Article15 November 2000free access The structural basis for the recognition of acetylated histone H4 by the bromodomain of histone acetyltransferase Gcn5p David J. Owen David J. Owen MRC Laboratory of Molecular Biology, Hills Road, Cambridge, CB2 2QH UK Search for more papers by this author Prisca Ornaghi Prisca Ornaghi Centro di studio per gli Acidi Nucleici, CNR, c/o Dipartimento di Genetica e Biologia Molecolare, Università 'La Sapienza', P.le A.Moro 5, 00185 Roma, Italy Search for more papers by this author Ji-Chun Yang Ji-Chun Yang MRC Laboratory of Molecular Biology, Hills Road, Cambridge, CB2 2QH UK Search for more papers by this author Nicholas Lowe Nicholas Lowe MRC Laboratory of Molecular Biology, Hills Road, Cambridge, CB2 2QH UK Search for more papers by this author Philip R. Evans Philip R. Evans MRC Laboratory of Molecular Biology, Hills Road, Cambridge, CB2 2QH UK Search for more papers by this author Paola Ballario Paola Ballario Centro di studio per gli Acidi Nucleici, CNR, c/o Dipartimento di Genetica e Biologia Molecolare, Università 'La Sapienza', P.le A.Moro 5, 00185 Roma, Italy Search for more papers by this author David Neuhaus David Neuhaus MRC Laboratory of Molecular Biology, Hills Road, Cambridge, CB2 2QH UK Search for more papers by this author Patrizia Filetici Patrizia Filetici Centro di studio per gli Acidi Nucleici, CNR, c/o Dipartimento di Genetica e Biologia Molecolare, Università 'La Sapienza', P.le A.Moro 5, 00185 Roma, Italy Search for more papers by this author Andrew A. Travers Corresponding Author Andrew A. Travers MRC Laboratory of Molecular Biology, Hills Road, Cambridge, CB2 2QH UK Search for more papers by this author David J. Owen David J. Owen MRC Laboratory of Molecular Biology, Hills Road, Cambridge, CB2 2QH UK Search for more papers by this author Prisca Ornaghi Prisca Ornaghi Centro di studio per gli Acidi Nucleici, CNR, c/o Dipartimento di Genetica e Biologia Molecolare, Università 'La Sapienza', P.le A.Moro 5, 00185 Roma, Italy Search for more papers by this author Ji-Chun Yang Ji-Chun Yang MRC Laboratory of Molecular Biology, Hills Road, Cambridge, CB2 2QH UK Search for more papers by this author Nicholas Lowe Nicholas Lowe MRC Laboratory of Molecular Biology, Hills Road, Cambridge, CB2 2QH UK Search for more papers by this author Philip R. Evans Philip R. Evans MRC Laboratory of Molecular Biology, Hills Road, Cambridge, CB2 2QH UK Search for more papers by this author Paola Ballario Paola Ballario Centro di studio per gli Acidi Nucleici, CNR, c/o Dipartimento di Genetica e Biologia Molecolare, Università 'La Sapienza', P.le A.Moro 5, 00185 Roma, Italy Search for more papers by this author David Neuhaus David Neuhaus MRC Laboratory of Molecular Biology, Hills Road, Cambridge, CB2 2QH UK Search for more papers by this author Patrizia Filetici Patrizia Filetici Centro di studio per gli Acidi Nucleici, CNR, c/o Dipartimento di Genetica e Biologia Molecolare, Università 'La Sapienza', P.le A.Moro 5, 00185 Roma, Italy Search for more papers by this author Andrew A. Travers Corresponding Author Andrew A. Travers MRC Laboratory of Molecular Biology, Hills Road, Cambridge, CB2 2QH UK Search for more papers by this author Author Information David J. Owen1, Prisca Ornaghi2, Ji-Chun Yang1, Nicholas Lowe1, Philip R. Evans1, Paola Ballario2, David Neuhaus1, Patrizia Filetici2 and Andrew A. Travers 1 1MRC Laboratory of Molecular Biology, Hills Road, Cambridge, CB2 2QH UK 2Centro di studio per gli Acidi Nucleici, CNR, c/o Dipartimento di Genetica e Biologia Molecolare, Università 'La Sapienza', P.le A.Moro 5, 00185 Roma, Italy *Corresponding author. E-mail: [email protected] The EMBO Journal (2000)19:6141-6149https://doi.org/10.1093/emboj/19.22.6141 PDFDownload PDF of article text and main figures. ToolsAdd to favoritesDownload CitationsTrack CitationsPermissions ShareFacebookTwitterLinked InMendeleyWechatReddit Figures & Info The bromodomain is an ∼110 amino acid module found in histone acetyltransferases and the ATPase component of certain nucleosome remodelling complexes. We report the crystal structure at 1.9 Å resolution of the Saccharomyces cerevisiae Gcn5p bromodomain complexed with a peptide