Structure of the RXR–RAR DNA-binding complex on the retinoic acid response element DR1
2000; Springer Nature; Volume: 19; Issue: 5 Linguagem: Inglês
10.1093/emboj/19.5.1045
ISSN1460-2075
AutoresFraydoon Rastinejad, Trixie Wagner, Qiang Zhao, Sepideh Khorasanizadeh,
Tópico(s)Antioxidant Activity and Oxidative Stress
ResumoArticle1 March 2000free access Structure of the RXR–RAR DNA-binding complex on the retinoic acid response element DR1 Fraydoon Rastinejad Corresponding Author Fraydoon Rastinejad Department of Pharmacology, X-ray Crystallography Laboratory, University of Virginia, Charlottesville, VA, 22908 USA Department of Biochemistry and Molecular Genetics, School of Medicine, University of Virginia, Charlottesville, VA, 22908 USA Search for more papers by this author Trixie Wagner Trixie Wagner Department of Pharmacology, X-ray Crystallography Laboratory, University of Virginia, Charlottesville, VA, 22908 USA Search for more papers by this author Qiang Zhao Qiang Zhao Department of Pharmacology, X-ray Crystallography Laboratory, University of Virginia, Charlottesville, VA, 22908 USA Search for more papers by this author Sepideh Khorasanizadeh Corresponding Author Sepideh Khorasanizadeh Department of Biochemistry and Molecular Genetics, School of Medicine, University of Virginia, Charlottesville, VA, 22908 USA Search for more papers by this author Fraydoon Rastinejad Corresponding Author Fraydoon Rastinejad Department of Pharmacology, X-ray Crystallography Laboratory, University of Virginia, Charlottesville, VA, 22908 USA Department of Biochemistry and Molecular Genetics, School of Medicine, University of Virginia, Charlottesville, VA, 22908 USA Search for more papers by this author Trixie Wagner Trixie Wagner Department of Pharmacology, X-ray Crystallography Laboratory, University of Virginia, Charlottesville, VA, 22908 USA Search for more papers by this author Qiang Zhao Qiang Zhao Department of Pharmacology, X-ray Crystallography Laboratory, University of Virginia, Charlottesville, VA, 22908 USA Search for more papers by this author Sepideh Khorasanizadeh Corresponding Author Sepideh Khorasanizadeh Department of Biochemistry and Molecular Genetics, School of Medicine, University of Virginia, Charlottesville, VA, 22908 USA Search for more papers by this author Author Information Fraydoon Rastinejad 1,2, Trixie Wagner1, Qiang Zhao1 and Sepideh Khorasanizadeh 2 1Department of Pharmacology, X-ray Crystallography Laboratory, University of Virginia, Charlottesville, VA, 22908 USA 2Department of Biochemistry and Molecular Genetics, School of Medicine, University of Virginia, Charlottesville, VA, 22908 USA *Corresponding authors. E-mail: [email protected] or E-mail: [email protected] The EMBO Journal (2000)19:1045-1054https://doi.org/10.1093/emboj/19.5.1045 PDFDownload PDF of article text and main figures. ToolsAdd to favoritesDownload CitationsTrack CitationsPermissions ShareFacebookTwitterLinked InMendeleyWechatReddit Figures & Info The 9-cis retinoic acid receptor (retinoid X receptor, RXR) forms heterodimers with the all-trans retinoic acid receptor (RAR) and other nuclear receptors on DNA regulatory sites composed of tandem binding elements. We describe the 1.70 Å resolution structure of the ternary complex of RXR and RAR DNA-binding regions in complex with the retinoic acid response element DR1. The receptors recognize identical half-sites through extensive base-specific contacts; however, RXR binds exclusively to the 3′ site to form an asymmetric complex with the reverse polarity of other RXR heterodimers. The subunits associate in a strictly DNA-dependent manner using the T-box of RXR and the Zn-II region of RAR, both of which are reshaped in forming the complex. The protein–DNA contacts, the dimerization interface and the DNA curvature in the RXR–RAR complex are distinct from those of the RXR homodimer, which also binds DR1. Together, these structures illustrate how the nuclear receptor superfamily exploits conformational flexibility and locally induced structures to generate combinatorial transcription factors. Introduction The 9-cis retinoic acid receptor (retinoid X receptor, RXR) is an important member of the nuclear receptor family because it forms heterodimers with many other receptors, including the all-trans