INTRODUCTION

Top Abstract Introduction Materials and methods Results Discussion References

The mdm2 oncogene was originally identified as a gene that is amplified and overexpressed in a tumorigenic derivative of mouse 3T3 cells (3T3DM), with the amplified sequences being located on extrachromosomal double minute particles (8). Subsequent studies revealed that overexpression of the mdm2 gene was responsible for transformation of these cells (19). Amplification and overexpression of the mdm2 gene have been detected in a number of human sarcomas (41, 49), suggesting that this oncogene plays a role in human carcinogenesis. The product of the mouse mdm2 gene is a protein with a predicted molecular mass of 54 kDa, although it migrates as a ~95-kDa protein in sodium dodecyl sulfate (SDS) gels (4).

mdm2 associates with wild-type and certain mutant p53 proteins (34, 47), and an excess of mdm2 can abrogate transcriptional activation by wild-type p53 (47). In addition, the binding of mdm2 to p53 results in a decrease in p53 levels through enhanced degradation (33, 40) by a proteosome-mediated process (40). Thus, overexpression of mdm2 serves as a negative regulator of p53 function. The mdm2 gene is regulated by wild-type p53 through an intronic sequence which contains a p53 DNA-binding region and functions as a p53 response element (69). This results in an autoregulatory loop in which mdm2 complexes with p53, thereby reducing the extent of its own expression (5, 67).

An interesting property of the mdm2 gene is that it can generate multiple transcripts which may differ in coding potential. Sequence analysis of mdm2 clones isolated from murine (19) and human (49) cDNA libraries indicates that the mdm2 gene can generate at least seven distinct mRNA species. The mdm2 splice variants differ in their ability to inhibit p53-mediated transactivation (31). Thus, the existence of multiple mdm2 proteins raises the possibility that mdm2 may elicit effects in cells independently of its known effect on p53. This is suggested by studies indicating that mdm2 can overcome a G₁ cell cycle arrest mediated by members of the retinoblastoma gene family (16, 68) and that expression of mdm2 can activate E2F1/DP1 (46) and the cyclin A gene promoter (44). This is also supported by studies of mdm2 expression in mammary tissue of p53^+/+ and p53^/ mice indicating that mdm2 can regulate DNA synthesis independently of its ability to inhibit p53 activity. Recent studies have also indicated that expression of mdm2 can be modulated by factors other than p53 (e.g., fibroblast growth factor [58]), suggesting that mdm2 may act and be regulated independently of p53.

The thyroid hormones influence a variety of physiological processes, including cell growth and metabolism in mammals, initiation of metamorphosis in amphibia, and development of the vertebrate nervous system (53). Most, if not all, of these actions are mediated by thyroid hormone (L-triiodothyronine; T3) nuclear receptors (T3Rs). The T3Rs are encoded by two genes ( and ) and are expressed as several isoforms (T3R1, T3R1, and T3R2) (43). The T3Rs are members of the thyroid hormone/retinoid receptor subfamily of nuclear hormone receptors, which includes the retinoic acid receptors (RARs), the retinoid X receptors (RXRs), the vitamin D receptor (VDR), the peroxisome proliferation activation receptors (PPARs), and orphan receptors such as chicken ovalbumin upstream promoter transcription factor (COUP-TF) (12, 24).

T3Rs activate transcription through DNA sequences referred to as thyroid hormone response elements (TREs). Naturally occurring TREs are organized as imperfect invert repeats and/or direct repeats (DRs) of the optimized AGGTCA half-site (7, 63). TREs have been identified in a wide variety of genes, including the long terminal repeat (LTR) of Moloney murine leukemia virus (55), the promoter and third intron of the rat growth hormone gene (54), and the promoters of the malic enzyme (13) and human -myosin heavy-chain (62) genes, and within the NF-B motifs of the human immunodeficiency virus type 1 (HIV-1) LTR (15). Certain TREs are also regulated by other members of the T3R/RAR subfamily (e.g., the rat growth hormone TRE) (62).

