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Article |
UBF levels determine the number of active ribosomal RNA genes in mammals
Correspondence to Ross D. Hannan: ross.hannan{at}petermac.org
In mammals, the mechanisms regulating the number of active copies of the
200 ribosomal RNA (rRNA) genes transcribed by RNA polymerase I are unclear. We demonstrate that depletion of the transcription factor upstream binding factor (UBF) leads to the stable and reversible methylation-independent silencing of rRNA genes by promoting histone H1–induced assembly of transcriptionally inactive chromatin. Chromatin remodeling is abrogated by the mutation of an extracellular signal-regulated kinase site within the high mobility group box 1 domain of UBF1, which is required for its ability to bend and loop DNA in vitro. Surprisingly, rRNA gene silencing does not reduce net rRNA synthesis as transcription from remaining active genes is increased. We also show that the active rRNA gene pool is not static but decreases during differentiation, correlating with diminished UBF expression. Thus, UBF1 levels regulate active rRNA gene chromatin during growth and differentiation.
Abbreviations used in this paper: AgNOR, argyrophilic NOR; ChIP, chromatin immunoprecipitation; ETS, external transcribed spacer; GAPDH, glyceraldehyde 3-phosphate dehydrogenase; HMG, high mobility group; IGS, intergenic spacer; MeDIP, methylated DNA immunoprecipitation; MEF, mouse embryonic fibroblast; MPRO, murine promyelocytic; MSCV, murine stem cell virus; NOR, nucleolar organizing region; NoRC, nucleolar remodeling complex; Pol I, polymerase I; pRT, pRevTRE; qChIP, quantitative ChIP; qRT-PCR, quantitative real-time PCR; r-chromatin, ribosomal gene chromatin; rDNA, ribosomal DNA; rRNA, ribosomal RNA; rUBF, rattus UBF; shRNA, short hairpin RNA; shRNAmir, shRNA–micro RNA; SS, serum starvation; UBF, upstream binding factor; UCE, upstream control element.
© 2008 Sanij et al. This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.jcb.org/misc/terms.shtml). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 3.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/3.0/).
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Introduction |
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A typical human cell contains 200 copies of the rRNA genes arranged in tandemly repeated arrays located in nucleolar organizing regions (NORs). Remarkably, despite rRNA gene transcription being limiting for growth, >50% of the rRNA genes are believed to be transcriptionally silent at any one time (for review see Grummt and Pikaard, 2003). The epigenetic mechanisms controlling the activity status of individual ribosomal genes and the reasons why a majority is silenced in higher eukaryotes remain unresolved questions (Huang et al., 2006).
One factor whose function has been linked to regulation of the rRNA gene locus is upstream binding factor (UBF). UBF belongs to the sequence-nonspecific class of high mobility group (HMG) proteins and appears to function exclusively in Pol I transcription (for review see Moss et al., 2007). UBF consists of two polypeptides (UBF1 and 2), which form hetero- and homodimers and arise from alternative splicing of a single transcript (O'Mahony and Rothblum, 1991). Although UBF1 supports robust rRNA gene transcription, UBF2 is fivefold less active (Hannan et al., 1996), but the underlying mechanisms that confer poor transcriptional activity to UBF2 are unclear. In one model, UBF acts through its multiple HMG boxes to induce looping of DNA. This creates the enhancesome, a nucleosome-like structure thought to be responsible for the ability of UBF to modulate rRNA gene transcription (Stefanovsky et al., 2001a,b). Early studies suggested that UBF1 acts predominantly at the promoter in the recruitment of SL1 (selectivity factor 1) and Pol I and in the formation of the preinitiation complex (Smith et al., 1990; McStay et al., 1991; Jantzen et al., 1992). More recently, additional roles have been ascribed to UBF1, including regulation of promoter escape (Panov et al., 2006) and transcription elongation (Moss et al., 2006). Importantly, the association of UBF1 with rRNA genes in vivo is not restricted to the promoter but extends across the entire transcribed portion and to a lesser extent to the intergenic spacer (IGS; Fig. 1, C and D; O'Sullivan et al., 2002). Indeed, consistent with its ability to modify DNA conformation, the inclusion of rRNA gene sequences with high affinity for UBF into ectopic sites on human chromosomes results in the formation of NOR-like structures indicative of "open" chromatin (Mais et al., 2005). In addition, targeting UBF1 to regions of heterochromatin is sufficient to induce large-scale chromatin decondensation (Chen et al., 2004). Together, these data suggest that UBF1 binding throughout the rRNA gene repeat might contribute to the formation of the active chromatin state of rRNA genes. However, direct experiments to demonstrate this function on endogenous rRNA genes and information on the relative contribution of the two UBF isoforms in chromatin remodeling are lacking.