corresponding to residues 15–29 of histone H4 acetylated at the ζ-N of lysine 16. We show that this bromodomain preferentially binds to peptides containing an N-acetyl lysine residue. Only residues 16–19 of the acetylated peptide interact with the bromodomain. The primary interaction is the N-acetyl lysine binding in a cleft with the specificity provided by the interaction of the amide nitrogen of a conserved asparagine with the oxygen of the acetyl carbonyl group. A network of water-mediated H-bonds with protein main chain carbonyl groups at the base of the cleft contributes to the binding. Additional side chain binding occurs on a shallow depression that is hydrophobic at one end and can accommodate charge interactions at the other. These findings suggest that the Gcn5p bromodomain may discriminate between different acetylated lysine residues depending on the context in which they are displayed. Introduction The recognition of specific modifications in the N- and C-terminal tails of the nucleosomal histones has been postulated to be one of the key interactions determining the transcriptional competence of chromatin (Strahl and Allis, 2000). One such modification is the acetylation of particular lysine residues in the N-terminal regions of histones H3 and H4. This type of modification has long been correlated with the activation of transcription (reviewed by Turner, 1991; Grunstein, 1997; W.L.Cheung et al., 2000; Kouzarides, 2000; Sterner and Berger, 2000). Histone acetylation is mediated by acetyltransferases including Gcn5p (Brownell et al., 1996), p300/CBP (Bannister and Kouzarides, 1996; Ogryzko et al., 1996), P/CAF (Yang et al., 1996) and TAFII250 (Mizzen et al., 1996). The selectivity of these enzymes depends on both their substrates and their environment within the cell. Free Gcn5p preferentially acetylates Lys14 of free histone H3 and to a lesser extent Lys8 and Lys16 of free histone H4 (Kuo et al., 1996). However, Gcn5p by itself is unable to modify nucleosomal histones (Kuo et al., 1996). Such an ability is conferred by association with other proteins in large macromolecular histone acetylation complexes such as the ADA and SAGA complexes (Grant et al., 1997). In these complexes the pattern of lysine modification by Gcn5p is altered (Grant et al., 1997). In addition to its histone acetyltransferase (HAT) domain, Gcn5p contains a C-terminal domain that is also found both in other HATs, including P/CAF, p300/CBP and TAFII250, and in the ATPase subunit of certain chromatin remodelling complexes, including RSC, SWI/SNF and their homologues (Haynes et al., 1992; Jeanmougin et al., 1997). This conserved 110 amino acid module is termed the bromodomain and was originally identified as a sequence motif common to the Drosophila brahma and female–sterile homeotic proteins, the yeast SWI2/SNF2 proteins and the human CCG1 protein (Tamkun et al., 1992). The name is derived from brahma by analogy to the chromodomain. Several lines of evidence suggest that the bromodomain may be directly involved in chromatin remodelling, particularly that associated with transcriptional activation. In the absence of Gcn5p, the nuclease-sensitive region of the HIS3 promoter is invaded by nucleosomes and the gene is repressed (Filetici et al., 1998). Efficient activation of HIS3 gene transcription specifically requires the bromodomain of Gcn5p in addition to the HAT domain (Marcus et al., 1994), although the former module is not required for the interaction of Gcn5p with ADA2, a component of the ADA complex. Similarly, Syntichaki et al. (2000) demonstrated that the Gcn5p bromodomain was not required in vivo for Gcn5p-mediated histone acetylation at a synthetic promoter, but was necessary for subsequent Swi2p-dependent nucleosome remodelling and consequent transcriptional activation. At the yeast PHO5 and PHO8 promoters, loss of Gcn5p HAT activity prevents the complete chromatin remodelling associated with sub-maximal and maximal activation, respectively (Gregory et al., 1998, 1999), while no remodelling is observed at PHO8p in the absence of active Swi2 (Gregory et al., 1999). At the HO promoter, the Swi2p-containing SWI–SNF remodelling complex recruits the SAGA