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FHL2, a novel tissue-specific coactivator of the androgen receptor

2000; Springer Nature; Volume: 19; Issue: 3 Linguagem: Inglês

10.1093/emboj/19.3.359

1460-2075

Müller Jm,

Hormonal and reproductive studies

Article1 February 2000free access FHL2, a novel tissue-specific coactivator of the androgen receptor Judith M. Müller Judith M. Müller Universitäts-Frauenklinik, Abteilung Frauenheilkunde und Geburtshilfe I, Klinikum der Universität Freiburg, Breisacherstrasse 117, 79106 Freiburg, Germany Search for more papers by this author Ulrike Isele Ulrike Isele Universitäts-Frauenklinik, Abteilung Frauenheilkunde und Geburtshilfe I, Klinikum der Universität Freiburg, Breisacherstrasse 117, 79106 Freiburg, Germany Search for more papers by this author Eric Metzger Eric Metzger Universitäts-Frauenklinik, Abteilung Frauenheilkunde und Geburtshilfe I, Klinikum der Universität Freiburg, Breisacherstrasse 117, 79106 Freiburg, Germany Search for more papers by this author Annette Rempel Annette Rempel Universitäts-Frauenklinik, Abteilung Frauenheilkunde und Geburtshilfe I, Klinikum der Universität Freiburg, Breisacherstrasse 117, 79106 Freiburg, Germany Search for more papers by this author Markus Moser Markus Moser Institut für Pathologie, Klinikum der RWTH Aachen, Pauwelstrasse 30, 52074 Aachen, Germany Search for more papers by this author Armin Pscherer Armin Pscherer Institut für Pathologie, Klinikum der RWTH Aachen, Pauwelstrasse 30, 52074 Aachen, Germany Search for more papers by this author Tobias Breyer Tobias Breyer Abteilung Innere Medizin III, Kardiologie und Angiologie, Klinikum der Universität Freiburg, Hugstetterstrasse 55, 79106 Freiburg, Germany Search for more papers by this author Christian Holubarsch Christian Holubarsch Abteilung Innere Medizin III, Kardiologie und Angiologie, Klinikum der Universität Freiburg, Hugstetterstrasse 55, 79106 Freiburg, Germany Search for more papers by this author Reinhard Buettner Reinhard Buettner Institut für Pathologie, Klinikum der RWTH Aachen, Pauwelstrasse 30, 52074 Aachen, Germany Search for more papers by this author Roland Schüle Corresponding Author Roland Schüle Universitäts-Frauenklinik, Abteilung Frauenheilkunde und Geburtshilfe I, Klinikum der Universität Freiburg, Breisacherstrasse 117, 79106 Freiburg, Germany Search for more papers by this author Judith M. Müller Judith M. Müller Universitäts-Frauenklinik, Abteilung Frauenheilkunde und Geburtshilfe I, Klinikum der Universität Freiburg, Breisacherstrasse 117, 79106 Freiburg, Germany Search for more papers by this author Ulrike Isele Ulrike Isele Universitäts-Frauenklinik, Abteilung Frauenheilkunde und Geburtshilfe I, Klinikum der Universität Freiburg, Breisacherstrasse 117, 79106 Freiburg, Germany Search for more papers by this author Eric Metzger Eric Metzger Universitäts-Frauenklinik, Abteilung Frauenheilkunde und Geburtshilfe I, Klinikum der Universität Freiburg, Breisacherstrasse 117, 79106 Freiburg, Germany Search for more papers by this author Annette Rempel Annette Rempel Universitäts-Frauenklinik, Abteilung Frauenheilkunde und Geburtshilfe I, Klinikum der Universität Freiburg, Breisacherstrasse 117, 79106 Freiburg, Germany Search for more papers by this author Markus Moser Markus Moser Institut für Pathologie, Klinikum der RWTH Aachen, Pauwelstrasse 30, 52074 Aachen, Germany Search for more papers by this author Armin Pscherer Armin Pscherer Institut für Pathologie, Klinikum der RWTH Aachen, Pauwelstrasse 30, 52074 Aachen, Germany Search for more papers by this author Tobias Breyer Tobias Breyer Abteilung Innere Medizin III, Kardiologie und Angiologie, Klinikum der Universität Freiburg, Hugstetterstrasse 55, 79106 Freiburg, Germany Search for more papers by this author Christian Holubarsch Christian Holubarsch Abteilung Innere Medizin III, Kardiologie und Angiologie, Klinikum der Universität Freiburg, Hugstetterstrasse 55, 79106 Freiburg, Germany Search for more papers by this author Reinhard Buettner Reinhard Buettner Institut für Pathologie, Klinikum der RWTH Aachen, Pauwelstrasse 30, 52074 Aachen, Germany Search for more papers by this author Roland Schüle Corresponding Author Roland Schüle Universitäts-Frauenklinik, Abteilung