test Browse by Author Names Browse by Titles of Works Browse by Subjects of Works Browse by Issue Dates of Works

Advanced Search
& Collections
Issue Date   
Sign on to:   
Receive email
My Account
authorized users
Edit Profile   
About T-Space   

T-Space at The University of Toronto Libraries >
School of Graduate Studies - Theses >
Doctoral >

Please use this identifier to cite or link to this item: http://hdl.handle.net/1807/17313

Title: Role of Frequenin1 and Frequenin2 in Regulating Neurotransmitter Release and Nerve Terminal Growth at the Drosophila Neuromuscular Junction
Authors: Dason, Jeffrey
Advisor: Atwood, Harold
Charlton, Milton
Department: Physiology
Keywords: Frequenin
Neuronal Calcium Sensor
synaptic transmission
Issue Date: 26-Feb-2009
Abstract: Frequenin (Frq) and its mammalian homologue, Neuronal Calcium Sensor 1 (NCS-1), are calcium-binding proteins, which regulate neurotransmitter release. However, reports are contradictory, and little is known about Frq's cellular mechanisms. The Drosophila nervous system can be used to gain a better understanding of the function of Frq. There are two Frq-encoding genes in Drosophila. The temporal and spatial expression patterns of the two genes are very similar, and the proteins they encode, Frq1 and Frq2, are 95% identical in amino acid sequence. Loss-of-function phenotypes were studied using three different procedures: creating a deletion designed to remove the entire frq1 gene and part of the frq2 gene; using an interfering C-terminal peptide to prevent Frq binding to its intracellular targets; and using RNAi to reduce frq1 and frq2 transcript levels. Deletion of the entire frq1 gene and part of the frq2 gene resulted in impaired neurotransmitter release and enhanced nerve terminal growth. To discriminate chronic from acute loss-of-function effects, the effects of transgenic expression and forward-filling an interfering C-terminal peptide into presynaptic terminals were compared. In both cases, a reduction in quantal content per bouton occurred, demonstrating that this trait does not result from homeostatic adaptations during development. The chronic treatment also enhanced nerve terminal growth. Conversely, gain-of-function conditions yielded an increase in quantal content and a reduction in nerve terminal growth. Frqs' effects on transmitter output were not due to changes in the number of active zones, nor were they due to changes in the size of the readily releasable pool of vesicles. Oregon Green 488 BAPTA-1 conjugated to 10 kDa Dextran was forward-filled into presynaptic boutons to detect changes in presynaptic Ca2+ signals. Ca2+ responses to presynaptic nerve impulses demonstrated that Frq modulates neurotransmitter release by regulating Ca2+ entry. Gain-of-function phenotypes remained present in a PI4KB null background, demonstrating that Frq's effects were not due to an interaction with PI4KB. All effects seen for all studies were identical for both Frqs, indicating that the two Frq proteins are likely functionally redundant. Overall, Frqs have two distinct functions: one on neurotransmission, primarily by regulating Ca2+ entry, and another on axonal growth and synaptic bouton formation.
URI: http://hdl.handle.net/1807/17313
Appears in Collections:Doctoral
Department of Physiology - Doctoral theses

Files in This Item:

File Description SizeFormat
Dason_Jeffrey_S_200811_PhD_thesis.pdf3.63 MBAdobe PDF

This item is licensed under a Creative Commons License
Creative Commons

Items in T-Space are protected by copyright, with all rights reserved, unless otherwise indicated.