Brown adipose and muscle tissues can increase energy expenditure via adapti
ve thermogenesis, thereby protecting against obesity. Mouse peroxisome prol
iferator activated receptor gamma coactivator 1 (Pgcl) has been reported to
enhance the expression of uncoupling protein-1, a key mediator of thermoge
nesis in brown adipose tissue (Puigserver et at, 1998, Cell 92, 829-839). W
e report here the characterization of the human PPARGC1 gene. PPARGC1 spans
a genomic region of similar to 67 kb, is composed of 13 exons, and encodes
a 91-kDa protein that exhibits 94% amino acid identity with the mouse orth
olog. mRNA species, transcribed from the TATA-less promoter, are 6.4 and 5.
3 kb in length due to utilization of two polyadenylation signals. Northern
blotting revealed expression of both transcripts in heart, skeletal muscle,
and kidney and to a lesser extent in liver, brain, and pancreas as well as
in the perirenal adipose tissue of a pheochromocytoma patient. PPARGCI was
mapped to chromosome 4p15.1, a region that has been associated with basal
insulin levels in Pima Indians. Hence, PPARGC1 expression might influence i
nsulin sensitivity as well as energy expenditure, thereby contributing to t
he development and pathophysiology of human obesity. (C) 1999 Academic Pres
s.