Frauenheilkunde und Geburtshilfe I, Klinikum der Universität Freiburg, Breisacherstrasse 117, 79106 Freiburg, Germany Search for more papers by this author Author Information Judith M. Müller1, Ulrike Isele1, Eric Metzger1, Annette Rempel1, Markus Moser2, Armin Pscherer2, Tobias Breyer3, Christian Holubarsch3, Reinhard Buettner2 and Roland Schüle 1 1Universitäts-Frauenklinik, Abteilung Frauenheilkunde und Geburtshilfe I, Klinikum der Universität Freiburg, Breisacherstrasse 117, 79106 Freiburg, Germany 2Institut für Pathologie, Klinikum der RWTH Aachen, Pauwelstrasse 30, 52074 Aachen, Germany 3Abteilung Innere Medizin III, Kardiologie und Angiologie, Klinikum der Universität Freiburg, Hugstetterstrasse 55, 79106 Freiburg, Germany ‡J.M.Müller, U.Isele and E.Metzger contributed equally to this work *Corresponding author. E-mail: [email protected] The EMBO Journal (2000)19:359-369https://doi.org/10.1093/emboj/19.3.359 PDFDownload PDF of article text and main figures. ToolsAdd to favoritesDownload CitationsTrack CitationsPermissions ShareFacebookTwitterLinked InMendeleyWechatReddit Figures & Info The control of target gene expression by nuclear receptors requires the recruitment of multiple cofactors. However, the exact mechanisms by which nuclear receptor–cofactor interactions result in tissue-specific gene regulation are unclear. Here we characterize a novel tissue-specific coactivator for the androgen receptor (AR), which is identical to a previously reported protein FHL2/DRAL with unknown function. In the adult, FHL2 is expressed in the myocardium of the heart and in the epithelial cells of the prostate, where it colocalizes with the AR in the nucleus. FHL2 contains a strong, autonomous transactivation function and binds specifically to the AR in vitro and in vivo. In an agonist- and AF-2-dependent manner FHL2 selectively increases the transcriptional activity of the AR, but not that of any other nuclear receptor. In addition, the transcription of the prostate-specific AR target gene probasin is coactivated by FHL2. Taken together, our data demonstrate that FHL2 is the first LIM-only coactivator of the AR with a unique tissue-specific expression pattern. Introduction Steroid hormone receptors such as the androgen receptor (AR) constitute a subfamily of the nuclear receptor superfamily of ligand-activated transcription factors that play important roles in development, differentiation and homeostasis (Wilson et al., 1991; Cato and Peterzierl, 1998). Members of the steroid receptor family bind as dimers to palindromic or direct repeat response elements (Evans, 1988; Beato et al., 1995). They share a common modular structure and are composed of several domains that mediate DNA binding, dimerization, ligand binding and transcriptional activity (Mangelsdorf et al., 1995). The ligand binding domain (LBD) performs a number of functions including ligand binding, transcriptional activation or repression and contributes to receptor dimerization. Upon ligand binding several major structural changes are induced within the LBD of nuclear receptors (Moras and Gronemeyer, 1998). One obvious difference between the unliganded (apo)- and liganded (holo)-LBD structures is a positional reorientation of helix 12 (H12) (Moras and Gronemeyer, 1998). H12 is indispensable for the transcriptional activation function (AF) of the LBD and harbours the so-called AF-2 AD core motif (Moras and Gronemeyer, 1998). Like other steroid receptors the AR contains an additional N-terminal ligand-independent activation function, the AF-1 (Evans, 1988; Beato et al., 1995). Recent data show direct interaction between the N- and the C-terminus of the AR, supporting the requirement of both the AF-1 and the AF-2 for transcriptional activation (Jenster et al., 1995; Doesburg et al., 1997; Ikonen et al., 1997). It is suggested that the ligand-induced conformational changes of the LBD in concert with physical interactions with the N-terminus result in the formation of novel surfaces, which allow direct protein–protein interactions of the liganded AR with transcriptional cofactors. Distinct classes of ligand-dependent transcriptional cofactors have been described. They include CBP/p300, the p160 family, pCAF/GCN5 and TRAP/DRIP (Xu et al., 1999). According