The mechanisms that establish cell-specific patterns of neurotransmitter expression are largely unknown. This research will examine (i) the factors that govern the initial expression of particular neuropeptides during embryogenesis; and (ii) the factors that modulate that expression during post-embryonic life. These studies focus on the simple nervous system of the moth in which neurons and their precursor cells are individually identifiable and can be examined with a variety of cellular and molecular approaches throughout their development. In particular, two previously generated monoclonal antibodies recognize cardioactive neuropeptides that are expressed by different identified neurons at various stages of embryonic and postembryonic development. Using these and other cellular and immunological techniques, the potential contributions of cellular environment and invarient cell lineages in directing the fate of these individual peptidergic neurons can be elucidated with great precision. In order to study the developmental regulation of neuropeptide expression in greater molecular detail, the monoclonal antibodies will be used to purify these neuropeptides. Recombinant DNA techniques will then be used to isolate the genes that encode them. Structural information derived from these experiments will facilitate the study of the cell-specific patterns of neuropeptide gene expression in a relatively simple and highly accessible developing central nervous system.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Research Project (R01)
Project #
5R01NS021749-02
Application #
3403272
Study Section
Neurological Sciences Subcommittee 1 (NLS)
Project Start
1985-07-01
Project End
1988-06-30
Budget Start
1986-07-01
Budget End
1987-06-30
Support Year
2
Fiscal Year
1986
Total Cost
Indirect Cost
Name
Washington University
Department
Type
Schools of Medicine
DUNS #
062761671
City
Saint Louis
State
MO
Country
United States
Zip Code
63130
Diao, Feici; Mena, Wilson; Shi, Jonathan et al. (2016) The Splice Isoforms of the Drosophila Ecdysis Triggering Hormone Receptor Have Developmentally Distinct Roles. Genetics 202:175-89
Beebe, Katherine; Park, Dongkook; Taghert, Paul H et al. (2015) The Drosophila Prosecretory Transcription Factor dimmed Is Dynamically Regulated in Adult Enteroendocrine Cells and Protects Against Gram-Negative Infection. G3 (Bethesda) 5:1517-24
Hadži?, Tarik; Park, Dongkook; Abruzzi, Katharine C et al. (2015) Genome-wide features of neuroendocrine regulation in Drosophila by the basic helix-loop-helix transcription factor DIMMED. Nucleic Acids Res 43:2199-215
Park, Dongkook; Li, Peiyao; Dani, Adish et al. (2014) Peptidergic cell-specific synaptotagmins in Drosophila: localization to dense-core granules and regulation by the bHLH protein DIMMED. J Neurosci 34:13195-207
Taghert, Paul H; Nitabach, Michael N (2012) Peptide neuromodulation in invertebrate model systems. Neuron 76:82-97
Park, Dongkook; Hou, Xiaowen; Sweedler, Jonathan V et al. (2012) Therapeutic peptide production in Drosophila. Peptides 36:251-6
Mills, Jason C; Taghert, Paul H (2012) Scaling factors: transcription factors regulating subcellular domains. Bioessays 34:10-6
Park, Dongkook; Hadži?, Tarik; Yin, Ping et al. (2011) Molecular organization of Drosophila neuroendocrine cells by Dimmed. Curr Biol 21:1515-24
Hamanaka, Yoshitaka; Park, Dongkook; Yin, Ping et al. (2010) Transcriptional orchestration of the regulated secretory pathway in neurons by the bHLH protein DIMM. Curr Biol 20:9-18
Park, Dongkook; Taghert, Paul H (2009) Peptidergic neurosecretory cells in insects: organization and control by the bHLH protein DIMMED. Gen Comp Endocrinol 162:2-7

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