retinoic acid receptor (RAR), vitamin D3 receptor (VDR), thyroid hormone receptor (TR), the peroxisome proliferator activated receptor (PPAR) and the nerve growth factor induced-B (NGFI-B) receptor (Leblanc and Stunnenberg, 1995; Mangelsdorf and Evans, 1995; Mangelsdorf et al., 1995). RAR and RXR, each of which have α, β and γ isotypes, transduce the retinoid signal into a variety of genetic responses, and their functions underlie the essential role played by retinoids in the development and homeostasis of vertebrates (Chambon, 1996). A consensus sequence 5′-AGGTCA-3′ is the core recognition element for the entire family of nearly 150 non-steroid nuclear receptors to which RXR and RAR belong (Mangelsdorf and Evans, 1995). However, RXR and RAR alone display negligible binding to this consensus site as monomers (Leid et al., 1992). Heterodimerization increases their joint affinity and selectivity for retinoic acid response elements (RAREs), which are composed of both binding sites arranged in tandem. The RXR–RAR heterodimer binds more efficiently to RAREs than either of the homodimeric forms of RXR or RAR (Leid et al., 1992). The core sequence of the DNA-binding domain (DBD) is highly conserved in the nuclear receptor superfamily, with >40% amino acid identity over a 67-residue region. This sequence is comprised of two zinc-nucleated modules and two α-helices that fold into a single globular domain. The use of a highly conserved receptor DBD together with a single major core binding sequence raises an important question as to how diverse signaling pathways are created in this transcription factor superfamily (Gronemeyer and Moras, 1995). Formation of combinatorial transcription factors involving RXR is one important mechanism by which complex DNA sites can be employed with greater selectivity (Yu et al., 1991; Bugge et al., 1992; Kliewer et al., 1992b; Marks et al., 1992). The functional consequence of forming receptor heterodimers is that in some cases two distinct ligands can co-regulate transcription from a single gene-regulatory element (Forman et al., 1995). Importantly, the DBDs of the nuclear receptors can generate the same pattern of DNA selectivity and dimerization as the full-length receptors (Mader et al., 1993; Perlmann et al., 1993; Zechel et al., 1994). A second dimerization function in the ligand-binding domains of some receptors has no selective role for response element recognition, but can further stabilize some dimeric assemblies (Perlmann et al., 1996). All RXR heterodimers preferentially bind response elements composed of two AGGTCA sites arranged in a direct repeat configuration with characteristic inter-half-site spacings of 1–5 bp (these are known as DR1–DR5, respectively; Umesono et al., 1991; Mangelsdorf and Evans, 1995). Interestingly, the sequence of the spacer is less critical than its size for discrimination. The selective recognition of DRs based on inter-half-site spacings has been formalized in a 1–5 rule that defines the highest affinity binding sites for each RXR heterodimer (Umesono et al., 1991; Mangelsdorf and Evans, 1995). However, the binding repertoire for other members of the nuclear superfamily extends beyond the usage of direct repeat geometry, as some factors bind efficiently to inverted and everted repeats of core hexamer (Mangelsdorf and Evans, 1995). The multiple arrangements with which the same consensus AGGTCA sequence is utilized in this family suggest that combinatorial nuclear receptors possess a remarkable readout mechanism that allows them to decipher the geometry of a binding site in addition to its sequence. An associated feature of any asymmetric response element is the polarity adopted by the subunits of the bound receptor heterodimer. The non-symmetric RXR–RAR complexes allow the position of each receptor to be distinguished as upstream or downstream, even though the two hexameric binding sites may have an identical sequence. The RXR–RAR complex, therefore, can adopt different polarities when bound to its various response elements, and these alternative arrangements have been shown to confer different functions on the heterodimer in terms of hormone and co-repressor binding (Kurokawa et al., 1994, 1995). A previous structural analysis of the RXR–TR DBD complex bound to