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Journal of Neuroscience, Vol 5, 903-910, Copyright © 1985 by Society for Neuroscience
Choline acetyltransferase and acetylcholine levels in Drosophila melanogaster: a study using two temperature-sensitive mutants
PM Salvaterra and RE McCaman
Choline acetyltransferase (ChAT, acetyl-CoA-choline-O- acetyltransferase,
EC 2.3.1.6) activity was measured in homogenates prepared from wild type
(Canton S) and two temperature-sensitive presumed ChAT structural gene
mutants (Chats1 and Chats2; originally described by Greenspan, R. (1980) J.
Comp. Physiol. 137: 83-92) of Drosophila melanogaster. Wild type flies
grown at 32 degrees C for 12 or 24 hr showed increased ChAT activity,
whereas Chats1 and Chats2 flies showed a progressive decrease in enzyme
activity at 32 degrees C (restrictive temperature) when compared to flies
reared at 18 degrees C (permissive temperature). Acetylcholine (ACh) and
choline levels were determined in formic acid-acetone extracts of
individual fly heads, and the ACh levels showed the same variation with
time at 32 degrees C as did the ChAT activity. In contrast, choline levels
did not vary in any regular pattern. Acetylcholinesterase (EC 3.1.1.7)
activity did not vary during heat treatment (except for Chatts2 flies held
at 32 degrees C for 24 hr, where a decrease was observed) indicating that
this treatment may be specific for ChAT. We conclude that ChAT activity is
strongly correlated with ACh levels in Drosophila heads and may thus have
an important regulatory role in determining the levels of ACh available for
physiological function. We also report on the preliminary characterization
of ChAT in both Chats mutants and compare the biochemical properties to
those of wild type enzyme. Isoelectric focusing profiles of ChAT from both
Chats mutants revealed enzymes with altered patterns compared to wild type,
indicating that the mutations are most probably in the structural
gene.(ABSTRACT TRUNCATED AT 250 WORDS)
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