Rhythmic control of AANAT translation by hnRNP Q in circadian melatonin production

Genes Dev. 2007 Apr 1;21(7):797-810. doi: 10.1101/gad.1519507.

Abstract

The circadian rhythm of pineal melatonin requires the nocturnal increment of serotonin N-acetyltransferase (arylalkylamine N-acetyltransferase [AANAT]) protein. To date, only limited information is available in the critical issue of how AANAT protein expression is up-regulated exclusively at night regardless of its species-specific mRNA profiles. Here we show that the circadian timing of AANAT protein expression is regulated by rhythmic translation of AANAT mRNA. This rhythmic control is mediated by both a highly conserved IRES (internal ribosome entry site) element within the AANAT 5' untranslated region and its partner hnRNP Q (heterogeneous nuclear ribonucleoprotein Q) with a peak in the middle of the night. Consistent with the enhancing role of hnRNP Q in AANAT IRES activities, knockdown of the hnRNP Q level elicited a dramatic decrease of peak amplitude in the AANAT protein profile parallel to reduced melatonin production in pinealocytes. This translational regulation of AANAT mRNA provides a novel aspect for achieving the circadian rhythmicity of vertebrate melatonin.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 5' Untranslated Regions / metabolism
  • Animals
  • Arylalkylamine N-Acetyltransferase / genetics*
  • Arylalkylamine N-Acetyltransferase / metabolism
  • Base Sequence
  • Circadian Rhythm / physiology*
  • Heterogeneous-Nuclear Ribonucleoproteins / metabolism*
  • Humans
  • Melatonin / biosynthesis*
  • Models, Biological
  • Models, Genetic
  • Molecular Sequence Data
  • Pineal Gland / metabolism
  • Protein Biosynthesis*
  • RNA, Messenger / metabolism
  • Rats
  • Sheep

Substances

  • 5' Untranslated Regions
  • Heterogeneous-Nuclear Ribonucleoproteins
  • RNA, Messenger
  • Aanat protein, rat
  • Arylalkylamine N-Acetyltransferase
  • Melatonin