In this study, we report that T3R can stimulate the native mdm2 gene in a T3-dependent fashion. Stimulation was found to occur via a TRE(s) which we localized to the first intron of the mdm2 gene. Similar results were found with homologous sequences from the human mdm2 gene (70). In contrast with T3R, no ligand-dependent stimulation was found with RAR, RXR, VDR, or PPAR, although constitutive activation was found to occur with COUP-TFI. Two T3R-responsive DNA elements were identified in the mdm2 intron and further mapped to sequences within the putative p53 binding sites. Our findings, which indicate that T3R can regulate the mdm2 gene independently of p53, may provide an explanation for certain known effects of T3 and T3R on cell proliferation (22, 32) and in the promotion of tumor development (29).

(This study was done by J.-S.Q. and Y.Y. in partial fulfillment of the requirements for a Ph.D. degree from the Sackler Institute for Graduate Biomedical Science at the New York University School of Medicine.)

	MATERIALS AND METHODS

Top Abstract Introduction Materials and methods Results Discussion References

Cell culture and transfection. HeLa cells and GH4C1 rat pituitary cells were cultured and transfected by electroporation as previously described (1, 22). p53-null (10)1 cells (67) were transfected by calcium phosphate precipitation. The chloramphenicol acetyltransferase (CAT) reporter vectors and other plasmids used are described below. After incubation for 48 h with or without the indicated ligand(s), cells were harvested for assay of CAT activity by a thin-layer chromatography assay (1, 22). Acetylated and unreacted [¹⁴C]chloramphenicol were excised from the thin-layer plate and quantitated in a liquid scintillation counter. The amount of protein used in the assays was adjusted to keep the percent conversion of [¹⁴C]chloramphenicol below 40%, which is in the linear range. CAT activity values were normalized to represent the percentage of [¹⁴C]chloramphenicol acetylated by a specific amount of cell protein in 16 h at 37°C. All experiments were performed with duplicate or triplicate flasks, which showed variations of less than 10%, and each experiment was repeated at least three times with similar results.

Cloning and plasmid construction. The full-length chicken T3R (cT3R) cDNA corresponding to amino acids 1 to 408, cloned into a pEXPRESS (pEX) vector (pEX-cT3R), has been described previously (25). pRSVT7-cT3R(21-408), pEX-cT3R(31-408), pEX-cT3R(51-408), pRSV-T7-cT3R(21-30/51-408), and pRSV-T7-cT3R(13-20/51-408) have been described previously (14, 30, 57). Human T3R1 (hT3R1) (28) and rat T3R2 (rT3R2) (35) were also expressed from pEX vectors. Wild-type and mutant human p53 plasmids, pC53-SN3 and pC53(V143A) (gifts from Bert Vogelstein), respectively, utilize a pCMV-Neo-Bam vector (3) or a T7 polymerase-transcribed pBluescript vector. The 59-nucleotide murine p53 response element sequence (TGGTCAAGTTGGGACACGTCCggcgtcggctgtcggagGAGCTAAGTCCTGACATGTCT [uppercase corresponds to Seq1 and Seq2]) from the first intron of the murine mdm2 gene (67) was cloned into the HindIII site at position 88 of MTV-CAT, which lacks the glucocorticoid response elements of the mouse mammary tumor virus LTR (63). This vector has been termed MTV-m59-CAT. 5'-TGGTCAAGTTGGGACACGTCC-3' (Seq1) and 5'-GAGCTAAGTCCTGACATGTCT-3' (Seq2) from the 59-bp element were cloned upstream of nucleotide 88 in MTV-CAT and have been termed MTV-Seq1-CAT and MTV-Seq2-CAT, respectively. The homologous 59-bp p53 response element from the human mdm2 gene (70) was also cloned at position 88 of MTV-CAT (MTV-h59-CAT). Cosx1CAT, which contains a 1-kb fragment from the first intron of the murine mdm2 gene subcloned upstream from the adenovirus major late TATA box-terminal deoxynucleotidyltransferase (TdT) initiation signal-CAT gene sequence (p1634CAT) (67), was a gift from Arnold J. Levine. Various deletion mutants containing different fragments of the mdm2 first-intron region cloned into the p1634CAT vector (H0.5NCAT, HX0.5CAT, BN300CAT, BA200CAT, and BP100CAT) (67) were also generously provided by Arnold J. Levine. A COUP-TFI-expressing Rous sarcoma virus vector that has been described elsewhere (11) was obtained from Ming-Jer Tsai.

