INTRODUCTION

Top Abstract Introduction Materials and Methods Results Discussion References

Once segmental boundaries are established by the early patterning mechanisms, the products of the homeotic selector genes specify the characteristic features of each body segment of the developing Drosophila embryo. The genes that are required for the maintenance of the differential expression patterns of these key developmental regulators have been divided into two groups: the trithorax group (trxG) maintains the active state, while the Polycomb group (PcG) is responsible for keeping the target genes in a repressed state (reviewed in references 34 and 37). Indeed, maintaining cells in a determined state, as defined by the specific expression pattern of key regulatory factors, crucially depends on the appropriate action of the PcG and trxG. Embryos with mutant PcG genes show a general misexpression of target genes outside their usual expression boundaries (47, 53), leading to dramatic transformations of the body pattern. Conversely, mutations in trxG genes lead to a down-regulation of homeotic genes. Members of both groups were found to play equally important roles in mammalian development (reviewed in references 14 and 51).

Combinations of PcG alleles show synergistic effects, suggesting that their products interact in multimeric complexes. Indeed, the Polycomb (PC), Polyhomeotic (PH), Posterior sex combs (PSC), and other PcG proteins are parts of a complex consisting of about 20 proteins (12, 16, 19, 43, 49). PcG proteins share binding sites on Drosophila polytene chromosomes (9, 12, 22), indicating that many target genes are coregulated. Several PcG proteins carry conserved regions, such as the SET, WD-40, or SPM domains and RING- or PHD-finger motifs, which are thought to mediate protein-protein interactions. PC itself contains two regions that are conserved in the vertebrate homologues: the 50-amino-acid N-terminal chromodomain and a C-terminal region of 28 amino acids (see Fig. 1). Mutations in the chromodomain prevent the interaction of PC with PH (49) and abolish PC binding to its target sites on salivary-gland chromosomes (25). The C-terminal part of PC is necessary for the repression of reporter constructs in transgenic flies (28) or in mammalian tissue culture cells (8). Recently it has been shown that the C-terminal parts of the mouse PC homologue M33 and the human homologue hPc2 are necessary for the repressive action of these proteins (40, 42). The deletion of this portion has no effect on the recruitment of PC to the target genes (25). Thus, PC seems to be divided into at least two functionally distinct domains: the chromodomain, which is crucial for the integration of PC in the PcG complex and for its targeting, and the C-terminal part, which mediates regulative interactions that are necessary for the repressive function of the PcG complexes (8, 28).

PcG proteins silence chromosomal regions by being targeted to DNA elements termed PREs (PcG response elements). PREs have been identified as cis-regulatory DNA elements, important for the PcG-dependent maintenance of the transcriptionally inactive state of homeotic genes. The integration of PREs into polytene chromosomes results in an ectopic binding of PcG proteins at the site of the transgene as well as in the silencing of an associated reporter gene (54). Recently, the product of the PcG gene pleiohomeotic (pho) was shown to encode a Drosophila YY1 homologue (7). Since PHO is a sequence-specific DNA binding protein, it is an excellent candidate for a targeting anchor for PcG complexes to PREs (7, 26). PREs apparently serve as nucleation sites that recruit PcG complexes and lead to a spreading of repressive chromatin structures into neighboring genes. This spreading may lead to packaging of regulatory units into structures that are inaccessible to the transcriptional machinery (54). Indeed, analysis of Drosophila tissue culture cells and embryonic chromatin by chromatin immunoprecipitation after cross-linking indicates that the PC protein associates with a broader chromatin domain of several kilobase pairs of DNA around PREs, in obvious contrast to the sequence-specific DNA-binding GAGA factor, which is strictly found at GAGA consensus sites in PREs (32, 48). This suggests that the PC protein interacts directly or via other subunits in the PcG complex with the nucleosomal backbone independently of the underlying DNA sequence to generate silenced higher-order structures. This structural model resembles that proposed for telomeric silencing and the repression of inactive mating type cassettes in yeast (15). SIR3 and SIR4, which both belong to a set of proteins that are required for these silencing processes, interact with the N-terminal domains of histones H3 and H4 (17). This interaction is thought to mediate the spreading of SIR complexes along the chromosome, creating a higher-order structure that is inaccessible to activators and the transcriptional machinery.

