hct-1 (hippocampal transcript) was detected in a differential screen o
f a rat hippocampal cDNA library. Expression of hct-1 was enriched in
the formation but was also detected in rat liver and kidney, though at
much lower levels; expression was barely detectable in testis, ovary,
and adrenal. In liver, unlike brain, expression was sexually dimorphi
c; hepatic expression was greatly reduced in female rats. In mouse, br
ain expression was widespread, with the highest levels being detected
in corpus callosum; only low levels were detected in liver. Sequence a
nalysis of rat and mouse hct-1 cDNAs revealed extensive homologies wit
h cytochrome P450s (CYPs), a diverse family of heme-binding monooxygen
ases that metabolize a range of substrates including steroids, fatty a
cids, and xenobiotics. Among the CYPs, hct-1 is most similar (39% at t
he amino acid sequence) to cholesterol 7 alpha-hydroxylase (CYP7) and
contains a postulated steroidogenic domain present in other steroid-me
tabolizing CYPs but clearly represents a type of CYP not previously re
ported. Genomic Southern analysis suggests that a single gene correspo
nding to hct-1 is present in mouse, rat, and human. hct-1 is unusual i
n that, unlike all other CYPs described, the primary site of expressio
n is in the brain. Similarity to CYP7 and other steroid-metabolizing C
YPs may argue that hct-1 (CYP7B) plays a role in steroid metabolism in
brain, notable because of the documented ability of brain-derived ste
roids (neurosteroids) to modulate cognitive function in vivo.