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Metabolic Research Unit (P.W., P.N., J.S., C.A., W.-J.F.,
M.P.N., P.J.K.) University of California School of
Medicine San Francisco, California 94143-0540
Department
of Pathology (D.C., S.-M.H., S.S., M.R.S.) University of Southern
California Los Angeles, California 90033
Department of
Physiology and Biophysics (E.M., B.S.K.) University of Illinois
Urbana, Illinois 61801
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ABSTRACT |
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 TOP ABSTRACT INTRODUCTIONRESULTSDISCUSSIONMATERIALS AND METHODSREFERENCES |
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contains two transactivation
functions, a weak constitutive activation function (AF-1) and a
hormone-dependent activation function (AF-2). AF-2 works by recruiting
a large coactivator complex, composed of one or more p160s,
CREB-binding protein (CBP)/p300, and P/CAF (p300 and CBP-associated
factor), via direct contacts with the p160s. We report here that
independent AF-1 activity also requires p160 contacts. Unlike AF-2,
which binds signature NR boxes in the center of the p160 molecule, AF-1
binds to sequences near the p160 C terminus. We propose that the
ability of AF-1 and AF-2 to interact with separate surfaces of the same
coactivator is important for the ability of these transactivation
functions to synergize. |
INTRODUCTION |
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TOPABSTRACTINTRODUCTIONRESULTSDISCUSSIONMATERIALS AND METHODSREFERENCES |
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(hereafter ER) and ß (ERß) (1, 2, 3). Both estrogen receptors (ERs)
are members of the nuclear receptor family of conditional transcription
factors (4, 5). In the absence of estrogen, the ERs are held in the
nucleus in a complex with molecular chaperonins, such as HSP90. Upon
estrogen binding, the receptors dissociate from the heat shock protein
(HSP) complex and bind, as homodimers or heterodimers (6, 7), to
a specific estrogen response element (ERE). From this location on DNA,
the receptor enhances transcription from the nearby promoter.
Transactivation is best understood within the context of the
-receptor. It is mediated by two activation functions, a weak
constitutive activation function, AF-1, that lies within the ER
N-terminal (AB) domain and a stronger estrogen-dependent activation
function, AF-2, that lies within the ER ligand-binding domain (LBD)
(8, 9, 10, 11, 12, 13, 14). Together, AF-1 and AF-2 synergize strongly to give the final
overall level of estrogen activation. The ER transactivation functions
are believed to work by binding coactivators and bringing them to the
promoter (15, 16, 17, 18). The AF-2 surface consists of a cluster of residues
from helices 3, 5, and 12 (13, 19), that form a hydrophobic patch on
the surface of the liganded LBD (19A ). This hydrophobic patch
binds a family of related proteins called the p160s, which include
GRIP1/TIF2 (20, 21, 22), SRC-1 (23), and RAC3/p/CIP/ACTR/AIB1
(24, 25, 26, 27). In each case, AF-2 recognizes a specific signature motif
(LXXLL), termed the NR box, that is found repeated throughout the p160s
(22, 25, 28, 29, 30), and also within proteins that act as AF-2 repressors,
such as RIP140 (28, 31) and TIF1 (32). GRIP1, for example, and its
human homolog TIF2, contain three separate NR boxes (I, II, and
III, respectively), of which NR boxes II and III are the most
important for ER binding (22, 29). The p160s, in turn, interact with
other coactivator proteins, including CREB-binding protein
(CBP)/p300 (22, 25, 33, 34) and p300 and CBP-associated factor
(P/CAF) (26, 35, 36). Together, this large coactivator complex,
whose subunits possess both histone acetyl-transferase activity (26, 35, 37, 38, 39) and the capacity to bind the basal transcription machinery
(40, 41), is responsible for the ability of AF-2 to stimulate gene
expression.
ER-AF-1, by contrast, is poorly understood. AF-1 usually displays little independent activity and serves only to synergize with AF-2 (10, 12, 14). For unknown reasons, however, AF-1 can also show strong independent activity in some cell types and on some promoters (12). Residues that are important for AF-1 activity are dispersed throughout a large region of the AB domain between amino acid 41 and amino acids 120–150, depending upon the cell type (13, 42, 43). Within this region, motifs that contribute to AF-1-independent activity (amino acids 41–64, hereafter Box 1) and synergism with the LBD (amino acids 87–108, hereafter Box 2) have been identified (44). AF-1 is also strong under conditions of mitogen-activated protein (MAP) kinase pathway stimulation (45, 46, 47, 48). Several serine residues (S104, S106, S118) that are phosphorylated by MAP kinases, or cyclin-dependent kinases (49), have been identified, with the latter accounting for more than 90% of total ER phosphorylation (45, 46, 50). Each phosphorylated serine contributes to overall AF-1 activity (45, 46). Despite all this information, the AF-1 protein target or targets remain unknown. Furthermore, the reasons why AF-1 synergizes with AF-2 in some contexts, yet works independently in others, are also unknown.
While the exact nature of the prospective AF-1 coactivator complex is poorly defined, several lines of evidence suggest that it shares features with the AF-2 coactivator complex. First, AF-1 can mask weak mutations in AF-2, suggesting that AF-1 can compensate for reduced p160 recruitment (13). Second, AF-1 and AF-2 squelch each others activity, suggesting that they compete for common limiting target molecules (51). Third, the transcriptional activity of isolated AF-1 can be enhanced by introducing the free ER-LBD into the same cells (52). This activity requires that the LBD be liganded to estrogen and possesses an intact AF-2 surface. Furthermore, enhancement of AF-1 activity by the free LBD is potentiated by exogenous SRC-1 (53). Thus, the free LBD utilizes the AF-2 surface and p160 contacts to participate in the AF-1 coactivator complex.
In this paper, we ask whether AF-1 and AF-2 might indeed bind a similar complement of coactivator proteins. We find that overexpression of p160 proteins, especially GRIP1, increases the transcriptional activity of AF-1. Furthermore, AF-1 interacts with sequences near the GRIP1 C terminus, and this region is needed for the ability of GRIP1 to potentiate AF-1. We propose that p160s are a direct target for both AF-1 and AF-2.
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RESULTS |
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TOPABSTRACTINTRODUCTIONRESULTSDISCUSSIONMATERIALS AND METHODSREFERENCES |
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In the absence of exogenous GRIP1, wild-type ER elicited a strong
estrogen response, but no tamoxifen response, from the
ERE-coll-CAT promoter (Fig. 1A
). This is
consistent with previous observations that show that AF-1 has little
independent activity at classical EREs in Hela cells (10, 12, 55). In
the presence of exogenous GRIP1, ER gave enhanced estrogen response but
also gave significant activity both in the presence of tamoxifen and
absence of ligand. The ability of GRIP1 to enhance the activity of
tamoxifen-liganded ER was more clearly seen when we used an ER variant
(ER-V400). This ER variant binds more tightly to the HSP complex than
its wild-type counterpart and therefore lacks most of the spontaneous
ligand-independent activity that ER usually displays in tissue
culture (56, 57). Here, GRIP1 potentiated the estrogen response of
ER-V400 and also elicited a large increase in tamoxifen response
without the corresponding increase in basal activity. The tamoxifen
response of ER-V400 was dependent upon the amounts of transfected GRIP1
and approached 40% of overall estrogen response at high amounts of
GRIP1 (Fig. 1B). Several alternate ERE-responsive promoters also showed
enhanced tamoxifen response in the presence of GRIP1 (Fig. 1C). We
conclude that GRIP1 enhances the transcriptional activity of tamoxifen
and estrogen-liganded ER.