Gel mobility shift assays. cT3R was expressed in Escherichia coli and purified to apparent homogeneity as described previously (23). Following the purification, the amount of cT3R was estimated with L-[¹²⁵I]T3 (23). Double-stranded oligonucleotides complementary to Seq1 and Seq2, as mentioned above, were synthesized and annealed. These oligonucleotides are flanked by HindIII cohesive ends, permitting cloning and end labeling. cT3R was incubated with ³²P-labeled Seq1 or Seq2 as described previously (23). The 30-µl incubation mixture contained 25 mM Tris (pH 7.8), 0.5 mM EDTA, 80 mM KCl, 1 mM dithiothreitol, 100 ng of aprotinin, 0.25 µg of poly(dI-dC), 0.05% (vol/vol) Triton X-100, 10% (vol/vol) glycerol, and various amounts of receptor, with or without 1 µM T3. For studies involving heterodimer binding to Seq1, the incubation mixture contained 15 fmol of reticulosyte lysate-synthesized cT3R and 25 fmol of baculovirus-expressed murine RXR (mRXR) as previously described (1). Samples were analyzed by electrophoresis at 4°C in nondenaturing SDS-5% polyacrylamide gels in buffer containing 10 mM Tris, 7.5 mM acetic acid, and 40 µM EDTA (pH 7.8) (23). The gels were dried and autoradiographed.

Western blot analysis of mdm2. GH4C1 cells were cultured in hormone-depleted medium (22) for 24 h. The cells were then incubated with 500 nM T3 for 4 days, 2 days, or 1 day before the cells were harvested for assay of mdm2. Some cells were incubated without T3 for the 4-day period. At the time of harvest, the cells were about 70 to 80% confluent. Cells were then washed twice with phosphate-buffered saline, scraped from the dishes, and lysed in RIPA buffer (50 mM Tris-HCl [pH 7.5], 5 mM EDTA [pH 8.0], 0.5% Nonidet P-40, 0.5% deoxycholic acid, 0.1% SDS, 150 mM NaCl), supplemented with 1 mM phenylmethylsulfonyl fluoride, 1 µg of aprotinin per ml, 2 µg of leupeptin per ml, and 1 µg of pepstatin per ml, for 30 min on ice with frequent vortexing. Lysates were then clarified by microcentrifugation, and a small aliquot of each was removed for determination of the protein concentration. Equal quantities of lysate protein were separated in an SDS-10% polyacrylamide gel. Verification of the efficiency of transfer to nitrocellulose and the equality of loaded protein quantities were determined by staining the membrane with 0.5% Ponceau S in 10% acetic acid and by probing the blots with antiactin antibody. Blots were washed in H₂O and then incubated overnight at 4°C in blocking buffer (5% nonfat dry milk in Tris-buffered saline [TBS]) and then with anti-mdm2 monoclonal antibody 2A10 (a gift from Arnold J. Levine), which recognizes the central region (amino acids 294 to 339) of hmdm2 and reacts with mdm2 proteins from a variety of species. Blots were also probed with a monoclonal antibody (Ab-1; Oncogene Science) that recognizes only the N terminus of mdm2. Blots were washed four times with TBS supplemented with Triton X-100 and then twice with unsupplemented TBS. Blots were then incubated at room temperature for 1 h with peroxidase-labeled goat anti-mouse immunoglobulin G second antibody (Kirkegaard & Perry Laboratories, Inc.) at 0.2 µg/ml, washed four times with TBS, and then visualized with an enhanced chemiluminescence detection system (E. I. Dupont de Nemours & Co.).

	RESULTS

Top Abstract Introduction Materials and methods Results Discussion References

The mdm2 gene is stimulated by T3 in GH4C1 cells. T3 is known to stimulate the growth of GH4C1 cells and related rat pituitary cell lines which express T3Rs (9, 22). This growth-stimulatory effect of T3 has been shown to result from an effect on the G₁ phase of the cell cycle (32). Since these cells express functional p53 (52), and p53 is known to influence the length of G₁, we assessed whether T3 might act to inhibit p53-mediated responses in GH4C1 cells. Since the expression of mdm2 is a sensitive indicator of p53 activity, we studied the effect of T3 on mdm2. Western blotting studies indicate that GH4C1 cells express three forms of mdm2 which range from 85 to 95 kDa (Fig. 1). This is consistent with previous reports indicating that the mdm2 gene encodes a number of alternatively spliced mRNAs that give rise to several isoforms of mdm2 protein in the cell (31, 50). The mdm2 isoforms, particularly the 85-kDa form, were stimulated rather than inhibited by T3, suggesting that T3R acts indirectly (i.e., via p53) or directly to activate the mdm2 gene.