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Results |
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Quantitative chromatin immunoprecipitation (ChIP [qChIP]) analysis was used to examine the effect of UBF1/2 depletion on the level of UBF associated with the rRNA genes. Consistent with recent experiments (O'Sullivan et al., 2002), we found that UBF1/2 is enriched not only at the proximal promoter but also across the transcribed portion of the 45S rRNA gene (Fig. 1, C and D). Depletion of UBF1/2 reduced the levels of UBF1/2 associated with the rRNA genes by a mean of 60% (Fig. 1 D). Immunofluorescence microscopy of NIH3T3 fibroblasts in interphase demonstrated a significant reduction in both the number of UBF-positive nucleoli and the intensity of UBF immunostaining (Fig. 1, E and F) after inducible UBF1/2 knockdown using retroviral delivery of a tetracycline-inducible UBF1/2 short hairpin RNA (shRNA; Dickins et al., 2007).
Next, we directly examined the effect of UBF depletion on the relative proportion of active and inactive (silent) ribosomal genes using psoralen, a DNA cross-linking agent. Active rRNA genes have an open chromatin structure that is accessible to psoralen and associated with nascent rRNA transcripts. Conversely, the silent genes are inaccessible to psoralen and associated with regularly spaced nucleosomes. After psoralen cross-linking, the active and inactive rRNA genes can be distinguished with Southern blotting by their differing rates of migration (Conconi et al., 1989; Dammann et al., 1993). Strikingly, psoralen analysis of the rRNA genes demonstrated a 70% reduction in the number of active genes with a reciprocal increase in the fraction of silenced genes (47.4 and 52.6% to 18.8 and 81.2%) after UBF knockdown in NIH3T3 cells (Fig. 2, A and B).
The change in the proportion of active genes was not a result of off-target effects, as silencing of UBF1/2 using siRNAs to different regions of the UBF1/2 coding sequence (Fig. S1, A and B) also reduced the number of active ribosomal genes (Fig. 2 A, lanes 4–6), whereas siRNA targeting EGFP or glyceraldehyde 3-phosphate dehydrogenase (GAPDH) had no effect on the ratio of active to inactive genes (Fig. 2, A and C). UBF1/2 knockdown also increased the percentage of silenced rRNA genes in cells arrested in G0–G1 phase after serum starvation (SS; Fig. 2 D, SS 24 h) and also in cells in early G1 (Fig. 2 D, +Serum 6 h). Thus, silencing of rRNA genes (rDNA) after depletion of UBF is not dependent on growth factors or chromatin remodeling during S phase. We further examined the effect of UBF depletion using argyrophilic NOR (AgNOR) staining of nucleoli from interphase NIH3T3 cells. Nucleolar fibrillar centers contain undercondensed and thus transcriptionally competent rRNA genes. Like mitotic NORs, they can be silver stained because of their association with the Pol I transcription machinery (Roussel and Hernandez-Verdun, 1994; Weisenberger and Scheer, 1995; Heliot et al., 1997). AgNOR staining of the nucleoli demonstrated an 60–70% decrease in the overall intensity of silver staining and number of fibrillar centers after UBF1/2 knockdown (Fig. 2 E). The strong correlation between decreased AgNOR staining and UBF depletion is consistent with experiments demonstrating that UBF is responsible for recruiting a majority of the Pol I transcription machinery to the rDNA repeats (Mais et al., 2005). Together, these data provide strong evidence that the association of UBF with rRNA genes is necessary for maintenance of the open chromatin structure found in active NORs.