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). We asked whether GRIP1 would enhance the
activity of mouse ERs (mORs) with either a truncation of the AB
domain that eliminates AF-1 (mOR
AF-1), a double-point mutation that
eliminates AF-2 (mORmAF-2), or both (mORAF-1/mAF-2) (13). In the
absence of exogenous GRIP1, wild-type mOR elicited a strong estrogen
response from the ERE-coll-CAT promoter. This response was reduced 50%
by the AF-1 deletion and eliminated by the AF-2 mutation, consistent
with the idea that estrogen response in the absence of GRIP1
predominantly reflects AF-2 activity. In the presence of GRIP1,
wild-type mOR gave enhanced estrogen response and significant activity
both in the presence of tamoxifen and absence of ligand, just as did
the human ER. The AF-1 deletion (mORAF-1) retained strong activity
in the presence of estrogen and absence of ligand, but showed no
activity in the presence of tamoxifen. In contrast, the AF-2 mutant
(mORmAF-2) gave strong tamoxifen and estrogen responses, but gave no
activity in the absence of ligand. The double mutant (mORAF-1/mAF-2)
showed no activity under any conditions. Thus, the spontaneous
ligand-independent activity that is obtained in the presence of
exogenous GRIP1 requires AF-2, and not AF-1. We speculate that this
AF-2 dependent, ligand-independent, activity reflects stabilization of
an ER-LBD conformation that resembles that of the estrogen-liganded
receptor by exogenous GRIP1. We also conclude that GRIP1 enhances the
activity of the tamoxifen-liganded ER by enhancing the activity of
AF-1 and not by enhancing the activity of AF-2.
p160s and p160-Associated Proteins Enhance AF-1 Activity
We next asked whether other coactivators would
also enhance AF-1 activity. The p160 protein RAC3 enhanced both
estrogen and tamoxifen response at an ERE, and SRC-1a showed similar
but weaker activity (Fig. 2A). This
weak activity of SRC-1a is consistent with previous observations that
show that this coactivator possesses little activity in HeLa cells
(58), perhaps because SRC-1a contains an inhibitory function within its
C-terminal domain (30). The AF-2 repressor RIP140 failed to enhance
tamoxifen response. Of the p160-associated proteins, CBP and p300
enhanced estrogen and tamoxifen induction, especially in combination
with GRIP1 (Fig. 2B). P/CAF only weakly enhanced tamoxifen activation
(data not shown).
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). In accordance with their effects on tamoxifen-liganded ER,
GRIP1, RAC3, and SRC-1a each enhanced AF-1-dependent transcription from
a GAL4-responsive reporter gene. CBP, p300, and, to a lesser extent,
P/CAF enhanced the transcriptional activity of AF-1. As expected, each
of the coactivators also enhanced the estrogen-dependent activity of a
GAL4-LBD fusion protein. Thus, the p160s and p300/CBP, and perhaps
P/CAF, are involved in transactivation by both AF-1 and AF-2.
An Extended Region of AF-1 Is Required for GRIP1 Action
We next examined which region of AF-1 was needed for GRIP1 action.
Three subregions of the AB domain have previously been implicated in
AF-1 activity (see Fig. 3). Box 1 (amino
acids 41–64) is needed for tamoxifen activation in MDA-231 breast
cells (44). Box 2 (amino acids 87–108) is required for synergism with
AF-2 in the same cell type. Sequences surrounding the main
phosphorylated serine residue at position 118 [kinase target region
(KTR), amino acids 108–129], also contribute to AF-1 activity (43).
To test whether these subregions were needed for GRIP1 action, we
transfected mutant human ERs into HeLa cells and assessed their ability
to activate ERE-dependent transcription in the presence or absence of
GRIP1 (Fig. 3A). In each case, the ERs contained mutations within the
AB domain (amino acids 1–184), but retained an intact DBD and LBD. For
simplicity, we compared the activity of mutant and wild-type ERs in the
absence or presence of GRIP1 (see Fig. 1A) and set activity of
wild-type ER at 100%.
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, first column). Tamoxifen response in the presence of
GRIP1 also required an extended region of the AB domain, but especially
sequences in and around box 1 (Fig. 3A, second column). ERs lacking
sequences upstream of amino acid 41 (n21, n41) showed normal, or
enhanced, tamoxifen response, but an ER with an N-terminal deletion
that eliminated box 1 (n87) showed markedly reduced tamoxifen response.
ERs lacking box 1 and box 2 (n101, n109), or all three subregions
(n117), gave further stepwise reductions in tamoxifen response. ERs
lacking sequences downstream of amino acid 129 (n50/141c; 129–178)
showed modestly enhanced tamoxifen response, but ERs with further
C-terminal deletions that eliminate the KTR (114–178), or both the
KTR and box 2 (93–178, 80–145), again showed reduced tamoxifen
activation. Finally, an ER specifically lacking box 1 (41–64)
showed markedly reduced tamoxifen activation, and an ER specifically
lacking box 2 (87–108) showed a more modest reduction in tamoxifen
activation. Thus, GRIP1 action requires each of the three AF-1
subregions and, especially, sequences within box 1.
We then specifically addressed the role of the AF-1 phosphorylation
sites. An ER with an alanine substitution at serine 118 (S118A)
actually showed enhanced tamoxifen activation in the presence of GRIP1
(Fig. 3A). Similarly, introduction of alanine residues at each MAP
kinase target serine (S104, S106, S118) also enhanced GRIP1 activation
of a GAL4-AB fusion protein (Fig. 3B). Thus, GRIP1 action at AF-1 is
independent of the phosphorylation sites.
Next, we compared the effect of GRIP1 on the ER AB-DBD region (AB-DBD),
which only contains AF-1, with a similar ER truncation that contained
an in- frame insertion of the VP16 activation function, just downstream
of box 1 (V281C, Fig. 3C) (55, 59). As expected, GRIP1 enhanced the
weak AF-1 activity that was obtained with the AB-DBD truncation. In
contrast, GRIP1 had no effect on the stronger activity that was
obtained with the VP16-ER fusion protein. Thus, insertion of a
heterologous transactivation function into the AB domain abolishes the
effect of GRIP1, supporting the notion that integrity of the proximal
part of AF-1 (box 1) is essential for GRIP1 action. Together, our
results show that GRIP1 enhancement of AF-1 activity requires an
extended region of the AB domain and, especially, sequences in and
around box 1.
