E. Hintermann et al., CLONING OF AN ARYLALKYLAMINE N-ACETYLTRANSFERASE (AANAT1) FROM DROSOPHILA-MELANOGASTER EXPRESSED IN THE NERVOUS-SYSTEM AND THE GUT, Proceedings of the National Academy of Sciences of the United Statesof America, 93(22), 1996, pp. 12315-12320
In insects, neurotransmitter catabolism, melatonin precursor formation
, and sclerotization involve arylalkylamine N-acetyltransferase (aaNAT
, EC 2.3.1.87) activity, It is not known if one or multiple aaNAT enzy
mes are responsible for these activities. We recently have purified an
aaNAT from Drosophila melanogaster, Here, we report the cloning of th
e corresponding aaNAT cDNA (aaNAT1) that upon COS cell expression acet
ylates dopamine, tryptamine, and the immediate melatonin precursor ser
otonin. aaNAT1 represents a novel gene family unrelated to known acety
ltransferases, except in two weakly conserved amino acid motifs. In si
tu hybridization studies of aaNAT1 mRNA in embryos reveal hybridizatio
n signals in the brain, the ventral cord, the gut, and probably in oen
ocytes, indicating a broad tissue distribution of aaNAT1 transcripts,
Moreover, in day/night studies we demonstrate a diurnal rhythm of mela
tonin concentration without a clear-cut change in aaNAT1 mRNA levels.
The data suggest that tissue-specific regulation of aaNAT1 may be asso
ciated with different enzymatic functions and do not exclude the possi
bility of additional aaNAT genes.