Literature DB >> 27856350

Achilles is a circadian clock-controlled gene that regulates immune function in Drosophila.

Jiajia Li1, Erin E Terry1, Edith Fejer2, Diana Gamba1, Natalie Hartmann1, Joseph Logsdon1, Daniel Michalski1, Lisa E Rois1, Maria J Scuderi2, Michael Kunst3, Michael E Hughes4.   

Abstract

The circadian clock is a transcriptional/translational feedback loop that drives the rhythmic expression of downstream mRNAs. Termed "clock-controlled genes," these molecular outputs of the circadian clock orchestrate cellular, metabolic, and behavioral rhythms. As part of our on-going work to characterize key upstream regulators of circadian mRNA expression, we have identified a novel clock-controlled gene in Drosophila melanogaster, Achilles (Achl), which is rhythmic at the mRNA level in the brain and which represses expression of antimicrobial peptides in the immune system. Achilles knock-down in neurons dramatically elevates expression of crucial immune response genes, including IM1 (Immune induced molecule 1), Mtk (Metchnikowin), and Drs (Drosomysin). As a result, flies with knocked-down Achilles expression are resistant to bacterial challenges. Meanwhile, no significant change in core clock gene expression and locomotor activity is observed, suggesting that Achilles influences rhythmic mRNA outputs rather than directly regulating the core timekeeping mechanism. Notably, Achilles knock-down in the absence of immune challenge significantly diminishes the fly's overall lifespan, indicating a behavioral or metabolic cost of constitutively activating this pathway. Together, our data demonstrate that (1) Achilles is a novel clock-controlled gene that (2) regulates the immune system, and (3) participates in signaling from neurons to immunological tissues. Copyright Â
© 2016 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Achilles; Antimicrobial peptides; Bacterial infection; CG17386; Circadian clock; Drosophila; Fat body; Gene expression; Genomics; Immunity; RNA-binding protein; RNA-seq

Mesh:

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Year:  2016        PMID: 27856350      PMCID: PMC5316375          DOI: 10.1016/j.bbi.2016.11.012

Source DB:  PubMed          Journal:  Brain Behav Immun        ISSN: 0889-1591            Impact factor:   7.217


  73 in total

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