Electroretinogram recordings to screen for modifiers of Neuronal Communication defects in fruit flies
Scope of the method
- Human health
- Other
- Basic Research
- In vivo
Description
- Neuronal communication
- brain
- neuronal health
- electrical field potentials
- eye
- genetic screen
- electrophysiology
- Drosophila melanogaster
- mutations
- molecular biology
- Life science
- Biomedicine
- cell biology
- biomolecular chemistry
- neuroscience
- biotechnology
The most commonly used readout for eye function in fruit flies is the electroretinogram (ERG). While ERGs are applied to study phototransduction, they also constitute a robust assay to assess neuronal communication between photoreceptors and second-order brain neurons. Using glass electrodes placed on the eye, the response of the eye and the brain on a light pulse is recorded. The electrical field potential that is recorded during a light flash consists of an ON and OFF transient when the light is turned on and off respectively, and a depolarization of the photoreceptors. In flies expressing for example human mutant Tau, these on and off transient are reduced indicating defects in neuronal communication between the eye and the brain. This ERG readout in Tau mutant flies is used to screen for modifiers that can rescue neuronal communication defects in Tau mutant flies.
Electroretinogram set up
- Published in peer reviewed journal
Pros, cons & Future potential
Easy to learn, quick method: hundred flies can be easily screened daily.
We use the method to study defects in neuronal communication but the assay can also be used in eye research.
References, associated documents and other information
-Assaying Mutants of Clathrin-Mediated Endocytosis in the Fly Eye Lauwers, Elsa; Verstreken, Patrik; Swan, LE (Editor) CLATHRIN-MEDIATED ENDOCYTOSIS: METHODS AND PROTOCOLS; 2018; Vol. 1847; pp. 109 - 119
-Reduced synaptic vesicle protein degradation at lysosomes curbs TBC1D24/sky-induced neurodegeneration Ana Clara Fernandes, Valerie Uytterhoeven, Sabine Kuenen, Yu-Chun Wang, Jan R Slabbaert, Jef Swerts, Jaroslaw Kasprowicz, Stein Aerts, Patrik Verstreken J Cell Biol 2014 Nov 24;207(4):453-62. doi: 10.1083/jcb.201406026.
-Shawn, the Drosophila Homolog of SLC25A39/40, Is a Mitochondrial Carrier That Promotes Neuronal Survival Jan R Slabbaert , Sabine Kuenen , Jef Swerts , Ine Maes, Valerie Uytterhoeven, Jaroslaw Kasprowicz, Ana Clara Fernandes, Ronny Blust, Patrik Verstreken J Neurosci. 2016 Feb 10;36(6):1914-29. doi: 10.1523/JNEUROSCI.3432-15.2016.
-Loss of skywalker reveals synaptic endosomes as sorting stations for synaptic vesicle proteins Valerie Uytterhoeven, Sabine Kuenen, Jaroslaw Kasprowicz, Katarzyna Miskiewicz, Patrik Verstreken Cell. 2011 Apr 1;145(1):117-32. doi: 10.1016/j.cell.2011.02.039.
-Neuronal identity defines α-synuclein and tau toxicity Roman Praschberger, Sabine Kuenen, Nils Schoovaerts, Natalie Kaempf, Jeevanjot Singh, Jasper Janssens, Jef Swerts, Eliana Nachman, Carles Calatayud, Stein Aerts, Suresh Poovathingal, Patrik Verstreken Neuron. 2023 May 17;111(10):1577-1590.e11. doi: 10.1016/j.neuron.2023.02.033. Epub 2023 Mar 21.
Contact person
Valerie UytterhoevenOrganisations
VIB - KU LeuvenCenter for Brain and Disease Research
Laboratory of Neuronal Communication
Belgium
Flemish Region
Neurosciences - KU Leuven
Department of Neurosciences
Laboratory of Neuronal Communication (VIB-KU Leuven)
Belgium
Flemish Region
Katholieke Universiteit Leuven (KUL)
Department of Neurosciences
Laboratory of Neuronal Communication (VIB-KU Leuven)
Belgium
Flemish Region