Melatonin synthesis in retina: cAMP-dependent transcriptional regulation of chicken arylalkylamine N-acetyltransferase by a CRE-like sequence and a TTATT repeat motif in the proximal promoter

J Neurochem. 2011 Oct;119(1):6-17. doi: 10.1111/j.1471-4159.2011.07397.x. Epub 2011 Aug 22.

Abstract

Arylalkylamine N-acetyltransferase (AANAT) is the key regulatory enzyme controlling the daily rhythm of melatonin biosynthesis. In chicken retinal photoreceptor cells, Aanat transcription and AANAT activity are regulated in part by cAMP-dependent mechanisms. The purpose of this study was to identify regulatory elements within the chicken Aanat promoter responsible for cAMP-dependent induction. Photoreceptor-enriched retinal cell cultures were transfected with a luciferase reporter construct containing up to 4 kb of 5'-flanking region and the first exon of Aanat. Forskolin treatment stimulated luciferase activity driven by the ∼4 kb promoter construct and by all 5'-deletion constructs except the smallest, Aanat (-217 to +120)luc. Maximal basal and forskolin-stimulated expression levels were generated by the Aanat (-484 to +120)luc construct. This construct lacks a canonical cyclic AMP-response element (CRE), but contains two other potentially important elements in its sequence: an eight times TTATT repeat (TTATT₈) and a CRE-like sequence. Electrophoretic mobility shift assays, luciferase reporter assays, chromatin immunoprecipitation, and siRNA experiments provide evidence that these elements bind c-Fos, JunD, and CREB to enhance basal and forskolin-stimulated Aanat transcription. We propose that the CRE-like sequence and TTATT₈ elements in the 484 bp proximal promoter interact to mediate cAMP-dependent transcriptional regulation of Aanat.

Publication types

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

MeSH terms

  • 5' Flanking Region / genetics
  • Animals
  • Arylalkylamine N-Acetyltransferase / biosynthesis*
  • Arylalkylamine N-Acetyltransferase / genetics
  • Cell Nucleus / metabolism
  • Cells, Cultured
  • Chick Embryo
  • Chromatin Immunoprecipitation
  • Cyclic AMP / physiology*
  • Cyclic AMP Response Element-Binding Protein / physiology*
  • DNA Primers
  • Electrophoretic Mobility Shift Assay
  • Gene Expression Regulation, Enzymologic
  • Luciferases / genetics
  • Melatonin / biosynthesis*
  • Melatonin / genetics
  • Mutagenesis, Site-Directed
  • Promoter Regions, Genetic / genetics
  • Proto-Oncogene Proteins c-fos / biosynthesis
  • Proto-Oncogene Proteins c-jun / biosynthesis
  • RNA, Small Interfering
  • Repetitive Sequences, Nucleic Acid
  • Retina / metabolism*
  • Transfection

Substances

  • Cyclic AMP Response Element-Binding Protein
  • DNA Primers
  • Proto-Oncogene Proteins c-fos
  • Proto-Oncogene Proteins c-jun
  • RNA, Small Interfering
  • Cyclic AMP
  • Luciferases
  • Arylalkylamine N-Acetyltransferase
  • Melatonin