We report the molecular cloning of a beta3-adrenergic receptor [beta3-
AR] cDNA from human brown adipose tissue. The cDNA-encoded protein is
identical to the previously cloned beta3-AR but with 6 additional amin
o acids at the C-terminus. The C-terminus is shared by the beta3 recep
tors expressed in human neuroblastoma cells [SK-N-MC] [Mol. Pharmacol.
42 (1992) 964 970]. Furthermore, using a polymerase chain reaction st
rategy we have cloned and sequenced the beta3-AR introns. Sequence ana
lysis demonstrates that the human beta3-AR gene comprises at least 3 e
xons and 2 introns and that the most abundant beta3-AR transcripts enc
ode a protein with an exon 3-derived C-terminus. Interestingly, althou
gh a similar organization has been found in rodent genes, the rat beta
3-AR transcripts encode a receptor with an exon 2-derived C-terminus.