View larger version (36K): [in this window] [in a new window]   FIG. 1.   The mdm2 gene is stimulated by T3 in GH4C1 cells. GH4C1 cells were cultured in hormone-depleted medium (22, 27) for 24 h. The cells were then incubated with (+) or without () 500 nM T3 for 4 days, 2 days, or 1 day before the cells were harvested for assay of mdm2. Day 0 cells were incubated without T3 for the entire 4-day period. Equal quantities of cell lysate protein were separated in an SDS-10% polyacrylamide gel. After transfer to nitrocellulose membranes, the samples were blotted with anti-mdm2 monoclonal antibody 2A10, which recognizes the central region of the mdm2 protein.

The first intron of the mdm2 gene contains a ligand-dependent TRE. The first intron of the mdm2 gene contains a p53 binding site which, when placed upstream of a minimal promoter, can stimulate a reporter gene in a p53-dependent fashion (38, 67). To determine whether T3R regulates mdm2 without indirectly affecting p53, T3-dependent stimulation of Cosx1CAT was analyzed in HeLa cells, which express very little if any p53 (56). Cosx1CAT contains a 1-kb DNA fragment from the first intron of the mdm2 gene cloned just upstream of the adenovirus major late TATA box and TdT initiator sequence which is linked to the CAT reporter gene (67). HeLa cells were transfected with Cosx1CAT with or without vectors expressing cT3R. T3 stimulated expression of Cosx1CAT about 15-fold (Fig. 2). Expression of the control minimal-promoter CAT reporter gene, which lacks the 1-kb mdm2 intronic region (p1634CAT) (not shown), was not altered by T3. This suggests that T3R can activate the mdm2 gene independently of p53 and that the first intron of the mdm2 gene contains a response element(s) for T3R in addition to a response element(s) for p53.

View larger version (26K): [in this window] [in a new window]   FIG. 2.   The first intron of the mdm2 gene contains a T3-dependent response element. HeLa cells were transfected by electroporation with 5 µg of Cosx1CAT or the indicated deletion mutants of Cosx1CAT with 4 µg of a vector expressing cT3R. Cosx1CAT contains a 1-kb XhoI-XhoI fragment from the first intron of the murine mdm2 gene cloned upstream from the adenovirus major late TATA box-TdT initiation signal-CAT gene sequence (67). Following transfection, cells were incubated for 48 h without or with 500 nM T3 prior to determination of CAT activity.

The mdm2 TRE is embedded within the p53-responsive sequence. The TRE within the mdm2 gene was mapped to an 85-bp HincII-PvuII sequence in the first intron of mdm2 (Fig. 2). T3-dependent stimulation by cT3R was found only with constructs containing this 85-bp sequence, which has been reported to also contain the p53 response element of the gene (67). To further map the TRE, a 59-bp putative p53 response sequence (Fig. 3) from the 85-bp HincII-PvuII region of the murine mdm2 gene was cloned at nucleotide 88 of MTV-CAT to create MTV-m59-CAT. This 59-bp sequence can be divided into two regions (Seq1 and Seq2) (Fig. 3), which were individually cloned at position 88 of MTV-CAT, resulting in MTV-Seq1-CAT and MTV-Seq2-CAT, respectively. Underlined in Seq1 and Seq2 of Fig. 3 are hexanucleotide sequences which show a high degree of homology to those found in known TREs (6, 10, 15).

View larger version (15K): [in this window] [in a new window]   FIG. 3.   Nucleotide sequences of Seq1 and Seq2 of the 59-bp intronic p53 response element of the mdm2 gene. Underlined are hexanucleotide sequences showing a high degree of homology to known native TREs, suggesting that the TRE in Seq1 is organized as a DR+4 TRE. The sequence underlined in Seq2 has on its complementary strand AGGACT. This is identical to sequences found in a TRE from the human thyroid-stimulating hormone  gene (10) and from the TRE sequences at positions 88 to 83 and 102 to 97 of the NF-B binding sites of the HIV-1 LTR (15).