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rRNA gene silencing in response to UBF depletion does not require NoRC-mediated chromatin-remodeling events
The chromatin-remodeling complex NoRC recruits DNA methyltransferases and histone deacetylases to the rRNA gene promoter–proximal terminator, contributing to the formation of a closed nucleosomal structure (Santoro and Grummt, 2005). In particular, NoRC-induced DNA methylation of a CpG dinucleotide at –133 in the core region of the rRNA gene promoter has been implicated in silencing of murine rRNA genes (Santoro and Grummt, 2001) and also has been shown to reduce UBF binding to the rRNA gene promoter. We examined the methylation status of the CpG dinucleotide at –133 in response to acute UBF1/2 depletion by Southern analysis of genomic DNA digested with the enzymes HpaII and MspI. These enzymes demonstrate differential sensitivity to methylation (Fig. 4 A; Santoro and Grummt, 2001), and the analysis revealed that 48% of the ribosomal genes were unmethylated at the CpG dinucleotide –133 in exponentially growing NIH3T3 cells (Fig. 4, B and C), which is in accordance with the aforementioned psoralen data and previous experiments (Santoro and Grummt, 2001).
This percentage was not affected by depletion of UBF1/2 or UBF1 only (Fig. 4, B and C; and Fig. S1). We extended this analysis across the entire rRNA gene using methylated DNA immunoprecipitation (MeDIP; Fig. 4 D) but failed to observe a significant change in CpG methylation at any of the amplicons upon UBF depletion. Moreover, ChIP analysis demonstrated that enrichment of SNF2H, a component of the NoRC complex (Strohner et al., 2001; Santoro et al., 2002; Percipalle et al., 2006), was not significantly altered at the rDNA promoter and transcribed region in response to UBF depletion (Fig. 4 E). In addition, the levels of histone marks associated with NoRC-dependent gene silencing such as H3K9Me2 and H3K9Me3 (Fig. 4, F–H) were unchanged after UBF depletion. Thus, the loss of UBF is sufficient to induce a closed r-chromatin state without the need for increased rDNA methylation and other NoRC-mediated chromatin-remodeling events.
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Using ChIP-CHOP, we found that immunoprecipitated UBF was almost exclusively associated with active, unmethylated rRNA gene promoters (>90%; Fig. 6 D). In contrast, immunoprecipitated histone H1 was almost entirely associated with the silenced, methylated rRNA gene promoters (>90%; Fig. 6 D). Thus, the rRNA genes are either associated with UBF or histone H1; they are mutually exclusive. UBF1/2 knockdown led to a twofold increase in the amount of H1 at the promoter and transcribed portion of the total pool of rRNA genes (Fig. 6 E). ChIP-CHOP demonstrated that this enrichment occurred on the unmethylated fraction of genes (Fig. 6, D and E). These would, presumably, correspond to the fraction of newly silenced genes depleted of UBF. Together, these results suggest a model in which direct association of UBF with the unmethylated rRNA genes prevents the assembly of transcriptionally inactive higher order chromatin structures catalyzed by linker histone H1.
UBF1 overexpression does not increase UBF loading on the rRNA genes
Our aforementioned data and previously published experiments (Santoro and Grummt, 2001) demonstrate that UBF does not bind to methylated rRNA genes. When considered with the UBF rescue experiments in Fig. 5, the data suggest a model whereby methylated rRNA genes are permanently silenced because of their inability to load UBF, which is required for rDNA activation. Consistent with this model, three- to fourfold overexpression of Flag-tagged UBF1 (Fig. 7 A) failed to significantly increase the amount of UBF1 at the promoter, transcribed, and IGS regions of the rDNA (Fig. 7 B).
In addition, ChIP-CHOP experiments revealed that in control as well as UBF1-overexpressing cells, immunoprecipitated UBF was almost exclusively associated with unmethylated rDNA promoters (Fig. 7 C). Thus, UBF cannot be loaded onto the methylated pool of rRNA genes. Surprisingly, despite the inability to increase the net loading of UBF onto the rRNA genes, overexpression of UBF1 induced a modest but statistically significant increase in the proportion of active genes from 45.8 to 60.4% (Fig. 7 D). One explanation for the increase in active gene number without more UBF loading is that overexpression of UBF1 increases the preponderance of UBF1–UBF1 homodimers, which our data (Fig. 3) indicate would be more active in r-chromatin remodeling than UBF1–UBF2 or UBF2–UBF2 dimers.
