@article {46601,
	title = {A small group of neurosecretory cells expressing the transcriptional regulator apontic and the neuropeptide corazonin mediate ethanol sedation in Drosophila.},
	journal = {The Journal of Neuroscience},
	volume = {33},
	year = {2013},
	month = {2013 Feb 27},
	pages = {4044-54},
	abstract = {<p>In the fruit fly Drosophila melanogaster, as in mammals, acute exposure to a high dose of ethanol leads to stereotypical behavioral changes beginning with increased activity, followed by incoordination, loss of postural control, and eventually, sedation. The mechanism(s) by which ethanol impacts the CNS leading to ethanol-induced sedation and the genes required for normal sedation sensitivity remain largely unknown. Here we identify the gene apontic (apt), an Myb/SANT-containing transcription factor that is required in the nervous system for normal sensitivity to ethanol sedation. Using genetic and behavioral analyses, we show that apt mediates sensitivity to ethanol sedation by acting in a small set of neurons that express Corazonin (Crz), a neuropeptide likely involved in the physiological response to stress. The activity of Crz neurons regulates the behavioral response to ethanol, as silencing and activating these neurons affects sedation sensitivity in opposite ways. Furthermore, this effect is mediated by Crz, as flies with reduced crz expression show reduced sensitivity to ethanol sedation. Finally, we find that both apt and crz are rapidly upregulated by acute ethanol exposure. Thus, we have identified two genes and a small set of peptidergic neurons that regulate sensitivity to ethanol-induced sedation. We propose that Apt regulates the activity of Crz neurons and/or release of the neuropeptide during ethanol exposure.</p>
},
	keywords = {Animals, Animals, Genetically Modified, Behavior, Animal, Brain, DNA-Binding Proteins, Dose-Response Relationship, Drug, Drosophila, Drosophila Proteins, Ethanol, Gene Expression Regulation, Green Fluorescent Proteins, Hypnotics and Sedatives, Metamorphosis, Biological, Mutation, Neurons, Neuropeptides, Neurosecretory Systems, RNA, Messenger, Transcription Factors},
	issn = {1529-2401},
	doi = {10.1523/JNEUROSCI.3413-12.2013},
	author = {McClure, Kimberly D and Heberlein, Ulrike}
}
