Abstract

Chloride intracellular channels (CLICs) are a unique family of evolutionarily conserved metamorphic proteins, switching between stable conformations based on redox conditions. CLICs have been implicated in a wide variety biological processes including ion channel activity, apoptosis, membrane trafficking, and enzymatic oxidoreductase activity. Understanding the molecular mechanisms by which CLICs engage in these activities is an area of active research. Here, the sole Drosophila melanogaster ortholog, Clic, was targeted for RNAi knockdown to identify genes and biological processes associated with Clic expression. Clic knockdown had a substantial impact on global transcription, altering expression of over 7% of transcribed Drosophila genes. Overrepresentation analysis of differentially expressed genes identified enrichment of Gene Ontology terms including Cytoplasmic Translation, Oxidation-Reduction Process, Heme Binding, Membrane, Cell Junction, and Nucleolus. The top term, Cytoplasmic Translation, was enriched almost exclusively with downregulated genes. Drosophila Clic and vertebrate ortholog Clic4 have previously been tied to ethanol sensitivity and ethanol-regulated expression. Clic knockdown-responsive genes from the present study were found to overlap significantly with gene sets from 4 independently published studies related to ethanol exposure and sensitivity in Drosophila. Bioinformatic analysis of genes shared between these studies revealed an enrichment of genes related to amino acid metabolism, protein processing, oxidation-reduction processes, and lipid particles among others. To determine whether the modulation of ethanol sensitivity by Clic may be related to co-regulated oxidation-reduction processes, we evaluated the effect of hyperoxia on ethanol sedation in Clic knockdown flies. Consistent with previous findings, Clic knockdown reduced acute ethanol sedation sensitivity in flies housed under normoxia. However, this effect was reversed by exposure to hyperoxia, suggesting a common set of molecular-genetic mechanism may modulate each of these processes. This study suggests that Drosophila Clic has a major influence on regulation of oxidative stress signaling and that this function overlaps with the molecular mechanisms of acute ethanol sensitivity in the fly.

Highlights

  • Chloride intracellular channels (CLICs) are a family of evolutionarily conserved proteins with unique metamorphic properties and a host of highly diverse, yet poorly understood biological functions

  • Our findings provide validation for published roles for CLICs, identify potentially novel functions and genetic interactions that shed light on the nature of chloride intracellular channel biology, and show a remarkable conservation of transcriptome responses to Clic knockdown, genes involved in oxidative stress and molecular mechanisms relating to ethanol sedation sensitivity in Drosophila

  • To better understand the mechanisms of Clic modulation of ethanol behaviors, we sought to identify genes dysregulated by Clic knockdown

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Summary

Introduction

Chloride intracellular channels (CLICs) are a family of evolutionarily conserved proteins with unique metamorphic properties and a host of highly diverse, yet poorly understood biological functions. The biological functions of CLICs have been difficult to ascertain, but insight has been gained through knockout models in mice and C. elegans. Work in knockout models has been complemented by in vitro studies and the overall list of functions associated with CLICs includes roles in ion channel activity [6,7,8], membrane trafficking [9, 10], apoptosis [11, 12], TGF-beta signaling [5, 13, 14], tubulogenesis [2, 3, 9], innate immunity [15, 16], and oxidoreductase enzymatic activity [17] among others. Little progress has been made in identifying the molecular mechanisms by which CLICs engage in these diverse biological processes and much remains to be elucidated

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