Regulation of circadian rhythm and sleep by miR-375-timeless interaction in Drosophila

FASEB J. 2020 Dec;34(12):16536-16551. doi: 10.1096/fj.202001107R. Epub 2020 Oct 20.

Abstract

MicroRNAs are important coordinators of circadian regulation that mediate the fine-tuning of gene expression. Although many studies have shown the effects of individual miRNAs on the circadian clock, the global functional miRNA-mRNA interaction network involved in the circadian system remains poorly understood. Here, we used CLEAR (Covalent Ligation of Endogenous Argonaute-bound RNAs)-CLIP (Cross-Linking and Immuno-Precipitation) to explore the regulatory functions of miRNAs in the circadian system by comparing the miRNA-mRNA interactions between Drosophila wild-type strain W1118 and a mutant of the key circadian transcriptional regulator Clock (Clkjrk ). This experimental approach unambiguously identified tens of thousands of miRNA-mRNA interactions in both the head and body. The miRNA-mRNA interactome showed dramatic changes in the Clkjrk flies. Particularly, among ~300 miRNA-mRNA circadian relevant interactions, multiple interactions involving core clock genes pdp1, tim, and vri displayed distinct changes as a result of the Clk mutation. Based on the CLEAR-CLIP analysis, we found a novel regulation of the circadian rhythm and sleep by the miR-375-timeless interaction. The results indicated that Clk disruption abolished normal rhythmic expression of miR-375 and the functional regulation occurred in the l-LNv neurons, where miR-375 modulated the circadian rhythm and sleep via targeting timeless. This work provides the first global view of miRNA regulation in the circadian rhythm.

Keywords: miR-375; CLEAR-CLIP; circadian rhythm; miRNAs; sleep.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • CLOCK Proteins / metabolism
  • Circadian Clocks / physiology*
  • Circadian Rhythm / physiology*
  • Drosophila Proteins / metabolism*
  • Drosophila melanogaster / metabolism*
  • Gene Expression / physiology
  • Gene Expression Regulation / physiology
  • Male
  • MicroRNAs / metabolism*
  • Motor Activity / physiology
  • Neurons / metabolism
  • RNA, Messenger / metabolism
  • Sleep / physiology*

Substances

  • Drosophila Proteins
  • MicroRNAs
  • RNA, Messenger
  • CLOCK Proteins