ER AF-1 Binds p160s
We then asked whether the AB domain binds p160s (Fig. 4A). In vitro translated GRIP1
and SRC-1a bound to both the AB domain and the ER-LBD in a
glutathione-S-transferase (GST) pull-down assay. Over the
course of this study, the bacterially expressed AB domain retained
about 5–20% of the amounts of GRIP1 and SRC-1a that were retained by
equimolar amounts of bacterially expressed LBD. We were unable to
demonstrate binding of the AB domain to CBP (data not shown). We
conclude that the AB domain, like the LBD, binds p160s.
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). An AB domain fusion protein with an N-terminal
deletion to amino acid 37 (38–161) bound GRIP1, but AB domains with
larger N-terminal deletions (55–161; 67–184; 82–161) failed to bind
GRIP1. Two AB fusion proteins with C-terminal deletions (1–145;
1–116) each bound GRIP1 efficiently. Indeed, the latter showed
enhanced binding relative to the native AB domain. An AB fusion protein
with a further deletion (5–90) retained some, albeit reduced, GRIP1
binding, but two portions of the AB domain that overlap sequences 5–90
(1–67 or 55–90) failed to bind GRIP1. Similar results were obtained
with SRC-1a (data not shown). Thus, an extended region of the AB domain
(amino acids 38–116), and especially sequences between amino acids
38–55 and upstream of amino acid 90, were needed to bind p160s. We
conclude that both GRIP1 enhancement of AF-1 activity (Fig. 3A, second
column), and GRIP1 binding (Fig. 4), require a similar region of the AB
domain, and, especially, sequences in and around box 1. This suggests
that AF-1, like AF-2, works by binding p160 proteins.
AF-1 Binds the GRIP C Terminus
We next asked how AF-1 recognized GRIP1 (Fig. 5A). Competition experiments revealed
that a specific peptide that was homologous to GRIP1 NR box III
blocked GRIP1 binding to the LBD but failed to block GRIP1 binding to
the AB domain, or to the p160-binding region of CBP (35) (Fig. 5B).
Similar results were also obtained with a peptide homologous to NR box
II (data not shown), or when SRC-1a was substituted for GRIP1
and tested with either peptide (data not shown). Thus, the AB domain
recognizes a region of GRIP1 and SRC-1a that is distinct from the NR
boxes.
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). The
AB domain failed to bind GRIP1 truncations lacking amino acids beyond
positions 400, 765, 920, or 1121, respectively, but did bind a GRIP1
fragment containing amino acids 920-1291 and, more weakly, to a
fragment containing amino acids 1282–1462. In contrast, the LBD bound
all C-terminal truncations that contained intact NR boxes (1–765;
1–920; 1–1121), but failed to bind either C-terminal GRIP1 fragment.
As predicted, the AB domain bound to a GRIP1 NR box mutant (boxes II
and III mutated) efficiently, and the LBD bound this molecule
only weakly. Experiments using GST-GRIP1 fragments also indicated that
GRIP1 sequences downstream of amino acid 1121, and especially sequences
1121–1282, were needed for ER binding (data not shown). These results
confirm that AF-1 recognizes GRIP1 at a site that, most likely, lies
between amino acids 1121 and 1462 and is distinct from the NR box
cluster. Amino acids 1121–1282, which contribute most to AF-1 binding,
overlap a glutamine rich (Q-rich) domain that is conserved throughout
the p160 family (26).
We then confirmed the location of the putative GRIP1 AB domain-binding
site in a yeast two-hybrid system (Fig. 5D). A GAL4-AB fusion protein
weakly enhanced transcription of a GAL4-responsive
ß-galactosidase gene in yeast, relative to the levels of
transcription obtained with the GAL4-DBD alone (data not shown). This
is consistent with previous studies indicating AF-1 is weakly active in
yeast cells (12). ER-AF-1 activity was unaffected by coexpression of
the GAL4 acid activation domain (GAL-AD), but was enhanced by
coexpression of GAL4-AD/full-length GRIP1 or SRC-1a fusion proteins. A
GAL-AD/GRIP1 fusion protein, containing C-terminal amino acids
1121–1462, also enhanced AF-1 activity. In contrast, a GAL-AD/GRIP1
fusion protein containing amino acids 730-1121 did not enhance AF-1
activity. Similarly, GAL-AD fusions to GRIP1 amino acids 563-1121 and
1–766 also failed to enhance AF-1 activity (data not shown). We stress
that the GAL-AD/GRIP1 fusions containing GRIP1 fragments 730-1121 (20),
563-1121, and 1–766 (data not shown) all strongly enhanced the
activity of a GAL-ER-LBD fusion protein in yeast, in agreement with the
fact that each of these fragments contains NR boxes, and confirming
that these fragments are efficiently expressed in yeast cells. Thus,
GRIP1 (and SRC-1a) target the GAL4-AD to the AB domain in yeast, and
this activity is specifically recapitulated by the GRIP1 C terminus.
Furthermore, both the GST pull-down and yeast two-hybrid assays
indicate that the C-terminal region of GRIP1 is the only region that
interacts with the ER-AB domain in these systems.
AF-1 Function Requires the GRIP1 C Terminus
We next tested whether the GRIP1 C terminus was needed for AF-1
activity in mammalian cells. We coexpressed GAL4-AB or GAL4-LBD fusion
proteins with either wild-type GRIP1, a GRIP1 truncation that cannot
bind AF-1 (GRIP-1121C), or a GRIP1 molecule with NR box mutations
(NR box mutant) (Fig. 6A). The GRIP1
truncation, GRIP-1121C, was completely deficient for AF-1
enhancement, but showed increased AF-2 enhancement relative to
wild-type GRIP1. In contrast, the GRIP1 NR box mutant strongly enhanced
AF-1 activity, but failed to enhance AF-2 activity. Thus, GRIP1 needs
an intact C terminus to enhance AF-1, but this region is dispensable
for GRIP1 enhancement of AF-2. Furthermore, NR boxes II and III
are not needed for GRIP1 enhancement of AF-1 activity.
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1121C) would affect the
activity of full-length ER (Fig. 6B). For these experiments we used a
promoter that shows some tamoxifen activation in the absence of
exogenous p160s (ERE-II-LUC; Fig. 6B, inset). As expected,
GRIP-1121C enhanced the action of the estrogen-liganded ER at the
ERE-II-LUC promoter, although this response was somewhat lower than
that obtained with wild-type GRIP1. In contrast, GRIP-1121C
eliminated the tamoxifen response that was seen in the absence of
exogenous p160s (see inset). A combination of wild-type
GRIP1 and GRIP-1121C gave increased estrogen response relative to
the responses obtained with wild-type GRIP1 cotransfected with empty
expression vector. [Note that this enhanced estrogen response occurs
because wild-type GRIP1 and the GRIP-1121C truncation both activate
isolated AF-2; therefore, this transfection contains more coactivator
protein that is capable of activating AF-2 than the transfection
containing wild-type GRIP1 alone]. Nonetheless, the tamoxifen response
that was obtained with this combination of coactivators was
significantly reduced relative to wild-type GRIP1 alone, showing that
the GRIP-1121C truncation also inhibited the enhanced tamoxifen
response that was obtained in the presence of exogenous GRIP1. We
conclude that the GRIP1 C terminus is needed for enhancement of AF-1
activity and that GRIP-1121C acts as a dominant negative for
tamoxifen response. Because GRIP-1121C is weakened in its ability to
enhance estrogen response in the presence of full-length ER, yet
strengthened in its ability to enhance isolated AF-2, we also suggest
that the GRIP1 C terminus is needed for AF-1/AF-2 synergism.
