Polycomb Recruiters Inside and Outside of the Repressed Domains

The establishment and stable inheritance of individual patterns of gene expression in different cell types are required for the development of multicellular organisms. The important epigenetic regulators are the Polycomb group (PcG) and Trithorax group (TrxG) proteins, which control the silenced and active states of genes, respectively. In Drosophila, the PcG/TrxG group proteins are recruited to the DNA regulatory sequences termed the Polycomb response elements (PREs). The PREs are composed of the binding sites for different DNA-binding proteins, the so-called PcG recruiters. Currently, the role of the PcG recruiters in the targeting of the PcG proteins to PREs is well documented. However, there are examples where the PcG recruiters are also implicated in the active transcription and in the TrxG function. In addition, there is increasing evidence that the genome-wide PcG recruiters interact with the chromatin outside of the PREs and overlap with the proteins of differing regulatory classes. Recent studies of the interactomes of the PcG recruiters significantly expanded our understanding that they have numerous interactors besides the PcG proteins and that their functions extend beyond the regulation of the PRE repressive activity. Here, we summarize current data about the functions of the PcG recruiters.


Introduction
During development of the multicellular organisms, individual patterns of gene expression are established in each cell type and stably transmitted through many consecutive cell divisions [1]. The precise control of gene expression in each tissue involves an antagonism between the Polycomb transcriptional repressors (PcG) and the Trithorax activator proteins (TrxG), which regulate the activity of the facultative heterochromatin and the developmentally regulated euchromatin, respectively [2][3][4][5].
The antagonism between the PcG and TrxG proteins was first demonstrated in Drosophila through studies on the Hox genes that specify the correct segmentation pattern of the body [3,[5][6][7]. Mutations in the PcG-encoding genes lead to characteristic homeotic transformations due to an overexpression of the Hox genes, while mutations in the TrxGencoding genes dominantly suppress these phenotypes. The loss-of-function mutations in the TrxG-encoding genes can also cause homeotic transformations, but they instead occur due to insufficient expression of the Hox genes [3,[5][6][7]. The subsequent studies have shown that, besides the Hox genes, the PcG/TrxG proteins control transcription of many developmental genes involved in different cellular processes and dysfunctions of genes encoding the PcG/TrxG proteins lead not only to various developmental abnormalities but to cancer as well [8][9][10][11][12][13].
In Drosophila, the PcG/TrxG group proteins are recruited to the specialized DNA regulatory sequences-the Polycomb response elements (PREs) [6,[14][15][16]. It was shown that PREs act as silencers and maintain repression of reporter genes throughout development in transgenes, thus constituting independent subunits of repression. However, at least some The Trithorax (Trx) and Trithorax-related (Trr) proteins are histone methyltransferases that catalyze the H3K4me1/2 modification characteristic for the active chromatin regions [50][51][52] and they are subunits of the COMPASS-like complexes [2,53].
The CBP protein, encoded by the nejire gene, is an acetyltransferase that performs histone modifications at a subset of histone positions, including the H3K27ac modification, a hallmark of the active chromatin [54]. Histone acetylation reduces the strength of the nucleosome-DNA interaction and leads to a decompactization of the chromatin [55].
In Drosophila, Trx, Trr, and CBP, as well as the H3K4me1/2 and H3K27ac modifications, are co-localized on the active enhancers and at the regions of PcG protein recruitment outside of the H3K27me3 domains [50][51][52]54].

PcG Recruiters
PREs can be located at different distances from the target genes, both in the immediate vicinity of the transcription start site and at a distance of thousands of base pairs. Structurally, they are DNA fragments of several hundred base pairs in length. Like other regulatory elements, they are DNA regions with a reduced density of nucleosomes and are hypersensitive to DNase I. PREs contain binding sites for the PcG recruiters. The sites for the PcG recruiters in each particular PRE can be present in different combinations, in different numbers and positions relative to each other.
In Drosophila, Trx, Trr, and CBP, as well as the H3K4me1/2 and H3K27ac modifications, are co-localized on the active enhancers and at the regions of PcG protein recruitment outside of the H3K27me3 domains [50][51][52]54].