complex (Cosma et al., 1999; Krebs et al., 1999) prior to activation. Taken together these observations suggest a model which proposes that transcriptional activation at certain promoters requires the concerted action of both the SAGA and SWI–SNF complexes, both of which contain bromodomains. This correlation of bromodomain function with chromatin remodelling suggested that this module might target different activities to nucleosomes (Winston and Allis, 1999). Consistent with this finding, three binding studies showed that the bromodomain interacted with the N-terminal regions of histones H3 and H4. However, while Ornaghi et al. (1999) demonstrated that the Gcn5p bromodomain bound specific unmodified sequences of histone H4, both Dhalluin et al. (1999) and Jacobson et al. (2000) showed that the P/CAF bromodomain and the TAFII250 dibromodomain, respectively, exhibited a strong preference for acetylated histone tails. The solution structure of the P/CAF bromodomain (Dhalluin et al., 1999) and the crystal structure of the TAFII250 dibromodomain (Jacobson et al., 2000) revealed that the bromodomain is a conserved four-helix bundle with a pronounced cleft between two loops. Dhalluin et al. (1999) proposed, on the basis of interactions with analogues to N-acetyl lysine, that this cleft was the primary recognition site for the acetylated histone tails, although N-acetyl lysine by itself did not bind to the P/CAF bromodomain. In this paper we report the crystal structure of a complex between an acetylated peptide from histone H4 and the Gcn5p bromodomain at a resolution of 1.9 Å. We show that the binding site for N-acetyl lysine is a deep cleft containing a number of conserved residues, including at its mouth three tyrosine residues proposed to be involved in histone tail binding from NMR studies (Dhalluin et al., 1999). The structure explains the molecular basis for the selective binding of this modified amino acid. We also show that additional interactions between the peptide and the domain can explain the binding of unmodified histone tails and may provide a means for discriminating between different sequences adjacent to N-acetylated lysines. Results and discussion Binding of a peptide from histone H4 depends on N-acetylation of lysine To test the binding selectivity of the Gcn5p bromodomain we used a 15 amino acid peptide corresponding to residues 15–29 of histone H4 (Figure 1). This sequence was chosen because it contained a lysine residue (Lys16) that can be acetylated in vivo and also because when unacetylated it interacts preferentially with the Gcn5p bromodomain in vitro (Ornaghi et al., 1999). Figure 1.Sequence of the Gcn5p bromodomain used for crystallization and for NMR spectroscopy. Highly and absolutely conserved residues in the bromodomain are marked by one and two asterisks, respectively. Amino acids encoded by the vector are in lower case. Residues directly contacting the N-acetyl lysine in the peptide are indicated by closed circles and residues contacting other parts of the peptide by open circles. The nomenclature for the secondary structure follows that of Dhalluin et al. (1999). αZ′ is a short α-helix that is present in all bromodomain structures but was previously unnamed. α- and 310-helices are indicated by dark grey and light grey boxes, respectively. Download figure Download PowerPoint We acquired and assigned the HSQC spectrum of the free bromodomain and then titrated the protein with acetylated and non-acetylated versions of the peptide. The acetylated, but not the non-acetylated, peptide induced a number of distinct chemical shift changes in the resonances of backbone amide groups of the bromodomain (Figure 2). These shift differences gradually increased throughout the titration, which was taken to a maximum acetylated peptide:bromodomain ratio of 5:1. We conclude from these data that the bromodomain has a strong preference for the acetylated, relative to the non-acetylated, peptide. The data also show that the peptide and the bromodomain are in fast exchange between free and bound states on the NMR chemical shift timescale. Figure 2.The Gcn5p bromodomain binds specifically to an H4 peptide containing N-acetyl lysine. Superimposed (15N, 1H) HSQC spectra of free bromodomain and bromodomain plus unacetylated peptide (left) and free bromodomain and bromodomain plus acetylated peptide (right). In both cases, the spectrum for the free bromodomain is shown in black and that complexed with the peptide in red. Download figure Download PowerPoint Signals for 109 and 108 backbone amide groups were assigned for the free protein and complex, respectively. There are 114 non-proline residues present in the domain, and the two N-terminal residues gave no backbone amide signals. Other absences were the NH signals of residues Asn407, Gly408 and Ser412 in the free protein and additionally of Tyr413 in the complex, probably reflecting the mobility of the BC loop [in the nomenclature of Dhalluin et al. (1999)]. The residues exhibiting changed chemical shifts on addition of the peptide were concentrated in two regions of sequence particularly including loops ZA and BC and the α-helical regions immediately flanking the BC loop (Figure 3), both spatially located at one end of the molecule (Figure 4D). The number of changed chemical shifts observed in the presence of the H4 15–29 peptide, acetylated at position 16, although generally congruent with those observed by Dhalluin et al. (1999), on addition of an H4 peptide corresponding to residues 1–12 in which Lys8 was acetylated, was significantly greater, suggesting that the H4 15–29 peptide is involved in more extensive interactions. This inference is consistent with the binding studies of Ornaghi et al. (1999), who observed that the Gcn5p bound the unacetylated H4 peptide containing residues 16–34, but not that containing residues 1–16. Figure 3.Histogram of chemical shift changes induced on addition of H4 peptide acetylated at Lys16. 1H and 15N changes are denoted by filled and open bars, respectively. Download figure Download PowerPoint Figure 4.Overall structure and peptide binding. (A) Ribbon diagram showing the bundle of four main α-helices, Z, A, B and C, with the Nζ-acetyl lysine side chain of the peptide bound in a deep slot at the top of the bundle. The ribbon is coloured from green (N-terminus) to gold (C-terminus). (B) 'Top' view of the molecular surface coloured by hydrophobic potential (dark green marks favourable regions for hydrophobic interaction; grey, less favourable; light green, intermediate). The five visible residues of the peptide fit into a shallow groove, with the acetyl lysine side chain in a deep slot. The hydrophobic surface at the base of the pocket formed by Phe352 and Val356, as well as that lining the side of the pocket formed by Pro351, Val 356, Tyr364 and Tyr413, are not easily visible in this view. (C) The same view as (B), showing the underlying helices coloured as in (A). (D) Mapping of backbone NH chemical shift changes onto residues 329–438 of the peptide backbone of the Gcn5p bromodomain in the same orientation as (B) and (C). 1H and 15N changes are indicated in red and blue, respectively. The colours are merged so that the shade reflects the relative contributions of the two shift changes and the intensity reflects the magnitude of the changes. Residues for which no backbone amide groups were assigned are shown in yellow (see text). Download figure Download PowerPoint Crystal structure of a Gcn5p bromodomain–acetylated H4 peptide complex The crystal structure of the Gcn5p bromodomain–H4 peptide complex was solved at a resolution of 1.9 Å using phasing from a single mercury derivative. No electron density was found for the first 10 N-terminal residues and the C-terminal residue of the bromodomain construct, and also for the C-terminal 10 residues of the peptide corresponding to histone H4 positions 20–29. The structure of the bromodomain from Gcn5p was, as expected from previous structures solved (Dhalluin et al., 1999; Jacobson et al., 2000), a four-helical bundle (Figure 4A). A number of conserved, mainly hydrophobic residues, but also some hydrophilic ones including Asn402, are involved in forming and stabilizing the hydrophobic core of the domain. A surface representation shows a narrow cleft with a cavity at the bottom formed by the ZA and BC loops (Figure 4B). Hydrophobic surface