RRC ID 56566
Author Ri H, Lee J, Sonn JY, Yoo E, Lim C, Choe J.
Title Drosophila CrebB is a Substrate of the Nonsense-Mediated mRNA Decay Pathway that Sustains Circadian Behaviors.
Journal Mol Cells
Abstract Post-transcriptional regulation underlies the circadian control of gene expression and animal behaviors. However, the role of mRNA surveillance via the nonsense-mediated mRNA decay (NMD) pathway in circadian rhythms remains elusive. Here, we report that Drosophila NMD pathway acts in a subset of circadian pacemaker neurons to maintain robust 24 h rhythms of free-running locomotor activity. RNA interference-mediated depletion of key NMD factors in timeless-expressing clock cells decreased the amplitude of circadian locomotor behaviors. Transgenic manipulation of the NMD pathway in clock neurons expressing a neuropeptide PIGMENT-DISPERSING FACTOR (PDF) was sufficient to dampen or lengthen free-running locomotor rhythms. Confocal imaging of a transgenic NMD reporter revealed that arrhythmic Clock mutants exhibited stronger NMD activity in PDF-expressing neurons than wild-type. We further found that hypomorphic mutations in Suppressor with morphogenetic effect on genitalia 5 (Smg5 ) or Smg6 impaired circadian behaviors. These NMD mutants normally developed PDF-expressing clock neurons and displayed daily oscillations in the transcript levels of core clock genes. By contrast, the loss of Smg5 or Smg6 function affected the relative transcript levels of cAMP response element-binding protein B (CrebB ) in an isoform-specific manner. Moreover, the overexpression of a transcriptional repressor form of CrebB rescued free-running locomotor rhythms in Smg5-depleted flies. These data demonstrate that CrebB is a rate-limiting substrate of the genetic NMD pathway important for the behavioral output of circadian clocks in Drosophila.
Volume 42(4)
Pages 301-312
Published 2019-4-30
DOI 10.14348/molcells.2019.2451
PII molcells.2019.2451
PMID 31091556
PMC PMC6530642
MeSH Animals Animals, Genetically Modified CLOCK Proteins / genetics Circadian Clocks* Cyclic AMP Response Element-Binding Protein / metabolism* Drosophila / genetics* Drosophila / metabolism Drosophila Proteins / genetics Drosophila Proteins / metabolism* Endoribonucleases / genetics Endoribonucleases / metabolism Mutation* Neurons / metabolism Neuropeptides / genetics Neuropeptides / metabolism Nonsense Mediated mRNA Decay* Nuclear Proteins / genetics Nuclear Proteins / metabolism RNA Processing, Post-Transcriptional Signal Transduction Trans-Activators / metabolism*
IF 3.533
Times Cited 1
Resource
Drosophila 6369R-1 6369R-3