Structure and E3-ligase activity of the Ring–Ring complex of Polycomb proteins Bmi1 and Ring1b
2006; Springer Nature; Volume: 25; Issue: 11 Linguagem: Inglês
10.1038/sj.emboj.7601144
ISSN1460-2075
AutoresGretel Buchwald, Petra van der Stoop, Oliver Weichenrieder, Anastassis Perrakis, Maarten van Lohuizen, Titia K. Sixma,
Tópico(s)Ubiquitin and proteasome pathways
ResumoArticle18 May 2006free access Structure and E3-ligase activity of the Ring–Ring complex of Polycomb proteins Bmi1 and Ring1b Gretel Buchwald Gretel Buchwald Division of Molecular Carcinogenesis and Center for Biomedical Genetics, Netherlands Cancer Institute, Amsterdam, Netherlands Search for more papers by this author Petra van der Stoop Petra van der Stoop Division of Molecular Genetics and Center for Biomedical Genetics, Netherlands Cancer Institute, Amsterdam, The Netherlands Search for more papers by this author Oliver Weichenrieder Oliver Weichenrieder Division of Molecular Carcinogenesis and Center for Biomedical Genetics, Netherlands Cancer Institute, Amsterdam, Netherlands Search for more papers by this author Anastassis Perrakis Anastassis Perrakis Division of Molecular Carcinogenesis and Center for Biomedical Genetics, Netherlands Cancer Institute, Amsterdam, Netherlands Search for more papers by this author Maarten van Lohuizen Maarten van Lohuizen Division of Molecular Genetics and Center for Biomedical Genetics, Netherlands Cancer Institute, Amsterdam, The Netherlands Search for more papers by this author Titia K Sixma Corresponding Author Titia K Sixma Division of Molecular Carcinogenesis and Center for Biomedical Genetics, Netherlands Cancer Institute, Amsterdam, Netherlands Search for more papers by this author Gretel Buchwald Gretel Buchwald Division of Molecular Carcinogenesis and Center for Biomedical Genetics, Netherlands Cancer Institute, Amsterdam, Netherlands Search for more papers by this author Petra van der Stoop Petra van der Stoop Division of Molecular Genetics and Center for Biomedical Genetics, Netherlands Cancer Institute, Amsterdam, The Netherlands Search for more papers by this author Oliver Weichenrieder Oliver Weichenrieder Division of Molecular Carcinogenesis and Center for Biomedical Genetics, Netherlands Cancer Institute, Amsterdam, Netherlands Search for more papers by this author Anastassis Perrakis Anastassis Perrakis Division of Molecular Carcinogenesis and Center for Biomedical Genetics, Netherlands Cancer Institute, Amsterdam, Netherlands Search for more papers by this author Maarten van Lohuizen Maarten van Lohuizen Division of Molecular Genetics and Center for Biomedical Genetics, Netherlands Cancer Institute, Amsterdam, The Netherlands Search for more papers by this author Titia K Sixma Corresponding Author Titia K Sixma Division of Molecular Carcinogenesis and Center for Biomedical Genetics, Netherlands Cancer Institute, Amsterdam, Netherlands Search for more papers by this author Author Information Gretel Buchwald1, Petra van der Stoop2, Oliver Weichenrieder1, Anastassis Perrakis1, Maarten van Lohuizen2 and Titia K Sixma 1 1Division of Molecular Carcinogenesis and Center for Biomedical Genetics, Netherlands Cancer Institute, Amsterdam, Netherlands 2Division of Molecular Genetics and Center for Biomedical Genetics, Netherlands Cancer Institute, Amsterdam, The Netherlands *Corresponding author. Division of Molecular Carcinogenesis and Center for Biomedical Genetics, Netherlands Cancer Institute, Plesmanlaan 121, 1066 CX Amsterdam, Netherlands. Tel.: +31 20 5121959; Fax: +31 20 5121954; E-mail: [email protected] The EMBO Journal (2006)25:2465-2474https://doi.org/10.1038/sj.emboj.7601144 PDFDownload PDF of article text and main figures. ToolsAdd to favoritesDownload CitationsTrack CitationsPermissions