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PMID: 10084686 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Cell type-specific regulatory sequences control expression of the Drosophila FMRF-NH2 neuropeptide gene.

Journal of neurobiology ·Vol. 38 ·No. 4 ·1999-03-00 ·Pages 507-20

Benveniste RJ, Taghert PH

Abstract

The FMRFamide (dFMRFa) neuropeptide gene is expressed in about 17 diverse cell types in the Drosophila central nervous system. This expression pattern is generated by transcriptional control elements that are distributed over 8 kilobases of dFMRFa DNA. Previous studies identified one enhancer within the dFMRFa 5' region that is both necessary and sufficient to drive reporter transgene expression in one of the 17 dFMRFa cell types, the OL2 neurons. We now report the presence of two additional, non-overlapping enhancers within the gene: One drives expression by the six Tv neuroendocrine cells, and another in the four X and X2 interneurons. We also show that the Tv neuron-specific enhancer itself has complex organization, with several positively and negatively acting cis elements. Together, these results describe the organization of what is likely to be a prototypic neuronal gene promoter: an assemblage of multiple, independent, cell type-specific enhancers, each consisting of multiple quantitative elements.

MeSH Terms
Animals Animals, Genetically Modified Base Sequence Drosophila/genetics Enhancer Elements, Genetic FMRFamide/biosynthesis,genetics Gene Expression Regulation Genes, Reporter Interneurons/metabolism Larva Neurons/metabolism Neurosecretory Systems/metabolism Recombinant Proteins/biosynthesis Regulatory Sequences, Nucleic Acid Transcription, Genetic
Chemicals
Recombinant Proteins FMRFamide
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Benveniste R J
Department of Anatomy and Neurobiology, Washington University School of Medicine, Saint Louis, Missouri 63110, USA.
Taghert P H
Article Info
Journal
Journal of neurobiology
Abbr.
J Neurobiol
ISSN
0022-3034
Published
1999-03-00
Pages
507-20
Language
English
Region
United States
NLM ID
0213640
Subset
IM
Grants
DS NIH HHS · NINDS21749 · United States
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