a thyroid response element DR4 allowed the direct visualization of the polarity associated with that complex (Rastinejad et al., 1995). The asymmetric assembly was established through the cooperation between DBD subunits, which occurs only when the inter-half-site spacing is 4 bp in length and RXR is positioned upstream of TR (Rastinejad et al., 1995). The response element repertoire of the RXR–RAR complex is considerably less selective than that of the RXR–TR complex, which was restricted to a single direct repeat element (DR4). In fact, the RXR–RAR heterodimer mediates transcriptional control through DR1, DR2 and DR5 sequences found in naturally occurring RAREs (Mangelsdorf et al., 1991; Predki et al., 1994; Chambon, 1996). The multiple high-affinity DNA-binding targets suggest a large degree of versatility on the part of their DBDs in forming favorable interaction surfaces, each of which has a distinct effect on target gene regulation (Kurokawa et al., 1995; Chambon, 1996). To explore how the joint assembly of RXR and RAR on DNA is mediated, we determined the 1.7 Å crystal structure of the ternary complex containing RXR and RAR DBDs bound to the DR1 element, the sequence first identified in the promoter of the cytosolic retinol-binding protein II gene (Mangelsdorf et al., 1991). In vivo, RXR–RAR heterodimers on DR1 repress transcription in both the absence and presence of their hormones (Kurokawa et al., 1995). In examining the structure of the complex, we asked how the DR1 specifies the polar assembly of the RXR and RAR DBDs, how cooperativity and target selectivity are achieved, and how DNA-induced changes in the secondary and tertiary structures of RXR and RAR promote the assembly of their complex. Results Overview of the structure The protein and DNA constructs used in co-crystallization are shown in Figure 1A and B. The polypeptides were designed to support the ability of RXR and RAR to form cooperative interactions on DR1. Using these constructs, the heterodimer of RXR and RAR DBDs gives half-maximal DR1 binding when each protein is at a concentration of ∼300–350 nM (data not shown). In contrast, the DBD of RXR alone shows a >10-fold reduction in binding to DNA sites containing a single AGGTCA sequence (Leid et al., 1992; Lee et al., 1993; Zhao et al., 2000). The T-box sequence of RXR, which has the sequence KREAVQEER at the C-terminal extension of the DBD, is required for the formation of the RXR homodimer DR1 complex, as well as the formation of other heterodimeric complexes when RXR occupies the site downstream of DR1 (Wilson et al., 1992; Predki et al., 1994; Ijpenberg et al., 1997). Figure 1.The protein and DNA constructs used in structure determination. (A) The DNA-binding regions of RXR (residues 129–212) and RAR (residues 82–167) used for co-crystallization. The polypeptides contain two zinc-nucleated modules whose coordinating cysteines are indicated in yellow. Each protein contains two α-helices (α1, α2) in its core domain. A third α-helix, α3, in the T-box of RXR (underlined) is seen in the absence of DNA, but is disrupted upon DNA binding (Holmbeck et al., 1998a,b). Disordered residues not found in the electron density maps are indicated by the small letters. The numbering of the amino acids is referenced to the first Zn-coordinating cysteine (1) for simplicity. (B) The 15 bp DR1 sequence with the consensus recognition half-sites and spacer sequence shown in white and black boxes, respectively. The 5′ overhangs, indicated by the small letters, are not seen in the electron density maps. (C) 2Fo − Fc map revealing the identity of the RAR subunit. RAR is distinguished by clear densities for sites such as Ser16 and Pro(−1). (D) 2Fo − Fc map showing how RXR can be distinguished by unambiguous density at sites such as Tyr16, His(−2) and Ile(−1) Download figure Download PowerPoint There is a good structural overlap between the backbone atoms of RXR and RAR DBDs in their homologous 67-residue core sequences, and this fold is shared with the corresponding DBD structures of TR, RevErb, estrogen receptor (ER), glucocorticoid receptor (GR), NGFI-B and by extension the entire nuclear receptor family (Luisi et al., 1991; Schwabe et al., 1993; Rastinejad, et al., 1995; Zhao et al., 1998; Meinke and Sigler, 1999). To