We tested the ability of the PC protein to interact with purified histones or reconstituted nucleosomes in vitro. Our data indicate that PC binds to nucleosomes via its conserved C-terminal domain and recruits other PcG proteins. Furthermore, we found a strong interaction of PC with cruciform (four-way junction) DNA (crDNA), suggesting an involvement of highly bent DNA in the PC-nucleosome interaction. This interaction of a PcG protein with nucleosomes may be important for the association of the PcG complex with extended chromosomal regions.

	MATERIALS AND METHODS

Top Abstract Introduction Materials and Methods Results Discussion References

Cloning, bacterial expression, and purification of PC-calmodulin-binding protein (CBP) fusion proteins. The respective coding regions for the different PC derivatives (Fig. 1) were obtained from the PC cDNA by PCR amplification with Pfu polymerase (Stratagene) and the following primers: primer N (5'-CGAATTCGCCATGGCTATGACTGGTCGAGGCAAGG-3'), primer N-trunc (5'-CCATATCGGGATCCGAGTCCAAGCGTCAGCGCA-3'), primer C-trunc (5'-CGAATTCGGGATCCGCATTTGGCCGGCAGCCAG-3'), primer C (5'-CGAATTCGGGATCCAGCTACTGGCGACGAATCG-3'), and primer C-2 (5'-CCATATCGGAATTCCGAAGCTCAAGCTACTGGC-3').

View larger version (16K): [in this window] [in a new window]   FIG. 1.   The conserved domain of the PC protein and the protein fusions used for the analysis. The three prominent regions of PC are indicated: the chromodomain, the two repeats of 10 and 8 histidines, and the C terminus, which is involved in repression. PC-Wt features the whole sequence of PC. PC-Lo carries a deletion of 24 amino acids in the chromodomain, PC-Ct has a C-terminal truncation of 42 amino acids, and PC-Ltr is a combination of both. PC-Nt has a large N-terminal truncation, deleting the chromodomain and the His repeats. All fusion proteins carry the 35 amino acids of CBP either as C-terminal fusions (PC-Wt, PC-Lo, PC-Ct, and PC-Ltr) or as N-terminal fusions (PC-Nt).

Purification of Drosophila core histones. The core histones were isolated essentially as described previously (44). To prepare the chromatin from nuclei, 50 g of early (0 to 90 min after egg laying) Drosophila embryos were homogenized in a Yamamoto homogenizer with six complete strokes at 1,000 rpm in 40 ml of glycine buffer (15 mM HEPES-KOH [pH 7.6], 10 mM KCl, 5 mM MgCl₂, 0.05 mM EDTA, 0.25 mM EGTA, 1 mM dithiothreitol [DTT], 0.2 mM phenylmethylsulfonyl fluoride [PMSF], 10% [vol/vol] glycerol) including one tablet of Complete protease inhibitor (Boehringer). The suspension was centrifuged at 10,000 × g for 10 min. The nuclei were washed with 25 ml of sucrose buffer (15 mM HEPES-KOH [pH 7.6], 10 mM KCl, 5 mM MgCl₂, 0.05 mM EDTA, 0.25 mM EGTA, 350 mM sucrose, plus Complete) and respun (this step was repeated once). The nuclei were resuspended in 40 ml of sucrose buffer including 3 mM CaCl₂ and 300 U of micrococcal nuclease/ml and were incubated for 10 min at 26°C. The reaction was stopped by adding 800 µl of 0.5 M EDTA. The suspension was centrifuged 10 min at 10,000 × g, and the pelleted nuclei were resuspended in 6.0 ml of TE, pH 7.5 (10 mM Tris [pH 7.5], 1 mM EDTA, including 0.02 mM PMSF, 1 mM DTT, and Complete). The nuclear suspension was then homogenized in a Potter-Elvehjem homogenizer (six complete strokes) and centrifuged (for 30 min at 12,000 rpm in a Sorvall HB-4 at 4°C), and the supernatant was transferred to a fresh tube. This soluble chromatin solution was used for further purification of the histones by the procedure of Simon and Felsenfeld (44).

