NAT1/DAP5/p97 and atypical translational control in the Drosophila Circadian Oscillator

Genetics. 2012 Nov;192(3):943-57. doi: 10.1534/genetics.112.143248. Epub 2012 Aug 17.

Abstract

Circadian rhythms are driven by gene expression feedback loops in metazoans. Based on the success of genetic screens for circadian mutants in Drosophila melanogaster, we undertook a targeted RNAi screen to study the impact of translation control genes on circadian locomotor activity rhythms in flies. Knockdown of vital translation factors in timeless protein-positive circadian neurons caused a range of effects including lethality. Knockdown of the atypical translation factor NAT1 had the strongest effect and lengthened circadian period. It also dramatically reduced PER protein levels in pigment dispersing factor (PDF) neurons. BELLE (BEL) protein was also reduced by the NAT1 knockdown, presumably reflecting a role of NAT1 in belle mRNA translation. belle and NAT1 are also targets of the key circadian transcription factor Clock (CLK). Further evidence for a role of NAT1 is that inhibition of the target of rapamycin (TOR) kinase increased oscillator activity in cultured wings, which is absent under conditions of NAT1 knockdown. Moreover, the per 5'- and 3'-UTRs may function together to facilitate cap-independent translation under conditions of TOR inhibition. We suggest that NAT1 and cap-independent translation are important for per mRNA translation, which is also important for the circadian oscillator. A circadian translation program may be especially important in fly pacemaker cells.

Publication types

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

MeSH terms

  • Animals
  • Biological Clocks / genetics*
  • Brain / metabolism
  • Circadian Rhythm / genetics*
  • Drosophila / genetics*
  • Drosophila / metabolism*
  • Drosophila Proteins / genetics
  • Drosophila Proteins / metabolism*
  • Eukaryotic Initiation Factor-4G / genetics
  • Eukaryotic Initiation Factor-4G / metabolism*
  • Gene Knockdown Techniques
  • Light
  • Neuropeptides / metabolism
  • Period Circadian Proteins / metabolism
  • Protein Biosynthesis*
  • RNA Helicases / metabolism
  • TOR Serine-Threonine Kinases / metabolism

Substances

  • Drosophila Proteins
  • Eukaryotic Initiation Factor-4G
  • NAT1 translation factor, Drosophila
  • Neuropeptides
  • PER protein, Drosophila
  • Period Circadian Proteins
  • pdf protein, Drosophila
  • TOR Serine-Threonine Kinases
  • Bel protein, Drosophila
  • RNA Helicases