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15% in response to depletion of UBF, which is fourfold less than the decrease in number of active genes (70% decrease; Fig. 2, A and B).
This suggests that the rate of transcription on the remaining active genes was increased. Consistent with this, ChIP analysis using antibodies to the largest subunit of Pol I (RPA194) demonstrated that UBF1/2 knockdown led to a twofold increase in Pol I loading on the remaining 15% of active rRNA genes (Fig. 8 D). This would maintain a nearly constant transcriptional output. We also examined Pol I transcription elongation rates, which are regulated by UBF and are limiting for rRNA gene transcription (Stefanovsky et al., 2006a). In vivo elongation rates were determined as we previously described (Stefanovsky et al., 2006a) using [3H]uridine pulse labeling (Fig. 8, E and F). If slowing of elongation in response to UBF depletion occurs, it would lead to an observable lag before the linear phase of label incorporation is reached. However, if the elongation rates are similar, no lag should be apparent. When 45S rRNA labeling was followed with time in NIH3T3 cells, no difference in the initial incorporation curves in the control siRNA-EGFP– and -UBF1/2–transfected cells was observed (Fig. 8 F), suggesting that UBF depletion did not affect elongation rates. Thus, increased Pol I loading per gene in the absence of appreciable changes in elongation suggests that initiation rates must have increased on the genes remaining active after UBF knockdown.
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Discussion |
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Through its HMG boxes, UBF has been shown to bend 140 bp of DNA into a near 360° loop. This protein DNA structure, coined the enhancesome, is central to the ability of UBF to regulate Pol I transcription at the level of elongation (Stefanovsky et al., 2006a). Our data demonstrate that mutations that block the ability of UBF1 to bend DNA and form the enhancesome in vitro also severely reduce the ability of UBF to define a unique psoralen-accessible chromatin structure across the rRNA gene in vivo, suggesting that these two processes are linked. Specifically, a UBF1 mutant (UBF-T117E) that mimics extracellular signal-regulated kinase phosphorylation at threonine 117 and is thus defective in the ability to form a functional enhancesome (Stefanovsky et al., 2001a,2001b, 2006b) was unable to prevent the loss of active genes. In contrast, the equivalent nonphosphorylatable mutant (UBF-T117A) that retains its ability to form the enhancesome in vitro was able to remodel r-chromatin to the same extent as recombinant wild-type UBF.
Interestingly, although the T117A mutant is able to function in enhancesome formation, it, like the T117E mutant, is severely compromised in its ability to regulate transcription by Pol I compared with wild-type UBF1 (Stefanovsky et al., 2001b). However, we do not think this demonstrates that transcription and chromatin remodeling can be separated. Rather, we conclude that psoralen cross-linking measures the number of actively transcribed genes but does not differentiate between highly transcribed genes (i.e., rescue with wild-type UBF1) and poorly transcribed genes (i.e., rescue with T117A). This is consistent with the observation that the number of active genes, as determined by psoralen cross-linking, does not vary between exponentially growing cells and serum-starved cells, although clearly the rate of transcription on the latter pool of rRNA genes is considerably repressed (Stefanovsky and Moss, 2006).
Our data also demonstrate that UBF1 and its natural splice variant UBF2 possess distinct abilities to remodel r-chromatin. UBF1 was able to efficiently replace endogenous UBF1/2 to maintain rRNA genes in an open chromatin state. In marked contrast, UBF2 exhibited little, if any, chromatin remodeling capability. UBF2 contains a 27–amino acid deletion in HMG box 2, which reduces the DNA-binding capacity of this domain (Stefanovsky and Moss, 2008). Thus, reminiscent of the aforementioned UBF1 mutants, UBF2 may function poorly in remodeling r-chromatin as a result of an inability to bend and loop DNA as efficiently as UBF1 (Stefanovsky and Moss, 2008). Moreover, these data also suggest that in vivo variations in UBF2 levels might function to fine tune the number of active rRNA genes by forming less active UBF2–UBF2 homodimers or UBF1–UBF2 heterodimers.
