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 language | English |
|---|---|
| Pages (from-to) | 189-197 |
| Number of pages | 9 |
| Journal | Molecular Brain Research |
| Volume | 63 |
| Issue number | 1 |
| DOIs | |
| State | Published - 10 Dec 1998 |
Keywords
- C3H/HeJ
- Circadian
- Cryptic splice acceptor site
- Pineal
- Retina
- RNA splicing
Fingerprint
Dive into the research topics of 'Natural melatonin 'knockdown' in C57BL/6J mice: Rare mechanism truncates serotonin N-acetyltransferase'. Together they form a unique fingerprint.Cite this
- APA
- Author
- BIBTEX
- Harvard
- Standard
- RIS
- Vancouver