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Logo of bmcmbBioMed Centralsearchsubmit a manuscriptregisterthis articleBMC Molecular Biology
BMC Mol Biol. 2007; 8: 40.
Published online May 22, 2007. doi:  10.1186/1471-2199-8-40
PMCID: PMC1887537

Coordinated regulation of Myc trans-activation targets by Polycomb and the Trithorax group protein Ash1

Abstract

Background

The Myc oncoprotein is a transcriptional regulator whose function is essential for normal development. Myc is capable of binding to 10% of the mammalian genome, and it is unclear how a developing embryo controls the DNA binding of its abundant Myc proteins in order to avoid Myc's potential for inducing tumorigenesis.

Results

To identify chromatin binding proteins with a potential role in controlling Myc activity, we established a genetic assay for dMyc activity in Drosophila. We conducted a genome-wide screen using this assay, and identified the Trithorax Group protein Ash1 as a modifier of dMyc activity. Ash1 is a histone methyltransferase known for its role in opposing repression by Polycomb. Using RNAi in the embryo and Affymetrix microarrays, we show that ash1 RNAi causes the increased expression of many genes, suggesting that it is directly or indirectly required for repression in the embryo, in contrast to its known role in maintenance of activation. Many of these genes also respond similarly upon depletion of Pc and pho transcripts, as determined by concurrent microarray analysis of Pc and pho RNAi embryos, suggesting that the three are required for low levels of expression of a common set of targets. Further, many of these overlapping targets are also activated by Myc overexpression. We identify a second group of genes whose expression in the embryo requires Ash1, consistent with its previously established role in maintenance of activation. We find that this second group of Ash1 targets overlaps those activated by Myc and that ectopic Myc overcomes their requirement for Ash1.

Conclusion

Genetic, genomic and chromatin immunoprecipitation data suggest a model in which Pc, Ash1 and Pho are required to maintain a low level of expression of embryonic targets of activation by Myc, and that this occurs, directly or indirectly, by a combination of disparate chromatin modifications.

Background

Cancer can arise in many ways, one of the most potent being deregulation of the myc proto-oncogene. Myc is a transcription factor, and its C-terminal domain is required for dimerization with its partner Max and its subsequent binding to DNA. It also possesses an N-terminal trans-activation domain that is required for both Myc's biological activities of transcriptional activation and repression. Activation by Myc involves binding to the nuclear protein TRRAP, which recruits histone acetyltransferase complexes to Myc activation targets. Subsets of target genes include those that mediate cell cycle progression, cell growth, genomic instability, angiogenesis, and inhibit differentiation [1-3]. Myc also acts as a repressor of a different set of targets, in addition to interfering with the function of activators such as Miz1 [4,5]. Myc binding to DNA is dependent on chromatin context, such that Myc sites having certain chromatin modifications are almost always bound, and Myc sites lacking those certain modifications are rarely bound by Myc [6].

Experiments in mammalian systems have answered many questions regarding Myc biology, though their limitations in broad based discovery led us to investigate Myc biology in Drosophila. The dMyc protein is highly similar to c-Myc in the residues required for DNA binding, and the gene has a similar exon and intron structure [7,8]. dMyc can functionally replace c-Myc in transformation assays with activated Ras and in rescue experiments with mouse cells null for c-myc [8,9]. In Drosophila, dMyc regulates RNA Pol I production of ribosomal RNAs, is required for oogenesis and larval growth, and overexpression of dmyc in clones of the Drosophila imaginal disc confers a growth advantage to cells having greater amounts of dmyc expression than their neighbors [10-14].

In a transgenic mouse model using induction of Myc in hepatocytes, the ability of Myc to induce proliferation and tumorigenesis was shown to vary greatly depending on the age of the mouse at the time Myc was induced, suggesting that the differentiation states of cells can mediate the response to Myc [15]. In Drosophila, differentiated or undifferentiated cell states are maintained by the Polycomb Group (PcG) and Trithorax Group (TrxG) of proteins, which are thought to bind to repressed or activated loci, and thus to stabilize patterns of gene expression [16,17]. We reported previously that repression by Myc in Drosophila requires Polycomb, a chromatin-binding transcriptional repressor [18]. Previously characterized phenotypes manifested in PcG mutants reflect a loss of repression of homeotic genes, and the members of the PcG group were additionally defined by their ability to enhance each other's dominant phenotypes [19,20] (and references within). Conversely, mutant phenotypes of members of the TrxG reflect a loss of activation of homeotic genes, and these mutations behave as suppressors of mutations in Pc. Many of the members of the PcG of proteins have been found in two separate protein complexes, PRC1 and PRC2, neither of which bind to DNA alone. PRC1 includes Pc, Ph, Psc and dRing1; PRC2 includes Esc; a histone methyltransferase, E(z); and Su(z)12. PcG proteins bind to hundreds of sites in the genomes of mammals and Drosophila [21-25], and repression of homeotic genes mediated by PcG proteins is experimentally linked to cis regulatory elements known as PREs (Polycomb Response Elements, reviewed in [26,27]). The PcG proteins Pho and dSfmbt bind to sites within PREs, recruiting PRC2, followed by recruitment of PRC1 [28-32]. TrxG proteins bind to over 100 sites on polytene chromosomes and can be found in nucleosome remodeling complexes such as the BAP complex (Brahma Associated Protein complex: Brahma, Moira, Osa and Snr1). Trx and Ash1 (absent, small or homeotic discs 1) are SET domain histone methyltransferases (reviewed in [33]).

Repression by Myc requires Pc for many targets, which includes the dmyc locus itself [18]. In the present study, we describe a novel genetic assay that we use to find additional Drosophila gene products involved in repression of the dmyc gene. Using this assay, we screened the Drosophila genome for modifiers of dmyc expression. We then used RNAi to deplete levels of our genetic modifiers, Ash1 and Pho, in the embryo and used Affymetrix microarrays to analyze gene expression changes in these embryos with or without ectopic Myc. Our genetic and genomic data allow us to describe the role of Pho and Ash1 in Myc-mediated repression and in control of Myc trans-activation targets in the embryo. These data provide the first evidence for a functional link between canonical Pc and Trx Group proteins.

Results

Pho and Psc are involved in repression of dmyc

Pc binds to methylated histone H3 at lysine 27 (H3K27), mediating repression of many genetic loci by Myc [18]. In an investigation of other PcG gene products potentially involved in this repression by Myc and Pc, we chose three candidates to test: Posterior sex combs (Psc), which is in a core repressive complex with Pc [34]; E(z), which is a histone methyltransferase that methylates histone H3 lysine 27 and recruits Pc repression [35-37]; and Pho, which is one of two DNA-binding proteins of the group and recruits E(z) [28,30-32]. Our strategy for testing Psc, E(z) and Pho involved a genetic test for modification of expression at the dmyc locus. Each of two different P element insertions in the dmyc locus, dmycBG02383 and dmycBG00605, provides two reporters for dmyc expression: a promoterless yeast Gal4 gene that is expressed by the upstream dmyc promoter, and a Drosophila eye color mini-white gene whose expression is influenced by the regulation of the locus (Figure (Figure1A)1A) [38,39].

Figure 1
A P element insertion in the dmyc locus is a reporter for dmyc activity. (A) A diagram indicating the exons (green rectangles) and introns (thick blue line) of the dmyc gene on the X chromosome. A pGT1 insertion in the second intron (dmycBG02383, top) ...