GRIP1 Is a Weak Activator of ERß AF-1
Previous observations have suggested that ERß, unlike ER(),
shows little activity in the presence of tamoxifen (60, 61). We
therefore examined the role of p160s in ERß function. Wild-type GRIP1
strongly enhanced the activity of unliganded and estrogen-liganded
ERß (Fig. 7A), consistent with similar
results that were obtained with SRC-1 (60), but only weakly increased
the activity of tamoxifen-liganded ERß. In parallel, GRIP1 markedly
increased the activity of tamoxifen-liganded ER() and failed to
affect the activity of an ER truncation lacking of the AB domain
(ERAB). Thus, ERß lacks an efficient AF-1 activity that responds
to GRIP1.
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). A GRIP1 fragment overlapping the
NR boxes (563–1121) bound ERß, but only in the presence of estrogen
and not tamoxifen. In contrast, a GRIP1 C-terminal fragment
(1121–1462) bound weakly to ERß but strongly to the ER() control.
As expected, ERAB also showed markedly reduced binding to this
C-terminal fragment (data not shown). Thus, the strength of the
interaction of the C terminus of GRIP1 with the two isoforms of ER
parallels the ability of GRIP1 to potentiate the activity of either
tamoxifen-liganded ERß or ER(). This result further underlines the
importance of the interactions between the ER() AB domain and the
GRIP1 C terminus. |
DISCUSSION |
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TOPABSTRACTINTRODUCTIONRESULTSDISCUSSIONMATERIALS AND METHODSREFERENCES |
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AF-1 function. We find that AF-1 activity, in the context of
tamoxifen-liganded ER or the isolated AB domain, is strongly enhanced
by overexpression of p160s and CBP/p300 and, somewhat weakly, by
overexpression of P/CAF. We find that the AB domain binds GRIP1 and
SRC-1a. Furthermore, a similar extended region of the AB domain is
required for GRIP1 potentiation of AF-1 activity in vivo and
for GRIP1 binding in vitro. We were also able to identify a
GRIP1 truncation that does not bind the AB domain and acts as a
specific dominant negative for tamoxifen-liganded ER, either in the
absence of exogenous p160s or the presence of overexpressed GRIP1. We
therefore propose that AF-1 action requires a p160/p300 complex and
that direct contacts with p160s are essential for recruitment of this
complex. Our study complements a recently published study which shows
that microinjection of anti-p160 or anti-CBP antibodies block tamoxifen
response in cells (HepG2) where AF-1 activity is high (62).
GRIP1 strongly enhances independent AF-1 activity. In the absence of
GRIP1, however, AF-1 largely serves to synergize with AF-2. We suggest
that AF-1/p160 interactions may also play a role in AF-1/AF-2
synergism. ER N-terminal deletions have similar effects on estrogen
response in the absence of GRIP1 and tamoxifen activation in the
presence of GRIP1. Likewise, box 1 (amino acids 41–64), which is
responsible for tamoxifen activation in breast cells (44), is needed
both for AF-1/AF-2 synergism in the absence of GRIP1 and tamoxifen
activation in the presence of GRIP1. Finally, the GRIP1 truncation
(1121C), which does not bind the AB domain, does not potentiate the
activity of estrogen-liganded ER as strongly as wild-type GRIP1, yet
potentiates the activity of isolated AF-2 better than wild-type GRIP1
(Fig. 6). Thus, GRIP-1121C is defective for potentiation of
independent AF-1 activity and AF-1/AF-2 synergism. Together, these
results suggest that the ability of AF-1 and AF-2 to bind separate
surfaces of the same coactivator is important for the ability of these
transactivation functions to synergize.
While we, and others (62), have readily detected protein-protein interactions between ER AF-1 and p160s, two other groups failed to do so. One set of authors failed to see interaction between AF-1 and TIF-2 in a yeast two-hybrid system (22). In that study, rather than full-length TIF-2 fused to the GAL-AD, the authors used a TIF-2 fragment spanning amino acids 624-1288. Another set of authors failed to see interactions between mouse AF-1 and SRC-1 in GST pull-downs (30). While we have no explanation for this discrepancy, we note that the second set of authors did see that a C-terminal fragment of SRC-1, which overlaps the Q-rich domain, bound full-length mouse ER in an AF-2-independent manner. We speculate that this interaction may be similar to the one that we have described in this paper.
The idea that both AF-1 and AF-2 directly bind p160s may account for several unexplained observations. First, AF-1 can compensate for weak AF-2 mutations (13). This could be explained if AF-1/p160 contacts assist weakened AF-2 interactions with p160s. Indeed, the ability of AF-1 to mask AF-2 mutations is lost in AB domain truncations that, we now know, lack the ability to bind GRIP1. Second, AF-1 and AF-2 squelch each others activity (51). This could be explained if AF-1 and AF-2 were both able to bind and to sequester limiting target p160s molecules. Third, free ER-LBD can enhance the activity of isolated AF-1 in trans (53). This could be explained if the LBD binds the NR boxes of p160s that, themselves, are bound to AF-1. Fourth, it has been previously shown that SRC-1 enhances the ability of tamoxifen-liganded ER to activate the C3 complement promoter in CV-1 cells (58). This could be explained if SRC-1 were simply enhancing AF-1 activity. Finally, our results may explain why tamoxifen behaves as a complete antagonist of ERß action at EREs (60, 61). GRIP1 potentiates the activity of tamoxifen-liganded ERß weakly and the GRIP1 C-terminus binds ERß weakly. The lack of ERß-AF-1 activity may reflect poor interaction between ERß and the GRIP1 C terminus.
GRIP1 Action and GRIP1 Binding Are Mediated By A Similar Region of
AF-1
In this study we asked which regions of the AB domain were needed
for GRIP1 stimulation of AF-1 activity and for direct GRIP1 binding by
the AB domain. We found marked similarities between AF-1 and the
p160-binding unit. First, a similar extended region of the AB domain is
required for GRIP1 activation (amino acids 41–129) and GRIP1 binding
(amino acids 38–116). Second, box 1 (amino acids 41–64), which is
also required for tamoxifen response in breast cells (44), is important
for both GRIP1 activation and GRIP1 binding. Third, the kinase target
residue serine 118 is dispensable for both GRIP1 action and GRIP1
binding. Lastly, sequences toward the C terminus of the AB domain
inhibit both GRIP1 activation and GRIP1 binding. These results strongly
suggest that GRIP1 activation of AF-1 is mediated by GRIP1 binding. We
speculate that this extended region of the AB domain forms a folded
AF-1 structure that, like AF-2 (19A ), contains p160-binding residues
along the length of its primary sequence. Our data particularly
implicate box 1 in GRIP1 activation and GRIP1 binding. While we favor
the possibility that box 1 contains residues that contact GRIP1, it
remains possible that mutations in box 1 are particularly deleterious
to overall AF-1 structure. It will be important to identify and mutate
specific residues on the surface of the folded AF-1 structure to fully
define the p160-binding site.