to the current model these cofactors are organized in multi-protein complexes and facilitate the access of nuclear receptors and the RNA polymerase II core machinery to their target DNA by chromatin remodelling and histone modification. Most of these coactivator complexes not only interact with members of the nuclear receptor family, but also with several other sequence-specific DNA-binding transcription factors (Xu et al., 1999). Under various experimental conditions nuclear receptors are capable of recruiting any of the different cofactor complexes. However, in vivo, only distinct complexes may be required for selective and tissue-specific gene activation (Xu et al., 1999). This raises the question of how target gene selection, and tissue- and development-specific gene activation are achieved in the organism. One attractive possibility to regulate transcription in a specific manner is the restricted expression of cofactors, such as the cold-inducible PPARγ coactivator PGC-1 (Puigserver et al., 1998). These tissue-specific cofactors may allow the recruitment of distinct transcriptional complexes tethered to DNA via the nuclear receptor, finally resulting in selective expression of target genes. During embryogenesis the AR is essential for the development and differentiation of sexual organs (Jenster, 1999). The development and maintenance of the prostate require androgens and the AR (Trapman and Brinkmann, 1996; Jenster, 1999). The AR also controls the production of proteins that are secreted in the prostatic fluid such as prostate-specific antigen or probasin (Matuo et al., 1985; Sinha et al., 1987; Jenster, 1999). In the prostate, the AR is expressed in the epithelial cells, the secretory cells of the prostate, which respond to androgens (Aumüller et al., 1998). Interestingly, the prostate-specific probasin gene is a selective target gene of the AR, whereas other steroid hormone receptors such as the glucocorticoid receptor fail to activate probasin (Claessens et al., 1996). According to the current model, the AR also plays an important role in the development of prostate cancer, since growth and survival of primary prostatic cancer cells are largely dependent on androgens (Gregory et al., 1998). Consequently, androgen ablation therapies are used clinically for treating patients with prostate cancer. Expression of the AR is also detected in many other tissues, mainly in male sexual organs, but for example also in liver and cardiac muscle (Schleicher et al., 1989; Kimura et al., 1993). The physiological function of the AR in these tissues still needs to be defined in detail. However, the observation that androgens can mediate cardiac hypertrophy suggests a role of the AR in heart function (Marsh et al., 1998). The receptors for glucocorticoids (GR), progesterone (PR) and mineralocorticoids (MR) recognize the same DNA element as the AR (Cato and Peterzierl, 1998). In situations where ligands for all steroid receptors are present, differential receptor regulation is necessary to control target gene expression selectively. This could be achieved by interaction with specific coregulators. As demonstrated for most of the other nuclear receptors the AR interacts with ubiquitously expressed coactivators such as members of the p160 family or CBP/p300 (Aarnisalo et al., 1998; Berrevoets et al., 1998). Additional coactivators of the AR have been described. However, for none of these AR cofactors has a selective interaction with the AR been demonstrated, and most of these cofactors also interact with related steroid receptors (Moilanen et al., 1998; Alen et al., 1999; Fujimoto et al., 1999; Heinlein et al., 1999; Hsiao and Chang, 1999; Hsiao et al., 1999; Kang et al., 1999). Therefore, differential regulation of target genes by the nuclear receptors remains unclear. Although it is suggested that AR activation requires the interaction of the N- and C-terminus, all screens for AR cofactors have been performed with isolated receptor domains so far. In order to identify AR cofactors that bind to the surface generated by the interaction of the holo-LBD together with the N-terminus, we employed a modified yeast two-hybrid system. As the bait protein we used a human AR in which the DNA-binding domain (DBD) was replaced