identify the polarity associated with the complex, specific and unambiguous assignments of RXR and RAR in the electron density maps were required. The polypeptides differ in 34 amino acid positions within the region −2 to 75, but most of these residues are conservative substitutions or solvent-exposed positions that are not fully ordered. The high-resolution X-ray data proved helpful in this regard. Figure 1C and D shows that the electron densities belonging to Y16 and its counterpart S16 are unambiguous, allowing the protein electron density containing the former to be assigned to RAR and the latter to RXR. Similarly, the identification of non-conserved residues that precede the core DBD, such as His(−2), Ile(−1) and Pro(−1), also proved helpful. These and other observations are consistent with the binding of RAR and RXR to the upstream and downstream half-sites, respectively. Figure 2 shows the overall structure of the complex. The observed mode of polarity agrees with a previous biochemical study that examined DR1 binding by full-length RAR and RXR polypeptides (Kurokawa et al., 1994). The binding of RXR at the downstream site is uniquely associated with DR1 elements, since most RXR heterodimers studied to date, including the two other RXR–RAR heterodimers on DR2 and DR5, the RXR–VDR heterodimer on DR3, the RXR–TR and RXR–Liver X receptor (LXR) heterodimers on DR4, and the RXR–NGFI-B interactions on DR5, use the opposite polarity, in which RXR binds exclusively at the upstream position. However, the DR1 sequence also supports the cooperative binding of RXR–PPAR with 3′ RXR binding as observed in the current structure (Ijpenberg et al., 1997). The unique asymmetry is a consequence of the subunit's ability to form productive protein–protein contacts in one orientation and not the other. Figure 2.Overall structure of the ternary complex. (A) Top view looking down the 5′ end of the DNA. The DNA phosphates and the zinc atoms are shown in red and white, respectively. The DNA recognition helices (α1) of RXR and RAR are partly invisible in this orientation as they insert into the major grooves of DR1. The C-terminally positioned T-box of RXR points towards the RAR Zn-II module to mediate the subunit interactions. (B) Side view showing the complementary surfaces formed between RAR and RXR and the polarity associated with the complex. Figures are made with the program GRASP (Nicholls et al., 1991). Download figure Download PowerPoint The characteristic spacing of the DR1 response element sets the rotation and translation geometry by which the RXR and RAR subunits must interact while maintaining a favorable registration with respect to the hexameric half-site. The minor groove of the DR1 reaches its narrowest point (5.6 Å) at the spacer base pair 8, precisely where the two proteins meet. The DNA helical axis deviates a total of 6° from that of standard B-DNA. The two AGGTCA sequences are contacted in the major groove by the recognition helix of each DBD (α1 in Figure 1A). These contacts account for all of the major groove interactions of the RXR–RAR complex. In their complex, ∼3500 Å2 of water-accessible surface area is buried, 1900 Å2 of which derives from the RXR–DNA interactions and 1600 Å2 of which is from the RAR–DNA interface. These values are in line with other protein–DNA interactions that involve similar sized recognition modules and DNA-binding sites (Nadassy et al., 1999). The heterodimerization interface and its DNA dependence RXR and RAR DBDs do not form homo- or heterodimeric associations in the absence of specific response elements. Figure 3A shows that the contacts between RXR and RAR in their complex take advantage of the polar functional groups in the minor grooves of base pairs 8 and 9, as well as the well ordered hydration spine associated with DNA structure (Shui et al., 1998). The intimate role of the DNA in aligning the subunits explains why stable interactions between RXR and RAR DNA-binding regions are not possible off DNA. The minor groove compression at the protein–protein junction (base pair 8) is electrostatically favorable, bringing the negatively charged DNA phosphates into closer proximity with the guanidino group of Arg75. This compression, as well as hydrogen-bonding with Gln72 and the ordered water