The fact that a large region of the AB domain is required for GRIP1
action raises the question of whether AF-1 might bind other target
proteins. Our in vitro binding studies reveal that sequences
within box 1 are absolutely required for GRIP1 binding (Fig. 4), yet
ERs with deletions of box 1 (41–64; n87, Fig. 3) retain 17–29% of
the GRIP1-induced tamoxifen response. One explanation for this
discrepancy is that, because transcriptional activity was determined in
the presence of AF-2, then residual interaction between GRIP1 and the
LBD masks the phenotypes of the AF-1 deletions. Alternatively, the AF-1
mutants might fold differently in vivo and in
vitro. More interestingly, if regions of AF-1 downstream of box 1
make contacts with other constituents of the coactivator complex, such
as p300 or P/CAF, then transfected GRIP1 might stimulate AF-1 activity
through these intermediate proteins, even in the absence of its own
binding site.
Two other lines of evidence point to the existence of alternate AF-1 targets. While the AF-1 phosphorylation sites themselves are dispensable for GRIP1 action, they are needed for AF-1 activity under conditions of MAP kinase stimulation (Refs. 45, 46 and W. J. Feng, P. Webb, J. Li, M. Karin, J. D. Baxter, and P. J. Kushner, manuscript submitted). This suggests that the AF-1 phosphorylation sites make contacts with other proteins. The existence of a subregion of the AB domain that inhibits GRIP1 action is also suggestive. Previous reports have indicated that tamoxifen- liganded ER binds the corepressors N-COR and SMRT (63) and that the overall level of activity of tamoxifen-liganded ER is regulated by the levels of corepressors (58, 62, 64, 65). Indeed, one group has shown that ER/corepressor interactions involve serine 118 (64). We are exploring the possibility that the inhibitory region of the AB domain binds corepressors.
The GRIP1 C Terminus Is Needed for AF-1 Activity
AF-1/GRIP1 interaction requires sequences at the GRIP1 C terminus
and especially sequences that overlap the Q-rich domain. This region is
conserved within the p160 family, suggesting that it may also be
involved in the interaction of other p160s with the AB domain. The
exact nature of the AF-1- binding site in the GRIP1 C terminus is
likely to be complex. While the Q-rich domain is essential for strong
AF-1 binding, a GRIP1 fragment (1282–1462), which is downstream of the
Q-rich region, also binds weakly to AF-1. Thus, the AF-1-binding site
may be spread across a large region of GRIP1. We also find that the AB
domain readily binds free GRIP1 in GST pull-down assays, but the
reciprocal interaction between tethered GRIP1 and the free AB domain is
weak (data not shown). We do see strong hormone-independent binding of
full-length ER to the GRIP C terminus in GST pull-down assays (Fig.
8B), and this binding requires the AB
domain (data not shown). Thus, contributions from the rest of the ER
molecule assist AF-1/GRIP1 interactions. One explanation for this
phenomenon is that interaction between the GRIP1 C terminus and ER-AF1
requires receptor dimerization functions, as does interaction between
the p160 NR box region and ER-AF2 (30). Another explanation is that the
ER DBD-LBD region contributes weak GRIP1 contacts that help stabilize
the AF-1/GRIP1 interaction. We are actively investigating these
possibilities.
Our work does not address whether AF-1 binding is the only role of the
GRIP1 C terminus in AF-1 activity. Recent studies have suggested that
transcription factors may bind the same coactivator, but require
different functions within that coactivator (66, 67). It is therefore
possible that AF-1 and AF-2 bind p160s but, at the same time, require
different p160 functions. TIF2 (the human homolog of GRIP1) has two
independent transactivation functions, AD1 and AD2 (22). AD1, which
binds CBP/p300, lies downstream of the AF-2-binding site (NR boxes) in
the middle of the p160 molecule. Intriguingly, AD2, whose target is
unknown, lies downstream of the AF-1-binding site within the TIF2 C
terminus. Likewise, p160 HAT activity (26, 39), which is dispensable
for AF-2 (66, 67), maps to the same p160 Q-rich region that is involved
in AF-1 binding. Finally, SRC-1a contains an inhibitory function within
its C terminus (30). A GRIP1 (1121C) truncation activated isolated
AF-2 better than wild-type GRIP1, suggesting that the GRIP1 C terminus
may also contain inhibitory sequences. AF-1 action could specifically
require any of these C-terminal GRIP1 functions.
The Choice Between AF-1/AF-2 Synergism and Independent AF1 Activity
May Be Regulated by p160s
GRIP1 enhances the ability of AF-1 to work independently of AF-2.
This suggests a simple hypothesis to explain why AF-1 synergizes with
AF-2 in some cells, but works independently in others. We propose that
the relatively weak AF-1/p160 contacts ordinarily support the stronger
interaction of the ER-LBD with p160s, and this explains why AF-1
synergizes with AF-2. At increased p160 levels, however, AF-1/p160
contacts become sufficient to recruit p160s independently. Thus, the
balance between AF-1/AF-2 synergism and AF-1 independent activity would
be regulated by p160 levels. In a sense, the behavior of AF-1 in this
model is analogous to the previously described behavior of weak AF-2
mutations that reduce GRIP1 binding, and whose phenotype is suppressed
at high levels of GRIP1 (19A, 68).
It was previously suggested that the agonist/antagonist behavior of tamoxifen in breast cells is influenced by cell-specific differences in factors that interact with subregions of the AB domain, such as box 1 (44). The results presented here suggest that those factors are p160 proteins. It is known that p160 levels are increased in certain breast and ovarian cancers because one of the p160 genes, AIB1, lies in an area of the genome that is commonly amplified in tumors (27). We have previously examined the properties of ERE-coll-CAT in MCF-7 and MDA-MB-453 breast cells that, we now know, contain amplified AIB1 (55). In accordance with our latest hypothesis, we found strong AF-1 activity. The similarity between the behavior of AF-1 in MDA-MB-231 cells (53) and HeLa cells in the presence of GRIP1 (present paper) may suggest that MDA-MB-231 cells also contain amplified AIB1. It will be interesting to test how p160 overexpression might affect the tamoxifen or estrogen responsiveness of genes with different promoter architectures, such as spaced half-sites (69) or AP-1 sites (55), whose transcription may correlate better with estrogen and antiestrogen effects on growth.
|
MATERIALS AND METHODS |
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TOPABSTRACTINTRODUCTIONRESULTSDISCUSSIONMATERIALS AND METHODSREFERENCES |
|---|
ER expression vectors have been previously described. For ease of
comparison, we have given ER expression vectors a consistent
nomenclature. The previous names and sources of each construct are as
follows: SG5-ER = HEG0; SG5-ERV400 = HE0 (57); n21; n41
= E41; n87 = A87; n109 = M109; ERAB; 41–64; 87–108
(44), n101 = HE302; n117 = HE303; n50/141c = HE344/368;
129–178 = HE316 (43). MORAF-1 = mOR121–599;
MORmAF-2 = mORL543A,L544A; MORAF-1/mAF-2 =
MOR121–599/543A,L544A (13).