We first determined whether these reporters were sensitive to the regulation of the dmyc gene, using the phenomenon of dmyc autorepression. In this assay, ectopic dmyc leads to a reduction in the expression from the endogenous locus [18]. We obtained high levels of ectopic Myc in embryos with the dmycBG02383 allele (see Methods for genotypes and crosses). We collected RNA from dmycBG02383 embryos with or without ectopic dmyc and used RT-PCR to amplify transcripts from the Gal4 and mini-white reporters, the first exon of dmyc (which amplifies only the endogenous transcript and not the exogenous transcript), and a loading control, dRas. Expression of endogenous dmyc in embryos with the P-element insertion is normal, and Northern blotting indicates that the mature transcript size is the same as in wild type (Figure (Figure1B1B and data not shown). Endogenous dmyc expression detected by RT-PCR in embryos with ectopic Myc was close to zero (Figure (Figure1B),1B), indicating that autorepression is intact in dmycBG02383 embryos. Phosphorimaging data revealed a reproducible reduction in both mini-white and Gal4 expression in embryos with ectopic dmyc (Figure (Figure1B).1B). The effect was small but striking, given that the embryos contain sources of mini-white and Gal4 in addition to those from the insertion in dmyc (i.e. the two transgenes that we used to provide ectopic dmyc, UAS dmyc and Gal4, both have mini-white associated with them). These results provided the molecular validation for our genetic strategy, linking dmyc regulation to the expression of the reporters within the locus.

We reasoned that reducing the dosage of a gene involved in dmyc repression might elevate the mini-white expression above that normally observed in dmycBG00605 and dmycBG02383 flies. Therefore, we generated flies with mutations in candidate dmyc repressors combined with the dmyc reporters and examined levels of mini-white expression (see Methods for genetic crosses and scoring procedures). Heterozygosity (i.e. one mutant chromosome and one wild type chromosome) for a Pc mutation did not increase mini-white levels of dmycBG02383 males, but did affect mini-white levels of dmycBG00605 (16% dark Pc3 males versus 0 dark non-mutant control male siblings, Table Table1).1). Heterozygosity for a Psc mutation affected both insertions in dmyc, increasing the mini-white levels compared to those of the non-mutant siblings in both cases (60% dark for dmycBG02383, 44% dark for dmycBG00605, 18% dark for the non-mutant controls, Figure Figure2A2A and Table Table1).1). Males heterozygous for either of two different loss-of-function alleles of E(z), E(z)5 and E(z)61, did not increase mini-white levels of either insertion in dmyc; E(z) males and non-mutant male siblings had indistinguishable mini-white intensities. Males heterozygous for a hypomorphic mutation in pho, pho1, had greater numbers of males with dark eyes than their non-mutant siblings, with 57% of pho1 heterozygotes having dark eyes compared to 5% of the non-mutant flies having dark eyes (Figure (Figure2B2B and Table Table1).1). Therefore, we considered dmycBG00605 to be the more sensitive reporter for dmyc expression because it revealed regulation by Pc. Psc and pho mutations affected both insertions, suggesting their involvement in Pc/Myc repression. However, neither insertion was affected by E(z) mutations, suggesting that E(z) may not be involved in repression by Myc or that mutations in E(z) are not haploinsufficient with respect to Myc activity.

Table 1
Deficiencies and mutants that behave as genetic repressors of dmyc
Figure 2
Psc,pho and ash1 behave as genetic repressors of the dmyc locus. (A) Male siblings are shown, both hemizygous for dmycBG02383, and either heterozygous for Psc1 (left), or the balancer chromosome (CyO). (B) Male siblings are shown, both hemizygous for ...

Pho participates with Pc in repression of Myc targets

The Pho protein is thought to recruit Pc to PREs [30-32] and in that way facilitates Pc's repressive activity. Requirements for Pho activity might therefore be expected to parallel those for Pc with respect to repression by Myc, as suggested by our mini-white assay described above. To examine this possibility, we injected embryos with dsRNA directed at pho, reducing transcript levels 6-fold (Figure (Figure3A).3A). We also induced RNAi for pho in embryos with ectopic Myc to examine the role that Pho has in Myc function. In addition to pho RNAi, we repeated the Pc RNAi experiment (4-fold reduction in Pc levels) for comparison using the Drosophila Genome 2.0 Affymetrix arrays (Figure (Figure3A).3A). As described previously [18], we also injected embryos with buffer for our controls, injected 200 embryos for each array hybridization, and duplicated the entire experiment, for a total of 400 injected embryos analyzed per genetic condition. We injected pre-cellularization embryos, and allowed them to age for 20 hours at 18°C before isolating RNA. This technique of using RNAi rather than known mutations in pho and Pc for our microarray analysis has several advantages. First, variability between genetic backgrounds is eliminated, since genetically identical mothers provided the embryos for our experiments from array to array, no matter what gene we depleted by RNAi or whether the fathers provided ectopic Myc or not (Figure (Figure4).4). Second, transgene expression is constant from chip to chip because we used the identical Gal4 source and UAS-dmyc for all experiments, without concern for the logistics of combining three different genetic situations in one set of embryos. Third, because we reduced both maternal and zygotic transcripts by RNAi, our experiments did not require that we generate germ line clones to eliminate the maternal contribution of transcripts.

Figure 3
Pho behaves similarly to and differently from Pc with respect to Myc activity. For all scatter-plot graphs, the diagonal blue lines indicate zero change and 2-fold changes in either direction. Our thresholds for labeling genes as increasing or decreasing ...
Figure 4
Biological replicates of microarray hybidizations are highly comparable. Normalized intensities for all 18660 transcripts on the Affymetrix Drosophila Genome 2.0 array are graphed for one replicate on the X axis, and the second replicate is the Y axis. ...

Our experiments reveal 329 target genes that appear to be repressed by Pho in normal embryos, since their levels increase following pho RNAi (see Methods for list generation). A larger number of Pc repression targets were identified following Pc RNAi (625, Table Table2),2), and consistent with the view that Pc and Pho work together, the two groups of targets show substantial overlap; 146 of the 329 pho targets are also Pc targets (Figure (Figure3D).3D). That the remaining 183 Pho targets do not appear to overlap Pc targets may reflect the limitations of the threshold techniques used to identify targets in our experiments. It may also reflect differences of specific targets in their sensitivity to reductions in Pc and Pho (see Discussion). The shared regulatory roles of Pc and Pho extend beyond normal development to those 57 genes that are repressed in embryos following ectopic Myc accumulation (Figure (Figure3B).3B). 26 of these are no longer repressed to the same degree in the absence of Pho, and 25 are no longer repressed to the same degree in the absence of Pc (in the combined condition of ectopic Myc and RNAi of Pc or pho, Figure Figure3C3C and Table Table3).3). These genes that fail to be repressed in the absence of Pc or Pho do not overlap completely. 15 are affected by Pc and Pho similarly, 10 are affected by Pc and not Pho, and 10 are affected by Pho and not Pc. We conclude that normal levels Pho and Pc are required for Myc's repressive activity, though not necessarily at the same time.