NoRC activity is not required for sustained silencing of ribosomal genes in response to UBF depletion
Importantly, our data demonstrate that ribosomal genes pseudosilenced in response to UBF depletion do not require increased CpG methylation or histone deacetylation across the rDNA repeats. These data are consistent with a model in which rRNA genes loaded with UBF are open; rRNA genes devoid of UBF are closed regardless of their CpG methylation status. In this model, the chromatin-remodeling complex NoRC lies upstream of UBF in the rRNA gene–silencing program, most likely by controlling the local r-chromatin landscape, including CpG methylation, to regulate the overall level of UBF binding to the rRNA genes (Santoro and Grummt, 2001).
Our data also demonstrate that rRNA genes pseudosilenced by UBF depletion do not become CpG methylated even after many generations, and, thus, the silencing is stable and can be reversed by restoring UBF levels. This suggests that UBF does not normally function to prevent "constitutive" NoRC-mediated methylation of rRNA genes, which is consistent with a model in which epigenetic silencing of genes through CpG methylation and UBF exclusion only occurs during defined stages during development.
Our data also allow us to make some conclusions about the mechanism by which UBF facilitates decondensation and formation of an active chromatin environment at rRNA genes. First, it is apparent that the UBF–DNA complexes and the core histones can coexist on rRNA genes. We found no evidence that UBF depletion was associated with increases in the total level of the core histones associated with the rRNA genes, which would be expected if UBF chromatin remodeling functioned to eject nucleosomes from DNA. These findings do not necessarily imply that the histones associated with active rRNA genes are nucleosomal. Indeed, much earlier experiments suggested that actively transcribed ribosomal genes remain associated with core histones, but in an unfolded "half-histone" state (Prior et al., 1983).
Second, rRNA gene silencing through loss of UBF leads to significant increases in the level of linker histone H1 associated with the new fraction of silenced genes. Thus, the combined data argue strongly that UBF contributes to the open r-chromatin structure by preventing the assembly of transcriptionally inactive higher order chromatin structures catalyzed by linker histone H1 binding.
Regulation of rRNA synthesis at the level of rate per gene rather than number of active genes
Another important finding of our study is that the reduction in the number of inactive genes through the depletion of UBF does not lead to a commensurate decrease in net cellular rRNA gene transcription rates. This was because the density of Pol I loading on the remaining active genes was increased, thus maintaining rRNA synthesis rates per cell. Such a phenomenon has been observed in yeast where artificially reducing the rRNA gene copy number from 143 to 42 does not affect growth rates because the mean number of polymerases per rRNA gene increases to maintain transcription output (French et al., 2003). Interestingly, upon UBF knockdown, a pool of unmethylated rRNA genes exhibited increases in markers of gene activation (acetylated H3K9 and di- and trimethylated H3K4) at their promoter regions (Fig. 9, A–C). It is probable that these changes are functionally associated with the increased Pol I loading.
UBF regulates the active ribosomal gene pool during differentiation
The prevailing view is that the relative amounts of active and inactive ribosomal genes are stably maintained as a result of CpG methylation of a fixed number of rRNA repeats (Conconi et al., 1989; Stefanovsky and Moss, 2006). In contrast, our experiments demonstrate that the number of silenced genes increases markedly during granulocyte differentiation. Furthermore, the silencing correlates with a reduction in UBF levels and UBF loading on the rDNA repeat but not promoter methylation of rRNA genes, suggesting that the loss of UBF is causative in the rRNA gene inactivation. Furthermore, as we and others have shown that reduced UBF expression is common during the terminal differentiation of many cell types (Larson et al., 1993; Datta et al., 1997; Alzuherri and White, 1999; Poortinga et al., 2004; Li et al., 2006; Liu et al., 2007), it is likely that down-regulation of UBF is a widespread mechanism for the silencing of active rRNA genes during development.