potential mapping showed the sides to be hydrophobic in nature, indicating its suitability as a site of hydrophobic contact mediating protein–peptide interactions. The structure was determined in a complex with a peptide corresponding to residues 15–29 of histone H4. The peptide binds in an extended conformation across the patch of high hydrophobic surface potential with specificity being provided by the interactions of N-acetyl lysine at H4 position 16 and the side chains at positions 18 and 19 (Figures 4B, C and 5A). This 'peptide-surface' or 'pronged plug in socket' type of interaction between a small folded domain and a linear peptide is common. Such interactions have been described between SH2 or PTB domains and phosphotyrosine-containing peptides (Eck et al., 1993, 1996; Waksman et al., 1993; Zhou et al., 1995), PDZ domains with C-terminal xS/TxV sequences (Doyle et al., 1996), μ2 subunit of AP2 with YxxΦ internalization motifs (Owen and Evans, 1998) and the clathrin N-terminal β-propeller with the LΦxΦD/E clathrin box motifs (ter Haar et al., 2000). The peptide is spatially complementary with the groove in which it lies (Figure 4B), but its backbone makes only one direct H-bond with the protein surface. Figure 5.Details of the peptide binding site. (A) Schematic view of interactions, with water molecules represented as W. (B) The N-acetyl lysine slot showing the ring of water molecules around the acetyl group at the base of the slot, and the hydrophobic walls left and right. (C) The binding groove for the (K + 2) and (K + 3) peptide residues lies across the 405–408 loop between αB and αC. His(K + 2) packs against Phe367, and Arg(K + 3) forms hydrogen bonds back to the protein backbone. The peptide backbone forms four hydrogen bonds to the protein, three of them via water molecules. Download figure Download PowerPoint The major binding determinant is the acetylated lysine. This sits in the deep cleft, which is accessible to solvent on one side (Figure 4B). The walls of the cleft, which pack against the aliphatic part of the N-acetyl lysine side chain, are composed of Val361 and Tyr364 on one side and Pro351 and Tyr413 on the other. This accounts for its high hydrophobic potential. The interaction that plays the major role in orientating the N-acetyl group such that its carbonyl points towards the hydrophobic interior of the protein is a H-bond formed between the amide nitrogen of Asn407 and the oxygen of the acetyl carbonyl group (Figures 5B, C and 6). The carbonyl group and amide nitrogen from the N-acetyl group also form H-bonds to a number of well-ordered water molecules, which participate in a network of H-bonds between each other and carbonyl groups and side chains of the protein, in particular the carbonyl group of Pro351 and the hydroxyl group of Tyr364 (Figures 5A and 6). The methyl of the N-acetyl group is surrounded at the base of the pocket by the exposed hydrophobic surfaces of Phe352 and Val356. An unacetylated lysine residue that is positively charged would have no compensatory negative charge to interact within this hydrophobic environment and consequently its binding would be considerably less energetically favourable. This would explain both the failure to observe chemical shifts on addition of the unacetylated peptide at a concentration of 5 mM (Figure 2) and also the >20-fold weaker binding measured for the binding of an unacetylated as opposed to an acetylated lysine-containing peptide to the TAFII250 dibromodomain (Jacobson et al., 2000). Figure 6.The Nζ-acetyl lysine binding site, showing electron density from the final 2mFo – DFc map. Nitrogen atoms are black and oxygen atoms are grey. The acetyl group is surrounded by a ring of water molecules (grey balls) at the base of the slot, and the carbonyl oxygen of the acetyl forms a hydrogen bond to the side chain of Asn407. An unacetylated lysine could not form these hydrogen bonds, and would introduce an unpaired charge into the slot. Download figure Download PowerPoint Specificity for the sequence surrounding the N-acetyl lysine comes from the binding of side chains at the K + 2 and K + 3 positions, where K defines the position of the acetylated lysine. The side chains