Cloning, sequencing and expression of cDNA for a novel subunit of acetylcholine receptor from calf muscle

Abstract

The nicotinic acetylcholine receptor (AChR) from fish electric organ has a subunit structure of α₂βγδ, and this is thought to be also the case for the mammalian skeletal muscle AChR^1–3. By cloning and sequencing the complementary or genomic DNAs, we have previously elucidated the primary structures of all four sub-units of the Torpedo californica electroplax^4–6 and calf muscle AChR^7–10 and of the α- and γ-subunits of the human muscle AChR^7,11; the primary structures of the γ-subunit of the T. californien AChR¹² and the α-subunit of the Torpedo marmorata AChR^13,14 have also been deduced elsewhere. We have now cloned DNA complementary to the calf muscle messenger RNA encoding a novel polypeptide (the ε-subunit) whose deduced amino-acid sequence has features characteristic of the AChR subunits and which shows higher sequence homology with the γ-subunit than with the other subunits. cDNA expression studies indicate that the calf ε-subunit, as well as the calf γ-subunit, can replace the Torpedo γ-subunit to form the functional receptor in combination with the Torpedo α-, β- and δ-subunits.