The level of rRNA gene silencing during granulocyte differentiation is similar to that observed during UBF depletion in NIH3T3 cells. However, UBF depletion did not change rRNA gene transcription rates significantly. Thus, although rRNA gene silencing may be required for the down-regulation of Pol I transcription during differentiation, it is not sufficient to regulate this process. Interestingly, our preliminary experiments show that during granulocyte differentiation, in addition to UBF, the expression of a majority of the other components of the Pol I complex is down-regulated (unpublished data). We propose that this results in limiting amounts of the Pol I complex, which prevents increased loading of Pol I on the remaining active rRNA genes after UBF depletion. This would ensure that rRNA gene silencing during differentiation leads to decreased rRNA synthesis rates. Future studies are needed to determine whether coordinate regulation of Pol I transcription factors and modulation of the number of active rRNA genes is a general mechanism to effect long-term changes in rRNA gene transcription rates during differentiation.
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Materials and methods |
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-tubulin and GAPDH were obtained from Sigma-Aldrich and Abcam, respectively. In-house rabbit anti–Pol I, -UBF1/2, and –rabbit sera were used for Western and ChIP assays (Poortinga et al., 2004).
RNAi
siRNAs encoding the sequences of EGFP or UBF were synthesized by Sigma-Aldrich. A complementary sequence of each oligonucleotide was designed to produce a two-nucleotide overhang at both of the 3' ends of the duplex. The oligonucleotide RNA sequences and positions on UBF1/2 are marked in Fig. S1. ON-TARGETplus siCONTROL GAPDH siRNA was purchased from Thermo Fisher Scientific. Short hairpin–targeting UBF1/2 sequences (Fig. S1) were subcloned into the tetracycline-regulated retroviral vector TMP containing the entire micro-RNA cassette.
Cell culture, transfection, and retroviral infection
NIH3T3 cells were cultured in DME with 10% FBS at 37°C. Lipofectamine reagent (Invitrogen) was used to transfect siRNA at 25 nM according to the manufacturer's protocol, and cells were harvested 48 h after transfection unless otherwise specified. For inducible RNAi targeting UBF, NIH3T3 cells were stably cotransduced with the pRevTet-On tetracycline transactivator (Clontech Laboratories, Inc.) and TMP-UBF shRNA–micro RNA#1 (shRNAmir#1) retroviral vectors. Single clones were isolated and selected with 1 µg/ml doxocyclin to induce UBF1/2 knockdown. To establish cell lines overexpressing rattus UBF 1 (rUBF1), NIH3T3 cells were stably transduced with rUBF1–murine stem cell virus (MSCV)–GFP and empty MSCV-GFP retroviral vectors. Cells were sorted for high GFP expression using flow cytometry. The tetracycline-regulated rat UBF1, UBF2, rUBF1-T117E, and rUBF1-T117A NIH3T3 MEF cell lines were established using a RevTet-Off expression system (Clontech Laboratories, Inc.). NIH3T3 MEF cells expressing the RevTet-Off–responsive elements were infected with pRevTRE (pRT)-UBF recombinant viruses. The MPRO granulocyte cell line was generated from whole bone marrow of mice and maintained in culture as described previously (Walkley et al., 2004). Differentiation of MPRO cells into mature granulocytes was induced by stimulation with 10–6 M of the retinoid agonist AGN 194204 for 4 d (McArthur et al., 2002).
ChIP
ChIP was performed as described previously (Poortinga et al., 2004; Walkley et al., 2004). Cross-linking was achieved with 0.6% formaldehyde and assays performed using 106 cells per immunoprecipitation. For all ChIPs, 4 µg of purified antibody or 8 µl of sera was used per immunoprecipitation. Samples were analyzed in triplicate using the SYBR green dye on the ABI Prism 7000 (Applied Biosystems). To calculate the percentage of total DNA bound, unprecipitated input samples from each condition were used as reference for all qRT-PCR reactions. Primer sequences are listed in Table S1 (available at http://www.jcb.org/cgi/content/full/jcb.200805146/DC1). ChIP-CHOP assays were performed by digesting DNA with HpaII before qRT-PCR. The relative level of HpaII resistance was calculated after normalization to mock-digested DNA.