Coactivator expression vectors (GRIP1, RAC3, SRC-1a, RIP-140, p300, CBP, and P/CAF) have each been previously described (24, 29, 33, 34, 35, 39, 72).
Cell Culture and Transfection
HeLa cells were maintained and transfected as previously
described (55). Unless otherwise indicated, the transfections contained
5 µg CAT or luciferase reporter, 1 µg pJ3 ß-galactosidase
control, 1 µg ER expression vector, and 5 µg coactivator expression
vector. Cell lysates were prepared 20–40 h after transfection and CAT,
luciferase, and ß-galactosidase assays were performed using standard
methods (55). In each case CAT and luciferase activities were corrected
for variations in transfection efficiency using the
ß-galactosidase activity.
GST-Fusion Proteins
GST-AB and GST-LBD fusions have been previously described (55).
GST AB truncations were prepared by amplification of AB sequences with
standard PCR methods and the resulting fragments were cloned in frame
into pGEX-5x-1 using appropriate restriction sites. GST-AB fragment
1–67 was prepared by digesting GST-AB with NotI and
self-ligating. Fragment 65–184 was prepared by cloning the
excised NotI fragment from GST-AB into pGEX-5X-2.
The GST-GRIP1 fragments were amplified by standard PCR methods and cloned into pGEX-2TK (563–1121) as a BamHI/EcoRI fragment or pGEX-4T1 (1121–1462) as a EcoRI/XhoI fragment.
In Vitro Translation Vectors
GRIP1, GRIP1 NR mutant, and SRC-1a transcription/translation
vectors have been previously described (29, 39). GRIP1 C-terminal
truncations (400, 765, 920) were prepared by restriction digestion and
run-off transcription/translation. The GRIP1 C-terminal truncation
1121C was prepared by digesting full-length GRIP1 with
XhoI and XbaI and inserting a comparable fragment
from an original partial GRIP1 cDNA clone 730-1121 (20). GRIP1
fragments 920-1291 and 1282–1462 were prepared by standard PCR
methods. In both cases, the 5'-oligonucleotide used for amplification
contained an in-frame Kozak consensus sequence. These fragments were
inserted into pSG5 between the EcoRI and BamHI
sites.
Protein-Binding Assays
GST-pull downs were performed as previously described (55).
Production and use of competitor peptides and yeast two-hybrid assays
are described elsewhere (29). For these studies a cDNA fragment coding
for the ER-AB domain (amino acids 1–184) was PCR amplified and cloned
into the EcoRI/BamHI sites of pGBT9 (CLONTECH,
Palo Alto, CA). GRIP1 and SRC-1a/GAL4-AD fusions were also previously
described (29).
|
ACKNOWLEDGMENTS |
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FOOTNOTES |
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This work was supported by grants from the California Breast Cancer Research Program (to P.J.K., P.W., and M.S.) and from the NIH (to P.J.K., M.S., and B.K.)
Received for publication April 17, 1998. Revision received June 2, 1998. Accepted for publication July 2, 1998.
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REFERENCES |
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TOPABSTRACTINTRODUCTIONRESULTSDISCUSSIONMATERIALS AND METHODSREFERENCES |
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 S. A. Ghali, B. Gottlieb, R. Lumbroso, L. K. Beitel, Y. Elhaji, J. Wu, L. Pinsky, and M. A. Trifiro The Use of Androgen Receptor Amino/Carboxyl-Terminal Interaction Assays to Investigate Androgen Receptor Gene Mutations in Subjects with Varying Degrees of Androgen Insensitivity J. Clin. Endocrinol. Metab., May 1, 2003; 88(5): 2185 - 2193. [Abstract] [Full Text] [PDF]
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B. J. Cheskis, N. J. McKenna, C.-W. Wong, J. Wong, B. Komm, C. R. Lyttle, and B. W. O'Malley Hierarchical Affinities and a Bipartite Interaction Model for Estrogen Receptor Isoforms and Full-length Steroid Receptor Coactivator (SRC/p160) Family Members J. Biol. Chem., April 4, 2003; 278(15): 13271 - 13277. [Abstract] [Full Text] [PDF]
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P. Webb, P. Nguyen, and P. J. Kushner Differential SERM Effects on Corepressor Binding Dictate ERalpha Activity in Vivo J. Biol. Chem., February 21, 2003; 278(9): 6912 - 6920. [Abstract] [Full Text] [PDF]
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M. Maira, C. Martens, E. Batsche, Y. Gauthier, and J. Drouin Dimer-Specific Potentiation of NGFI-B (Nur77) Transcriptional Activity by the Protein Kinase A Pathway and AF-1-Dependent Coactivator Recruitment Mol. Cell. Biol., February 1, 2003; 23(3): 763 - 776. [Abstract] [Full Text]
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R. Kumar and E. B. Thompson Transactivation Functions of the N-Terminal Domains of Nuclear Hormone Receptors: Protein Folding and Coactivator Interactions Mol. Endocrinol., January 1, 2003; 17(1): 1 - 10. [Abstract] [Full Text] [PDF]
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S. Zhou, G. Turgeman, S. E. Harris, D. C. Leitman, B. S. Komm, P. V. N. Bodine, and D. Gazit Estrogens Activate Bone Morphogenetic Protein-2 Gene Transcription in Mouse Mesenchymal Stem Cells Mol. Endocrinol., January 1, 2003; 17(1): 56 - 66. [Abstract] [Full Text] [PDF]
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 R. Schiff, S. Massarweh, J. Shou, and C. K. Osborne Breast Cancer Endocrine Resistance: How Growth Factor Signaling and Estrogen Receptor Coregulators Modulate Response Clin. Cancer Res., January 1, 2003; 9(1): 447s - 454s. [Abstract] [Full Text]
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V. Christiaens, C. L. Bevan, L. Callewaert, A. Haelens, G. Verrijdt, W. Rombauts, and F. Claessens Characterization of the Two Coactivator-interacting Surfaces of the Androgen Receptor and Their Relative Role in Transcriptional Control* J. Biol. Chem., December 13, 2002; 277(51): 49230 - 49237. [Abstract] [Full Text] [PDF]
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Y. He, D. Szapary, and S. S. Simons Jr. Modulation of Induction Properties of Glucocorticoid Receptor-Agonist and -Antagonist Complexes by Coactivators Involves Binding to Receptors but Is Independent of Ability of Coactivators to Augment Transactivation J. Biol. Chem., December 13, 2002; 277(51): 49256 - 49266. [Abstract] [Full Text] [PDF]
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C. Teyssier, D. Chen, and M. R. Stallcup Requirement for Multiple Domains of the Protein Arginine Methyltransferase CARM1 in Its Transcriptional Coactivator Function J. Biol. Chem., November 22, 2002; 277(48): 46066 - 46072. [Abstract] [Full Text] [PDF]