Table 2
Numbers of genes responding to ectopic Myc, ash1 RNAi (ash1-), (pho-), Pc RNAi (Pc-), and Myc combined with each
Table 3
Gene list matrix

We examined the possibility that Pc mediates its repressive effects upon dMyc targets by utilizing previously characterized Polycomb Responsive Elements (= PREs). The location of both Pc and Myc repressed genes, however, provides no evidence of close proximity to each other (Figure (Figure5A).5A). Because we were able to map target genes to chromosomes using Genespring with Affymetrix Drosophila Genome 1 data and not Genome 2.0, we used our previous set of Pc repressed genes to compare to the locations of likely PREs [18]. We compared the genomic locations of 214 Pc repressed genes to the genomic locations of experimentally determined Pc binding sites [24,25,40]. 13 of the 214 Pc responsive genes in our data overlap Pc binding sites, and 30 of the remaining 214 are within two cytological number divisions of Pc binding sites for one set of published data (i.e. gene at 61C7 and Pc binding at 61C9 or closer) [40]. Compared to a different set of published Pc binding sites, 8 of 214 Pc responsive genes of our set are within Pc binding sites [25]. The overlap is small, though interestingly, the overlap of the two previously published Pc binding sites with each other is also small: just 1 of 43 genes with Pc binding sites in our set is common to the data sets of both Schwartz et. al. and Tolhuis et. al. A third set of mapped Pc binding sites describes many fewer Pc binding sites, and two of those overlap our Pc responsive genes [24]; these two are also described as being Pc binding sites by Swartz et. al. (Figure (Figure5B).5B). We conclude that Pc binding is dynamic, with no absolute set of Pc binding sites. Each set of data is a snapshot of the current and changing position of Pc, and our gene expression data is consistent with the dynamic and possibly stochastic nature of Pc binding to the genome.

Figure 5
Pc and Myc responsive genes are not clustered near genomic Pc binding sites. (A) Chromosomes of the Drosophila genome are shown, with a vertical blue bar above or below (plus or minus strand, respectively) each chromosome to indicate Myc repressed genes. ...

Our previous experiments indicated that many of the genes activated by Myc are normally repressed by Pc [18]. We were curious whether Pho repression overlapped Myc activation to the same extent. The levels of 680 transcripts increase with ectopic Myc. Of the 329 genes whose levels increase with pho RNAi, 260 are among the 680 Myc activation targets (Table (Table3,3, Figure Figure3E).3E). Therefore, a substantial role for Pho in normal embryos is to repress genes that can be activated by ectopic Myc.

We examined our embryonic Myc activation targets for the presence of transcription factor binding sites. Using P-Match to search our sequences for known transcription factor binding sites within the Transfac database [41], we found 0 of 680 Myc induced targets that have canonical vertebrate Myc-binding E-boxes from the 0 position through the first exon. E-boxes in Drosophila are most likely to be found from -50 to +50, with the majority between 0 and 50 [42]. The lack of E-boxes may simply reflect the nature of our embryonic Myc targets, which exclude those that are maternally deposited because those transcripts are present in both our experimental and control embryos. It is possible that our zygotic Myc targets are part of a different set that are induced by non-canonical binding sites. Among Drosophila genes bound by dam-Myc, 95% of the sites identified at those loci were not the canonical CACGTG [43]. We did find, however, many Myc activated transcripts with vertebrate YY1 sites, which is the homolog of Drosophila Pho. The mammalian transcription factor YY1 is able to bind to PREs and recruit Pc repression in Drosophila [44], and 32 of 680 Myc activated genes have YY1 sites. To determine the significance of this number, we used P-Match to search the sequences of 50 random Drosophila genes, and 3 of those have YY1 sites as well. Therefore, we considered the appearance of 32 YY1 sites in our set of 680 Myc activated genes to be similar to what is found randomly.

Mutations in ash1 cause increased expression of the dmyc gene

To search for other components that might mediate a Pho/Myc/Pc interaction, we conducted an unbiased genetic screen of large deletions on the Second and Third Chromosomes (comprising 80% of the Drosophila genome). Because dmycBG02383 flies have a darker eye color that is easier to score than dmycBG00605, we used dmycBG02383 in our screen. Out of a total of 154 Deficiency mutants (Dfs), 16 scored as decreasing mini-white levels of dmycBG02383 and 15 scored as increasing mini-white expression (screen scheme is shown in Figure Figure1C).1C). Among the latter Dfs, we were particularly interested in the overlapping region of Df(3L)kt02 and Df(3L)XS533 because it includes ash1, a histone methyltransferase [45,46]. We tested specific ash1 mutants for their ability to recapitulate the phenotype seen in the two overlapping deficiencies and found that 69% of ash1RE418 mutant males had darker mini-white compared to 8% of their non-mutant siblings (Figure (Figure2C2C and Table Table1).1). To be sure that the mutations that scored as affecting the insertion in dmyc were indeed affecting dmyc expression and not mini-white in general, we conducted independent control crosses of a mini-white P element insertion (pGT1) on the X chromosome, BG00979, to every mutation and deficiency that scored positive in our assay. We found that 2 deficiencies affected this non-dmyc mini-white insertion and ruled them out. The rest, including Pc, Psc,pho and ash1, did not affect mini-white levels of the non-dmyc associated insertion (data not shown). Therefore, our genetic assay provided a DNA binding protein (Pho) and a histone methyltransferase (Ash1) as potential mediators of Myc-Pc activity.

Depletion of Ash1 and Pc in the embryo results in similar gene expression changes

Although Ash1 appears to be involved in repression of dmyc with Pho and Pc in our mini-white assay, it is known as a Trithorax Group gene. Ash1 mutant phenotypes and genetic interactions suggest that, at least with respect to homeotic loci, it works in opposition to the activity of the Pc Group [47-51]. To examine the full range of functions for Ash1, beyond regulation of the homeotic selector genes, we conducted microarray experiments comparing gene expression changes between embryos with wild type and reduced levels of ash1. We injected embryos with dsRNA directed at ash1, reducing transcript levels 2-fold (Figure (Figure3A).3A). We also induced RNAi for ash1 in embryos with ectopic Myc to examine the role that Ash1 has in Myc function. The experiments were conducted the same way as described above for pho RNAi.

We first characterized Ash1's potential repressive activity in the embryo, determining whether ash1 RNAi causes increased expression of certain transcripts and whether those targets overlap Myc or Pc activities. We found that levels of 239 genes increase with ash1 RNAi, suggesting that Ash1 behaves directly or indirectly as a repressor in the embryo (Table (Table2,2, Figure Figure6A).6A). 142 of these 239 genes are activated by Myc (Figure (Figure6B,6B, purple). The overlap parallels our previous findings with Pc and Pho, and suggests that, in the embryo, a significant role of Ash1, Pho and Pc is to control the expression of targets that are activated by ectopic Myc. In addition, we found that 130 of the 239 Ash1 repression targets are also Pc repression targets (Figure (Figure6C,6C, purple). This overlap is at least as large as that observed for Pho and Pc and provides the first molecular link between Pc and a TrxG protein in repression. This link may be the result of either direct or indirect activities of Pc and Ash1. The overlap of Pc/Pho and Ash1 repression targets is not limited to genes activated by Myc. 66 of the 97 non-Myc targets repressed by Ash1 are also repressed by Pc or Pho.

Figure 6
Ash1 protein's activities overlap those of Pc and Myc. (A) Expression levels of 8865 genes are plotted by their basal levels along the X axis and their levels upon ash1 RNAi along the Y axis. Red dots indicate genes whose levels rise with ash1 RNAi, and ...

The genetic assay that revealed that Ash1 is involved in Myc biology was one assessing repression of the dmyc locus. Therefore, we examined the 57 Myc repressed genes for any requirement of Ash1 in that repression. In an embryo with ectopic Myc and ash1 RNAi, 47 of those genes remain repressed (Table (Table3)3) suggesting that Ash1 is required for Myc repression at only a small fraction of its targets (i. e., 10/57 = 18%). In contrast, 25 of the same 57 Myc repressed targets were no longer repressed to the same degree when Pc levels were reduced. This effect is more pronounced than that of Ash1 and may indicate a more direct role for Pc in Myc repression. These numbers do not represent absolute repression by Ash1 and Pc, however, given that the RNAi depletion of these transcripts was not complete. In fact, Pc levels were reduced 2 fold more than ash1 transcripts, as measured by microarray.

