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J. Biol. Chem., Vol. 275, Issue 27, 20928-20934, July 7, 2000
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§,
,
From the Nuclear receptors regulate transcription in
direct response to their cognate hormonal ligands. Ligand binding leads
to the dissociation of corepressors and the recruitment of
coactivators. Many of these factors, acting in large complexes, have
emerged as potential chromatin remodelers through intrinsic histone
modifying activities. In addition, other ligand-recruited complexes
appear to act more directly on the transcriptional apparatus. The DRIP complex is a 15-subunit complex required for nuclear receptor transcriptional activation in vitro. It is recruited to the
receptor in response to ligand through specific interactions of one
subunit, DRIP205. We present evidence that DRIP205 interacts with
another member of the steroid receptor subfamily, estrogen receptor
(ER). This interaction occurs in an agonist-stimulated fashion which in
turn is inhibited by several ER antagonists. In vivo, a
fragment of DRIP205 containing only its receptor interacting region
acts to selectively inhibit ER's ability to activate transcription in
response to estradiol. These observations suggest a key role for the
DRIP coactivator complex in estrogen-ER signaling.
Cell Biology Program, Memorial
Sloan-Kettering Cancer Center, Sloan-Kettering Division, Cornell
University, Graduate School of Medical Sciences, New York, New York
10021 and ¶ Wyeth Ayerst Research, Nuclear Receptors Department,
Radnor, Pennsylvania 19087
To whom correspondence should be addressed: Cell Biology
Program, Memorial Sloan-Kettering Cancer Center, Box 470, 1275 York Ave., New York, NY 10021. Tel.: 212-639-2976; Fax: 212-717-3298; l-freedman@ski.mskcc.org.
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