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How transcription affects the way specific genes are arranged within the nucleus remains to be fully understood. We examine here whether transcription occurs in discrete sites (factories) containing the required machinery and whether these sites specialize in transcribing different genes. We cotransfected plasmids encoding a common origin of replication but different transcription units into cells, where they are assembled into minichromosomes that the cellular machinery replicates and transcribes. In cells containing thousands of minichromosomes, we found (using fluorescence in situ hybridization) active templates concentrated in only a few factories that transcribe particular units depending on the promoter type and the presence of an intron. Close proximity between similar transcription units, whether on two different minichromosomes or on host chromosomes and minichromosomes, is confirmed using chromosome conformation capture. We conclude that factories specialize in producing a particular type of transcript depending on promoter type and whether or not the gene contains an intron.
It is widely assumed that RNA polymerases diffuse to their target promoters, wherever those promoters might be in the nuclei, before initiating. However, recent evidence suggests that polymerases active on different genes cluster into “factories.” Clustering ensures high local concentrations and, thus, efficient interaction, and a promoter would then have to diffuse to a factory before it could be transcribed (Cook, 1999). Nucleolar factories containing polymerase I provide the prototypic example; only ribosomal DNA associated with a nucleolus is transcribed, and newly made ribosomal RNA is surrounded by all the machinery required for assembly into a ribosome. Active forms of polymerases II and III are also concentrated in factories (Pombo et al., 1999), and the application of new techniques show that their templates tend to cluster when transcribed. For example, the mouse Hbb-b1 (β-globin) gene lies 40–60 kbp from its locus control region (LCR) on the genetic map and ~25 Mbp from Eraf. But in 3D nuclear space, chromosome conformation capture (3C) and FISH reveal that Hbb1 lies close to the LCR and Eraf, as well as many other parts of the genome, but only when contacting regions are transcribed (Osborne et al., 2004; Simonis et al., 2006). The LCR seems to nucleate a “hub” or factory that ties the locus in loops and facilitates expression of globin-related genes (Chakalova et al., 2005; de Laat, 2007; Ohlsson and Gondor, 2007). Other evidence points to factories specializing in the transcription of specific gene subsets (Pombo et al., 1998; Frey et al., 1999; Thompson et al., 2003; Bartlett et al., 2006; Osborne et al., 2007).
We used replicating minichromosomes as probes to examine whether transcription occurs in factories. Using FISH and 3C, we found that although a cell may contain thousands of minichromosomes, essentially all nascent minichromosomal RNA is concentrated in a few foci: the factories. These factories specialize in producing particular types of transcripts depending on the promoter type and whether or not the gene contains an intron.
Our strategy (Fig. 1 A) was to cotransfect plasmids encoding the SV40 origin of replication (ori) and different transcription units into a monkey line that expresses the SV40 T antigen (Mellon et al., 1981). Previous work has shown that the plasmid DNA is assembled into nucleosomes, and the resulting minichromosomes are replicated and transcribed by the cellular machinery (Mellon et al., 1981; Jackson and Cook, 1993; Dean, 1997). We then examined if transcribing minichromosomes are spread throughout nuclei or concentrated in the same or different factories. Plasmids are named by promoter type, coding sequence, and whether or not they contain an intron and a 3′ end (Fig. 1 B). For example, plasmid IICMV,EGFPV,pA possesses the polymerase II cytomegalovirus (CMV) promoter driving EGFP with an intron (V) and polyadenylation (pA) signal, whereas 0,EGFP,pA lacks a promoter and intron.