ShareFacebookTwitterLinked InMendeleyWechatReddit Figures & Info Polycomb group proteins Ring1b and Bmi1 (B-cell-specific Moloney murine leukaemia virus integration site 1) are critical components of the chromatin modulating PRC1 complex. Histone H2A ubiquitination by the PRC1 complex strongly depends on the Ring1b protein. Here we show that the E3-ligase activity of Ring1b on histone H2A is enhanced by Bmi1 in vitro. The N-terminal Ring-domains are sufficient for this activity and Ring1a can replace Ring1b. E2 enzymes UbcH5a, b, c or UbcH6 support this activity with varying processivity and selectivity. All four E2s promote autoubiquitination of Ring1b without affecting E3-ligase activity. We solved the crystal structure of the Ring–Ring heterodimeric complex of Ring1b and Bmi1. In the structure the arrangement of the Ring-domains is similar to another H2A E3 ligase, the BRCA1/BARD1 complex, but complex formation depends on an N-terminal arm of Ring1b that embraces the Bmi1 Ring-domain. Mutation of a critical residue in the E2/E3 interface shows that catalytic activity resides in Ring1b and not in Bmi1. These data provide a foundation for understanding the critical enzymatic activity at the core of the PRC1 polycomb complex, which is implicated in stem cell maintenance and cancer. Introduction The Ring-domain proteins Ring1b and Bmi1 are important members of Polycomb group (PcG) proteins that adjust chromatin conformation and mediate target gene repression. During development, PcG proteins and their counteracting Trithorax-group (Trx-G) antirepressor complexes are responsible for stable maintenance of correct transcription patterns of specific key regulators such as homeotic genes. They possess an epigenetic transcriptional memory function during development and cell proliferation, which is not only required for correct cell behaviour and body plan but also later in life to maintain cell fate and to prevent oncogenic cell transformations (reviewed in Jacobs and van Lohuizen, 2002; Orlando, 2003; Lund and van Lohuizen, 2004a). Absence of Bmi1 leads to a defect in stem cell self-renewal (Park et al, 2003; Leung et al, 2004; Bruggeman et al, 2005), illustrating a crucial role in maintenance of cell fate also at the cellular level. PcG proteins assemble into at least two biochemically and functionally distinct complexes. The initiation complex Polycomb repressive complex 2 (PRC2) and the maintenance complex PRC1 are involved in developmentally regulated and tissue-specific transcriptional silencing of Hox genes in flies and mammals (Lund and van Lohuizen, 2004b; Cernilogar and Orlando, 2005). In human cells, the PRC1 core complex contains stoichiometric amounts of RING1B (RNF2), RING1A (RING1), BMI1, EDR1 (HPH1) and CBX4 (HPC2), whereas the PRC2 core complex consists of EED, EZH2 and SUZ12 (Orlando, 2003; de Napoles et al, 2004; Lund and van Lohuizen, 2004b; Wang et al, 2004). Gene duplication has generated the RING1A and RING1B pair and the BMI1 and MEL18 pair. Although these proteins have very high sequence similarity, they appear to fulfil different functions. The PRC1 protein Bmi1 was originally identified as an oncogene, which, when overexpressed, collaborates with c-Myc to induce the formation of B-cell lymphomas (reviewed in Jacobs and van Lohuizen, 2002). Next to BMI1, it has become evident that deregulation of several other PcG genes may play a role in a variety of human tumours such as different types of leukaemia, medulloblastoma, breast cancer and non-small-cell lung cancer (Raaphorst, 2005). When compared to other PRC1 core proteins, Bmi1 appears to fulfil a unique role in that its levels are tightly regulated and it displays strong dosage sensitivity: even two-fold changes in protein