by the Gal4 DBD. We cloned a LIM-only protein identical to a previously reported protein FHL2/DRAL with unknown function (Genini et al., 1997; Chan et al., 1998). Our data show that FHL2 is a selective agonist-dependent coactivator of the AR, but not of other nuclear receptors. FHL2 interacts specifically with the AR in vitro and in vivo. FHL2 harbours a strong, autonomous transactivation function and selectively increases the transcriptional activity of the AR in an agonist- and AF-2-dependent manner. FHL2 is therefore the first LIM-only coactivator for a particular member of the nuclear receptor family. Expression analysis of FHL2 mRNA shows strong expression in the ventricles of the heart. Substructure analysis demonstrates FHL2 protein expression in the myocardium of the heart, as well as in the epithelial cell layer of the prostate. Moreover, protein expression of the AR and FHL2 overlaps in the nuclei of these secretory and androgen-sensitive cells of the prostate. Expression of FHL2 results in an agonist- and AR-dependent transcriptional coactivation of the prostate-specific AR target gene probasin, suggesting an important role for the AR–FHL2 complex in prostate function. Results Yeast two-hybrid screen We employed a modified yeast two-hybrid system to identify proteins that interact with the human AR (Wilson et al., 1991). As the bait a hybrid protein (AGA) was used in which the Gal4 DBD replaces the AR DBD (Figure 1A). This approach was chosen in order to isolate AR cofactors, which bind to the surface generated by the interaction of the holo-LBD together with the N-terminus. The transcriptional activity of the bait protein AGA in yeast, especially in the yeast strain HF7c that we used for the two-hybrid assays, is very weak. The screening of a human prostate library was performed in the presence of the synthetic AR agonist R1881. We identified a 1.4 kb cDNA containing an 840 bp open reading frame. The cDNA encodes a protein of 279 amino acids with a predicted molecular weight of 32 kDa (Figure 1A). Sequence similarity searches revealed that it is identical to the previously reported protein FHL2/DRAL with unknown function (Genini et al., 1997; Chan et al., 1998). FHL2 is a LIM-only protein that contains four-and-a-half LIM domains. LIM domains are defined by double zinc finger motifs and mediate protein–protein interactions (Dawid et al., 1998; Jurata and Gill, 1998). Figure 1.FHL2 interacts with the AR in yeast in an agonist-dependent manner. (A) Schematic representation of the AGA bait protein and the FHL2 protein. (B) β-galactosidase activity in yeast expressing AGA and Gal4AD–FHL2 in the presence or absence of the agonist R1881 or the antagonist CPA (bar 2). Bars 1 and 3 show the negative and bar 4 shows the positive controls, respectively. Download figure Download PowerPoint To quantify the in vivo interaction between FHL2 and the AR in yeast, liquid β-galactosidase assays were performed (Figure 1B). FHL2 fused to the activation domain of the yeast transcription factor Gal4 associates with the AR bait protein AGA in an agonist-dependent manner, thereby increasing β-galactosidase reporter gene activity as strongly as the positive control. In the presence of the antagonist cyproterone acetate (CPA), the AR bait protein fails to interact with FHL2 (Figure 1B). Tissue-specific FHL2 mRNA expression To analyse the expression pattern of FHL2 mRNA, Northern blot analyses of human and mouse tissues were performed. Multiple tissue Northern blot analyses of human fetal RNA show specific expression of FHL2 in heart (Figure 2A). In addition, Figure 2A shows that FHL2 expression in mouse adult tissues is also restricted to heart and confirms FHL2 mRNA expression in adult human heart (Genini et al., 1997; Chan et al., 1998). To investigate FHL2 expression in human muscle tissues, an expression analysis of RNA from different adult human striated and smooth muscle tissues was performed (Figure 2A). FHL2 is exclusively expressed in heart muscle, since no FHL2 signal could be detected in skeletal muscle or in smooth muscle from different tissues including the stromal smooth muscle cells of the prostate (Figure 2A). To investigate further the expression pattern of FHL2 in human heart, mRNA from explanted