Sulfation is an important pathway in the metabolism of estrogens. We r
ecently cloned a human liver estrogen sulfotransferase (EST) cDNA. We
have now determined the structure and chromosomal localization of the
EST gene, STE, as a step toward molecular genetic studies of the regul
ation of EST in humans. STE spans approximately 20 kb and consists of
8 exons, ranging in length from 95 to 181 bp. The locations of most ex
on-intron splice junctions within STE are identical to those found in
a human phenol ST (PST) gene, STM, and in a rat PST gene, In addition,
the locations of five STE introns are also conserved in the human deh
ydroepiandrosterone (DHEA) ST gene, STD. The 5'-flanking region of STE
contains one CCAAT and two TATA sequences. The location of one of the
TATA box elements is in excellent agreement with the site of transcri
ption initiation as determined by 5'-rapid amplification of cDNA ends.
STE was mapped to human chromosome 4q13.1 by fluorescence in situ hyb
ridization, Cloning and structural characterization of STE will now ma
ke it possible to study potential molecular genetic mechanisms involve
d in the regulation of EST in human tissues. (C) 1995 Academic Press,
Inc.