible aid to localized signaling. Dev Biol 200:82-91
Wang, Y; Telfer, W H (1998) Cyclic-AMP-induced water uptake in a moth ovary: inhibition by bafilomycin and anthracene-9-carboxylic acid. J Exp Biol 201:1627-35
Wang, Y; Telfer, W H (1996) Cyclic nucleotide-induced termination of vitellogenin uptake by Hyalophora cecropia follicles. Insect Biochem Mol Biol 26:85-94
Pan, M L; Telfer, W H (1996) Methionine-rich hexamerin and arylphorin as precursor reservoirs for reproduction and metamorphosis in female luna moths. Arch Insect Biochem Physiol 33:149-62
Magee, J; Kraynack, N; Massey Jr, H C et al. (1994) Properties and significance of a riboflavin-binding hexamerin in the hemolymph of Hyalophora cecropia. Arch Insect Biochem Physiol 25:137-57
Prevost, C; Louise-May, S; Ravishanker, G et al. (1993) Persistence analysis of the static and dynamical helix deformations of DNA oligonucleotides: application to the crystal structure and molecular dynamics simulation of d(CGCGAATTCGCG)2. Biopolymers 33:335-50
Pan, M L; Telfer, W H (1992) Selectivity in storage hexamerin clearing demonstrated with hemolymph transfusions between Hyalophora cecropia and Actias luna. Arch Insect Biochem Physiol 19:203-21
Telfer, W H; Kunkel, J G (1991) The function and evolution of insect storage hexamers. Annu Rev Entomol 36:205-28

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