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M. E. Torres-Padilla, F. M. Sladek, and M. C. Weiss Developmentally Regulated N-terminal Variants of the Nuclear Receptor Hepatocyte Nuclear Factor 4alpha Mediate Multiple Interactions through Coactivator and Corepressor-Histone Deacetylase Complexes J. Biol. Chem., November 15, 2002; 277(47): 44677 - 44687. [Abstract] [Full Text] [PDF]
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M. Desclozeaux, I. N. Krylova, F. Horn, R. J. Fletterick, and H. A. Ingraham Phosphorylation and Intramolecular Stabilization of the Ligand Binding Domain in the Nuclear Receptor Steroidogenic Factor 1 Mol. Cell. Biol., October 15, 2002; 22(20): 7193 - 7203. [Abstract] [Full Text] [PDF]
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L. F. Su, Z. Wang, and M. J. Garabedian Regulation of GRIP1 and CBP Coactivator Activity by Rho GDI Modulates Estrogen Receptor Transcriptional Enhancement J. Biol. Chem., September 27, 2002; 277(40): 37037 - 37044. [Abstract] [Full Text] [PDF]
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M. Bommer, A. Benecke, H. Gronemeyer, and C. Rochette-Egly TIF2 Mediates the Synergy between RARalpha 1 Activation Functions AF-1 and AF-2 J. Biol. Chem., September 27, 2002; 277(40): 37961 - 37966. [Abstract] [Full Text] [PDF]
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S. E. Wardell, V. Boonyaratanakornkit, J. S. Adelman, A. Aronheim, and D. P. Edwards Jun Dimerization Protein 2 Functions as a Progesterone Receptor N-Terminal Domain Coactivator Mol. Cell. Biol., August 1, 2002; 22(15): 5451 - 5466. [Abstract] [Full Text] [PDF]
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P. Yi, S. Bhagat, R. Hilf, R. A. Bambara, and M. Muyan Differences in the Abilities of Estrogen Receptors to Integrate Activation Functions Are Critical for Subtype-Specific Transcriptional Responses Mol. Endocrinol., August 1, 2002; 16(8): 1810 - 1827. [Abstract] [Full Text] [PDF]
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S. Cheng, S. Brzostek, S. R. Lee, A. N. Hollenberg, and S. P. Balk Inhibition of the Dihydrotestosterone-Activated Androgen Receptor by Nuclear Receptor Corepressor Mol. Endocrinol., July 1, 2002; 16(7): 1492 - 1501. [Abstract] [Full Text] [PDF]
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A. Vottero, T. Kino, H. Combe, P. Lecomte, and G. P. Chrousos A Novel, C-Terminal Dominant Negative Mutation of the GR Causes Familial Glucocorticoid Resistance through Abnormal Interactions with p160 Steroid Receptor Coactivators J. Clin. Endocrinol. Metab., June 1, 2002; 87(6): 2658 - 2667. [Abstract] [Full Text] [PDF]
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 T. Barkhem, L.-A. Haldosen, J.-A. Gustafsson, and S. Nilsson pS2 Gene Expression in HepG2 cells: Complex Regulation through Crosstalk between the Estrogen Receptor alpha , an Estrogen-Responsive Element, and the Activator Protein 1 Response Element Mol. Pharmacol., June 1, 2002; 61(6): 1273 - 1283. [Abstract] [Full Text] [PDF]
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 D. P. McDonnell and J. D. Norris Connections and Regulation of the Human Estrogen Receptor Science, May 31, 2002; 296(5573): 1642 - 1644. [Abstract] [Full Text] [PDF]
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P. J. Shughrue, G. R. Askew, T. L. Dellovade, and I. Merchenthaler Estrogen-Binding Sites and Their Functional Capacity in Estrogen Receptor Double Knockout Mouse Brain Endocrinology, May 1, 2002; 143(5): 1643 - 1650. [Abstract] [Full Text] [PDF]
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D. Kressler, S. N. Schreiber, D. Knutti, and A. Kralli The PGC-1-related Protein PERC Is a Selective Coactivator of Estrogen Receptor alpha J. Biol. Chem., April 12, 2002; 277(16): 13918 - 13925. [Abstract] [Full Text] [PDF]
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C.-Y. Chang and D. P. McDonnell Evaluation of Ligand-Dependent Changes in AR Structure Using Peptide Probes Mol. Endocrinol., April 1, 2002; 16(4): 647 - 660. [Abstract] [Full Text] [PDF]
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P. Yi, M. D. Driscoll, J. Huang, S. Bhagat, R. Hilf, R. A. Bambara, and M. Muyan The Effects of Estrogen-Responsive Element- and Ligand-Induced Structural Changes on the Recruitment of Cofactors and Transcriptional Responses by ER{alpha} and ER{beta} Mol. Endocrinol., April 1, 2002; 16(4): 674 - 693. [Abstract] [Full Text] [PDF]
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Y. Shang and M. Brown Molecular Determinants for the Tissue Specificity of SERMs Science, March 29, 2002; 295(5564): 2465 - 2468. [Abstract] [Full Text] [PDF]
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B. He, J. T. Minges, L. W. Lee, and E. M. Wilson The FXXLF Motif Mediates Androgen Receptor-specific Interactions with Coregulators J. Biol. Chem., March 15, 2002; 277(12): 10226 - 10235. [Abstract] [Full Text] [PDF]
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J. M. Hall, D. P. McDonnell, and K. S. Korach Allosteric Regulation of Estrogen Receptor Structure, Function, and Coactivator Recruitment by Different Estrogen Response Elements Mol. Endocrinol., March 1, 2002; 16(3): 469 - 486. [Abstract] [Full Text] [PDF]
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I. T. R. Cavarretta, R. Mukopadhyay, D. M. Lonard, L. M. Cowsert, C. F. Bennett, B. W. O'Malley, and C. L. Smith Reduction of Coactivator Expression by Antisense Oligodeoxynucleotides Inhibits ER{alpha} Transcriptional Activity and MCF-7 Proliferation Mol. Endocrinol., February 1, 2002; 16(2): 253 - 270. [Abstract] [Full Text] [PDF]
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Z.-x. Zhou, B. He, S. H. Hall, E. M. Wilson, and F. S. French Domain Interactions between Coregulator ARA70 and the Androgen Receptor (AR) Mol. Endocrinol., February 1, 2002; 16(2): 287 - 300. [Abstract] [Full Text] [PDF]
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S. R. Lee, S. M. Ramos, A. Ko, D. Masiello, K. D. Swanson, M. L. Lu, and S. P. Balk AR and ER Interaction with a p21-Activated Kinase (PAK6) Mol. Endocrinol., January 1, 2002; 16(1): 85 - 99. [Abstract] [Full Text] [PDF]
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S. Fan, Y. X. Ma, C. Wang, R.-Q. Yuan, Q. Meng, J.-A. Wang, M. Erdos, I. D. Goldberg, P. Webb, P. J. Kushner, et al. p300 Modulates the BRCA1 Inhibition of Estrogen Receptor Activity Cancer Res., January 1, 2002; 62(1): 141 - 151. [Abstract] [Full Text] [PDF]