View this table: [in this window] [in a new window]   TABLE 4.   Transcriptional activation of MTV-m59-CAT by endogenous p53 and T3Rs in GH4C1 cellsa

T3R binds to Seq1 and Seq2 of the p53-responsive element. TREs of native genes are organized as DRs and/or inverted repeats of hexanucleotide half-sites separated by variously sized nucleotide gaps (6, 48, 64). The half-site sequences of native genes show significant diversity, indicating that the T3Rs are capable of activating a wide variety of structurally divergent TREs. To study the binding of T3R to the 59-bp sequence of the murine element, gel mobility shift assays were performed with ³²P-labeled Seq1 or Seq2 as the probe. cT3R bound to both Seq1 and Seq2 as monomers and homodimers, but it exhibited a higher degree of affinity for Seq1 (Fig. 4A and B). T3 increased the binding of monomers but decreased the binding of homodimers to both sequences (Fig. 4A and B). This effect of T3 is commonly seen with DR elements, suggesting that the Seq1 and Seq2 TREs have such an organization. T3Rs bind preferentially to DNA as heterodimers with the RXRs in vitro, and we and others have provided evidence that the T3R-RXR heterodimer is the functional form of the receptor on most native response elements in vivo (1, 51). The ability of cT3R and mRXR to bind as a heterodimer to Seq1 and Seq2 was studied. cT3R and mRXR bound as an abundant heterodimer to Seq1 (Fig. 4C), while the extent of heterodimer binding to Seq2 was very low (not illustrated), which paralleled the functional activity of T3-dependent stimulation of these sequences (Table 1).

View larger version (68K): [in this window] [in a new window]   View larger version (37K): [in this window] [in a new window]   FIG. 4.   Binding of T3R to Seq1 and Seq2 of the mdm2 p53 response sequence. Gel mobility shift assays were used to study the binding of purified cT3R, at 15 (+), 30 (++), or 45 (+++) fmol, to 32P-labeled Seq1 (A) or Seq2 (B) in the absence () or presence (+) of 1 µM T3. Shifted complexes are indicated by arrows. (C) Binding of 15 fmol of cT3R plus 25 fmol of mRXR. For the experiment in panel C, the cT3R used was synthesized in vitro, using rabbit reticulocyte lysate (2 µl) (1), while mRXR was synthesized by using a baculovirus (bv) expression vector (45). Two microliters of unprogrammed reticulocyte lysate was used as a control. The migration positions of cT3R monomers, homodimers, and cT3R-mRXR heterodimers have been previously established (1, 23).

A 10-amino-acid sequence in the A/B region of T3R, which is important for interaction with TFIIB, is also required for activation of mdm2. The domain structures of cT3R and p53 are illustrated in Fig. 5. The N-terminal A/B region is the least-conserved region among members of the thyroid/retinoid receptor subfamily and the T3R isoforms. The highly conserved 68-amino-acid C domain is organized into two zinc finger DNA-binding structures. High-affinity ligand binding requires the D, E, and F domains, a region which also contains the i and heptad repeats thought to be involved in protein-protein interactions (1, 24, 51). Amino acids 21 to 30 (DGKRKRKSSQ), in the A/B region, contain a cluster of five basic amino acids important for transcriptional activation of native TREs and for interaction with the general transcription factor TFIIB (30). This 10-amino-acid sequence also appears to be important for activation via the mdm2 intronic TRE (Fig. 6). Several N-terminal deletion mutants of cT3R were compared for their ability to transactivate Cosx1CAT. Transfection studies indicate that cT3R(21-408), but not cT3R(31-408), activated Cosx1CAT similarly to wild-type cT3R (Fig. 6). These results indicate that amino acids 21 to 31 are required for transcriptional stimulation by the mdm2 intronic TRE and that TFIIB likely plays a role in this activation. This was further confirmed by functional studies indicating that cT3R(21-30/51-408), but not cT3R(13-20/51-408), can stimulate Cosx1CAT (Fig. 6).

View larger version (30K): [in this window] [in a new window]   FIG. 5.   Domain structures of cT3R (A) and p53 (B). (A) cT3R, like other members of the nuclear receptor family, can be divided into six distinct regions (A to F) (18). The N-terminal A/B region is the least-conserved region among the nuclear hormone receptors. The highly conserved 68-amino-acid C domain (amino acids 51 to 119) is organized into two zinc finger DNA-binding structures. D, E, and F comprise the ligand-binding domain (amino acids 120 to 408) (37). (B) p53 can be divided into three regions. The N terminus (amino acids 1 to 43) contains a strong transcription regulatory region (20, 61, 69) and interacts with a number of proteins, including mdm2 (39). The central region (amino acids 100 to 300) contains the sequence-specific DNA-binding domain (69) and four regions (II to V) that are evolutionarily conserved within all vertebrate species (59). The C-terminal region contains an oligomerization domain that dictates the formation of stable p53 tetramers (amino acids 340 to 393) (60) and a nonspecific nucleic acid-binding domain (amino acids 330 to 393) (66).