Ectopic Myc replaces Ash1 in activation

Consistent with Ash1's known role in gene activation, levels of 159 genes decrease in response to ash1 RNAi (Figure (Figure6A,6A, Table Table2),2), an effect that is superficially similar to the positive role of Ash1 in regulating homeotic gene activity. 70 of these 159 genes are also Myc activation targets. In contrast, only 9 of 76 genes whose levels decrease with Pc RNAi are also Myc activated (Table (Table3).3). Similarly, just 4 of 69 genes whose levels decrease with pho RNAi are also Myc activated (Table (Table3),3), suggesting that Pc and Pho are unlikely to be functioning similarly to Ash1 with respect to gene activation. Given this overlap between activation targets of Myc and Ash1, we hypothesized that ectopic Myc might rescue the loss of activation that occurs with ash1 RNAi. If this were the case, we would expect that genes whose levels decrease with ash1 RNAi alone would in fact increase with ash1 RNAi and ectopic Myc. Consistent with this notion, we found that levels of 81 of these 159 genes are significantly elevated above basal levels in embryos with both ectopic Myc and ash1 RNAi, and expression of 68 genes is at basal levels (Figure (Figure6D).6D). Only 10 of the 159 genes whose levels are reduced with ash1 RNAi remain reduced in the presence of ectopic Myc. Therefore, a large majority of genes that are activated by Ash1 are not only Myc activated, but Myc can replace Ash1 in their activation. These results also suggest that, while Ash1 is important in the activation of these genes, they do not require wild type levels of Ash1 to be activated by Myc.

Ash1 is required for Myc activation

We were curious about the inverse, whether Ash1 is required for activation by Myc. Levels of 680 genes increase upon activation of ectopic Myc. In embryos with both ectopic Myc and ash1 RNAi, levels of 76 of these genes fail to increase at the same level (Figure (Figure7A).7A). None of these 76 genes is also regulated by Ash1 alone, suggesting that Ash1's regulation of these genes is limited to activation by Myc. Upon closer examination of the 76 genes, we found a cluster of 60 that are regulated by Pc and Pho (Figure (Figure7B,7B, generated by K-means clustering of Myc activation targets). The regulation of these genes by Pc and Pho is negative, in that the targets have elevated expression with Pc or Pho RNAi (Figure (Figure7B).7B). Therefore, many of these targets are normally repressed by Pc/Pho. Among the named genes in this group, several encode structural constituents, such as Ccp84Ac (larval cuticle), Dhc62B (Dynein Heavy chain 62B) and Actin 88F, and some are involved in metabolism, such as Glycogenin and Lipase1. One possible explanation for the regulation of these Myc targets is that the role of Ash1 is to oppose Pc/Pho repression, allowing Myc activation. In fact, Ash1 opposes Pc repression at homeotic loci [47]. Therefore, our data suggest that Ash1 also opposes Pc repression at loci activated by Myc (Figure (Figure7C7C).

Figure 7
Ash1 works against Pc/Pho repression to facilitate Myc activation. (A) Changes in expression of 77 genes are shown, log2 of ratios of expression over basal, for transcripts whose levels increase with ectopic Myc (blue bars). For each of the 77 genes, ...

Myc targets exhibit disparate histone modifications

In many of our experiments, Pc, Pho and Ash1 proteins facilitate Myc's activity as a repressor, but also appear to oppose its activity as an activator. In an attempt to understand how the same proteins cooperate with Myc to repress one set of targets and conversely work to repress a different set of Myc activation targets, we have to consider a major difference between Myc's targets of activation and repression: before Myc acts upon them, repression targets are necessarily being expressed while activation targets are largely unexpressed (Figure (Figure8A8A).

Figure 8
Myc targets of activation are methylated at both H3K4 and H3K27. (A) (Left) A graph showing basal levels of 680 Myc activated targets (blue, left bar, each gene is represented by a thin line) followed by their levels upon ectopic Myc activation (blue, ...

Myc's embryonic targets of activation, prior to induction of ectopic Myc, are expressed at low levels and our data show that Pc, Pho and Ash1 are required to maintain that pattern of expression. To examine Myc targets for hallmarks of both Ash1 and Pc activity, we used chromatin immunoprecipitation to examine the methylation of histone tails in wild type embryos. Because Ash1 methylates H3K4, a chromatin modification that correlates with mammalian targets of Myc activation [6], and Pho and Pc are involved in setting up and binding to H3K27 methylation, respectively, we used sequential chromatin immunoprecipitation to determine whether Myc activation targets in the embryo exhibit both methylation marks. Using chromatin from wild type embryos, obtained over a 24 hour room temperature collection, we immunoprecipitated with anti-dimethyl H3K4, purified the chromatin, and immunoprecipitated again with anti-trimethyl H3K27. We also performed the reciprocal experiment, beginning with anti-trimethyl H3K27 and following with anti-dimethyl H3K4 (See Methods, and [52]). We used PCR to detect three different genes that are Myc activated, Pc, Ash1 and Pho repressed (CG16712, fs(1)N, and alpha Tubulin 67C, Figure 8B–C). All three of these genes were amplified from our sequential ChIP DNA, arguing that they are modified on both H3K4 and H3K27. As a control, we examined a gene that is not regulated by Myc, Pc, Ash1 or Pho (Atg8a) and found it absent in our sequential ChIP DNA, though it is expressed at high levels in the embryo and methylated at H3K4 (Figure (Figure8C).8C). In addition, we tested two genes that are Pc and Myc repressed (CyP309a1, CG18108, respectively [18]), and they show both H3K4 and H3K27 methylation individually in chromatin from wild type embryos. This result is not unexpected, since we obtained the chromatin from all the cells of wild type embryos, so that different cells may be expressing or repressing each gene. We found that these loci are not methylated at both residues simultaneously, because we failed to amplify either gene from our sequential ChIP DNA (Figure 8B–C). These results, along with our genetic and genomic data, support a model for the control of Myc targets in the embryo, in which Ash1, Pc and Pho are required for the low levels of expression of these genes, reflected by the disparate chromatin methylation of targets of Myc activation (Figure (Figure8D).8D). Developmentally regulated genes in mammalian embryonic stem cells also exhibit low levels of expression prior to differentiation, corresponding to methylation of both H3K4 and H3K27 [52].

Myc repression targets, different from activation targets, are expressed in the embryo prior to ectopic Myc induction (Figure (Figure8A).8A). Bracken and colleagues have shown that PcG proteins bind at expressed loci prior to differentiation and repression, and those sites also have H3K27 methylation [22]. We have observed H3K27 methylation of Myc targets in wild type embryos (Figure 8B–C), suggesting that they are primed for repression, and upon ectopic Myc induction Pho and Pc work to repress these targets. The role of Ash1 in repression of these targets may be limited to the embryo, possibly to allow for trans-activation in the event of an activation signal, rather than a less reversible Pc-mediated silenced state (Figure (Figure8E8E).