molecules in the minor groove, reduces the conformational flexibility of Arg75, precisely orienting its side-chain to make van der Waals contact with Asn51 of RAR. The orientation of Asn51 with respect to the dimer interface is also restricted through hydrogen-bonding with DNA. An interaction between Glu73 of RXR, Val48 of RAR and bridging water gives rise to a secondary stabilizing interface between subunits. Figure 3.Stereo diagrams showing the contacts between the protein subunits. (A) The RXR–RAR interface involves the DNA minor groove and well ordered water molecules (red spheres). Dotted lines indicate hydrogen-bonding between atoms. The yellow spheres indicate the positions of the Zn-II atoms. Arg75 and Asn51 form complementary van der Waals interactions. (B) The corresponding region of the RXR–DBD homodimer interface on DR1 (Zhao et al., 2000). These and the following molecular display graphics were made using the program Ribbons (Carson and Bugg, 1986). Download figure Download PowerPoint In all, the subunit interactions lead to a total loss of less than ∼400 Å2 of solvent-accessible surface from both proteins. This suggests that the observed dimer interface is inferior to bona fide protein–protein interfaces, as these typically bury >700 Å2 of solvent-exposed area (Janin et al., 1998). However, the extent of the solvent-excluded surface is comparable to and in some cases even favorable relative to other transcription factor interfaces that form exclusively on DNA (Klemm and Pabo, 1996; Zhao et al., 1998, 2000; Fuji et al., 1999; Zheng et al., 1999). The interactions in the RXR–RAR complex are also distinct from those of the homo-cooperative complex of RXR, which forms on the same DR1 response element (see Figure 3B; Zhao et al., 2000). But in both cases, the subunits utilize the DNA infrastructure to stabilize their interactions. This observation suggests that these and other combinatorial RXR complexes do not pre-assemble their DNA-recognition surfaces in solution, but rather assemble only when an appropriate gene-regulatory site is available. Relation to other nuclear receptor assemblies on DR1 In both the homo- and heterodimeric complexes shown in Figure 3, the downstream RXR uses exclusively its T-box to mediate protein–protein interactions with the upstream Zn-II region. However, there are differences in terms of the induced T-box conformation, the protein–protein and the protein–DNA interactions in these assemblies. For example, the subunit interactions in the homodimer rely to some extent on hydrogen-bonding interactions between Glu74 from the T-box of the downstream subunit, and Gln49 and Arg52 from the Zn-II region of the upstream subunit (see Figure 3B). This is not possible in the RXR–RAR interaction, since RAR has a T49 in place of Q49, disabling the salt-bridge at the dimerization surface (Figure 3). The DR1 configuration is also used by the RXR–PPAR complex (Kliewer et al., 1992a; Gearing et al., 1993; Palmer et al., 1995; Ijpenberg et al., 1997). Interestingly, PPARα, PPARβ and PPARγ all contain the same Asn51 and Glu54 residues that provide the upstream contact surfaces shown in Figure 3A. In addition, an A·T base pair is also highly preferred in the DR1 spacer of PPAR response elements, suggesting the possibility of a similar role for the DNA minor groove in aligning subunit interactions (Ijpenberg et al., 1997). However, the binding site for RXR–PPAR is extended relative to that of the RXR–RXR and RXR–RAR, since PPAR also recognizes the minor grooves of 5′ flanking sequences using a C-terminal extension of its core DBD known as the GRIP-box (Ijpenberg et al., 1997; Zhao et al., 1998). These distinctions suggest that a graded affinity is associated with each of these RXR complexes, depending on the sequence of the spacer, the induced curvature in the DNA and the unique sequences flanking the DR1. Factors responsible for the cooperative assembly Figure 3A suggests that protein occupancy at one site can lead to facilitated binding at the second site via protein–protein interactions. An extended DNA-binding surface formed through tight protein–protein interactions can result in a considerable gain in DNA-binding cooperativity. However, given the limited extent of the subunit contacts, it is likely that