human hearts was subjected to Northern blot analysis. Figure 2B shows that FHL2 is mainly expressed in the right and left ventricles. A similar ventricle restricted expression pattern is observed in non-failing human hearts (data not shown). Figure 2.Analysis of FHL2 expression. (A) FHL2 is specifically expressed in the heart. Northern blots of human tissues (fetal, adult and adult muscle) and adult mouse tissues were probed with FHL2. β-actin was used as an internal control. (B) FHL2 is mainly expressed in the heart ventricles. Northern blot analysis of mRNA of left and right ventricles (LV, RV) and left and right atria (LA, RA) of an explanted human heart. GAPDH was used as a control. (C) FHL2 and AR protein expression in human heart. Extract (200 μg) from a left ventricle was analysed in a Western blot. Controls are shown in lane 2 (10 μg of 293 cell extract transfected with human AR) and lane 3 (100 ng of purified His-tagged FHL2). The upper panel was decorated with an α-AR antibody, the lower panel with an α-FHL2-specific antibody. (D) Immunohistochemical staining of FHL2 in cardiac muscle cells (a and b) or FHL2 and AR in prostate epithelium (c–f). Controls are shown in b, d and f. In the heart, FHL2 antibodies stained specifically myocardial fibres (my), but not vascular smooth muscle cells (sm) (a). Two hematoxilin–eosin stained arteriolae (at) shown in (a) entirely lack FHL2 immunoreactivity. Both cytoplasmic and nuclear FHL2 immunoreactivity was detected in the secretory epithelium of the prostate (c). AR immunoreactivity was confined to the nucleus of the secretory epithelium (e). Abbreviations: at, arteriola; br, brain; co, colon; ep, epithelial cells; ht, heart; kd, kidney; li, liver; lm, lumen; lu, lung; my, myofibres; pan, pancreas; pl, placenta; pr, prostate; skm, skeletal muscle; si, small intestine; sm, smooth muscle; sp, spleen; st, stomach; str, stroma; te, testis; ut, uterus. Download figure Download PowerPoint To analyse specifically protein expression of FHL2 in human tissues we generated a monoclonal antibody against FHL2. The α-FHL2 antibody is highly specific for FHL2 and does not interact with any other LIM domain-containing protein tested (data not shown). In human heart the α-Flirt antibody detects a protein of 32 kDa, as exemplified in an extract of the left ventricle (Figure 2C, lower panel). Notably, in the same heart extract AR protein is also observed with an α-AR-specific antibody (Figure 2C, upper panel), demonstrating coexpression of both proteins in heart. Additional immunohistochemical analyses show that FHL2 protein is specifically detected in myofibres of heart myocardium (Figure 2D, a and b). No FHL2 protein is detected in aorta, endo- or epicardium (data not shown). Furthermore, in the smooth muscle cells surrounding the arteriolae FHL2 protein is not expressed (Figure 2D, a). In the prostate FHL2 protein is detected in the epithelial cells (Figure 2D, c). In agreement with our Northern blot data (Figure 2B) FHL2 protein is not expressed in the stromal smooth muscle cells of the prostate. Importantly, in the secretory and androgen-sensitive epithelial cells nuclear FHL2 clearly colocalizes with nuclear AR immunoreactivity (Figure 2D, c and e). FHL2 binds selectively to the AR To analyse whether FHL2 fulfils the characteristics of a transcriptional coactivator we first investigated the AR–FHL2 protein–protein interaction. GST pulldown experiments were performed using GST–FHL2 and various in vitro translated [35S]methionine-labelled nuclear receptors (Figure 3A). Figure 3A shows that GST–FHL2 binds specifically to the full-length AR but fails to interact with the control GST protein. Although GST–FHL2 binds full-length AR both in the absence (data not shown) and in the presence of ligand, we included agonist in all further pulldown assays to ensure comparability. GST–FHL2 does not associate with the most homologous steroid hormone receptors GR, PR or MR in the presence of their cognate ligands. FHL2 also fails to associate with receptors of the retinoic acid receptor/thyroid hormone receptor subfamily (data not shown). These results indicate that the interaction between the AR and FHL2 is highly specific for this particular member of the nuclear receptor