Discussion

The requirement for Ash1 in activation and maintenance of non-activation

Our genetic assay for modification of expression of the dmyc locus enabled us to identify an unexpected interaction, namely that gene regulation by Ash1 in the embryo overlaps gene regulation by Myc, Pc and Pho. We found that a deletion of ash1 leads to greater expression of a mini-white reporter within the dmyc locus, which potentially reflects repression of dmyc in the eye imaginal disc. In addition, ash1 RNAi in the embryo causes the induction of 239 genes. Interestingly, homeotic transformations in flies mutant for ash1 are enhanced by mutations in Psc [53], a PcG gene that is part of the core repressive complex including Pc [34]. Thus, the current understanding of Ash1 as a nuclear protein involved in the complex regulation of cellular memory does not exclude the possibility that Ash1 may be involved in repression of certain genes, directly or indirectly. Ash1 was identified as a late larval lethal mutation with imaginal disc defects [54]. Expression of homeotic selector genes in ash1 mutants is affected differently in different cells, with stochastic loss of expression [48] apparently caused by ectopic silencing by Pc-G proteins [47]. Flies heterozygous for a mutation in ash1 show homeotic transformations when the fly is also heterozygous for another trxG mutation [51]. This intergenic non-complementation indicates that levels of TrxG proteins are important, which is supported by the large genomic effects we describe with just a 2-fold reduction in ash1 transcripts. The Ash1 protein is a SET domain histone methyltransferase that methylates lysines 4 and 9 of histone H3 and lysine 20 of histone H4, and these combined activities are correlated with active transcription [45,46]. Interestingly, methylation of histone H3 lysine 9 is reduced in the chromocenter of polytene chromosomes in ash1 mutants lacking the SET domain [46], and H3K9 methylation is associated with HP-1 binding and heterochromatin formation [55-57]. In addition, Ash1 binds to 108 bands on polytene chromosomes, several of which overlap or are adjacent to binding sites of Psc [50]. We found that among the 239 genes that are up-regulated with ash1 RNAi, 130 are also up-regulated with Pc RNAi, 139 are up-regulated with pho RNAi, with 73 of these genes common to all three. These results suggest that Ash1 methylation is not exclusive to transcriptional activation.

Ash1 also appears to be involved in activation of a different set of embryonic targets, and many of the genes in this set overlap Myc activation targets. In fact, we found that ectopic Myc can replace Ash1 in embryos with both ash1 RNAi and ectopic Myc by activating 76% of the genes whose expression decreases with ash1 RNAi alone. In addition, we argue that Ash1 is required in Myc activation of a subset of its targets, presumably by antagonizing Pc/Pho repression. H3K4 methylation is correlated with Myc binding to high affinity target sites, and this methylation occurs in the absence of Myc protein, suggesting that it is established and then Myc is able to bind [6]. Ash1 may function to maintain a favorable methylation state of Myc targets, allowing subsequent activation by Myc.

We found minimal direct overlap of Ash1 activation with Pc and Pho repression. Our threshold values for determining genes affected by each genetic condition likely caused false negative results; in addition, ash1 transcript levels were not depleted as effectively as Pc or pho levels. Our experiments were conducted with RNA from entire embryos, therefore we cannot determine the segment-specific regulation by the genes that we tested, and the overlap of Pc and Pho repression with Ash1 activation would be expected to occur in a segment-specific manner. Following that argument, the large overlap of Ash1, Pc and Pho repression targets may be related to universal genetic programs, including Myc transcriptional activation, in contrast to the cell-type specific programs, such as those under the control of homeotic genes.

Pho's activity overlaps Myc targets better than Pc targets

We found many of the transcripts that are de-repressed by pho RNAi overlap those that are de-repressed by Pc RNAi, but more of the Pho targets overlap those that are Myc activated than Pc repressed. Our stringent statistical requirement for the membership of any transcript in a list of genes that increase or decrease in response to a particular genetic condition may reduce our view of the overlap of genes regulated by both Pc and Pho. But a difference in the effects of loss of Pc and loss of Pho is not unprecedented. pho mutants have segmental transformations similar to those of Pc mutants, however these mutations have either little or no effect on expression of abd-A, abd-B or Ubx in embryos [20,58-60]. And yet, Pho is required for silencing of the iab-7 PRE [61] and is necessary, though not sufficient, for the silencing activity of the MCP element of the Abd-B gene [62]. Our data and the earlier experiments we described may reveal the redundancy of Pho and Pho-like, which is a homolog of Pho and binds to the same sequence [28,63]. Wang and colleagues found that Pho-like recruits PcG complexes just as Pho does in the wing imaginal disc [32].

Conclusion

Our data have revealed that there is tremendous overlap and plasticity of regulation by proteins whose functions have been thought to be disparate. We are left with a view of the embryonic genome in which the transcription factor Myc is capable of activation and repression of many loci, and its canonical binding site is less important than the influence of proteins whose role in biology is to maintain cell fates. The methylation status of chromatin surrounding Myc targets supports the notion that the nucleus of a wild type embryo is primed to control its response to a transcription factor such as Myc.

Methods

Fly strains and crosses

See Flybase for additional information about the mutants and insertions used. dmycBG02383, dmycBG00605, and BG00979 were generated by the Drosophila P-Screen/Gene Disruption Project.

For the RT-PCR data shown in Figure Figure1,1, we crossed females homozygous for dmycBG02383 on the X Chromosome and homozygous for a maternal tubulin Gal4 driver on the Second and Third chromosomes (matTub-Gal4VP16 67C;15) to males hemizygous for dmycBG02383 on the X Chromosome and homozygous for UAS-dmyc on the Third chromosome [64]. For control embryos lacking ectopic Myc, we crossed dmycBG02383 ; Gal4 driver females to their siblings. For ectopic expression of dmyc used in the microarray experiments, females homozygous for an armadillo-Gal4 driver [65] were crossed to males homozygous for UAS-dmyc [64]. Control embryos were collected from mothers and fathers homozygous for armadillo-Gal4.

For the mini-white assay for dmyc expression, we crossed females homozygous for each insertion on the X Chromosome to males heterozygous for Pc, Psc, E(z) and pho mutations and scored all the male progeny by their eye color (all the male progeny of the cross will be hemizygous for their mother's X chromosome, dmycBG02383 or dmycBG00605, and heterozygous for either a mutant chromosome or the balancer). We scored the males within a few hours of eclosing and grouped them based on intensity of mini-white expression. We counted the flies in each of three groups (light, dark, neither), and looked for differences in representation of males with the mutation versus males with the balancer chromosome (effectively wild type). We crossed dmycBG02383 homozygous females to males of the Bloomington stock center's deficiency collection that includes deletions spanning 80% of the Second and Third Chromosomes (Figure (Figure1C).1C). We scored F1 males as described for Pc, Psc, E(z) and pho mutations.

RNAi

We amplified 500 bp of 5' regions of the ash1 and pho cDNAs, and cloned the products using the pGem T Easy vector (Promega). We synthesized the sense and antisense transcripts separately using the dual promoters of pGem T Easy, SP6 and T7 polymerases (Ambion), and annealed the transcripts to each other. We injected a 5 μM solution of the dsRNA into dechorionated embryos, as previously described [66]. Injected embryos were washed off the cover slip with heptane to solubilize the glue and oil. We removed the heptane and froze the embryos before homogenization in TRIzol.

Injected embryos were all alive and undergoing germ band retraction (approximately mid-embryogenesis) before RNA isolation. None exhibited any mutant phenotype, including those with ectopic Myc, which is lethal by the end of embryogenesis.

RNA isolation and RT-PCR

We used TRIzol reagent (Invitrogen) to isolate total RNA from dechorionated embryos. RT-PCR reactions were performed using Invitrogen's SuperScript One Step RT-PCR system, as previously described [18]. Primer pairs for all amplification products spanned an intron to control for DNA contamination. We minimized amplification cycles in order to remain in the linear range of amplification.

Microarray data treatment

We began our analysis of the data by eliminating genes from our analysis whose levels were below a threshold. We determined that threshold using signals for negative controls on the arrays, such that genes whose levels were less than 2.5 times the signal for a negative control were not considered in our analysis. In the next step we normalized the raw data by averaging the signals of several Drosophila positive controls (4 different actin signals), comparing those averages across arrays (16 arrays, from biological replication of 8 samples), and multiplying all signals by a resulting chip-specific constant. We then averaged signals for each gene in biological replicates. We were left with data for eight experiments, normalized to be comparable.

