Human uncoupling protein 3 (UCP3) has two RNA transcripts that arise from t
he differential processing of the same gene product. One encodes the full l
ength protein (UCP3L) while the other encodes a truncated version (UCP3S) l
acking the sixth membrane spanning domain. The roles of the two isoforms ar
e not known, but a mutation that decreases the proportion of UCP3L decrease
s fat oxidation and increases susceptibility to obesity. In the ADP/ATP car
rier, a protein closely related to UCP3, the sixth membrane spanning domain
is required for insertion into the inner membrane. Therefore, defective me
mbrane insertion of UCP3S may account for the different effects of the two
isoforms in vivo. We investigated mitochondrial import of the two UCP3 isof
orms, When epitope-tagged versions of UCP3S and UCP3L were expressed in COS
7 cells, both were inserted into the mitochondrial inner membrane, Translat
ion in vitro followed by incubation with isolated mitochondria showed that
both isoforms were inserted into the inner membrane, however, the insertion
of UCP3S was significantly slower. (C) 2000 Federation of European Biochem
ical Societies.