at K – 1 and K + 1 make no contacts with the protein, while no density can be seen for any of the 10 residues following K + 3 and these are therefore not likely to be involved in binding to the bromodomain. In this peptide, the K + 2 residue is a histidine which sits in a shallow hydrophobic pocket formed by the side chains of Tyr406 and Phe367 (Figures 4B and 5C). A hydrophobic residue or an arginine at this position would also be expected to form an energetically beneficial interaction and indeed there are other examples, shown in Table I, where a hydrophobic residue, in particular leucine or proline, is found in a corresponding position relative to other acetylatable lysine residues. The K + 3 residue is an arginine and interacts with the protein via two H-bonds to the backbone carbonyl groups of Arg404 and Asn407 (Figure 5C). It is interesting to note that 5 Å away from the guanidinium group of the K + 3 side chain is a glutamate side chain (Glu409). If this were able to form an ionic interaction in vivo with the K + 3 arginine, it would increase the specificity for an arginine residue at this position. However, in the crystal structure there is a crystal contact at this point, in which the side chain of Asn345 from an adjacent molecule interacts with the K + 3 arginine. This would prevent the Glu409 side chain from interacting with the K + 3 arginine. Since it cannot form this interaction in the crystal, this glutamic acid residue is relatively mobile and has poor electron density. Table 1. Sequence context of acetylatable lysines in histones H3 and H4 from S.cerevisiae Histone Acetylatable lysine Sequence H3 9 RKSTG H3 14 GKAPR H3 18 RKQLA H3 23 SKAAR H4 5 GKGGK H4 8 GKGLG H4 12 GKGGA H4 16 AKRHR The table shows the sequences from K − 1 to K + 3, where K is the acetylatable lysine. Residues that could potentially make secondary interactions with the Gcn5p bromodomain are shown in bold. The identification of two interaction sites reconciles previous apparently disparate observations. Dhalluin et al. (1999) and Jacobson et al. (2000) reported that the bromodomain of P/CAF and the dibromodomain of TAF250, respectively, preferentially bound peptides from histones H3 and H4 that contain N-acetylated lysine residues. In contrast, Ornaghi et al. (1999) found that the bromodomain of Gcn5p selectively bound certain sequences from the N-terminal region of histone H4 when challenged with sequences in which the lysine residues were unmodified. The most likely explanation for these observations is that both Dhalluin et al. (1999) and Jacobson et al. (2000) measured the effect of the primary interaction of N-acetyl lysine with its binding cleft, while the results of Ornaghi et al. (1999) were dependent only on the secondary interaction. This interpretation is consistent with the observation that the strongest binding sequence selected by Ornaghi et al. (1999) contains H4 residues His18 and Arg19, which interact well with the secondary site. Arginine residues, which as discussed above could interact particularly favourably with the secondary site, were important for this binding. By comparison, the sequences following the other acetylatable lysines in histone H4 (Lys5, Lys8, Lys12, as well as Lys9, Lys18 and Lys23 in histone H3; Table II) would be expected to interact less favourably with the secondary site. This suggests that the Gcn5p bromodomain may discriminate between different acetylated lysines, depending on the sequence context in which they are found. Interestingly, the sequences following two of the three preferred substrates for free Gcn5p (Kuo et al., 1996), H4 Lys16 and H3 Lys14, are also those we would predict to interact most strongly with the Gcn5p bromodomain at the K + 2 and K + 3 positions. The hydrophobic part of the secondary binding site (see Figure 4B) is well conserved in other bromodomains, but the region interacting with Arg19 shows more variation, both in charge and hydrophobicity, raising the possibility that different bromodomains might target different acetylated lysine residues as a result of the interaction of the peptide K + 3 residue at this site. Table 2. Statistics on data collection and phasing Native EMTS Data