PcG Recruiters
PREs can be located at different distances from the target genes, both in the immediate vicinity of the transcription start site and at a distance of thousands of base pairs. Structurally, they are DNA fragments of several hundred base pairs in length. Like other regulatory elements, they are DNA regions with a reduced density of nucleosomes and are hypersensitive to DNase I. PREs contain binding sites for the PcG recruiters. The sites for the PcG recruiters in each particular PRE can be present in different combinations, in different numbers and positions relative to each other.
Each of the other five PcG recruiters has DNA-binding domains of distinct types ( Figure 2). Psq contains four HTH DNA-binding domains at the C-terminus. While the Psq DNA-binding domain type is different from that of GAF, it was also shown to recognize the (GA)n sequences [19,77,78]. Another similarity with GAF is the presence of the BTB/POZ domain at the N-terminus of Psq.
Zeste contains the Myb/SANT-like DNA-binding domain that binds YGAGYG [19,79,80]. Dsp1 contains two High mobility group (HMG) motifs. Initially, Dsp1 was reported to bind to the GAAAA sequence in the Fab7PRE in transgenic constructs [67]. However, the genome-wide Dsp1 binding site was identified as (GA)n [74]. It has been reported that the HMG proteins are able to bind DNA with no sequence specificity [81][82][83], suggesting that Dsp1 can mimic the overall Ph peak consensus, which was shown to be (GA)n as well. Interestingly, the most enriched ChIP-seq motifs for Spps and Zeste were also identified as (GA)n rich [19,20], indicating that the regions of their binding highly overlap with the (GA)n-rich sequences.
Grainy head (Grh) contains the Grh/CP2 DNA-binding domain that was first shown to bind to YNAACYGGTYYTGCGG in vitro [84]; a similar AACYNGTTT core was identified by a genome-wide study [85]. Adh transcription factor 1 (Adf1) contains an MADF DNAbinding domain at the N-terminus that binds ACGBCGRC (B = T, C, or G) [19]. In addition, Adf1 has a C-terminal BESS domain involved in self-dimerization and protein-protein interactions [86].

Role of PcG Recruiters in PcG Repression
The pho mutants die at the pharate adult stage and have sex combs on the second and third legs, demonstrating a classic homeotic PcG phenotype [87,88]. Accordingly, mutations of the pho gene lead to a derepression of the Hox genes [57,58,89]. pho mutations affect the ability of the transgenic PRE to repress reporter genes and so do mutations of its binding sites in the PRE [3,15,16]. However, Pho sites alone fail to make up a functional PRE [70,90] and, thus, require other proteins. For example, phol mutation does not have homeotic phenotype, but it enhances the pho mutation [58]. In addition, while the recruitment of the Pc (PRC1), E(z), and Su(z)12 (PRC2) to the bxdPRE is sensitive to the Pho knockdown by RNAi in Drosophila cells where Phol is absent, the double pho/phol mutations are required for the loss of Pc binding at the bxdPRE at the larval stage where both proteins are expressed [91]. Accordingly, both the Pho and Phol proteins are required for the binding of Pc, Psc, Scm, and E(z) to several sites on the larval polytene chromosomes [58].
The dsp1 mutants have a mixed PcG/TrxG phenotype, indicating that Dsp1 is most likely involved in both repression and activation of transcription [92]. Mutations of other PcG recruiters do not have a PcG homeotic phenotype, but the majority of them were shown to enhance mutations in the PcG core genes or pho, leading to more severe homeotic phenotypes. For example, the Trl [63,64,70], Psq [64,65], and Adf1 [69] mutations enhance PcG mutants, and the grh [68] mutation enhances PcG and pho mutants. The cg (encoding Combgap) [59] and Spps [60] mutations were shown not to affect the homeotic phenotype of pho mutants but enhance lethality.
Combgap, Spps, Crol, GAF, Psq, Zeste, Dsp1, and Grh were confirmed to be important for the functioning of transgenic PREs either by genetic tests and/or by mutations of their binding sites ( [61] and reviewed in [15]). For example, crol knockout and mutation of the Crol binding site decrease the silencing caused by transgenic evePRE and affect recruitment of Ph and Combgap [61]. Trl mutations decrease the silencing caused by the Fab7PRE [62]. Dsp1 binding to Fab7PRE was shown to be sensitive to dsp1 mutation on larval polytene chromosomes, and the Dsp1 G(A)n site affected recruitment of PRC1 (Ph) and PRC2 (E(z)) [67].