To compare changes in gene expression between genetic conditions, we generated ratios of expression for each genetic condition by dividing all signals by their corresponding signal in the Gal4 no RNAi sample. As described previously, we took the log2 for each ratio, found the mean of the ratios for each of seven lists of ratios, determined the standard deviation from the mean, and classified genes as changing up or down based on the standard deviation from the mean. Genes whose ratios were 1.5 times the standard deviation were classified as being induced or de-repressed, and genes whose ratios were -1.5 times the standard deviation were classified as being repressed or de-activated (in the cases of up with Pc- and Myc activated, we used 2 times the standard deviation, because levels for many more genes went up than down in those samples). Following this classification, we established lists for genes as follows: up with Myc, down with Myc, up with ash1-, down with ash1-, up with pho-, down with pho-, up with Pc-, down with Pc-, up with Myc ash1-, down with Myc ash1-, up with Myc pho-, down with Myc pho-, up with Myc Pc-, down with Myc Pc-. We generated these lists using normalized data in Excel, and loaded the raw data and our lists into GeneSpring for clustering and figure generation. Our complete data set is available in Additional file 1. Cel files and other file types containing the data are available upon request.

Chromatin immunoprecipitation

We performed single ChIPs as described previously [18], and sequential ChIPs as described by Bernstein and colleagues [52]. We used anti tri-methyl H3K27 (Upstate) at a 1:100 dilution, and anti di-methyl H3K4 (Upstate) at a 1:100 dilution, and used primers to amplify the 5'-most 400 bp of each gene. For single ChIPs we used 30 amplification cylces, and for sequential ChIP we used 35 cycles. Band intensities of PCR products were determined using an Alpha Innotec device and Fluor-Chem software.

Abbreviations

Pc = Polycomb

pho = pleiohomeotic

ash1 = absent, small or homeotic discs 1

dmyc = Drosophila myc gene; diminutive

dMyc = Drosophila Myc protein

RNAi = RNA interference

PcG = Polycomb Group

TrxG = Trithorax Group

PRE = Polycomb Response Element

PRC1 &2 = Polycomb Repressive Complexes 1&2

Df/Dfs = Deficiency/Deficiencies

H3K27 = histone H3 lysine 27

H3K9 = histone H3 lysine 9

Authors' contributions

JMG designed and performed experiments, analyzed data, and prepared the manuscript. EW and MDC assisted in experimental design and data interpretation, edited the manuscript, and provided funding. All authors have read and approve the final manuscript.

Supplementary Material

Additional file 1:

Microarray data. A tab-delimited txt file containing the Affymetrix intensities of our averaged, replicated chip hybridizations.

Acknowledgements

We are grateful to Allen Shearn and Peter Gallant for flies; the Bloomington Stock Center for the maintenance and design of the deficiency kit; the Drosophila Gene Disruption project for two insertions in dmyc; Ali Nouri, Girish Deshpande, Greg Shanower, Stefano DeRenzis and Trudi Schupbach for comments on the manuscript; and Mark Ptashne for helpful discussions about mechanisms of gene activation and repression. This work was supported by grants from the NCI to MDC and EW. EW is an investigator of the Howard Hughes Medical Institute.