collectiona resolution (Å) (outer bin) 19–1.87 (1.97) 19–1.85 (1.95) Rmergeb 0.073 (0.204) 0.042 (0.283) Rmeasc 0.079 (0.220) 0.052 (0.336) </σ()> 24.5 (8.7) 29.4 (6.7) completeness (%) 99.8 (99.5) 99.1 (95.2) multiplicity 7.4 (7.0) 6.7 (5.9) Wilson plot B (Å2) 19 22 MIR phasing no. of sites 1 Rderivd 0.078 Rcullise 0.92 phasing power: isomorphous 0.73 (0.91) (anomalous)f mean figure of merit 0.23 figure of merit after solvent flattening (all data) 0.80 Refinement R (Rfree)g 0.185 (0.204) (Å2) 20 Nreflections (Nfree) 11 944 (573) Natoms (Nwater) 1090 (109) r.m.s.d. bond length (Å) 0.013 r.m.s.d. bond angle (°) 1.3 no. of Ramachandran violations 0 a aValues in parentheses apply to the high resolution shell. b bRmerge = ΣΣi |Ih − Ihi|/ΣΣi Ih, where Ih is the mean intensity for reflection hi. c cRmeas = Σ √(n/n – 1)Σi |Ih – I hi|/ΣΣi Ih, the multiplicity weighted Rmerge (Diederichs and Karplus, 1997). d dRderiv = Σ|FPH – FP|/ΣFP e eRcullis = Σ||FPH – FP| – |FHcalc||/Σ|FPH – FP| f fPhasing power = <|FHcalc|/phase-integrated lack of closure>. g gR = Σ|FP − Fcalc|/ΣFP The asparagine residue corresponding to Asn407 is highly, but not absolutely, conserved in the bromodomain sequences reported so far, but is present in all GCN5 homologues. Where this residue is present we would expect that the interactions in the primary N-acetyl lysine binding site observed in this structure would also be conserved and, therefore, that the specificity for N-acetyl lysine binding should be maintained. So far, there are five examples of sequences homologous to the Gcn5p bromodomain in which the residue corresponding to Asn407 is different: in three of these cases, this residue is a serine, in the other two, a tyrosine. It should be noted that these are both residues that could potentially form H-bonds from their side chains to the N-acetyl lysine carbonyl group. However, the binding of N-acetyl lysine in such a non-asparagine pocket would be of a different strength to that of a pocket containing asparagine. Three of these deviations occur in open reading frames with more than one bromodomain, while the latter two, SP-140 and LYSP-100, are both components of distinct subnuclear structures (Bloch et al., 1996; Dent et al., 1996). These latter two also lack part of the highly hydrophobic lining to the cleft and could thus potentially recognize a different amino acid. We note, however, that neither of these domains has yet been shown functionally or structurally to be a true bromodomain. In addition to binding to the bromodomain of Gcn5p, the N-terminal regions of the histone tails also bind to the HAT domain. Recent crystal structures of the HAT domain include those of Saccharomyces cerevisiae Gcn5p (Trievel et al., 1999), the related Hat1p (Dutnall et al., 1998), and a complex between the Tetrahymena Gcn5p HAT domain and a histone H3 peptide (Rojas et al., 1999). In these examples, the proposed (Dutnall et al., 1998) and observed (Rojas et al., 1999) interaction of the peptide is considerably more extensive than that with the bromodomain, involving ∼10 amino acids bound in an extended cleft. There are many contacts with the main chain of the peptide, but interestingly, as for the Gcn5p bromodomain, residues corresponding to K + 2 and K + 3 in the H4 peptide make important contacts. In particular, in the histone H3 sequence 14-KGPR-17, Pro16 binds to a hydrophobic surface comprising a phenylalanine and an alanine residue, while Arg17 also makes hydrophobic contacts with a proline residue. The primary acetylation target of Gcn5p is nucleosomal histone H3 rather than histone H4 (Grant et al., 1997). The acetylation of Lys14 of H3 is also correlated with phosphorylation of Ser10 (P.Cheung et al., 2000; Clayton et al., 2000; Lo et al., 2000). It is an open question as to whether this additional modification influences or is influenced by the binding of the bromodomain. The recognition of N-acetyl lysine by the Gcn5p bromodomain differs from that of ω-acetyl histamine by the P/CAF bromodomain in two important respects. In the P/CAF–ω-acetyl histamine complex, intermolecular NOEs are observed between the side chain of Ala757 and the methyl group of the acetyl group in the a