Interactions between PcG Recruiters and PcG Core Complexes
In immunoprecipitation experiments, Pho was shown to interact with the Scm-related gene containing four malignant brain tumor (MBT) domains protein (Sfmbt) [93] (Figure 3). Structural analysis revealed that the spacer region of Pho forms a tight complex with the four MBT domains of Sfmbt [93]. Sfmbt is a PcG member, since mutations in the Sfmbt gene lead to misexpression of the Hox genes [94]. Since both Pho and Sfmbt are recruited to PREs, this protein pair was assigned to a separate complex named Pho repressive complex (PhoRC). Both Pho and Sfmbt have been shown to have a number of physical contacts with the PcG proteins ( Figure 3). Pho co-immunoprecipitates with the components of the PRC1 and PRC2 [95][96][97] and interacts directly with Ph and Pc [98] (PRC1) and E(z) and Esc [91] (PRC2). In turn, Sfmbt interacts with the Scm protein in the direct and indirect assays [95,99].
of their binding sites ( [61] and reviewed in [15]). For example, crol knockout and mutation of the Crol binding site decrease the silencing caused by transgenic evePRE and affect recruitment of Ph and Combgap [61]. Trl mutations decrease the silencing caused by the Fab7PRE [62]. Dsp1 binding to Fab7PRE was shown to be sensitive to dsp1 mutation on larval polytene chromosomes, and the Dsp1 G(A)n site affected recruitment of PRC1 (Ph) and PRC2 (E(z)) [67].

Interactions between PcG Recruiters and PcG Core Complexes
In immunoprecipitation experiments, Pho was shown to interact with the Scm-related gene containing four malignant brain tumor (MBT) domains protein (Sfmbt) [93] ( Figure 3). Structural analysis revealed that the spacer region of Pho forms a tight complex with the four MBT domains of Sfmbt [93]. Sfmbt is a PcG member, since mutations in the Sfmbt gene lead to misexpression of the Hox genes [94]. Since both Pho and Sfmbt are recruited to PREs, this protein pair was assigned to a separate complex named Pho repressive complex (PhoRC). Both Pho and Sfmbt have been shown to have a number of physical contacts with the PcG proteins ( Figure 3). Pho co-immunoprecipitates with the components of the PRC1 and PRC2 [95][96][97] and interacts directly with Ph and Pc [98] (PRC1) and E(z) and Esc [91] (PRC2). In turn, Sfmbt interacts with the Scm protein in the direct and indirect assays [95,99]. In addition to Pho, the Phol protein also interacts with Sfmbt. However, it was shown that Pho and Phol interact with Sfmbt in a mutually exclusive manner [94]. A quantitative analysis of the Phol complex in vivo has not yet been carried out, but Phol has been shown to interact with the Esc subunit of PRC2 in a pull-down assay [91].
For Spps, contacts with the PRC1 and PRC2 core subunits have not been described, but it is able to directly interact with the Scm protein [100].
Of the other PcG recruiters, Combgap [59], Crol [61], GAF [96], Psq [101], Zeste [32], Grh [97], and Adf1 [69] were co-purified with the PRC1 subunits. Of these, Zeste and Grh In addition to Pho, the Phol protein also interacts with Sfmbt. However, it was shown that Pho and Phol interact with Sfmbt in a mutually exclusive manner [94]. A quantitative analysis of the Phol complex in vivo has not yet been carried out, but Phol has been shown to interact with the Esc subunit of PRC2 in a pull-down assay [91].
For Spps, contacts with the PRC1 and PRC2 core subunits have not been described, but it is able to directly interact with the Scm protein [100].