Trypsin digestion of Drosophila core histones. Soluble chromatin was prepared as described above, except that no proteinase inhibitors were added to the buffers. To establish suitable digestion conditions, 10 µl of the soluble chromatin solution was adjusted to digestion buffer (10 mM Tris-HCl [pH 7.6], 70 mM NaCl, 0.1 mM EDTA) treated with 1, 2, 4, or 10 µg of trypsin (from a 10-mg/ml stock solution) in a final volume of 20 µl. The samples were incubated for 20 min at 26°C. The reactions were stopped by adding 100 µg of trypsin inhibitor (Boehringer), and the digested histones were analyzed on a sodium dodecyl sulfate (SDS)-15% polyacrylamide gel electrophoresis (PAGE) gel. These tailless histones form a stable digestion intermediate that is fairly resistant to further proteolysis. The optimal trypsin concentration for obtaining the typical pattern (see Fig. 3c or 6b) was used to digest the total chromatin solution under similar conditions. For partial trypsin treatment, an aliquot of the chromatin suspension was treated with the same amount of trypsin but at 4°C. The digested chromatin solution was then used for further purification of the histones by the procedure of Simon and Felsenfeld (44).

Far-Western blot analysis. Far-Western blot analysis was carried out as described by Edmondson et al. (11). Portions (1 or 5 µg) of purified core histones were separated on an SDS-15% PAGE gel and electroblotted to polyvinylidene difluoride membranes (Immobilon-P; Millipore). After transfer the blots were stained with Ponceau red, and the positions of the four histones were marked. Renaturation of the blots took place in phosphate-buffered saline (PBS)-0.05% Tween 20 (PBST) for 2 h at room temperature, and blocking in PBS-bovine serum albumin (BSA) (PBS, 2% BSA, 0.5% NP-40, 0.01% NaN₃) also took place for 2 h at room temperature. Blots were then incubated in a 50-ml conical tube with recombinant Pc-Wt (50 to 140 ng/cm² of blot) in 2 ml of PBS-BSA (including 1% normal goat serum) for 2 h at room temperature. Membranes were then washed five times with PBS, and bound PC was detected by antibody staining using ECL (Amersham).

Preparation of the DNA template. The fragments used for mononucleosome reconstitution were originally created for other purposes. Sixty base pairs of sequence from the Drosophila hsp26 promoter was engineered to contain two novel EcoRV restriction sites. The fragment was cloned between the EcoRI and HindIII sites of a modified pUC19 vector. Oligonucleotides were designed on the vector sequences to amplify 146- or 220-bp fragments containing the insert in the center. One biotinylated primer and one primer kinased with [-³²P]ATP were used for PCR amplification. The PCR products were separated on a 1.3% agarose gel and purified with the Qiaquick gel extraction kit (Qiagen).

Reconstitution of nucleosomal core particles. The nucleosomal templates were prepared by the procedures described in references 30 and 50. Each reconstitution mixture contained 2 to 10 µg of DNA (of which 200 ng was a biotinylated PCR fragment and the remainder was sheared herring sperm DNA), a slightly smaller amount (in mass) of purified Drosophila histones (intact or partially or fully trypsinized), 0.5 mg of chicken albumin (Sigma)/ml, and 0.05% NP-40. The reaction mixture was filled up to 50 µl with DB(2000) (2 M NaCl, 10 mM HEPES-KOH [pH 7.6], 1 mM EDTA, 1 mM -mercaptoethanol, 0.05% NP-40). The samples were dialyzed in collodion bags (Sartorius) twice for 1 h each time against 1 liter of DB(2000) at 4°C and then for 1 h against 1 liter of DB(1200) (1.2 M NaCl). The bags were then transferred into 500 ml of fresh DB(1200), and the salt concentration was reduced gradually to about 550 mM NaCl by pumping DB(550) into the beaker while pumping a corresponding volume of the mixed dialysis buffer out (pump speed, 2.0 ml/min for 18 h). Finally, the samples were dialyzed for 3 h against DB (no NaCl). The samples were collected and stored in siliconized tubes on ice. The reconstituted nucleosomes were analyzed after dialysis by 4% nondenaturing PAGE (electrophoretic mobility shift assay). The gel was run at 10 to 12.5 V/cm, dried on Whatman DE-81 paper, and analyzed by autoradiography.

