The mineralocorticoid receptor (MR), a member of the steroid receptor
family, acts as a transcription factor and mediates both aldosterone a
nd cortisol effects. Aldosterone specificity in some tissues results f
rom the inactivation of competing cortisol into cortisone by 11 beta-h
ydroxysteroid dehydrogenase. In other tissues MR and the glucocorticoi
d receptor show overlapping physiological effects or may act together
by forming a heterodimer. An additional MR splice variant (MR+4) has b
een found in different mRNA samples from rat tissues and human white b
lood cells, thereby implying additional modes of MR-regulated effects.
We therefore looked for the presence of these two MR-mRNA isoforms in
human classical aldosterone target tissues and various other tissues.
MR-mRNA was found in all samples investigated, thereby showing the ex
pression of MR to be more abundant than has been observed thus far. In
addition, the MR+4-mRNA variant was also found in all the tissues exa
mined.