Immunofluorescence and microscopy
Cells were fixed in 3% paraformaldehyde for 10 min at room temperature, permeabilized with ice-cold 0.05% Triton X-100 in PBS for 15 min, and blocked with 5% skim milk powder and 0.5% chicken serum in PBS for 30 min. Anti-UBF sera was used at 1:500 dilution and detected with Alexa Fluor 594 anti–rabbit secondary antibody (Invitrogen) at 1:1,000 dilution. DNA was counterstained with DAPI in ProLong Gold antifade reagent (Invitrogen). Images were acquired on a microscope (BX-51; Olympus) equipped with a camera (RT model 25.4; SPOT) using the UPlanAPO 60x NA 1.2 water immersion objective. Images were acquired using Advanced software (version 4.6.4.3; SPOT). All UBF images were taken at a 1-s exposure with a gain (excitation power) of two. Settings for adjusting the image after acquisition (i.e., 
adjust and background subtract settings) were identical for all images.
RNA extraction and expression analysis
Cells were lysed in 4 M guanidine thiocyanate, 25 mM sodium citrate, pH 7.0, 0.5% sarcosyl, and 0.1 M β-mercaptoethanol, and RNA was extracted according to standard methods. To estimate RNA recovery rate, a 32P-labeled RNA probe was mixed with RNA lysates before extraction. RNA amounts were quantitated and normalized to equal numbers of cells. First-strand cDNA was synthesized using a random hexamer primer and avian myeloblastosis virus reverse transcription (Promega) according to the manufacturer's protocol. qRT-PCR was performed as described in the ChIP section. Mouse 5' ETS primer sequences were previously published (Poortinga et al. 2004).
Sliver staining
AgNOR staining was performed as described previously (Ploton et al., 1984), and nucleoli were visualized using transmission EM.
Psoralen cross-linking assay
Cells were lysed in 10 mM Tris-HCl, pH 7.4, 10 mM NaCl, 3 mM MgCl2, and 0.5% NP-40, and nuclei were pelleted, resuspended in 50 mM Tris-HCl, pH 8.3, 40% glycerol, 5 mM MgCl2, and 0.1 mM EDTA, and irradiated in the presence of 4,5,8'-trimethylpsoralen (Sigma-Aldrich) with a 366-nm UV light box at a distance of 6 cm (Conconi et al., 1989). 200 µg/ml psoralen was added at 1:20 dilution every 4 min for a total irradiation time of 20 min. Genomic DNA was isolated, digested with SalI, and separated on a 0.9% agarose gel, and alkaline Southern blotting was performed. To reverse psoralen cross-linking, filters were treated with 254-nm UV rays at 1,875 x 100 µJ/cm2 using a UV cross-linker (Stratalinker 2400; Agilent Technologies). The membrane was then hybridized to a purified 32P (Amersham)-labeled rDNA as depicted in Fig. 2 A, visualized by scanning on a PhosphoImager (GE Healthcare), and quantitated using ImageQuant (TLv2005.04; GE Healthcare).
DNA methylation and MeDIP
Genomic DNA was digested with the methylation-sensitive enzyme HpaII or MspI (Santoro and Grummt, 2001). Southern blotting was performed using the aforementioned probe. MeDIP was performed by incubating 4 µg of heat-denatured sonicated, genomic DNA with 4 µg anti-5mC antibody for 2 h at 4°C in 0.14 M NaCl, 16.7 mM Tris, pH 8.0, and 0.05% Triton X-100. DNA–antibody complexes were incubated with protein A–Sepharose beads (Millipore) for 2 h at 4°C, and the precipitates were eluted in 50 mM Tris, pH 8.0, 10 mM EDTA, and 0.5% SDS. DNA was purified and analyzed by qRT-PCR, and the percentage of bound DNA was calculated after normalization to 20 ng of input DNA.
Online supplemental material
Figs. S1 and S2 describe siRNA oligonucleotide sequences and positions within the murine UBF1/2 coding regions. Table S1 includes ChIP RT-PCR primer sequences. Online supplemental material is available at http://www.jcb.org/cgi/content/full/jcb.200805146/DC1.
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Acknowledgments |
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This work was supported by grants from the National Health and Medical Research Council (NHMRC) of Australia and the Cancer Council Victoria to R.D. Hannan, R.B. Pearson, and G.A. McArthur and by a National Institutes of Health grant (5R01HL077814 USA) to L. Rothblum. R.D. Hannan, R.B. Pearson, and G.A. McArthur were supported by NHMRC fellowships.
Submitted: 23 May 2008
Accepted: 25 November 2008
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