The present study examined the tissue distribution of rat sulfotransfe
rase (SULT) mRNAs to assess the relative contribution of each tissue t
o the process of sulfation. The SULT isoforms examined were male-domin
ant SULTs (SULT1A1, SULT1C1, and SULT1E2), female-dominant SULTs (SULT
20/21, SULT40/41, and SULT60), and the recently cloned, nora sex-depen
dent SULT (SULT1B1). SULTs fall into two distinct classes based on sub
strate preference: phenol SULTs (SULT1A1, SULT1B1, SULT1C1, and SULT1E
2) and hydroxysteroid SULTs (SULT20/21, SULT40/41, and SULT60). The fo
llowing tissues were analyzed for SULT mRNA expression: liver, brain,
lung, heart, intestine, kidney, adrenal, prostate, testes, ovary, uter
us, and spleen by Northern blot analysis with [alpha-P-32]dATP-labeled
oligonucleotide probes specific for individual SULT mRNAs. Tissue exp
ression levels of each SULT were quantified and compared with liver ex
pression by phosphorautoradiographic analysis. Male-dominant SULT expr
ession was observed in many organs, where SULT1A1 was expressed in liv
er, brain, lung, heart, intestine, kidney, adrenal, testes, and spleen
; SULT1C1 expression was observed in liver, kidney, and spleen; and SU
LT1E2 expression was observed only in liver and heart. The female-domi
nant SULTs exhibited a more limited tissue distribution. Expression of
SULT20/21 and SULT60 was observed only in liver and adrenal gland, wh
ereas SULT40/41 expression was observed only in liver. SULT1B1 was exp
ressed to a similar extent in tissues of male and female rats and was
detected in liver, intestine, and kidney. Expression of SULT mRNAs in
liver was much higher than in other tissues, except for SULT1A1, which
exhibited substantial expression in lung, and SULT1B1, which was expr
essed at relatively high levels in intestine. These studies indicate t
hat liver is the most diverse organ with respect to expression of mult
iple SULT enzymes and is therefore the most significant organ involved
in sulfation. in contrast to liver, extrahepatic tissues express spec
ific SULT mRNAs, and this may be important for the physiological role
of each tissue.