expression have profound effects on biological outcome such as lymphoma formation (Jacobs et al, 1999). PcG complexes bind to chromatin and initiate and maintain gene repression, which is thought to be achieved by covalent modifications including methylation, deacetylation and ubiquitination of core histones (Francis et al, 2001; de Napoles et al, 2004; Wang et al, 2004; Cernilogar and Orlando, 2005). Recent evidence supports the role of RING1A, RING1B and BMI1 in the ubiquitination pathway of histone H2A (de Napoles et al, 2004; Fang et al, 2004; Wang et al, 2004). Ubiquitination is a form of post-translational modification in which a small 76 amino-acid protein, ubiquitin, is conjugated through its C-terminus to lysines on cellular proteins, where it provides a signal for degradation (K48 polyubiquitin chains) or a regulatory function (monoubiquitination and other chain types). Ubiquitin conjugation is mediated by a conserved E1–E2–E3 cascade of enzymatic reactions (Weissman, 2001; Pickart and Eddins, 2004) in which the E3 ligase catalyses the last step of ubiquitin conjugation by forming an isopeptide bond between a target lysine and the C-terminus of ubiquitin. (Laney and Hochstrasser, 1999; Pickart, 2001; Glickman and Ciechanover, 2002). RING1A, RING1B and BMI1 are essential for the function of the PRC1 complex, which acts as an ubiquitin E3 ligase that monoubiquitinates histone H2A at lysine 119 (Wang et al, 2004). Monoubiquitinated H2A and MacroH2A are enriched on the inactive female X-chromosome and are thought to be involved in its stable silencing (Fang et al, 2004; de Napoles et al, 2004; Hernandez-Munoz et al, 2005). Although both RING1A and RING1B have been implicated in monoubiquitination of H2A, RING1B appears to serve a predominant role in that loss of RING1B leads to major depletion of monoubiquitinated H2A, whereas loss of RING1A has only a minor effect. Interestingly, this also corresponds with the relative importance for development of these related Ring-domain proteins as Ring1a knockout mice only display minor skeletal aberrations, whereas loss of Ring1b leads to a full loss of PRC1 silencing resulting in early embryonic lethality (del Mar Lorente et al, 2000; Voncken et al, 2003). Both Bmi1 and Ring1b contain an N-terminal Ring-domain. Ring-domains interact directly with the E2-ubiquitin thiolester and catalyse the ubiquitin transfer from the E2 to the target (Joazeiro and Weissman, 2000), most likely by positioning the E2 close to the target (Zheng et al, 2000, 2002). Ring-domains and another type of E3-ligase, the U-box domains, are structurally related, but whereas the latter is stabilised by a set of hydrogen bonding and salt bridges, the Ring-domain is stabilised by chelation of Zn2+ (Joazeiro and Weissman, 2000; Hatakeyama et al, 2001; Ohi et al, 2003). Ring-domains can function in the context of larger complexes, such as the SCF complex, in the context of larger proteins, such as Cbl, or in the context of Ring–Ring complexes such as BRCA1/BARD1 (Freemont, 2000; Joazeiro and Weissman, 2000; Brzovic et al, 2001b). BMI1 and RING1A were shown to form a heterodimer both in vivo and in vitro (Satijn and Otte, 1999). Their Ring-domains promote this interaction and allows homodimerisation of each protein (Satijn and Otte, 1999), whereas the Ring-domain of Bmi1 is critical for its tumorigenic function (Alkema et al, 1997). Here we study the enzymatic activity, structure and complex-formation of the Ring1b/Bmi1 complex. Results and discussion H2A ubiquitination by Ring1b is enhanced by Bmi1 in vitro The importance of Ring1b for monoubiquitination of histone H2A by the core PRC1 complex was recently shown (Fang et al, 2004; Wang et al, 2004). We confirmed the ubiquitin-conjugating