Quantitative “blotting” and PCR show that the minichromosomal copy number increases progressively from the level seen at 8 h (when some naked input DNA remains), and by 24 h, at least 8,000 new copies are generated (Fig. 2 A). All plasmids replicate similarly (Fig. 2 A). Transcript copy numbers also increase, but promoters and introns affect levels (Fig. 2 B). DNA FISH reveals that most minichromosomes are concentrated in ~20 bright nuclear foci that increase in intensity (Fig. 2, C and D; Dean, 1997). Intensities are normalized relative to plastic beads (Fig. 2 C, inset), so results from different experiments can be compared. Fewer than 5% of the minichromosomes were concatenated and/or replicating (unpublished data; Jackson and Cook, 1993) and therefore bound either to one another or to replication factories. Therefore, something must confine the ~8,000 minichromosomes seen at 24 h to a few foci. As most are not diffusely spread, we can eliminate possibility 1 in Fig. 1 A.
We next examined whether minichromosomes are transcribed in factories. We transfect IICMV,DsRed,pA, which encodes both a CMV promoter (driving DsRed) and an SV40 early promoter, on the common backbone (driving Neor; Fig. 1 B); the latter is down-regulated under these conditions (Myers et al., 1981; Dynan and Tjian, 1985). RNA FISH shows that both DsRed and Neor transcripts are found mainly in the cytoplasm, but some are concentrated in nuclear foci against a general nuclear background (Fig. 3 A, i–iv; foci can only be seen clearly in the insets). Many studies have shown that such nuclear foci mark the high concentration of RNA at transcription sites, whereas the general background represents completed transcripts on their way to the cytoplasm (Dirks et al., 1993; Levsky et al., 2002). Immuno-FISH confirms that such foci colocalize with high concentrations of the active form of RNA polymerase II, which is detected using an antibody directed against phospho-Ser2 in the heptad repeats in the C-terminal domain of the largest catalytic subunit (Fig. S1, available at http://www.jcb.org/cgi/content/full/jcb.200710053/DC1). Most RNA in such foci is nascent (i.e., still associated with engaged polymerases), as transcripts leave transcription sites so soon after the polymerase terminates (Iborra et al., 1998).
We distinguished a nuclear focus from the background using two criteria. A focus should have an intensity greater than a threshold defined as follows. As some DsRed transcripts might be made by read-through from the SV40 promoter on the backbone (despite down-regulation and the presence of an efficient polyadenylation signal), we determined the extent of this using 0,EGFP,pA. As EGFP lacks a promoter, any EGFP RNA seen must result from read-through from the SV40 promoter. EGFP signal is again normalized relative to the intensity given by reference beads; it is just above (Fig. 3 B, red bars) the irreducible background caused by the autofluorescence seen in mock-transfected cells (Fig. 3 B; gray bars). We require foci to have intensities above a threshold just above the maximum signal given by this read-through (i.e., above the green dotted line in Fig. 3 B). We also require a focus to occupy >4 pixels (where a pixel is 100 × 100 nm and little signal is then discarded, as such foci contain >85% nuclear signal above the threshold). A nucleus transfected with IICMV,EGFP,pA typically contains 23 ± 6 foci (mean area of 7 ± 3 pixels) defined in this way. Such foci are not seen if cells are treated after fixation with RNase or before fixation with an inhibitor of RNA polymerase II: α-amanitin (Fig. 3 C).
Inspection of the two nuclear foci in the inset in Fig. 3 A (ii–iv) reveals that each contains red and green signal. We deem signals to colocalize if ≥25% of a focus of either color overlaps a focus of the other color; then, 95% EGFP foci colocalize with DsRed foci, and vice versa (Fig. 3 A, iv, bottom). As expected, two units on one minichromosome driven by similar viral promoters are transcribed in the same place. Transcripts from the (down-regulated) SV40 promoter are not considered from now on, as Neor probes are not used and read-through is below our threshold.
Two minichromosomes identical except for coding region were now compared: IICMV,EGFP,pA and IICMV,DsRed,pA (Fig. 3 A,v–viii). As before, transfected cells contained high concentrations of both types of mature mRNA in the cytoplasm as well as nuclear foci against the nuclear background. 78% of DsRed foci colocalize with EGFP foci, and vice versa; minichromosomes with identical promoters are transcribed in the same factories.