superfamily. Figure 3.FHL2 interacts with the AR in vitro and in vivo. (A) Selective interaction of FHL2 with the AR. GST pulldown assays were performed with in vitro translated, labelled AR, PR, GR or MR in the presence of their cognate ligands and GST–FHL2 fusion protein. GST protein was used as a control. (B) AR coimmunoprecipitates with FHL2 in the presence of the natural agonist DHT. Nuclear extracts of 293 cells transfected with AR and Flag-FHL2 were immunoprecipitated with α-Flag antibody. Ten percent of the extract used for immunoprecipitation was loaded as input in lanes 1 and 3. The immunoprecipitate (IP) is loaded in lanes 2 and 4. Western blots were either decorated with an α-Flag- or an α-AR-specific antibody. Download figure Download PowerPoint Association between the AR and FHL2 is also revealed by coimmunoprecipitation (Figure 3B). Nuclear extracts from 293 cells transfected with the AR and Flag-epitope-tagged FHL2 were immunoprecipitated using α-Flag antibody. Western blot analysis shows that the AR–Flag–Flirt complex is efficiently immunoprecipitated in the presence of the natural AR agonist dihydrotestosterone (DHT). No AR was found in immunoprecipitated complexes using untagged FHL2 (data not shown) or in the absence of agonist (Figure 3B), demonstrating specificity and agonist dependence of the AR–FHL2 interaction. Mapping of the AR and FHL2 interaction domains To delineate the domains in the AR that mediate the protein–protein interaction with FHL2 in vitro, GST pulldown experiments were performed (Figure 4). GST–FHL2 binds full-length AR, but interacts neither with the AR LBD (AR624–919) nor with the AR1–626, which lacks the LBD (Alen et al., 1999). This confirms that the interaction with FHL2 requires the structurally intact AR. When H12 of the AR LBD, which harbours the activation function 2 core motif, was deleted (ARΔH12), no interaction with FHL2 was observed (Figure 4A). In other nuclear receptors helix 3 (H3) is part of the coactivator binding surface (Nolte et al., 1998). To identify specific amino acids within the H3 region that could potentially affect interaction with FHL2, we assayed a series of point mutations in the AR H3 region (Alen et al., 1999). GST–FHL2 binds to the AR mutants K720A, W718A, A719K and to the double mutant V715A/V716A (data not shown). However, FHL2 did not bind the mutant ARL712R (Figure 4A). These results suggest that the H12 and the H3 regions of the AR are an important part of the FHL2 interaction surface. Figure 4.AR associates with FHL2 in an AF-2-dependent manner. (A) GST pulldown assays were performed using GST–FHL2 fusion protein and in vitro translated, labelled AR or AR mutants in the presence of the agonist R1881. (B) Interaction between the AR and either GST, GST–FHL2, GST–FHL2(1–162) or GST–FHL2(163–279) fusion proteins in the presence of the agonist R1881. Numbers above the scheme indicate the amino acid position. Download figure Download PowerPoint To determine which region of the FHL2 protein binds to the AR, a series of mutant GST–FHL2 proteins was tested for their ability to interact with full-length AR (Figure 4B). Deletion of either the FHL2 N-terminus or the C-terminal LIM domains 3–4 reduced but did not abolish the ability of the FHL2 protein to bind to the AR (Figure 4B). These results suggest that both the N- and C-terminal LIM domains contribute to the interaction with the AR. FHL2 contains an autonomous transcriptional activation domain Next, we investigated the transcriptional properties of FHL2 in transient transfection experiments. Since we could not observe DNA binding of FHL2 (data not shown), plasmids expressing the Gal4 DBD fused to full-length FHL2 (Gal–FHL2) were generated and tested in comparison with the known coactivators Gal–TIF2.1 (Voegel et al., 1996) and Gal–SRC1 (Onate et al., 1998). Figure 5 shows that FHL2 tethered to DNA robustly induces the transcriptional activity of the G5E1b-LUC reporter gene in various cell lines. Importantly, the activity of Gal–FHL2 and Gal–TIF2.1 is comparable, whereas Gal-SRC1 seems to be a weaker activator in the cell lines tested (Figure 5). Taken together, these data show that FHL2 contains an autonomous transcriptional activation function. Figure 5.FHL2 contains an autonomous