Connections between PcG Recruiters and TrxG Proteins
Several observations indicate that Dsp1, GAF, Zeste, and Pho/Phol PcG recruiters have TrxG-related activities. As mentioned above, dsp1 mutants have a mixed PcG/TrxG phenotype [92] and, in particular, resemble and enhance the Ubx loss-of-function phenotype. Enhancement of the Ubx phenotype is also observed in genetic experiments with the Trl gene. In addition, hypomorphic Trl alleles have loss-of-function transformations in segment A6 [105]. Zeste was shown to be necessary for the PRE-mediated inheritance of the active chromatin state of a small Fab7PRE fragment [106] and plays an activating role in the case of the bxdPRE element [107]. In the case of the Fab7PRE, Zeste sites were required for recruitment of the SWI/SNF TrxG Brm protein to the transgene [106]. In addition, Pho and Phol are required for the maintenance of both the repressed and active state of evePRE [108].
A number of PcG recruiters were shown to interact with the TrxG SWI/SNF ATPchromatin remodelers. GAF was shown to co-purify both with BAP and PBAP [104,109]. Pho [98], Psq [19], and, less efficiently, Combgap [19] and Zeste [110] were shown to precipitate with the BAP complex ( Figure 3). In our IP/LP-MS experiments, Psq interacted with the BAP proteins much more efficiently than with the PcG proteins, that were present only at background levels [19]. Also, Pho was shown to directly bind to Brm [98], and Zeste with Mor and Osa [110].
In addition, PcG recruiters were shown to co-purify with several other TrxG proteins [19,111]. In particular, Zeste and Psq efficiently precipitated the Fs(1)h TrxG protein [19], which was previously shown to co-purify with PRC1 and to be correlated with Pc and the H3K27ac modification genome-wide [21]. Fs(1)h also co-purified Pho and GAF proteins [21]. Importantly, Fs(1)h recognizes the same site as Zeste and, thus, has a potential to be directly bound to the PRE elements.

PcG Recruiters Are Localized Outside of H3K27me3 Domains Genome-Wide
The functional and physical connections of the PcG recruiters with the TrxG proteins indicate their importance for the PRE activating state and, potentially, a more global role in the activation of transcription. Accordingly, current data suggest that the binding of PcG core proteins, as well as PcG recruiters, is not restricted to the H3K27me3 domains [19][20][21][22][23][24]61]. There are also indications that PcG recruiters are important for the PcG recruitment outside of the H3K27me3 domains. In particular, it was confirmed for Spps, Pho [20], Combgap [20,59], and Crol [61] recruiters with respect to the Ph protein.
If we evaluate the level of overlap of the PcG recruiters with the PcG proteins, then about 80% of the Pho, Combgap [59], and Crol peaks [61] will overlap with Ph at the 3rd instar larval imaginal discs and brains and this will constitute over 60% of the Ph sites ( Figure 4A). In Drosophila S2 cells, approximately 80% of Combgap, Psq, and Zeste overlap with Ph. In the case of Adf1, the overlap with Ph is about 50% [19] (Figure 4A).
Accordingly, over 80% of peaks for PRC1 (Ph, Psc) and PRC2 (E(z)) fall outside of the H3K27me3 domains as well [20] (Figure 4C). For Pc, the percent of peaks outside of H3K27me3 was estimated to be about 65% [20] ( Figure 4C). The average Ph [23] and E(z) [20] binding levels are lower outside of the H3K27me3 domains. The E(z) was suggested to be inactive due to the presence of active chromatin marks [20]. However, additional studies are required to understand what can block E(z) H3K27me enzymatic activity.