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A. Warnmark, A. Wikstrom, A. P. H. Wright, J.-A. Gustafsson, and T. Hard The N-terminal Regions of Estrogen Receptor alpha and beta Are Unstructured in Vitro and Show Different TBP Binding Properties J. Biol. Chem., November 30, 2001; 276(49): 45939 - 45944. [Abstract] [Full Text] [PDF]
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R. Metivier, G. Penot, G. Flouriot, and F. Pakdel Synergism Between ER{alpha} Transactivation Function 1 (AF-1) and AF-2 Mediated by Steroid Receptor Coactivator Protein-1: Requirement for the AF-1 {alpha}-Helical Core and for a Direct Interaction Between the N- and C-Terminal Domains Mol. Endocrinol., November 1, 2001; 15(11): 1953 - 1970. [Abstract] [Full Text] [PDF]
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S. Nilsson, S. Makela, E. Treuter, M. Tujague, J. Thomsen, G. Andersson, E. Enmark, K. Pettersson, M. Warner, and J.-A. Gustafsson Mechanisms of Estrogen Action Physiol Rev, October 1, 2001; 81(4): 1535 - 1565. [Abstract] [Full Text] [PDF]
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M. Maggiolini, D. Bonofiglio, S. Marsico, M. L. Panno, B. Cenni, D. Picard, and S. Ando Estrogen Receptor alpha Mediates the Proliferative but Not the Cytotoxic Dose-Dependent Effects of Two Major Phytoestrogens on Human Breast Cancer Cells Mol. Pharmacol., September 1, 2001; 60(3): 595 - 602. [Abstract] [Full Text] [PDF]
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Z. Yang and M. L. Privalsky Isoform-Specific Transcriptional Regulation by Thyroid Hormone Receptors: Hormone-Independent Activation Operates through a Steroid Receptor Mode of Coactivator Interaction Mol. Endocrinol., July 1, 2001; 15(7): 1170 - 1185. [Abstract] [Full Text] [PDF]
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H. Liu, E.-S. Lee, A. D. L. Reyes, J. W. Zapf, and V. C. Jordan Silencing and Reactivation of the Selective Estrogen Receptor Modulator-Estrogen Receptor {{alpha}} Complex Cancer Res., May 1, 2001; 61(9): 3632 - 3639. [Abstract] [Full Text]
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W. Feng, P. Webb, P. Nguyen, X. Liu, J. Li, M. Karin, and P. J. Kushner Potentiation of Estrogen Receptor Activation Function 1 (AF-1) by Src/JNK through a Serine 118-Independent Pathway Mol. Endocrinol., January 1, 2001; 15(1): 32 - 45. [Abstract] [Full Text]
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R. M. Tolón, A. I. Castillo, A. M. Jiménez-Lara, and A. Aranda Association with Ets-1 Causes Ligand- and AF2-Independent Activation of Nuclear Receptors Mol. Cell. Biol., December 1, 2000; 20(23): 8793 - 8802. [Abstract] [Full Text]
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F. Schaufele, C.-y. Chang, W. Liu, J. D. Baxter, S. K. Nordeen, Y. Wan, R. N. Day, and D. P. McDonnell Temporally Distinct and Ligand-Specific Recruitment of Nuclear Receptor-Interacting Peptides and Cofactors to Subnuclear Domains Containing the Estrogen Receptor Mol. Endocrinol., December 1, 2000; 14(12): 2024 - 2039. [Abstract] [Full Text]
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 M. Dutertre and C. L. Smith Molecular Mechanisms of Selective Estrogen Receptor Modulator (SERM) Action J. Pharmacol. Exp. Ther., November 1, 2000; 295(2): 431 - 437. [Abstract] [Full Text]
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R. Métivier, F. G. Petit, Y. Valotaire, and F. Pakdel Function of N-Terminal Transactivation Domain of the Estrogen Receptor Requires a Potential {alpha}-Helical Structure and Is Negatively Regulated by the A Domain Mol. Endocrinol., November 1, 2000; 14(11): 1849 - 1871. [Abstract] [Full Text]
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F. Delaunay, K. Pettersson, M. Tujague, and J.-A. Gustafsson Functional Differences between the Amino-Terminal Domains of Estrogen Receptors alpha and beta Mol. Pharmacol., September 1, 2000; 58(3): 584 - 590. [Abstract] [Full Text]
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 K. P. Nephew, S. Ray, M. Hlaing, A. Ahluwalia, S. D. Wu, X. Long, S. M. Hyder, and R. M. Bigsby Expression of Estrogen Receptor Coactivators in the Rat Uterus Biol Reprod, August 1, 2000; 63(2): 361 - 367. [Abstract] [Full Text]
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J. Font de Mora and M. Brown AIB1 Is a Conduit for Kinase-Mediated Growth Factor Signaling to the Estrogen Receptor Mol. Cell. Biol., July 15, 2000; 20(14): 5041 - 5047. [Abstract] [Full Text]
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H. Fuse, H. Kitagawa, and S. Kato Characterization of Transactivational Property and Coactivator Mediation of Rat Mineralocorticoid Receptor Activation Function-1 (AF-1) Mol. Endocrinol., June 1, 2000; 14(6): 889 - 899. [Abstract] [Full Text]
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A. Bollig and R. J. Miksicek An Estrogen Receptor-{alpha} Splicing Variant Mediates Both Positive and Negative Effects on Gene Transcription Mol. Endocrinol., May 1, 2000; 14(5): 634 - 649. [Abstract] [Full Text]
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G. de Haan, S. Chusacultanachai, C. Mao, B. S. Katzenellenbogen, and D. J. Shapiro Estrogen Receptor-KRAB Chimeras Are Potent Ligand-dependent Repressors of Estrogen-regulated Gene Expression J. Biol. Chem., April 28, 2000; 275(18): 13493 - 13501. [Abstract] [Full Text] [PDF]
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Y. Xu, L. Klein-Hitpass, and M. K. Bagchi E1A-Mediated Repression of Progesterone Receptor-Dependent Transactivation Involves Inhibition of the Assembly of a Multisubunit Coactivation Complex Mol. Cell. Biol., March 15, 2000; 20(6): 2138 - 2146. [Abstract] [Full Text]
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S.-M. Huang and M. R. Stallcup Mouse Zac1, a Transcriptional Coactivator and Repressor for Nuclear Receptors Mol. Cell. Biol., March 1, 2000; 20(5): 1855 - 1867. [Abstract] [Full Text]
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D. Robyr, A. P. Wolffe, and W. Wahli Nuclear Hormone Receptor Coregulators In Action: Diversity For Shared Tasks Mol. Endocrinol., March 1, 2000; 14(3): 329 - 347. [Full Text]
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C. Leo, H. Li, and J. D. Chen Differential Mechanisms of Nuclear Receptor Regulation by Receptor-associated Coactivator 3 J. Biol. Chem., February 25, 2000; 275(8): 5976 - 5982. [Abstract] [Full Text] [PDF]
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