additional indirect effects must also contribute to cooperation between RXR and RAR. One such mechanism is adjacent DNA site stabilization, when binding of one subunit reduces the conformational flexibility at the adjacent site, thus pre-paying some of the entropic costs associated with its tight binding. It has been shown that the POU domains of Oct-1 use partially overlapping DNA contacts at the center of their octamer site to achieve cooperative binding, even though there is a total absence of protein–protein interactions (Klemm and Pabo, 1996). Similarly, Ubx–Exd subunits cooperate to a significant extent through their partially overlapping DNA contacts at the center of their binding site, which is enough to produce a cooperative enhancement even if their primary protein–protein interactions are removed (Chan et al., 1994; Passner et al., 1999; Piper et al., 1999). Tandem site stabilization may also enhance the assembly of RXR and RAR on DR1, given that the half-sites are separated by only 1 bp and that the subunits form overlapping contacts at the spacer (see section on DNA sequence recognition and Figure 5). Figure 4.Topological comparison of the RXR–RAR–DR1 complex with the (RXR)2–DR1 complex. (A) The superposition of the two complexes shows that the DNA structure and the subunit position at the 5′ (top) half-sites are different. (B) Superposition of the DNA molecules shows a divergence in the helical axes associated with DR1 in its complexes with the RXR homodimer and the RXR–RAR heterodimer. The divergence is most severe at the 5′ half-sites, which are occupied by different proteins in these complexes. (C) For comparison, the superposition of two crystallographically distinct RXR DBD homodimer–DR1 complexes, showing very close overlap throughout, despite different crystal packing environments (Zhao et al., 2000). Download figure Download PowerPoint The RXR and RAR proteins also cooperate through DNA- and dimerization-induced structural transitions in RXR that overcome an inhibition in its DNA binding. We have shown previously that the RXR T-box, in its α-helical structure off DNA (Holmbeck et al., 1998a), poses unfavorable contacts with the DNA via Glu74 and Glu75 and also blocks the DNA-binding surface in α1. A reconfiguration of the T-box structure overcomes both inhibitory effects in the RXR homodimer (Holmbeck et al., 1998b; Zhao et al., 2000). Interestingly, either of the two extended structures seen in downstream subunits (Figure 3) leads to an effective dimerization surface (one in the homodimer, the other in the heterodimer), and relieves the inhibitory effects on DNA binding. A similar mechanism by which the DNA element and a heterodimeric partner can help overcome an inhibitory DNA function associated with a transcription factor has also been described for the Hox–Exd complex (Chan et al., 1996). The role of DNA curvature Further cooperation in a ternary transcriptional complex is achieved when protein occupancy at the one DNA site induces structural distortions at the second site to accommodate protein binding better. The importance of even small DNA deformations, especially bends in the DNA helix, for fine-tuning protein–DNA interactions has been pointed out previously (Gewirth and Sigler, 1995; Dickerson, 1998; Dickerson and Chiu, 1998). The bending of the DNA has also been suggested to be responsible for the cooperative binding of the interferon regulatory factor 1 (IRF-1)–DNA complex, which does not use any contacts between DBDs in its cooperative assembly (Fuji et al., 1999). The utilization of this mechanism in achieving cooperativity in the RXR–RAR–DR1 is illustrated in Figure 4A and B, which shows that the DNA helical axis bends, especially at the 5′ binding site. This distortion appears to facilitate RAR and RXR interactions with their half-sites while being engaged as a heterodimer. Figure 5.DNA sequence recognition by RXR and RAR. (A) A view along the DNA-recognition helix (α1) of RAR showing residues Tyr13, Arg26, Lys22, Glu19 and Arg27 and their direct and water-mediated base contacts. Hydrogen-bonds and water molecules are shown as dotted blue lines and red spheres, respectively. The DNA sequence is numbered as in Figure 1B. (B) The corresponding view of the RXR interface. (C) Summary of the