PcG Recruiters at Active Promoters and Enhancers
Going back in history, GAF [112][113][114], Grh [84,115], Zeste [79,116], and Adf1 [117] were initially discovered as the promoter-bound activators of transcription. In particular, GAF, Grh, and Zeste together positively regulate the transcription of the Ubx gene [84,118,119]. Subsequent studies have shown that all currently known PcG recruiters can bind to the actively transcribed promoters [20,61,69,71,74,85,120]. A number of the PcG recruiters were confirmed to bind to the predicted enhancers (Combgap, Zeste, Psq, Adf1, GAF, and Grh) [19,85,121]. Grh [85] and Zeste [122,123] were confirmed to be functionally required for enhancer activity in a number of cases. Likewise, PRC1 has also been shown to be recruited to the promoters of active genes and to potential enhancers [23,24].
For several PcG recruiters, the estimated overlap was quantified. GAF binds to 20% of active promoters [120] and binds to 53% of HOT elements predicted to function as enhancers [121]. In the S2 cells, in the range of 19 to 41%, Combgap, Zeste, Psq, and Adf1 overlap with the promoters having H3K4me3 and, thus, are suggested to be active [19]. In addition, 8 to 13% of Combgap, Zeste, Psq, and Adf1 overlap with potential active enhancer regions [19] defined by the H3K27ac peaks that are bound by CBP and localized outside of TSS. A high degree of overlap with the predicted active enhancers is shown for Psq in Kc167 cells, where it was shown to overlap with the active histone modifications, CBP, and also with GAF and Pc [78].
In agreement with the functional overlap of the PcG recruiters with enhancers and promoters, the interactomes of the PcG recruiters contain many proteins implicated in the activities of these regulatory elements.

PcG Recruiters and Their Promoter Partners
The Pol II together with the general transcription factors (GTFs: TFIIA, TFIIB, TFIID (composed of TBP and more than 10 TAFs), TFIIE, TFIIF, and TFIIH) are recruited to the promoters and they are assembled into the preinitiation complex (PIC). A successful formation of the PIC leads to a rapid initiation of transcription. Pol II pauses after it produces an RNA of 20-60 nucleotides in length. Current data suggest that the pausing of Pol II at the early elongation is an obligate part of the transcription cycle; a step that is universally encountered by Pol II for the majority of even highly expressed genes. The promoter pausing is primarily mediated by an action of the NELF and DSIF complexes that stabilize Pol II at the pause region [124,125]. In addition, the M1BP DNA-binding factor, the RNA polymerase II-associated factor 1 complex (PAF1C), and TFIID were shown to be implicated in the promoter pausing [126].
Of the PcG recruiters, GAF is well known to be implicated in pausing for a large subset of genes, most of which are developmentally regulated [111,120,[127][128][129][130][131]. In total, GAF associates with about 20% of the Pol II-bound promoters and correlates with the highest levels of paused Pol II [120,128]. Of the promoter-associated proteins, GAF was shown to interact directly and in co-IP with Taf3 [132,133] and Taf4 [104,133] subunits of the TFIID complex [132] (Figure 3).
In a pull-down assay, Grh interacted with Taf2 and Taf6 TFIID subunits [134] (Figure 3). In IP/LC-MS, Combgap efficiently co-purified with a number of the TFIID subunits (Figure 3), including Taf4, Taf7, Taf8, and Taf9 [19]. In addition, Combgap shows stable association with the NELF complex ( Figure 3) and M1BP. We have recently shown that over 80% of Combgap overlaps with the NELF-A and NELF-B subunits, genome-wide. Moreover, Combgap is required for an effective NELF recruitment to two genes, CG4562 and Pp2B-14D, which are actively transcribed, as well as to the Poxm gene, which is under the H3K27me3 repression [19].
It was shown that, except for promoters, NELF [19,137] and DSIF (Spt5) [23,138] are bound to the PREs/enhancers. Moreover, the spt5 and nelf-A mutants enhance the PcG phenotype observed in pho mutant flies, suggesting an involvement of pausing factors in the PcG silencing [136]. Thus, both the PcG recruiters and the pausing proteins have a potential to be co-regulators of promoters and PREs/enhancers.
Not surprisingly, PRC1 is connected to promoter functioning as well. It was demonstrated that depletion of the PRC1 subunits by RNAi alters both phosphorylation of RNAP II and recruitment of the Spt5 subunit of the DSIF complex to the active genes [23] and decreases gene transcription [24].