transactivation function. The Gal–FHL2 fusion protein transactivates the G5E1b-LUC reporter gene in different cell lines (CV-1, 293 and HL-1). The coactivators Gal–TIF2.1 and Gal–SRC1a were used as controls. Download figure Download PowerPoint FHL2 acts as a coactivator of AR-dependent transcription To examine the potential regulation of the AR by FHL2 on a naturally occurring gene the MMTV promoter was chosen because the steroid hormone receptors AR, PR, GR and MR are known to regulate its expression in a ligand-dependent fashion (Schüle et al., 1990). Accordingly, we cotransfected each of these steroid hormone receptors together with FHL2 and the MMTV-LUC reporter gene into 293 cells (Figure 6A). Coexpression of the AR and FHL2 results in a ligand-dependent coactivation, which is not promoted in the presence of an AR antagonist. Importantly, the ligand-dependent transcriptional activity of GR, PR and MR remained unchanged in the presence of FHL2 (Figure 6A). The same result was obtained when the coactivation assay was performed with sub-saturating agonist concentrations for the various receptors (data not shown). In addition, the transcriptional activity of all other nuclear receptors tested, for example ERs, RXR, RAR, TR, VDR, GCNF and RORs, is not coactivated by FHL2 (data not shown). As expected, coactivation of AR is AF-2-dependent as demonstrated by the mutant ARΔH12 (Figure 6A). To compare the ability of FHL2 to coactivate the AR with the ability of previously described coactivators we tested TIF2, SRC1a or SRC1e together with the AR and the MMTV-LUC reporter gene in 293 cells. Figure 6B shows that similar to the other coactivators FHL2 potently coactivates the AR in an agonist-dependent manner. Figure 6.FHL2 is a specific coactivator of the AR. (A) FHL2 coactivates the AR in an agonist- and AF-2-dependent manner. Expression plasmids coding for AR, ARΔH12, PR, GR or MR were cotransfected with the MMTV-LUC reporter with or without FHL2 in 293 cells. (B) FHL2, TIF2, SRC1e or SRC1a coactivate the AR to a similar extent in 293 cells. (C) FHL2 functions as a coactivator of the AR-specific probasin-LUC reporter (PB-LUC). AR and FHL2 were cotransfected as indicated in the presence of two different AR agonists (R1881, DHT) or the antagonist CPA in CV-1 cells. Download figure Download PowerPoint FHL2 coactivates the transcription of the prostate-specific AR target gene probasin The promoter of the cellular probasin gene, which is expressed in the epithelial cells of the prostate, is selectively regulated by the AR (Claessens et al., 1996). Therefore, we tested FHL2 coactivator function on a probasin reporter (PB-LUC) (Figure 6C). FHL2 enhances the activity of the AR in the presence of either synthetic (R1881) or natural (DHT) agonists in CV-1 cells. Antagonists such as CPA, however, completely block transactivation. Taken together, these data clearly demonstrate that the coactivator function of FHL2 for the AR is AF-2- and agonist-dependent in different cell types and promoter environments (Figure 6B and C). The fact that FHL2 coactivates a well known AR target gene supports a role of the AR–FHL2 complex in prostate function. Discussion Recent studies suggest that tissue-restricted gene expression can be controlled by tissue-specific coactivators of transcription factors (Xu et al., 1999). Using a modified yeast two-hybrid screen we identified a novel tissue-specific coactivator of the AR. Sequence comparison showed that it is identical to the previously described FHL2/DRAL protein of unknown function (Genini et al., 1997; Chan et al., 1998). FHL2 is a LIM-only protein that contains four LIM domains and an N-terminal half LIM domain. LIM domains are characterized by a cysteine-composed double zinc finger motif: C-X2-C-X16–23-H-X2-(C/H)-X2-C-X2-C-X16–23-C-X2-(C/H/D) (Jurata and Gill, 1998). LIM domains can mediate protein–protein interaction with LIM domain-containing proteins or various other classes of proteins (Dawid et al., 1998). FHL2 is a selective coactivator of the AR We show that FHL2 is a bona fide coactivator of the AR. FHL2 interacts specifically with the AR in vitro and in vivo and harbours a strong, autonomous transactivation function. FHL2 selectively increases the transcriptional activit