Coupling of the reconstituted nucleosomes to Dynabeads and binding assays. For each 200 ng of biotinylated fragment, 40 µl of paramagnetic-bead solution (Dynabeads M-280; Dynal) was washed according to the specifications of the manufacturer. The beads were then carefully resuspended in the nucleosome solution derived from the salt gradient dialysis (in DB) and incubated overnight on a rotating wheel at 4°C. The beads were then washed three times with EX(120) (10 mM HEPES-KOH [pH 7.6], 10 mM KCl, 5 mM MgCl₂, 0.5 mM EGTA, 10 mM glycerol-phosphate, 10% glycerol, 1 mM DTT, 0.2 mM PMSF) containing 0.05% NP-40 and 0.25 mg of chicken albumin/ml. The coupled nucleosomes were resuspended in EX(120) at a final concentration of 1 to 10 ng/µl. The histone stoichiometry was analyzed by SDS-PAGE and subsequent silver staining.

Binding assay with histone-GST fusion proteins and crDNA molecules. Glutathione S-transferase (GST) and GST-histone fusions were expressed in Escherichia coli BL21 (DE3) as described elsewhere (45). GST or GST-histone fusion proteins bound to 20 µl of Glutathione Sepharose 4B (Pharmacia) were equilibrated for 10 min at room temperature in TNE(150) (20 mM Tris-HCl [pH 8], 150 mM NaCl, 1 mM EDTA, 0.1% Triton X-100, 1 mM DTT). After removal of the supernatant, 300 ng of recombinant PC was added in 50 µl of TNE(150) and the samples were incubated for an additional hour. Beads were then washed three times with 500 µl of TNE(150). Proteins were eluted twice in 100 µl of elution buffer (50 mM Tris-HCl [pH 8]-10 mM reduced glutathione), precipitated with methanol-chloroform (4:1), and redissolved in SDS-PAGE sample buffer. Samples were resolved by SDS-PAGE (8% polyacrylamide) and electroblotted, and bound PC was detected by antibody staining using ECL (Amersham).

	RESULTS

Top Abstract Introduction Materials and Methods Results Discussion References

PC protein interacts with core histones. Potential PC-histone interactions were first assayed by Far-Western blot analysis. PC was expressed as a fusion protein with CBP (calmodulin binding protein, a C-terminal fragment of the myosin light chain kinase) in E. coli and was purified by using a calmodulin affinity resin. Pc-Wt features all 390 amino acids of the PC protein plus 35 additional amino acids of the CBP tag (Fig. 1). Core histones were purified from Drosophila embryos by hydroxyapatite chromatography (44). We observed strong binding of PC to histone H3 and a weaker interaction with histones H4 and H2B (Fig. 2a). No signal was obtained without the addition of PC, excluding any cross-reactions of histones with our antibody. By reducing the concentration of PC in the assay (50 µg/cm² of filter), the binding was restricted mainly to H3 (Fig. 2b), whereas the binding to H4 and H2B was very weak. We never observed an interaction of PC with histone H2A. This indicates that the interaction of PC with histone H3 is preferred and most stable under the conditions of the assay. A general, nonspecific interaction of PC with the highly basic histones can be excluded. Furthermore, under the assay conditions we used, both the core histones and PC have a net positive charge (average isoelectric point [IEP] of all proteins, 9). Thus we conclude that the observed in vitro interaction of PC with histones is specific.

View larger version (61K): [in this window] [in a new window]   FIG. 2.   Far-Western blot analysis with Drosophila core histones and recombinant PC (Pc-Wt). (a) Histones (H1, 1 µg; H2, 5 µg) were separated on an SDS-15% PAGE gel, electroblotted, and renatured. The figure shows the resolved histones in a Coomassie blue-stained gel (Coom.), the blot stained with Ponceau red (Ponceau), and the blot after incubation with PC-Wt (150 ng/cm2) (+PC). After extensive washing, PC signals were detected with PC antiserum and visualized by ECL. (b) Purified core histones were treated as for panel a but were incubated with 50 ng of PC-Wt/cm2 (+PC) or without addition of protein (PC). The positions of the four core histones and the sizes of the molecular weight standards (M1 and M2) in kilodaltons are indicated.

Evidence for the interaction of PC and a PcG complex with nucleosomes. Since free histones are an unlikely target for PC in vivo, especially considering the presumptive role of this interaction in organizing chromatin, we examined in a second approach the ability of PC to interact with nucleosomal cores. Nucleosomes were reconstituted on a biotinylated 146-bp ³²P-labeled DNA fragment by a salt dialysis protocol from purified core histones (50) (Fig. 3a). The quality of the resulting nucleosome preparations was checked by a band shift assay (Fig. 3b). Samples that did not contain free DNA were coupled to paramagnetic beads, and an aliquot was analyzed by SDS-PAGE (Fig. 3c). All four core histones were present in roughly equal amounts, as expected.