PcG Recruiters and Mediator Complex
Mediator is a large co-activator complex consisting of about 30 subunits, named MED1-MED31, Cdk8, and cyclin C [139]. Mediator associates with enhancers and active promoters and a depletion of Mediator subunits reduces transcription of the enhancercontrolled genes [140][141][142][143].
Adf1 stands apart from other PcG recruiters in the way that it highly efficiently copurifies with the Mediator complex ( Figure 3). Moreover, over 55% of the Adf1 peaks overlap with the MED1 and MED30 Mediator subunits genome-wide [19]. This suggests that Adf1 might be involved in the recruitment of Mediator to the chromatin. Intriguingly, while not as efficient as Adf1, Fs(1)h [21] and, less so, Psq [19] were also shown to co-purify a number of Mediator subunits.

PcG Recruiters and Architectural Proteins
The architectural (also known as insulator or boundary) proteins interact with the regulatory elements-boundaries that can limit enhancer-promoter interactions and block the spread of the heterochromatin [144,145]. They are also required for the separation of the genomic domains into TADs and for the formation of the 3D chromatin structure [146].
Of the PcG recruiters, GAF was experimentally confirmed to be required for the boundary activity of particular insulators [111,144]. GAF can co-purify with a number of architectural proteins (Figure 3), including Mod(mdg4)2.2, CP190, Chro, and Su(Hw) [104]; of these, GAF directly interacts with Mod(mdg4)2.2 [147][148][149]. However, genome-wide it does not show an extended overlap with the architectural proteins [150], suggesting that it might function differently from the other architectural proteins. Accordingly, GAF was shown to be implicated in the activity of tethering elements required for proper enhancer-promoter and promoter-promoter interactions of the developmentally regulated genes [151][152][153].
While there is a huge overlap of Combgap, Zeste, Psq, and Adf1 with the boundary proteins genome-wide, it should be noted that CP190 frequently overlaps with promoters [150,155], and, moreover, boundaries are frequently found in close proximity to PREs [62,[156][157][158] and can stimulate the PRE repressive activity [159]. Thus, the genomewide functional consequences of the overlap with CP190 require more studies. In a recent study, Combgap sites were shown to be enriched at the Su(Hw)-indirect peaks [160], suggesting that, at least in some cases, the overlap can be a result of a non-direct recruitment to the regulatory elements. It will be important to estimate in the future the intensity of the peaks that overlap between the PcG recruiters and boundaries.
In accordance with the interactions between the PcG recruiters, for some of them, Pho, Combgap, Spps, Crol, Psq, Zeste, and Adf1, a significant genome-wide overlap was reported [19,20,59,61]. At the 3rd instar larval imaginal discs and brains, about 80% of Pho peaks co-localize with Combgap [20,59] and Crol [61], and this corresponds to~50% of Combgap and Crol peaks ( Figure 5). Crol displays 80% overlap with Combgap [61]. In addition, over 70% of the Spps sites overlap with Combgap, Pho, and Crol, and this corresponds to~20-40% of Combgap, Pho, or Crol peaks [20,61]. In Drosophila S2 cells, 88% of Psq peaks overlap with Combgap, while the majority of Zeste peaks overlapped with Combgap (90%) and Psq (88%) [19]. The overlap of PcG recruiter with Adf1 is lower, but still exceeds 50% in the case of Combgap and Zeste sites. It should be noted that, overall, the binding profiles of the PRE DNA-binding proteins are unique and each of the tested proteins has its own unique binding peaks [19,20,59] and if we calculate simultaneous overlap between a larger number of recruiters together, they would show a lower frequency. For example, simultaneous overlap for Combgap, Zeste, Psq, and Adf1 proteins identifies 1168 regions which correspond to 15% of Combgap, 24% of Adf1, 27% of Psq, and 56% of Zeste peaks [19].
In addition, it should be noted that the extent of overlap can be different within and outside of the H3K27me3 domains. For Spps-Pho, it was reported to be lower outside of the H3K27me3 domains-about 90% and 70% of Spps peaks overlap with Pho, inside and outside of the H3K27me3 domains, respectively [20]. Another study suggested a better overlap of Grh with GAF at Grh-repressed loci [85]. In any case, the total extent of the mutual overlap between the PcG recruiters is substantially high, which allows the proposal that at many loci inside and outside of the H3K27me3 domains they can function together.
