Acetylcholinesterase, an enzyme essential for the termination of the a
ction of acetylcholine, is encoded by a single gene. Alternative mRNA
processing gives rise to the expression of enzyme forms with three dis
tinct carboxyl-termini. These structural differences govern the cellul
ar disposition of the expressed enzyme but do not influence catalytic
activity. Alternative polyadenylation signals give rise to distinct 3'
non-coding regions which are likely to affect mRNA stability. Alterna
tive splicing also occurs at the 5' end of the gene where two promoter
regions can be identified. Hence, regulation of expression of the gen
e occurs at 3 levels, transcriptional through alternative promoters, t
ranslational by affecting mRNA stability and processing of distinct mR
NAs and post-translationally by giving rise to distinct peptide chains
which are processed differently. Recombinant DNA studies have also be
en extended to modifying protein structure through site-specific mutag
enesis and studying the function of the mutant enzymes.