4.7 Article

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

期刊

BRAIN BEHAVIOR AND IMMUNITY
卷 61, 期 -, 页码 127-136

出版社

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.bbi.2016.11.012

关键词

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

资金

  1. University of Missouri-St. Louis College of Arts and Science
  2. University of Missouri Research Board
  3. NIH [NIAMS 1R21AR069266-01A1]

向作者/读者索取更多资源

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. (C) 2016 Elsevier Inc. All rights reserved.

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