Previous studies have shown that the SA gene is expressed at higher le
vels in the kidney of genetically hypertensive rats than in control st
rains and that in hybrid crosses of genetically hypertensive rats and
normotensive controls, markers in or close to the SA gene cosegregate
with blood pressure. The present studies examine the localization of t
he SA gene product in the kidney by semiquantitative reverse transcrip
tion-polymerase chain reaction (RT-PCR). cDNA was prepared from microd
issected nephron segments from Sprague-Dawley (SD) rats, spontaneously
hypertensive rats (SHRs), and Wistar-Kyoto (WKY) rats, and RT-PCR was
performed using specific primers. In all three strains, SA gene mRNA
was found to be abundantly expressed in proximal tubules. SA PCR produ
ct was occasionally detected at approximately 100-fold lower abundance
in glomeruli, while no signal was obtained from the collecting duct,
thick ascending limb of the loop of Henle, or arcuate artery. Within t
he proximal tubule of normotensive rats, distribution of SA mRNA was f
ound to be strain dependent: in SD rats it was expressed at high level
s in the proximal convoluted tubule, whereas in WKY rats it was restri
cted to the proximal straight tubule. In SHRs, SA PCR product was dete
cted along the entire proximal tubule. Induction of hypertension by re
nal artery clamping (two-kidney, one-clamp Goldblatt model) did not al
ter the pattern of expression observed in the SD rat. These results in
dicate that an extension of SA gene expression to the full length of t
he proximal tubule accompanies spontaneous hypertension and that in no
nhypertensive animals the pattern of gene product expression is more r
estricted but shows substantial strain variability.