protein–DNA contacts of RAR. Bridging water molecules are shown as black circles. The base pairs in blue form the consensus AGGTCA recognition element. The gray circles indicate the DNA phosphates. (D) Summary of RXR–DNA interactions. The base pairs in orange form the consensus element. Download figure Download PowerPoint The comparison in Figure 4B demonstrates how structural versatility in DNA structure is exploited in accommodating two distinct types of receptor interactions with RXR. The RXR homodimer induces a 12° kink in DR1 compared with the RXR–RAR complex, which bends the DNA by 6°. These induced curvatures are a direct result of the distinct subunit associations on DR1, since the DNA sequences in the two complexes are otherwise identical along 14 out of 15 bp. The kinks in both cases are mainly localized to the central spacer, which adopts a different combination of tilt and roll angles to give rise to the 12 and 6° bends, respectively. Because the spacer is also the convergence point for the protein–protein interactions in each complex, the different helical distortions are a direct consequence of the dimerization arrangements. Figure 4C shows that two RXR homodimer–DR1 complexes from two different crystallographic environments (these being two distinct complexes in the asymmetric unit of the RXR–RXR–DNA crystals) are nearly superimposable with respect to their DNA curvatures (Zhao et al., 2000). This observation suggests that the distinct distortions observed in the helical axes of the RXR–RAR and RXR–RXR binding sites are not caused merely by their different crystallographic packing environments. Recognition of DNA sequence The DNA contacts for both proteins are shown in Figure 5. The base-specific contacts of RXR and RAR occur along 6 and 5 bp, respectively. In the RXR–DNA interface, two of the six base contacts occur along the minor grooves of base pairs 8 and 9. The pattern of major groove contacts for these proteins is similar, as shown in Figure 5A and B. The recognition helix of each receptor forms direct and water-mediated base contacts using Arg27, Lys22, Glu19 and Lys26/Arg26. RXR and RAR both also use a number of highly ordered water molecules to bridge their base-specific and phosphate interactions. In addition, RXR and RAR each form extensive backbone contacts along 7 bp of DNA (Figure 5C and D). We compared the DNA contacts with those seen in the RXR homodimer–DR1 complex (Zhao et al., 2000). In terms of the number of specific protein–DNA interactions, the RXR–RAR complex has a clear advantage over the homodimeric RXR complex. In the homodimer, the subunits together form specific contacts with only six positions along the entire DR1, compared with 11 contacts formed by the heterodimer. Moreover, the three base-specific contacts made by each RXR in the homodimer vary in each independent crystallographic representation of RXR (Zhao et al., 2000). The weak, and by comparison relaxed, binding of the homodimer to DR1 has also been demonstrated by biochemical studies (Dowhan et al., 1994; Yang et al., 1995; Castelein et al., 1996). Protein structural transitions in the complex The structures of the isolated RXR and RAR DBD polypeptides have previously been studied by NMR (Knegtel et al., 1993; Holmbeck et al., 1998a; van Tilborg et al., 1999). In comparing these protein structures with their counterparts bound to DR1, we asked what secondary and tertiary protein structural changes are associated with the formation of the complex. Figure 6 indicates that the two regions undergoing the most dramatic structural rearrangement in each subunit are the T-box and the Zn-II module, both of which interact to stabilize the RXR–RAR–DR1 complex and can adopt other conformations in different contexts (Holmbeck et al., 1998b; van Tilborg et al., 1999). The ability of the highly dynamic Zn-II region of RXR to facilitate the assembly of the RXR–RAR–DR5 complex was suggested in a recent dynamics study of these proteins (van Tilborg et al., 1999). Furthermore, the Zn-II regions of nuclear receptors can in some cases undergo transitions between helix and loop in binding and dissociating from DNA (Schwabe et al., 1993; Holmbeck et al., 1998a,b). Similarly, the T-box sequence
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