View larger version (47K): [in this window] [in a new window]   FIG. 3.   Reconstitution of nucleosomes. (a) Scheme illustrating the reconstitution protocol. Purified core histones (untreated, partially trypsinized, or fully trypsinized) and DNA template were mixed in a reconstitution buffer containing 2 M NaCl. During gradual reduction of the NaCl concentrations, histone octamers formed on the DNA fragment (see Materials and Methods). (b) The completeness of reconstitution was tested by analysis of the reconstituted nucleosomes on a native (band shift) gel. The 146-bp DNA fragment was radiolabeled with [-32P]ATP. The signals for the free DNA (dsDNA) and the nucleosomal DNA (wt, untreated; pt, partially trypsinized; ft, fully trypsinized) are indicated. Only nucleosome preparations that did not contain free DNA were coupled to paramagnetic beads and used for further experiments. An autoradiogram of the gel is shown. (c) Histone contents of the input material and the reconstituted nucleosomes. A silver-stained SDS-15% PAGE gel with 50 ng of input material (purified core histones) and 80 ng of coupled reconstituted nucleosomes is shown (abbreviations for the nucleosome preparations are as explained for panel b). (d) Reconstituted nucleosomes remain stable in the presence of EtBr. Two aliquots (80 ng) of nucleosomes (nu) on beads were incubated for 1 h in the presence of 50 µg of EtBr/ml (+EtBr) or without EtBr (EtBr) in binding buffer. After a wash, both samples were resolved by SDS-PAGE and silver stained. For reference an aliquot of the input material (50 ng) was included (in).

View larger version (61K): [in this window] [in a new window]   FIG. 4.   PC binding to reconstituted nucleosomes. (a) PC and PSC are coisolated with reconstituted nucleosomes. Portions (20 µl) of nuclear extract were incubated with immobilized nucleosomes (nu) reconstituted on 60 ng of DNA or an equivalent amount of free DNA template (ds). After extensive washing, the bound material was analyzed by SDS-PAGE. Bound proteins were visualized by Western blot analyses with antisera against the indicated proteins. On the left, 5 µl of extract was loaded (in) to indicate the presence of the relevant proteins in the input material. (b) Interaction of recombinant PC (Pc-Wt) with reconstituted nucleosomes. Portions (300 ng) of PC-Wt (input) were incubated with 20 ng of nucleosome-carrying DNA (nu) or a free DNA fragment (ds) coupled to paramagnetic beads in the presence or absence of EtBr (50 µg/ml). The assay was performed as for panel a. (c) Interaction of mutant PC derivatives with reconstituted nucleosomes. The assay was performed as for panel b. A 300-ng portion of each mutant PC derivative was used. (d) Interaction of mutant PC derivatives as in panel c with reconstituted nucleosomes in the presence of EtBr (50 µg/ml).

The PC C terminus mediates the nucleosome interaction. All Polycomb alleles examined so far show either point mutations in the chromodomain, deletions in the conserved region of the C terminus, or mutations that lead to frame shifts altering the C terminus (13). A third remarkable domain of PC, two stretches of histidines (see Fig. 1), has also been found conserved in the mouse homologue mPC2 (1). Deletions in the histidine repeats have little influence on PC binding on polytene chromosomes. Thus, it is thought that this region has a minor role in defining the PC target gene specificity (25) and might have other, not yet identified functions.

PC interacts with the N-terminal domains of the core histones. The N-terminal domains of the core histones protrude from the otherwise very compact histone octamer in the nucleosome and, therefore, are likely candidates for targets of interacting factors (23). Therefore we assayed the interaction of PC with GST fusion proteins of the N-terminal domains of the four core histones of yeast (17), comprising amino acids 1 to 35 (H4 and H2B), 1 to 34 (H2A), and 1 to 46 (H3). In addition, a derivative of the H4 peptide, where three lysines had been replaced by glycine [GST-H4(3K-G)], was assayed.