activity of Ring1b of H2A in vitro using purified mouse GST-Ring1b amino acids (aa 1–331) (Q9CQJ4) lacking eight residues at the C-terminus (Figure 1A) in a mixture of nucleosomal histones, recombinant ubiquitin, E1, UbcH5c as E2, ubiquitin and ATP (Figure 1B, lane 3). We then tested the effect of adding full-length Escherichia coli-expressed Bmi1 (P25916) to the reaction. Titration of Bmi1 into GST-Ring1b shows an activating effect of Bmi1 on histone H2A modification (Figure 1B, upper panel), whereas Bmi1 alone does not show any E3-ligase activity, as we observe no increase over background of monoubiquitinated histone H2A (Figure 1B, lower panel). This dose-dependent increase of Ring1b's target-specific E3-ligase activity is interesting as it may provide one possible explanation for the unique sensitivity of the cell to changes in the dose of Bmi1 in the PRC1 complex in vivo (Jacobs et al, 1999). Figure 1.Ring1b/Bmi1 and the minimal Ring1b/Bmi1 complex are catalytically active on histone H2A. GST-Ring1b, full-length Ring1b/Bmi1 (2 μM) or different Ring-domain constructs of Ring1b and Ring1a in complex with Bmi1109 (2 μM) were incubated in ligase buffer in the presence of 28 nM human E1, 1.5 μM UbcH5c, 22 μM ubiquitin, 3 mM ATP and 4.8 μM H2A (18 μg nucleosomes). The reaction mixture was incubated at 30°C for 1 h. Samples were analysed for ubiquitination by SDS–PAGE and Western blot as described in Materials and methods. (A) Proteins and complexes used in this study. (B) Bmi1 enhances ligase activity of GST-Ring1b in vitro and is not active by itself. Upper panel: Bmi1 was titrated to the indicated final concentration into 2 μM GST-Ring1b, E1, MgATP, UbcH5c and nucleosomes. Lower panel: titration of Bmi1 with the indicated final concentrations in the presence of E1, MgATP, UbcH5c and nucleosomes and in the presence of 2 μM GST-Ring1b in lane 7 and 8, respectively. Western blots against ubiquitin. (C, D) The short Ring–Ring complex, Ring1b159/Bmi1109, is catalytically active in the presence of human E1 and UbcH5c. (C) Western blot against ubiquitinated histone H2A (uH2A) and histone H2A (H2A). (D) Western blot against ubiquitin. Ubiquitinated H2A, ubiquitinated Ring1b and Bmi1 are indicated. *Indicates diubiquitin. (E) Ring1a can substitute for Ring1b and the Ring1a111/Bmi1109 complex is equally active as the minimal Ring1b114/Bmi1109 complex against H2A; Western blot against ubiquitin. *Indicates diubiquitin. Download figure Download PowerPoint We copurified a Ring1b/Bmi1 complex after individual expression of Ring1b (aa 1–331) and full-length murine Bmi1. This complex forms a heterotetramer, a dimer of heterodimers, as shown by gel filtration and multiangle static light scattering (MALLS) (138 kDa compared to a theoretical value of 150 kDa, data not shown). We confirmed that this complex is active in monoubiquitination of histone H2A with antibodies against ubiquitin, H2A and ubiquitin-H2A (Figure 1C). Besides the monoubiquitinated H2A, various ubiquitinated products are formed in these in vitro reactions. Antibodies against Ring1b and Bmi1 detect monoubiquitinated Ring1b and Bmi1, both running at ∼47 kDa (see Supplementary Figure 2). In addition, longer polyubiquitin chains are formed. The formation of these chains is not dependent on the presence of nucleosomes (Figure 1D, lane 8) and there is neither Ring1b nor Bmi1 in most of these products (Supplementary Figure 2), and also no Ubc5c (data not shown), indicating that these are unanchored polyubiquitin chains. A minimal Ring1b/Bmi1 complex is sufficient for the observed E3-ligase activity To define the E3-ligase activity within the Ring1b/Bmi1 complex, we used sequence alignment and secondary structure predictions aiming at a minimal catalytic domain. Domain