Isolation and characterization of full-length cDNA clones coding for cholinesterase from fetal human tissues.

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Abstract
To study the primary structure and regulation of human cholinesterases, oliogodeoxynucleotide probes were prepared according to a consensus peptide sequence present in the active site of both human serum pseudocholinesterase (BtChoEase; EC 3.1.18) and Torpedo electric organ "true" acetylcholinesterase (AcchoEase; EC 3.1.1.7). Using these probes, we isolated several cDNA clones from .lambda.gt10 libraries of fetal brain and liver origins. These include 2.4-kilobase cDNA clones that code for a polypeptide containing a putative signal peptide and the N-terminal, active site, and C-terminal peptides of human BtChoEase, suggesting that they code either for BtChoEase itself or for a very similar but distinct fetal form of chollinesterase. In RNA blots of poly(A)+ RNA from the cholinesterase-producing fetal brain and liver these cDNAs hybridized with a single 2.5-kilobase band. Blot hybridization to human genomic DNA revealed that these fetal BtChoEase cDNA clones hybridize with DNA fragments of the total length of 17.5 kilobases, and signal intensities indicated that these sequences are not present in many copies. Both the cDNA-encoded protein and its nucleotide sequence display striking homology to parallel sequences published for Torpedo AcChoEase. These findings demonstrate extensive homologies between the fetal BtChoEase encoded by these clones and other cholinesterases of various forms and species.