View larger version (51K): [in this window] [in a new window]   FIG. 5.   Binding of PC to N-terminal "tail" domains of histones. (a) PC-Wt (300 ng) was incubated with GST or with different GST fusion proteins (GST-H2A, -H2B, -H3, and -H4) immobilized on Sepharose beads. GST fusion proteins were used at a 125-fold excess with respect to PC. For comparison the input is shown (in). After extensive washing, the bound material was analyzed by SDS-PAGE and Western blotting with antisera against PC. (b) Tail interaction assay with PC-Wt as in panel a, but in the presence of EtBr (50 µg/ml). PC-Wt (300 ng) was incubated with a 100-fold molar excess of GST, GST-H3, or GST-H4 immobilized on Sepharose beads. (c) PC interacts preferentially with the histone H3 N-terminal domain. PC-Wt was incubated with GST, GST-H3, or GST-H4 at a 1-, 5-, 25-, or 125-fold molar excess of fusion protein over PC (1×, 5×, 25×, and 125×, respectively). In the rightmost lanes, the supernatant (Sup) (unbound fraction) of the second sample (GST-H3) was loaded for comparison. After washing, the bound material was analyzed by SDS-PAGE and Western blotting as before.

PC interacts with tailless nucleosomes and trypsin-treated histones. Proteolytic treatment of chromatin with trypsin leads to a shortening of the N-terminal domains of all four core histones and of the C-terminal domains of histones H3 and H2B, leaving the globular domains of the histones mainly intact (6). Mild trypsin treatment at 4°C (partial trypsinization) results mainly in digestion of the H3 tails (5) (see Fig. 3c and 6b). Stable nucleosomal core particles lacking the histone N termini can be reconstituted by using histones purified from trypsinized chromatin (2). We used fully and partially trypsinized purified histones for the nucleosome reconstitution as described above (Fig. 3a to c). With these "tailless" nucleosomes coupled to paramagnetic beads, we performed binding assays with recombinant PC. PC interacted with partially trypsinized core particles as well as with untreated core particles, whereas the interaction with fully trypsinized particles was slightly but significantly weaker (Fig. 6a). We also examined the binding of PC-Wt to isolated trypsinized histones in a far-Western analysis (Fig. 6b). PC showed a strong interaction with the globular domains of H3 and an increased interaction (compared to intact histones) with H2B and H4 after partial trypsin treatment (Fig. 6b). Finally, we also observed a significant interaction of PC with the globular domains of the fully trypsinized core histones (Fig. 6b). These results show that the N-terminal regions of the histones are apparently not necessary for the interaction of PC with the core particle, although PC is able to bind to isolated histone N termini.

View larger version (60K): [in this window] [in a new window]   FIG. 6.   Interaction of recombinant PC with reconstituted nucleosomes by using trypsinized histones. (a) The assay was performed like those described for Fig. 4 except that PC-Wt was also incubated with trypsinized nucleosomes (wt, untreated; pt, partially trypsinized; ft, fully trypsinized). Portions (300 ng) of PC-Wt (input [in]) were incubated with 20 ng of nucleosome-wrapped DNA (wt, pt, ft) or a free DNA fragment (ds) coupled to paramagnetic beads in the presence of EtBr (50 µg/ml). (b) Far-Western blot analysis of the interaction of recombinant PC with trypsinized histones. Nontrypsinized (wt), partially trypsinized (pt), and fully trypsinized (ft) histones were separated on an SDS-15% PAGE gel, electroblotted, and renatured. Left three panels, Coomassie stain of the input material. Note the band of digested H3 in the pt fraction below H2A. Right panel, blot after incubation with PC-Wt. PC interacts mainly with H3 and weakly with H4 and H2B (as shown in Fig. 2) when full-length histones are present (wt). After partial trypsin treatment, PC still interacts with the shortened H3 and interacts more efficiently with H2B and H4 (pt). PC can still interact with fully trypsinized proteins, though it is no longer possible to determine with which of the histones it interacts (ft).

PC interacts with crDNA. For mammalian histone H1 and HMG1, the interaction with nucleosome core particles depends on accessible linker DNA (31). In our experiments we observed no difference in the binding of PC to nucleosomes reconstituted on 146- or 220 (containing linker DNA)-bp fragments (data not shown). If the interaction of PC with nucleosomes involved a DNA component, we would expect this DNA to be highly distorted due to the nucleosome association.

