Document Detail


Drosophila sec10 is required for hormone secretion but not general exocytosis or neurotransmission.
MedLine Citation:
PMID:  12453153     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
The sec6/8, or exocyst, complex is implicated in trafficking of secretory vesicles to fusion sites in the plasma membrane. Genetic analyses have been done primarily in yeast, where mutation of the eight protein subunits similarly disrupts polarized vesicle fusion. The goal of this study was to assay the sec6/8 complex in Drosophila, and specifically to test its widely hypothesized functions in synaptogenesis and neurotransmission. We used a transgenic RNAi approach to remove the most highly conserved complex component, Drosophila sec10 (dSec10). Ubiquitous dSec10 RNAi resulted in early postembryonic lethality, demonstrating that dSec10 is essential. Surprisingly, tissue-specific dSec10 RNAi revealed no essential requirement in nervous system, musculature, gut or epidermis. Assays of polarized secretion in all these tissues failed to reveal any role for dSec10. In particular, the neuromuscular synapse showed no defects in morphogenesis or vesicle trafficking/fusion underlying neurotransmission. The essential requirement for dSec10 was restricted to the ring gland, the Drosophila organ specialized for endocrine function. The developmental arrest of dSec10 RNAi animals was partially rescued by feeding ecdysone, suggesting dSec10 mediates steroid hormone secretion. We conclude that dSec10 has no detectable role in most forms of polarized trafficking/exocytosis, including neurotransmission, but rather is essential for endocrine secretion.
Authors:
Hillary K Andrews; Yong Q Zhang; Nick Trotta; Kendal Broadie
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Publication Detail:
Type:  Journal Article; Research Support, U.S. Gov't, P.H.S.    
Journal Detail:
Title:  Traffic (Copenhagen, Denmark)     Volume:  3     ISSN:  1398-9219     ISO Abbreviation:  Traffic     Publication Date:  2002 Dec 
Date Detail:
Created Date:  2002-11-27     Completed Date:  2003-06-16     Revised Date:  2007-11-14    
Medline Journal Info:
Nlm Unique ID:  100939340     Medline TA:  Traffic     Country:  Denmark    
Other Details:
Languages:  eng     Pagination:  906-21     Citation Subset:  IM    
Affiliation:
Department of Biological Sciences, Vanderbilt University, Nashville, TN 37235-1634, USA.
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MeSH Terms
Descriptor/Qualifier:
Animals
Animals, Genetically Modified
Carrier Proteins / chemistry*,  physiology*
Drosophila / genetics*,  metabolism
Drosophila Proteins / chemistry*,  physiology*
Ecdysone / pharmacology
Electrophysiology
Exons
Expressed Sequence Tags
Green Fluorescent Proteins
Immunohistochemistry
In Situ Hybridization
Introns
Luminescent Proteins / metabolism
Mutation
RNA Interference
Recombinant Fusion Proteins / metabolism
Reverse Transcriptase Polymerase Chain Reaction
Signal Transduction
Time Factors
Transgenes
Grant Support
ID/Acronym/Agency:
R01 GM54544/GM/NIGMS NIH HHS
Chemical
Reg. No./Substance:
0/Carrier Proteins; 0/Drosophila Proteins; 0/Luminescent Proteins; 0/Recombinant Fusion Proteins; 0/sec10 protein, Drosophila; 147336-22-9/Green Fluorescent Proteins; 3604-87-3/Ecdysone

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