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J. Biol. Chem., Vol. 277, Issue 2, 1229-1234, January 11, 2002
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,
From the Department of Life Science, Pohang University of Science
and Technology, Pohang 790-784 and the Department of Biochemistry,
College of Medicine, University of Ulsan, Seoul 138-736, Korea
Transcriptional coactivators either bridge
transcription factors and the components of the basal transcription
apparatus and/or remodel the chromatin structures. We isolated a novel
nuclear protein based on its interaction with the recently described
general coactivator activating signal cointegrator-2 (ASC-2). This
protein CAPER (for coactivator of activating protein-1
(AP-1) and estrogen receptors (ERs))
selectively bound, among the many transcription factors we tested, the
AP-1 component c-Jun and the estradiol-bound ligand binding
domains of ER
and ER
. Interestingly, CAPER exhibited a cryptic
autonomous transactivation function that becomes activated only in the
presence of estradiol-bound ER. In cotransfections, CAPER
stimulated transactivation by ER
, ER
, and AP-1. Thus, CAPER may
represent a more selective transcriptional coactivator molecule that
plays a pivotal role for the function of AP-1 and ERs in
vivo in conjunction with the general coactivator ASC-2.
The nucleotide sequence(s) reported in this paper has been submitted to the GenBankTM/EBI Data Bank with accession number AY061882.
Current address: Dept. of Molecular Biology, Massachusetts General
Hospital, Boston, MA 02114.
§
To whom correspondence should be addressed: Dept. of Life Science,
Pohang University of Science and Technology, Pohang 790-784, Korea.
Tel.: 82-54-279-2129; Fax: 82-54-279-8374; E-mail
jaewoon@postech.ac.kr.
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