Several observations support a co-operative activity of the PcG recruiters. It was shown that Pho protein binding to a chromatinized PRE in vitro requires the assistance of GAF or Zeste proteins [165]. In another in vitro study, Pho and Grh facilitated each other's binding to the naked DNA [68]. In vivo, Spps was shown to be important for the Pho recruitment at subsets of sites genome-wide, independent of the H3K27me3 state [20]. Similar, Crol is important for Combgap binding at several sites in and out of H3K27me3 domains [61].
In addition to the co-operation, the activities of the PcG recruiters were proposed to be redundant and partially compensate for each other [15,20].
In connection with the potential network that can be formed by multiple interactions between the PRE DNA-binding proteins, their functional co-operation, and redundancy, we have proposed a model according to which the combination of the PRE DNA-binding factors at the PRE forms a "platform" that provides for an efficient recruitment of the core PcG/TrxG complexes [15]. We propose that this model can be relevant not only at the PREs, but also outside of the H3K27me3 domains as well. Figure 5. The genome-wide overlap between PcG recruiters. The total numbers of binding peaks for two selected PcG recruiters are shown for each line. The PcG recruiter 1 peaks (indicated on the left) that do not overlap with PcG recruiter 2 (indicated on the right) are colored in yellow, the PcG recruiters' peaks that overlap with each other are colored in red, and the PcG recruiter 2 peaks that do not overlap with PcG recruiter 1 are colored in blue. For the Pho overlap with Combgap, the data derived from two different studies are presented: 1 -[20]; 2 - [59]. The other designations are as in Figure 4.
Several observations support a co-operative activity of the PcG recruiters. It was shown that Pho protein binding to a chromatinized PRE in vitro requires the assistance of GAF or Zeste proteins [165]. In another in vitro study, Pho and Grh facilitated each other's binding to the naked DNA [68]. In vivo, Spps was shown to be important for the Pho recruitment at subsets of sites genome-wide, independent of the H3K27me3 state [20]. Similar, Crol is important for Combgap binding at several sites in and out of H3K27me3 domains [61].
In addition to the co-operation, the activities of the PcG recruiters were proposed to be redundant and partially compensate for each other [15,20].
In connection with the potential network that can be formed by multiple interactions between the PRE DNA-binding proteins, their functional co-operation, and redundancy, we have proposed a model according to which the combination of the PRE DNA-binding factors at the PRE forms a "platform" that provides for an efficient recruitment of the core PcG/TrxG complexes [15]. We propose that this model can be relevant not only at the PREs, but also outside of the H3K27me3 domains as well. Figure 5. The genome-wide overlap between PcG recruiters. The total numbers of binding peaks for two selected PcG recruiters are shown for each line. The PcG recruiter 1 peaks (indicated on the left) that do not overlap with PcG recruiter 2 (indicated on the right) are colored in yellow, the PcG recruiters' peaks that overlap with each other are colored in red, and the PcG recruiter 2 peaks that do not overlap with PcG recruiter 1 are colored in blue. For the Pho overlap with Combgap, the data derived from two different studies are presented: 1 -[20]; 2 - [59]. The other designations are as in Figure 4.

Conclusions
The current data suggest that the PcG recruiters, as well as PcG core proteins, bind to regions inside and outside of the H3K27me3 domains and participate in both the repression and activation of genes. Although much progress has been made toward an understanding of the role of the PcG recruiters in assembly of the PcG protein complexes genome-wide, many questions remain to be elucidated.
Multiple interactions between the PcG recruiters were identified and they show an extensive overlap with each other and with the PRC1 genome-wide. However, the currently described interactomes of the PcG recruiters, GAF, Combgap, Zeste, Psq, and Adf1, differ substantially from each other. This might suggest that each protein can attract a unique set of transcription factors to the DNA, and the presence of a binding site for a particular DNA-binding protein could subtly modulate the resulting activity of the DNA regulatory element. This can probably apply to both PREs and the other types of regulatory elements. The characterization of the interactomes of other PcG recruiters may provide a better understanding of the role of each of them in the genome-wide transcriptional regulation.