View larger version (31K): [in this window] [in a new window]   FIG. 6.   A 10-amino-acid sequence in the N-terminal A/B domain of cT3R is required for activation of the mdm2 TRE. HeLa cells were transfected by electroporation with 5 µg of Cosx1CAT alone or with 4 µg of vector expressing wild-type cT3R or the indicated N-terminal deletion mutants of cT3R. Following transfection, cells were incubated for 48 h without or with 500 nM T3 prior to determination of CAT activity.

The mdm2 p53/T3R response element is also activated by COUP-TFI but not by RAR, VDR, RXR, or PPAR. COUP-TFI was initially characterized by its binding to the COUP element (positions 90 to 70) (2, 65). Analysis of COUP-TFI binding sites revealed that COUP-TF could bind to many A/GGGTCA repeats with different spacings and orientations (12). COUP-TFI is known to repress hormonal induction of many target genes by VDR, T3R, and RAR (11). Transfer of the putative ligand binding domain of COUP-TFI to the GAL4 DNA binding domain suggested that it possesses an active silencing function within its C-terminal domain (11).

View larger version (30K): [in this window] [in a new window]   FIG. 7.   COUP-TFI activates the mdm2 p53 response sequence. HeLa cells were transfected by electroporation with 4 µg of the indicated reporters that contain different fragments of the first intron of the mdm2 gene and 4 µg of a pRSV control vector (COUPTFI) or pRSV-COUP-TFI (+COUPTFI). Following transfection, cells were incubated in hormone-depleted medium for 48 h prior to determination of CAT activity.

	DISCUSSION

Top Abstract Introduction Materials and methods Results Discussion References

Previous studies have shown that p53 stimulates the expression of the mdm2 gene through a p53 response sequence in the first intron of the mdm2 gene (38, 67). The segment conferring p53 responsiveness includes two elements which display significant homology to a consensus p53 binding site (17). These two elements have been termed Seq1 and Seq2 (Fig. 3). We showed that the 59-bp p53 DNA-binding site contains two TREs (Table 1) and that the major TRE in the 59-bp region is contained within Seq1. T3R binds as a monomer or homodimer with a higher affinity for Seq1 than for Seq2 (Fig. 4A and B), or it binds to Seq1 as a heterodimer with RXR. This difference in affinity for T3R parallels the difference in the abilities of Seq1 and Seq2 to function as TREs (Table 1). The strong TRE found in Seq1 resembles a DR with a 4-bp gap (DR+4), which is characteristic of many native TREs (Fig. 3). Inspection of Seq1 indicates that it contains the sequence TGGTCAagttGGGACA, which resembles an idealized TRE half-site (AGGTCA) organized as an imperfect DR with a 4-bp gap (DR+4). Examination of Seq2 indicated that it contains the sequence AGTCCT. The half-site on the complementary strand (AGGACT) is identical to half-sites found in a TRE from the human thyroid-stimulating hormone  gene (10) and in the TRE sequences at positions 88 to 83 and 102 to 97 of NF-B binding sites of the HIV-1 LTR (15).

Activation by wild-type p53 parallels the findings with T3R (i.e., the 59-bp fragment containing Seq1 and Seq2 is about as active as that containing only Seq1, and both are much more active than that containing only Seq2) (Table 1). This suggests that T3R and p53 may contact similar sequences in the 59-bp mdm2 sequence. This is further supported by the finding that expression of unliganded T3R blocks p53-mediated stimulation of MTV-m59-CAT (Table 3). All isoforms of T3R activate the mdm2 response sequence as well as the homologous sequence from the human mdm2 gene (Table 2). Hadzic et al. (30) showed that amino acids 21 to 30 (DGKRKRKSSQ) in the A/B region of cT3R contain a cluster of five basic amino acids that are important for transcriptional activation of native TREs and for interaction with the general transcription factor TFIIB. Similarly, this 10-amino-acid region was also found to be important for transcriptional activation of Cosx1CAT. The related receptors hRAR, hRXR, hPPAR, and hVDR do not transcriptionally activate these sequences, which is consistent with the apparent DR+4 organization of the TRE. In contrast, the orphan receptor COUP-TF, which commonly represses the activity of TREs, activates the mdm2 response sequence in Cosx1CAT (Fig. 7).

