2014
DOI: 10.1534/genetics.114.172023
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Potency of Transgenic Effectors for Neurogenetic Manipulation inDrosophilaLarvae

Abstract: Genetic manipulations of neuronal activity are a cornerstone of studies aimed to identify the functional impact of defined neurons for animal behavior. With its small nervous system, rapid life cycle, and genetic amenability, the fruit fly Drosophila melanogaster provides an attractive model system to study neuronal circuit function. In the past two decades, a large repertoire of elegant genetic tools has been developed to manipulate and study neural circuits in the fruit fly. Current techniques allow genetic … Show more

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Cited by 27 publications
(22 citation statements)
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References 67 publications
(68 reference statements)
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“…The antiserum was used in adult and larval Drosophila . Ablation of OA/TA neurons in the larval brain correlated with the absence of a specific staining for OA and TA neurons (Pech et al, ; Pauls et al, ).…”
Section: Methodsmentioning
confidence: 99%
“…The antiserum was used in adult and larval Drosophila . Ablation of OA/TA neurons in the larval brain correlated with the absence of a specific staining for OA and TA neurons (Pech et al, ; Pauls et al, ).…”
Section: Methodsmentioning
confidence: 99%
“…Synaptic inactivation by expression of shi ts1 is a highly effective means of inhibiting neurons in Drosophila (Kitamoto, 2001; Pauls et al, 2015; Thum et al, 2006) and has been used to study a variety of behaviors, including courtship, circadian behavior, memory, olfaction, 3rd instar larval locomotion, turning behavior and spatial orientation (Akalal et al, 2006; Hughes and Thomas, 2007; Kahsai et al, 2010; Keene et al, 2011; Okusawa et al, 2014; Pitman et al, 2006; Sakai and Kitamoto, 2006; Song et al, 2007; Suh et al, 2004). However, while shi ts1 can effectively inhibit chemical synapses, it is important to remember that it has no effect on electrical synapses.…”
Section: Discussionmentioning
confidence: 99%
“…Optogenetically bitter-stimulable offspring resulted from crossing Blooming Stock Center (BSC) line 57670 (genotype: w [*]; wg [Sp-1]/ CyO ; P{w[+mC]= Gr66a - GAL4 .1.8}1/ TM3 , Sb [1]), characterised by bitter-sensing neurons-restricted expression of Gal4 (Weiss et al 2011), to a UAS-ChannelRhodopsin2 construct-bearing line (w[*]; UAS - XXL - ChR2 / CyO : GFP ), a kind gift of Professor Christian Wegener. Please note that this type of ChR2 does not require all-trans-retinal in order to be activated by 480nm light (Pauls et al 2015; Dawydow et al 2014).…”
Section: Methodsmentioning
confidence: 99%