References

  • Cole MD, McMahon SB. The Myc oncoprotein: a critical evaluation of transactivation and target gene regulation. Oncogene. 1999;18:2916–2924. doi: 10.1038/sj.onc.1202748. [PubMed] [Cross Ref]
  • Patel JH, Loboda AP, Showe MK, Showe LC, McMahon SB. Analysis of genomic targets reveals complex functions of MYC. Nat Rev Cancer. 2004;4:562–568. doi: 10.1038/nrc1393. [PubMed] [Cross Ref]
  • Pelengaris S, Khan M, Evan G. c-MYC: more than just a matter of life and death. Nat Rev Cancer. 2002;2:764–776. doi: 10.1038/nrc904. [PubMed] [Cross Ref]
  • Adhikary S, Eilers M. Transcriptional regulation and transformation by Myc proteins. Nat Rev Mol Cell Biol. 2005;6:635–645. doi: 10.1038/nrm1703. [PubMed] [Cross Ref]
  • Mao DY, Barsyte-Lovejoy D, Ho CS, Watson JD, Stojanova A, Penn LZ. Promoter-binding and repression of PDGFRB by c-Myc are separable activities. Nucleic Acids Res. 2004;32:3462–3468. doi: 10.1093/nar/gkh669. [PMC free article] [PubMed] [Cross Ref]
  • Guccione E, Martinato F, Finocchiaro G, Luzi L, Tizzoni L, Dall' Olio V, Zardo G, Nervi C, Bernard L, Amati B. Myc-binding-site recognition in the human genome is determined by chromatin context. Nat Cell Biol. 2006;8:764–770. doi: 10.1038/ncb1434. [PubMed] [Cross Ref]
  • Gallant P, Shiio Y, Cheng PF, Parkhurst SM, Eisenman RN. Myc and Max homologs in Drosophila. Science. 1996;274:1523–1527. doi: 10.1126/science.274.5292.1523. [PubMed] [Cross Ref]
  • Schreiber-Agus N, Stein D, Chen K, Goltz JS, Stevens L, DePinho RA. Drosophila Myc is oncogenic in mammalian cells and plays a role in the diminutive phenotype. Proc Natl Acad Sci U S A. 1997;94:1235–1240. doi: 10.1073/pnas.94.4.1235. [PMC free article] [PubMed] [Cross Ref]
  • Trumpp A, Refaeli Y, Oskarsson T, Gasser S, Murphy M, Martin GR, Bishop JM. c-Myc regulates mammalian body size by controlling cell number but not cell size. Nature. 2001;414:768–773. doi: 10.1038/414768a. [PubMed] [Cross Ref]
  • de la Cova C, Abril M, Bellosta P, Gallant P, Johnston LA. Drosophila myc regulates organ size by inducing cell competition. Cell. 2004;117:107–116. doi: 10.1016/S0092-8674(04)00214-4. [PubMed] [Cross Ref]
  • Grewal SS, Li L, Orian A, Eisenman RN, Edgar BA. Myc-dependent regulation of ribosomal RNA synthesis during Drosophila development. Nat Cell Biol. 2005;7:295–302. doi: 10.1038/ncb1223. [PubMed] [Cross Ref]
  • Maines JZ, Stevens LM, Tong X, Stein D. Drosophila dMyc is required for ovary cell growth and endoreplication. Development. 2004;131:775–786. doi: 10.1242/dev.00932. [PubMed] [Cross Ref]
  • Moreno E, Basler K. dMyc transforms cells into super-competitors. Cell. 2004;117:117–129. doi: 10.1016/S0092-8674(04)00262-4. [PubMed] [Cross Ref]
  • Pierce SB, Yost C, Britton JS, Loo LW, Flynn EM, Edgar BA, Eisenman RN. dMyc is required for larval growth and endoreplication in Drosophila. Development. 2004;131:2317–2327. doi: 10.1242/dev.01108. [PubMed] [Cross Ref]
  • Beer S, Zetterberg A, Ihrie RA, McTaggart RA, Yang Q, Bradon N, Arvanitis C, Attardi LD, Feng S, Ruebner B, Cardiff RD, Felsher DW. Developmental context determines latency of MYC-induced tumorigenesis. PLoS Biol. 2004;2:e332. doi: 10.1371/journal.pbio.0020332. [PMC free article] [PubMed] [Cross Ref]
  • Levine SS, King IF, Kingston RE. Division of labor in polycomb group repression. Trends Biochem Sci. 2004;29:478–485. doi: 10.1016/j.tibs.2004.07.007. [PubMed] [Cross Ref]
  • Ringrose L, Paro R. Epigenetic regulation of cellular memory by the Polycomb and Trithorax group proteins. Annu Rev Genet. 2004;38:413–443. doi: 10.1146/annurev.genet.38.072902.091907. [PubMed] [Cross Ref]
  • Goodliffe JM, Wieschaus E, Cole MD. Polycomb mediates Myc autorepression and its transcriptional control of many loci in Drosophila. Genes Dev. 2005;19:2941–2946. doi: 10.1101/gad.1352305. [PMC free article] [PubMed] [Cross Ref]
  • Campbell RB, Sinclair DA, Couling M, Brock HW. Genetic interactions and dosage effects of Polycomb group genes of Drosophila. Mol Gen Genet. 1995;246:291–300. doi: 10.1007/BF00288601. [PubMed] [Cross Ref]
  • Simon J, Chiang A, Bender W. Ten different Polycomb group genes are required for spatial control of the abdA and AbdB homeotic products. Development. 1992;114:493–505. [PubMed]
  • Boyer LA, Plath K, Zeitlinger J, Brambrink T, Medeiros LA, Lee TI, Levine SS, Wernig M, Tajonar A, Ray MK, Bell GW, Otte AP, Vidal M, Gifford DK, Young RA, Jaenisch R. Polycomb complexes repress developmental regulators in murine embryonic stem cells. Nature. 2006;441:349–353. doi: 10.1038/nature04733. [PubMed] [Cross Ref]
  • Bracken AP, Dietrich N, Pasini D, Hansen KH, Helin K. Genome-wide mapping of Polycomb target genes unravels their roles in cell fate transitions. Genes Dev. 2006;20:1123–1136. doi: 10.1101/gad.381706. [PMC free article] [PubMed] [Cross Ref]
  • Lee TI, Jenner RG, Boyer LA, Guenther MG, Levine SS, Kumar RM, Chevalier B, Johnstone SE, Cole MF, Isono K, Koseki H, Fuchikami T, Abe K, Murray HL, Zucker JP, Yuan B, Bell GW, Herbolsheimer E, Hannett NM, Sun K, Odom DT, Otte AP, Volkert TL, Bartel DP, Melton DA, Gifford DK, Jaenisch R, Young RA. Control of developmental regulators by Polycomb in human embryonic stem cells. Cell. 2006;125:301–313. doi: 10.1016/j.cell.2006.02.043. [PMC free article] [PubMed] [Cross Ref]
  • Negre N, Hennetin J, Sun LV, Lavrov S, Bellis M, White KP, Cavalli G. Chromosomal Distribution of PcG Proteins during Drosophila Development. PLoS Biol. 2006;4:e170. doi: 10.1371/journal.pbio.0040170. [PMC free article] [PubMed] [Cross Ref]
  • Tolhuis B, de Wit E, Muijrers I, Teunissen H, Talhout W, van Steensel B, van Lohuizen M. Genome-wide profiling of PRC1 and PRC2 Polycomb chromatin binding in Drosophila melanogaster. Nat Genet. 2006;38:694–699. doi: 10.1038/ng1792. [PubMed] [Cross Ref]
  • Muller J, Kassis JA. Polycomb response elements and targeting of Polycomb group proteins in Drosophila. Curr Opin Genet Dev. 2006;16:476–484. doi: 10.1016/j.gde.2006.08.005. [PubMed] [Cross Ref]
  • Pirrotta V, Poux S, Melfi R, Pilyugin M. Assembly of Polycomb complexes and silencing mechanisms. Genetica. 2003;117:191–197. doi: 10.1023/A:1022992011833. [PubMed] [Cross Ref]
  • Brown JL, Mucci D, Whiteley M, Dirksen ML, Kassis JA. The Drosophila Polycomb group gene pleiohomeotic encodes a DNA binding protein with homology to the transcription factor YY1. Mol Cell. 1998;1:1057–1064. doi: 10.1016/S1097-2765(00)80106-9. [PubMed] [Cross Ref]
  • Klymenko T, Papp B, Fischle W, Kocher T, Schelder M, Fritsch C, Wild B, Wilm M, Muller J. A Polycomb group protein complex with sequence-specific DNA-binding and selective methyl-lysine-binding activities. Genes Dev. 2006;20:1110–1122. doi: 10.1101/gad.377406. [PMC free article] [PubMed] [Cross Ref]
  • Mohd-Sarip A, Cleard F, Mishra RK, Karch F, Verrijzer CP. Synergistic recognition of an epigenetic DNA element by Pleiohomeotic and a Polycomb core complex. Genes Dev. 2005;19:1755–1760. doi: 10.1101/gad.347005. [PMC free article] [PubMed] [Cross Ref]
  • Mohd-Sarip A, Venturini F, Chalkley GE, Verrijzer CP. Pleiohomeotic can link polycomb to DNA and mediate transcriptional repression. Mol Cell Biol. 2002;22:7473–7483. doi: 10.1128/MCB.22.21.7473-7483.2002. [PMC free article] [PubMed] [Cross Ref]
  • Wang L, Brown JL, Cao R, Zhang Y, Kassis JA, Jones RS. Hierarchical recruitment of polycomb group silencing complexes. Mol Cell. 2004;14:637–646. doi: 10.1016/j.molcel.2004.05.009. [PubMed] [Cross Ref]
  • Brock HW, Fisher CL. Maintenance of gene expression patterns. Dev Dyn. 2005;232:633–655. doi: 10.1002/dvdy.20298. [PubMed] [Cross Ref]
  • Francis NJ, Saurin AJ, Shao Z, Kingston RE. Reconstitution of a functional core polycomb repressive complex. Mol Cell. 2001;8:545–556. doi: 10.1016/S1097-2765(01)00316-1. [PubMed] [Cross Ref]