View larger version (20K): [in this window] [in a new window]   FIG. 7.   Interaction of recombinant Pc (Pc-Wt) with crDNA. (a) The four-way junction DNA molecule shown in the open conformation. Under the conditions of our experiment (5 mM MgCl2), the molecule had a distorted, stacked X-like structure. crDNA was formed by annealing the four oligonucleotides indicated. Oligonucleotide 1 (Oligo 1) was biotinylated for coupling to paramagnetic beads. (b) Binding assay with crDNA and PC. Equal amounts of crDNA (cr) and dsDNA (ds) (1.25 pmol of each) immobilized on paramagnetic beads were incubated with 300 ng (input [in]) of the different PC derivatives (PC-Wt, PC-Ct, PC-Lo, PC-Ltr, and PC-Nt). After extensive washing, the bound material was analyzed by using SDS-PAGE and Western blotting as before. PC proteins were used at a fivefold molar excess in this experiment. (c) Influence of EtBr on the PC-crDNA interaction. Left two lanes (EtBr), input of PC-Wt (300 ng) (in) and bound PC after incubation with 0.125 pmol of crDNA (cr). Right lanes (+EtBr), bound PC after incubation with 0.125, 0.3, and 1.5 pmol of crDNA in the presence of EtBr (50 µg/ml).

	DISCUSSION

Top Abstract Introduction Materials and Methods Results Discussion References

One of the models that try to explain the repressive function of the PcG complex assumes an effect on higher-order chromatin structures (33). A fundamental question arises of how such a chromatin modulator is targeted to specific chromosomal regions and how it is anchored at the nucleosomal fiber. In this report we show that PC itself interacts with the major chromatin components, the nucleosomes.

PcG proteins interact with nucleosomes mediated by the conserved C terminus of PC. Using far-Western blot analysis, we demonstrated the ability of PC to interact with histones, observing that it bound most stably to histone H3. PC in nuclear extracts, where it resides in a complex with other PcG proteins, also interacted with reconstituted nucleosome core particles. The associated binding of PSC demonstrated the interaction of the entire PcG complex. Two regions in the PC protein could be identified as mediating the nucleosome interaction. Binding via the chromodomain was affected by EtBr, which identifies DNA as one target of PC. The structure of the chromodomain of the mouse chromatin modifier protein 1 (MoMOD1) was determined by nuclear magnetic resonance spectroscopy (3). Ball and colleagues found an unexpected homology to two archaebacterial DNA-binding proteins but suggest, judging from structural comparisons, that the chromodomain functions as a protein interaction motif. Consistent with this is our previous finding that the chromodomain is required for the PC-PH interaction in the complex (49). Thus, in vivo the task of the chromodomain appears to be to generate the target site specificity through the other factors of the PcG complex (38), though it seems to posses a cryptic nucleic acid binding ability. However, many DNA binding moieties, e.g., the homeodomains, are also the target of protein-protein interactions (36).

Mechanism of PC-induced silencing. For the repressive action of PcG complexes, several models are currently being discussed. PcG complexes might directly enhance the chromatin packaging of putative target genes and thus block the access of activators or the transcriptional machinery to DNA. Alternatively, the interaction of PcG complexes with several PREs might lead to a large DNA-protein complex, thus preventing direct promoter enhancer looping interactions. A third possibility, which does not necessarily exclude the other two, suggests that binding of the PC complexes to PREs could tether target genes to inactive nuclear compartments. Our data cannot discriminate between these different models. However, our finding that a major member of the PcG complexPCdirectly interacts with nucleosomes supports previous data showing that PC is not only concentrated at PREs but is also found associated with extended chromatin regions around PREs (32, 48). It is conceivable, therefore, that PcG complexes interact with nucleosomes over larger regions, thus immobilizing nucleosomal structures, or influencing the folding of the nucleosomal array into higher-order structures. This hypothesis is further substantiated by the recent isolation of a PC-containing complex in Drosophila (43). PRC1 (Polycomb repressive complex 1) blocks the ability of nucleosomal arrays to be remodeled by the SWI-SNF complex. This anti-remodeling activity could be observed only upon preincubation of the nucleosomal array with PCR1. This suggests that a direct interaction of components of the PCR1 with the nucleosomes has to take place, competing with SWI-SNF added subsequently (43). Our finding that PC interacts with the nucleosomal core and might also have an affinity to the nucleosomal DNA opens the possibility that PC locks nucleosomes in a structure that prevents any remodeling activity. Alternatively, PC may compete with SWI-SNF for essential interaction surfaces on the nucleosome.