boundaries were set by the end of predicted secondary structure. We coexpressed GST-fusions of either Ring1b159 or Ring1b114 together with untagged Bmi1109 in E. coli. The minimal Ring1b/Bmi1 complexes were copurified using the GST-tag (for Ring1b) and the GST-tag was removed. The proteins did not dissociate during purification or tag removal, indicating a stable complex. Both minimal heterodimers eluted from a gel-filtration column at the apparent size of the heterodimer and there was no evidence for higher order complexes. We could show that these Ring–Ring complexes are active in monoubiquitinating H2A (Figure 1C–E) and that the reaction is dependent on the presence of the E1 and E2 enzymes. The fact that even these Ring–Ring complexes are fully active has implications for the binding site of the substrate. Traditionally, the Ring-domains are expected to bind to the E2 in ubiquitin conjugation, but in this case they must also be able to bind to target H2A in the nucleosome. The Ring-domain of Ring1a is equally active as E3 ligase Gene duplication in mammals has created a Ring1b homolog, the Ring1a protein, that is also present in the PRC1 complex in stoichiometric amounts (Satijn and Otte, 1999; Wang et al, 2004). We retrieved Ring1a sequences from several species that are up to 30 amino acids longer at their N-terminus than the commonly used murine sequence in the literature (Schoorlemmer et al, 1997). The alignment reveals that part of the novel N-terminal sequence (aa 11–30) of Ring1a is well conserved in Ring1b (Figure 3E). Figure 2.Specific E2 requirement for histone H2A ubiquitination by the Ring1b159/Bmi1109 complex. Western blots against ubiquitin showing the effect of different E2 enzymes on H2A ubiquitination and poly-ubiquitin chain formation. For conditions, see Figure 1 and Materials and methods. Download figure Download PowerPoint Figure 3.The crystal structure of the Ring1b/Bmi1 Ring–Ring complex. (A) Stereo ribbon representation of the crystal structure of the Ring1b159/Bmi1109 complex, with Ring1b in orange, Bmi1 in green. The Zn2+-ions and ligands are shown in grey. Site A is formed by Cys 51, 54, 72 and 75 in Ring1b and by Cys 18, 21, 39 and 42 in Bmi1. Site B is formed by Cys 67, 87, 90 and His 69 in Ring1b and by Cys 34, 53, 56 and His 36 in Bmi1. Transparent segments indicate disordered regions. (B) Both Ring motifs are very similar. Superposition of the Ring1b and Bmi1 Ring-domains. A three-residue insertion in the Bmi1 Ring-domain is indicated. (C, D) Details of the interface between Ring1b and Bmi1 (C) formed by the embracing arm of Ring1b and Bmi1's Ring-domain and kinked C-terminal helix, with important interactions indicated. (D) Close up view of the interface region formed by the helical bundle flanking the Ring-domains. Side chains of residues involved in the interaction according to analysis with PISA are shown. Arg 70 in Ring1b forms a salt bridge with Asp 72 in Bmi1, which is stabilised by lateral interactions with Phe 106 and Leu 75. (E) Sequence alignment of Ring-domain proteins in PRC1 with secondary structure indicated. Zn2+ binding site I is highlighted in blue and Zn2+ binding site II is highlighted in cyan. The autoubiquitination site in Ring1b is marked with a filled triangle. Sequence visible in the structure is underlined. Download figure Download PowerPoint We coexpressed and copurified a complex of the Ring-domains of Ring1a and Bmi1 (Ring1a111/Bmi1109), including this novel N-terminus. This complex is active as E3 ligase and basically indistinguishable from the Ring1b114/Bmi1109 heterodimer in ubiquitin conjugation of histone H2A, polyubiquitin chain formation and autoubiquitination (Figure 1E). In vivo, however, Ring1a and Ring1b are functionally