  • Cao R, Wang L, Wang H, Xia L, Erdjument-Bromage H, Tempst P, Jones RS, Zhang Y. Role of histone H3 lysine 27 methylation in Polycomb-group silencing. Science. 2002;298:1039–1043. doi: 10.1126/science.1076997. [PubMed] [Cross Ref]
  • Czermin B, Melfi R, McCabe D, Seitz V, Imhof A, Pirrotta V. Drosophila enhancer of Zeste/ESC complexes have a histone H3 methyltransferase activity that marks chromosomal Polycomb sites. Cell. 2002;111:185–196. doi: 10.1016/S0092-8674(02)00975-3. [PubMed] [Cross Ref]
  • Muller J, Hart CM, Francis NJ, Vargas ML, Sengupta A, Wild B, Miller EL, O'Connor MB, Kingston RE, Simon JA. Histone methyltransferase activity of a Drosophila Polycomb group repressor complex. Cell. 2002;111:197–208. doi: 10.1016/S0092-8674(02)00976-5. [PubMed] [Cross Ref]
  • Bellen HJ, Levis RW, Liao G, He Y, Carlson JW, Tsang G, Evans-Holm M, Hiesinger PR, Schulze KL, Rubin GM, Hoskins RA, Spradling AC. The BDGP gene disruption project: single transposon insertions associated with 40% of Drosophila genes. Genetics. 2004;167:761–781. doi: 10.1534/genetics.104.026427. [PMC free article] [PubMed] [Cross Ref]
  • Lukacsovich T, Asztalos Z, Awano W, Baba K, Kondo S, Niwa S, Yamamoto D. Dual-tagging gene trap of novel genes in Drosophila melanogaster. Genetics. 2001;157:727–742. [PMC free article] [PubMed]
  • Schwartz YB, Kahn TG, Nix DA, Li XY, Bourgon R, Biggin M, Pirrotta V. Genome-wide analysis of Polycomb targets in Drosophila melanogaster. Nat Genet. 2006;38:700–705. doi: 10.1038/ng1817. [PubMed] [Cross Ref]
  • Chekmenev DS, Haid C, Kel AE. P-Match: transcription factor binding site search by combining patterns and weight matrices. Nucleic Acids Res. 2005;33:W432–7. doi: 10.1093/nar/gki441. [PMC free article] [PubMed] [Cross Ref]
  • Hulf T, Bellosta P, Furrer M, Steiger D, Svensson D, Barbour A, Gallant P. Whole-genome analysis reveals a strong positional bias of conserved dMyc-dependent E-boxes. Mol Cell Biol. 2005;25:3401–3410. doi: 10.1128/MCB.25.9.3401-3410.2005. [PMC free article] [PubMed] [Cross Ref]
  • Orian A, van Steensel B, Delrow J, Bussemaker HJ, Li L, Sawado T, Williams E, Loo LW, Cowley SM, Yost C, Pierce S, Edgar BA, Parkhurst SM, Eisenman RN. Genomic binding by the Drosophila Myc, Max, Mad/Mnt transcription factor network. Genes Dev. 2003;17:1101–1114. doi: 10.1101/gad.1066903. [PMC free article] [PubMed] [Cross Ref]
  • Srinivasan L, Atchison ML. YY1 DNA binding and PcG recruitment requires CtBP. Genes Dev. 2004;18:2596–2601. doi: 10.1101/gad.1228204. [PMC free article] [PubMed] [Cross Ref]
  • Beisel C, Imhof A, Greene J, Kremmer E, Sauer F. Histone methylation by the Drosophila epigenetic transcriptional regulator Ash1. Nature. 2002;419:857–862. doi: 10.1038/nature01126. [PubMed] [Cross Ref]
  • Byrd KN, Shearn A. ASH1, a Drosophila trithorax group protein, is required for methylation of lysine 4 residues on histone H3. Proc Natl Acad Sci U S A. 2003;100:11535–11540. doi: 10.1073/pnas.1933593100. [PMC free article] [PubMed] [Cross Ref]
  • Klymenko T, Muller J. The histone methyltransferases Trithorax and Ash1 prevent transcriptional silencing by Polycomb group proteins. EMBO Rep. 2004;5:373–377. doi: 10.1038/sj.embor.7400111. [PMC free article] [PubMed] [Cross Ref]
  • LaJeunesse D, Shearn A. Trans-regulation of thoracic homeotic selector genes of the Antennapedia and bithorax complexes by the trithorax group genes: absent, small, and homeotic discs 1 and 2. Mech Dev. 1995;53:123–139. doi: 10.1016/0925-4773(95)00430-0. [PubMed] [Cross Ref]
  • Shearn A. The ash-1, ash-2 and trithorax genes of Drosophila melanogaster are functionally related. Genetics. 1989;121:517–525. [PMC free article] [PubMed]
  • Tripoulas N, LaJeunesse D, Gildea J, Shearn A. The Drosophila ash1 gene product, which is localized at specific sites on polytene chromosomes, contains a SET domain and a PHD finger. Genetics. 1996;143:913–928. [PMC free article] [PubMed]
  • Tripoulas NA, Hersperger E, La Jeunesse D, Shearn A. Molecular genetic analysis of the Drosophila melanogaster gene absent, small or homeotic discs1 (ash1) Genetics. 1994;137:1027–1038. [PMC free article] [PubMed]
  • Bernstein BE, Mikkelsen TS, Xie X, Kamal M, Huebert DJ, Cuff J, Fry B, Meissner A, Wernig M, Plath K, Jaenisch R, Wagschal A, Feil R, Schreiber SL, Lander ES. A bivalent chromatin structure marks key developmental genes in embryonic stem cells. Cell. 2006;125:315–326. doi: 10.1016/j.cell.2006.02.041. [PubMed] [Cross Ref]
  • Gildea JJ, Lopez R, Shearn A. A screen for new trithorax group genes identified little imaginal discs, the Drosophila melanogaster homologue of human retinoblastoma binding protein 2. Genetics. 2000;156:645–663. [PMC free article] [PubMed]
  • Shearn A, Rice T, Garen A, Gehring W. Imaginal disc abnormalities in lethal mutants of Drosophila. Proc Natl Acad Sci U S A. 1971;68:2594–2598. doi: 10.1073/pnas.68.10.2594. [PMC free article] [PubMed] [Cross Ref]
  • Bannister AJ, Zegerman P, Partridge JF, Miska EA, Thomas JO, Allshire RC, Kouzarides T. Selective recognition of methylated lysine 9 on histone H3 by the HP1 chromo domain. Nature. 2001;410:120–124. doi: 10.1038/35065138. [PubMed] [Cross Ref]
  • Lachner M, O'Carroll D, Rea S, Mechtler K, Jenuwein T. Methylation of histone H3 lysine 9 creates a binding site for HP1 proteins. Nature. 2001;410:116–120. doi: 10.1038/35065132. [PubMed] [Cross Ref]
  • Nakayama J, Rice JC, Strahl BD, Allis CD, Grewal SI. Role of histone H3 lysine 9 methylation in epigenetic control of heterochromatin assembly. Science. 2001;292:110–113. doi: 10.1126/science.1060118. [PubMed] [Cross Ref]
  • Gehring WJ. A recessive lethal [l(4)29] with a homeotic effect in D. melanogaster. Drosophila Information Services. 1970;45:103.
  • Girton JR, Jeon SH. Novel embryonic and adult homeotic phenotypes are produced by pleiohomeotic mutations in Drosophila. Dev Biol. 1994;161:393–407. doi: 10.1006/dbio.1994.1040. [PubMed] [Cross Ref]
  • Poux S, McCabe D, Pirrotta V. Recruitment of components of Polycomb Group chromatin complexes in Drosophila. Development. 2001;128:75–85. [PubMed]
  • Mishra RK, Mihaly J, Barges S, Spierer A, Karch F, Hagstrom K, Schweinsberg SE, Schedl P. The iab-7 polycomb response element maps to a nucleosome-free region of chromatin and requires both GAGA and pleiohomeotic for silencing activity. Mol Cell Biol. 2001;21:1311–1318. doi: 10.1128/MCB.21.4.1311-1318.2001. [PMC free article] [PubMed] [Cross Ref]
  • Busturia A, Lloyd A, Bejarano F, Zavortink M, Xin H, Sakonju S. The MCP silencer of the Drosophila Abd-B gene requires both Pleiohomeotic and GAGA factor for the maintenance of repression. Development. 2001;128:2163–2173. [PubMed]
  • Brown JL, Fritsch C, Mueller J, Kassis JA. The Drosophila pho-like gene encodes a YY1-related DNA binding protein that is redundant with pleiohomeotic in homeotic gene silencing. Development. 2003;130:285–294. doi: 10.1242/dev.00204. [PubMed] [Cross Ref]
  • Johnston LA, Prober DA, Edgar BA, Eisenman RN, Gallant P. Drosophila myc regulates cellular growth during development. Cell. 1999;98:779–790. doi: 10.1016/S0092-8674(00)81512-3. [PubMed] [Cross Ref]
  • Sanson B, White P, Vincent JP. Uncoupling cadherin-based adhesion from wingless signalling in Drosophila. Nature. 1996;383:627–630. doi: 10.1038/383627a0. [PubMed] [Cross Ref]
  • Kennerdell JR, Carthew RW. Use of dsRNA-mediated genetic interference to demonstrate that frizzled and frizzled 2 act in the wingless pathway. Cell. 1998;95:1017–1026. doi: 10.1016/S0092-8674(00)81725-0. [PubMed] [Cross Ref]

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