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Womens Health Research Institute, Wyeth-Ayerst Research, Radnor, Pennsylvania 19087
Address all correspondence and requests for reprints to: Dr. Heather A. Harris, Womens Health Research Institute, Wyeth-Ayerst Research, 145 King of Prussia Road, Radnor, Pennsylvania 19087. E-mail: harrish{at}war.wyeth.com
Estrogen receptor-ß (ERß) is a recently discovered member of the
steroid hormone superfamily. Because its distribution is distinct from
that of the classical estrogen receptor, and it is expressed in several
nonclassical estrogen target tissues (e.g. prostate and
bladder), its role in mediating the action of estrogen is unclear. One
approach to elucidating the function of this receptor is to identify
genes that it regulates. Using differential display, we profiled the
messenger RNAs regulated by 17ß-estradiol in SAOS-2 and LNCaPLN3
cells overexpressing ERß. Follow-up studies used cells expressing
either ER
or ERß. One gene, metallothionein II, was regulated by
both receptor subtypes in LNCaPLN3 cells, but only by ERß in SAOS-2
cells. Because cycloheximide blocks this response, induction is
probably mediated through regulation of at least one other protein.
Identification of endogenous genes that are regulated differentially by
ER
and ERß will be valuable tools in elucidating the function of
ERß and the mechanisms by which these two receptors regulate
transcription.
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