distinct, as most of the ubiquitinated H2A is depleted upon loss of Ring1b and only a low level of uH2A remains, which can be removed when Ring1a is additionally lost (Fang et al, 2004; de Napoles et al, 2004). Only a subset of E2s promotes Ring1b/Bmi1 ligase activity We tested Ring1b/Bmi1 ligase activity with a panel of available ubiquitin-conjugating E2 enzymes to see if the preference for UbcH5c that was reported by Wang et al (2004) for RING1B is conserved in the heterodimer. In Ring1b159/Bmi1109-dependent assays with nine different human E2s (UbcH5a, UbcH5b, UbcH5c, UbcH3, Rad6, E2-25K, UbcH6, UbcH7 and UbcH10), ubiquitination of histone H2A can only be observed in the presence of any UbcH5 subtype or UbcH6 (Figure 2). This is a common set of E2 enzymes that was also active in promoting E3-ligase activity of other proteins such as ARD1 (Vichi et al, 2005) or Topors (Rajendra et al, 2004). In the Ring1b/Bmi1 reactions, the processivity and selectivity of the different E2s varies: UbcH5c creates more polyubiquitin chains then UbcH5a and UbcH5b, whereas UbcH6 does not produce these at all. A physical interaction of Ring1b with E2-25K/Hip2 had been reported (Lee et al, 2001). We confirmed the existence of this E2/E3 complex in analytical gel-filtration experiments with Ring1b159/Bmi1109 but saw no stimulation of E2 catalytic activity compared to the E2 alone. None of the other E2s tested (UbcH5c, UbcH3, Rad6, Ubc9) formed a stable complex with Ring1b159/Bmi1109 in gel-filtration experiments. Thus, neither absence nor presence of a tight physical interaction correlates with catalytic activity in these E2/E3 pairs. A similar discrepancy between catalytic efficiency and binding has been noted previously for UbcH7 in complex with BRCA1/BARD1 (Brzovic et al, 2003). Autoubiquitination of Ring1b We observed monoubiquitination of both Ring1b and Bmi1, as confirmed by Western blot (Supplementary Figure 2). These products are also observed when nucleosomes are left out of the reaction (Figure 1D, lane 8). In the shorter Ring–Ring complexes Ring1b159/Bmi1109 (Figure 1D, lane 6) and Ring1b114/Bmi1109 (Figure 1E, lane 7), we could only detect modification of Ring1b, suggesting that Bmi1 is modified at a position outside of the Ring-domain. Mass-spectrometry after in-gel tryptic digestion identified Lys 112 of Ring1b as the site for auto-monoubiquitination of Ring1b159/Bmi1109 (data not shown). This site is found in the C-terminal α-helix of Ring1b that interacts with Bmi1 (see below, Figure 3D). The lysine residue is accessible for modification and the ubiquitin would not interfere with E2 interaction as predicted from known E2/E3 complexes (Zheng et al, 2000; Zhang et al, 2005). We mutated Lys 112 to arginine in Ring1b to test whether the autoubiquitination has an effect on E3-ligase activity of the heterodimeric Ring–Ring complex. This mutant showed no difference in target modification on nucleosomes. The analysis is complicated by the fact that even the mutant complex still creates ubiquitinated Ring1b product (Supplementary Figure 2B), indicating that another lysine in the Ring1b Ring-domain now becomes ubiquitinated. However, one of our later constructs of Ring1b, Ring1b16–114 (lacking the 15 N-terminal residues), is not autoubiquitinated. This complex also shows no difference in target ubiquitination when compared to Ring1b114/Bmi1109, (not shown) or Ring1a111/Bmi1109 (Figure 5A), suggesting that autoubiquitination of the Ring1b Ring-domain has no influence on catalytic activity of the Ring–Ring complex. Figure 4.Structural comparison of Ring1b/Bmi1 with Ring and U-box dimers. (A) Superposition of Ring1b/Bmi1 onto the four-helix bundle of BRCA1/BARD1 (blue). The Zn2+ atoms in Ring1b/Bmi1 (grey) and BRCA1/BARD1 (magenta) are also depicted. (B) Superposition of Ring1b/Bmi1 onto the U-box domain of the ChIP homodimer (blue). The interface in these dimers is made by the regions that flank the Ring-domains. Download figure Download PowerPoint Figure 5.Role of the N-terminus of Ring1a and Ring1b. (A) Assays performed with isolated Ring1a30–111 and Bmi1 and complexes of Ring1b/Bmi1, Ring1b16–114/Bmi1109 and Ring1a111/Bmi1109 using conditions as described in the legend of Figure 1 and Materials and methods; Western blot against ubiquitin. (B) Bmi1 was titrated to the indicated final concentration into 2 μM Ring1a30–111, E1, MgATP, UbcH5c and nucleosomes; Western blot against ubiquitin. (C) Titration of Bmi1 to the indicated final concentrations into 2 μM Ring1a30–111 or Ring1a111/Bmi1109, respectively, using the same conditions as described in (B); Western blot against ubiquitin. Download figure Download PowerPoint Only UbcH5c seems to promote polyubiquitination of Ring1b and Bmi1, whereas the other three E2s promote only monoubiquitination of the E3 proteins (see Supplementary Figure 2). This is most likely a function of the general processive nature of UbcH5c, as there seems to be no change in target modification compared to other E2s (Figure 2). Altogether these biochemical studies show no detectable effect of the autoubiquitination of either Ring1b or Bmi1, but the possibility remains that autoubiquitination of Ring1b at Lys 112 has a modulatory effect in vivo on the function of Ring1b within the larger Polycomb complex, for instance by affecting PRC1 complex formation. Crystal structure of the heterodimeric Ring1b/Bmi1 Ring–Ring complex We determined the crystal structure of the N-terminal Ring containing fragments of coexpressed Ring1b159/Bmi1109 that was active in histone H2A ubiquitination. The structure was determined at 2.0 Å using the anomalous diffraction of the four zinc atoms and one iodine from the solvent. The weak anomalous data collected at remote wavelengths gave sufficient phasing information to solve the structure and autotrace the model with ARP/wARP (see Supplementary Table 1 for data analysis and refinement statistics). The final refined model has an R-factor of 17.6 with Rfree of 21.3%. Electron density for the first 14 and the last 45 C-terminal residues of Ring1b is missing, most likely because this part of the protein is degraded during crystallisation, as revealed by SDS–PAGE. The Ring1b and Bmi1 structures contain the usual Ring motif with flanking N- and C-terminal helices (Figure 3). Both have an extension that forms a helix at the C-terminus of Bmi1 and a long loop at the N-terminus in Ring1b. The Ring motif is composed of two large Zn2+-binding loops, a short three-stranded antiparallel β-sheet, a central α-helix and a 310-helix (Figure 3A). The overall structure of the central Ring motif in both subunits of the heterodimer is similar to other Ring-domain structures (Bellon et al, 1997; Brzovic et al, 2001b), characterised by two large Zn2+-binding loops, in which eight Cys and His residues bind two Zn2+ ions in a so-called cross-brace arrangement. The first and third pair of Zn2+ ligands coordinate the first Zn2+ ion, whereas the second and fourth pair coordinate the second Zn2+ ion (Borden, 2000). The overlay of the Bmi1 and Ring1b Ring motifs shows that both structures are very similar in this region (Figure 3B, r.m.s.: 0.58 Å on 54 Cα atoms). The only difference can be observed in a loop extension of Bmi1 after the 310-helix, where it has three additional residues (aa 62–64) (Figure 3B). Comparison of the individual Bmi1 and Ring1b structures to the PDB using the DALI server (Holm and Sander, 1993) gives the highest similarity (z-score 10.6 for Bmi1, 9.6 for Ring1b) to the U-box