The mdm2 protooncogene is amplified in a variety of tumors and approximately 30% of sarcomas (41, 49). Overexpression of mdm2 inhibits the prolongation or blockade of G₁ progression mediated by p53 as well as the ability of p53 to suppress transformation of cells in culture (21). Although the action of mdm2 as an oncogene could occur solely by inhibiting the function of p53 (4, 67), it could also function through p53-independent pathways. This is supported by recent studies indicating that mdm2 can overcome the G₁ cell cycle arrest mediated by members of the retinoblastoma gene family (16, 68) and that expression of mdm2 can activate E2F1/DP1 (46) and the cyclin A gene promoter (44). The mdm2 gene encodes a number of alternatively spliced mRNAs that give rise to multiple protein forms (31, 50). Some isoforms lack the N-terminal epitopes required for the mdm2-p53 interaction (31, 50), which further implies a function for mdm2 in addition to its ability to block p53-mediated responses.

Landers et al. (42) found that high levels of mdm2 proteins are present in two choriocarcinoma cell lines that also overexpress wild-type p53. In this study, we found that GH4C1 cells, which appear to express functional p53 (Table 4), express high levels of mdm2 (Fig. 1). GH4C1 cells express T3R1, T3R1, and T3R2 (36). Several forms of mdm2, particularly the ~85-kDa form, were found to be stimulated by endogenous T3Rs when GH4C1 cells were treated with T3 (Fig. 1). This ~85-kDa form of mdm2 was not detected with monoclonal antibody Ab-1 (Oncogene Science), which recognizes the N terminus of mdm2 (data not shown), suggesting that the ~85-kDa form of mdm2 does not possess the N-terminal amino acid sequence required for interaction with p53. This suggests that the ~85-kDa form of mdm2 may mediate functions of mdm2 independently of its ability to block p53-mediated functions. Our results do not document that the regulation of mdm2 by T3R is through a direct pathway, because it takes at least 24 h to detect the stimulation (Fig. 1). However, one possible mechanism to account for the lag period in a direct activation pathway is that the mdm2 stimulated by T3 binds with endogenous p53, which in turn acts to decrease p53-mediated mdm2 stimulation (4, 67). This reduction in mdm2 stimulation by p53 offsets the initial extent of stimulation by T3R, resulting in an apparent lag in the time until stimulation by T3 is detected. This is consistent with the finding that endogenous levels of mdm2 appear to be sufficient to regulate p53 levels and that increased expression of mdm2 can reduce the level of p53 (40).

Our results also indicate that p53 independently transactivates Seq1 and Seq2 (Table 1), consistent with the prediction that both Seq1 and Seq2 resemble a p53 consensus sequence (4, 67). Interestingly, activation by Seq1 is similar to that found for the entire 59-bp response sequence, suggesting that Seq1 predominantly contributes to the response of the mdm2 element to p53. In addition, p53 and T3R appear to compete for the same or overlapping DNA sequences (Table 3). These results are consistent with a model in which T3R regulates the mdm2 gene, particularly in cells that lack or contain low levels of p53 or contain p53 mutants deficient in DNA binding. Mutations in the DNA binding region of p53 are common in human cancer, and the wild-type p53 allele is often concomitantly deleted. Our findings suggest that under these conditions, T3R or related factors such as COUP-TF may act to regulate the mdm2 gene. Such stimulation would also occur in cells containing levels of endogenous p53 which only partially compete with T3R or COUP-TF for the mdm2 gene-responsive sequence. This notion is supported by the finding that endogenous T3R can further activate MTV-m59-CAT in the presence of endogenous levels of p53 in GH4C1 cells (Table 4). The regulation of mdm2 by T3R and COUP-TF, as well as other, as-yet-undefined transcription factors, may provide a mechanism for the growth-promoting effects of the T3Rs or other factors on certain cell types as well as for the mdm2-mediated development of tumors in cells containing p53 mutants or low levels of p53.