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Natural melatonin 'knockdown' in C57BL/6J mice: Rare mechanism truncates serotonin N-acetyltransferase

Patrick H. Roseboom, M. a.Aryan Namboodiri, Drazen B. Zimonjic, Nicholas C. Popescu, Ignacio R. Rodriguez, Jonathan A. Gastel, David C. Klein*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

263 Scopus citations

Abstract

Pineal melatonin synthesis (serotonin → N-acetylserotonin → melatonin) is severely compromised in most inbred strains of mice, in many cases because serotonin is not acetylated by serotonin N-acetyltransferase (arylalkylamine N-acetyltransferase, AANAT). We have found that in the C57BL/6J strain, AANAT mRNA encodes a severely truncated AANAT protein, because a pseudo-exon containing a stop codon is spliced in. This is the first identification of a natural mutation which knocks down melatonin synthesis. The decrease in melatonin signaling may have been a selective factor in the development of laboratory strains of mice because melatonin can inhibit reproduction and modify circadian rhythmicity.

Original languageEnglish
Pages (from-to)189-197
Number of pages9
JournalMolecular Brain Research
Volume63
Issue number1
DOIs
StatePublished - 10 Dec 1998

Keywords

  • C3H/HeJ
  • Circadian
  • Cryptic splice acceptor site
  • Pineal
  • Retina
  • RNA splicing

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