protein CHIP (Zhang et al, 2005). High similarities were also identified for the U-box protein AtPub14 (Andersen et al, 2004), and for Ring-containing proteins such as the V(D)J recombination-activating protein Rag1 (Bellon et al, 1997), the breast and ovarian cancer tumour suppressor BRCA1 and its partner BARD1 (Brzovic et al, 2001b). Heterodimer formation The major part of the heterodimer interface between Ring1b and Bmi1 is formed by the N-terminal arm of Ring1b (residues 15–39) that bends away and loops around to embrace the Bmi1 Ring-domain, bending the C-terminal helix of Bmi1 (residues 85–103). It seems that this arrangement of the C-terminal helix in Bmi1 helps to position the N-terminus of Ring1b. The N- and C-terminal flanking regions of the central Ring motif (residues 50–103 of Ring1b and 17–72 of Bmi1) interact with each other and form a short four-helix bundle involving only 1–2 turns. Residues 45–49 and 104–114 of Ring1b form short antiparallel helices that interact with the two Ring-domain flanking helices of Bmi1 formed by residues 9–16 and 73–84. These interfaces agree with data that show that N- and C-terminal regions adjacent to the Ring-domains are critical for complex formation between RING1A (the closely related homologue of Ring1b) and BMI1 (Satijn and Otte, 1999). The total interface buries 2289 Å2 and is relatively hydrophilic. There are 15 salt bridges and 31 hydrogen bonds in the interface (Figure 3C and D) and Arg 70 in Ring1b forms a salt bridge with Asp 72 in Bmi1. Mutation of the equivalent arginine in dRing (R65C) caused loss of function in Drosophila (Fritsch et al, 2003) and abrogated the RING1B (R70C) enzymatic activity on H2A (Wang et al, 2004). This was interpreted as a loss of enzymatic activity, but the structure reveals that Arg 70 in Ring1b is buried in the dimer interface and is most likely critical for the interaction with Bmi1 (Figure 3D). This indicates how important the Ring1b interaction with Bmi1 is in vivo. Comparison to other dimeric Ring–Ring or U-box complexes The heterodimeric arrangement of the Ring1b/Bmi1 heterodimer strongly resembles the heterodimeric BRCA1/BARD1 complex (Brzovic et al, 2001b) (Figure 4A), whereas it is very different from the RAG1 dimer (Bellon et al, 1997). Alignment of Ring1b/Bmi1 on the four-helix bundle of BRCA1/BARD1 reveals that the Ring motifs have a very similar local arrangement and that the interaction is mainly defined by structural elements that flank the Ring motifs. However, whereas the main BRCA1/BARD1 dimerisation interface is formed by a four-helical antiparallel bundle, the Ring1b/Bmi1 heterodimer utilises a much shorter helical bundle and the embracing N-terminal loop of Ring1b to create the main interface with Bmi1. Nevertheless, both interfaces bury similar solvent-accessible surface areas (Brzovic et al, 2001b). In BRCA1/BARD1, the heterodimer interface is functionally extremely important, as many of the BRCA1 point mutations that are linked to breast cancer predisposition are found in the interface between the helices (Brzovic et al, 2001a). This correlates well with the positive effect that the dimerisation with Bmi1 has on the Ring1b activity and with the importance of the R65C mutation in dRing. The heterodimeric Ring–Ring complex of the tumour suppressor BRCA1 and BARD1 is also an E3 ligase and also monoubiquitinates histone H2A (Lorick et al, 1999; Hashizume et al, 2001; Mallery et al, 2002), but in contrast to the Ring1b/Bmi1 complexes the minimal interacting Ring-domains BRCA1 (1–109) and BARD1 (26–119) were not active in H2A ubiquitination (Mallery et al, 2002) although they form a stable complex (Brzovic et al, 2001b). Much larger Ring-containi
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