We next examined two very different polymerase II units. IICMV,DsRed,pA encodes a “standard” intronless unit, whereas IIU2,U2G,3′box encodes a structural U2 RNA (which can be differentiated from host U2 RNA because it is marked by a globin sequence) and possesses its own special enhancers, promoter, and 3′ end (Cuello et al., 1999; Smith and Lawrence, 2000; Matera et al., 2007). After cotransfection, most standard (DsRed) transcripts are cytoplasmic, whereas most U2G transcripts are nuclear. This is expected; standard messages are exported to accumulate in the cytoplasm, whereas U2G transcripts are detected using a probe complementary to sequences in the preU2 RNA that are removed rapidly and degraded (Medlin et al., 2003). Most nuclear RNA of both types is again found in foci, but now ≤6% foci colocalize (Fig. 4, A–D); U2G units are transcribed in different factories from CMV units, which is consistent with possibility 3 in Fig. 1 A. There are 23 ± 6 and 15 ± 4 DsRed and U2G nuclear foci of similar area (7 ± 3 pixels), respectively.
This experiment was repeated using IICMV,DsRed,pA and IIU2p−,U2G,3′box, the only difference being the replacement of 12 bp in the U2 promoter with an irrelevant sequence that destroys promoter activity (Cuello et al., 1999). No U2G transcripts were then detected (unpublished data), so those seen previously cannot be produced from a cryptic promoter.
The introduction of an intron also affects localization. Thus, transcripts copied from IICMV,DsRed,pA and IICMV,EGFPV,pA are both mainly cytoplasmic (Fig. 4, E–H), and quantitative RT-PCR (qRT-PCR) shows that those from the intron-containing unit are present in higher quantities (Fig. 2 B; Brinster et al., 1988). Protein levels are also higher, as the ratio of EGFP–DsRed (protein) fluorescence (detected using FACS) in cells transfected with IICMV,EGFPV,pA + IICMV,DsRed,pA is greater than that given by IICMV,EGFP,pA + IICMV,DsRed,pA (unpublished data). Both intron-containing and intronless nascent RNA is also found in ~20 nuclear foci of similar size and intensity (there are 21 ± 4 and 23 ± 6 intron-containing and intronless nuclear foci of 6 ± 3 and 7 ± 3 pixels, respectively.) Although flanked by the same promoter and 3′ signals, they are usually found in different factories (Fig. 4, E–H). Immuno-FISH shows that intron-containing foci colocalize more often with splicing factor SC-35 than their counterparts without introns; however, neither type of transcript generally colocalizes with the very brightest “splicing speckles,” which are known to be transcriptionally inactive (Fig. S2, available at http://www.jcb.org/cgi/content/full/jcb.200710053/DC1; see Lamond and Spector, 2003; Xie et al., 2006).
We next analyzed promoters transcribed by the three different nuclear polymerases. Few transcripts copied using the polymerase I promoter in I45S,EGFP,pA are found in prominent nucleoli (Fig. 4 K) or the cytoplasm; instead, most are found in 38 ± 13 large nuclear foci (area of 30 ± 13 pixels). These nuclear polymerase I transcripts often colocalize with upstream binding factor (UBF) and are still seen when transcription by polymerase II is inhibited with α-amanitin (Fig. S3, available at http://www.jcb.org/cgi/content/full/jcb.200710053/DC1). This is consistent with what has been seen previously. When UBF-binding sites are inserted ectopically into host chromosomes, they organize many nonnucleolar foci—or “pseudonucleoli”—which, in this case, are transcriptionally inactive, as they lack polymerase I promoters (Mais et al., 2005). However, few of our (nascent) polymerase I transcripts colocalize with (nascent) polymerase II transcripts (Fig. 4, I–L). Similarly, few transcripts copied from a polymerase III unit are cytoplasmic (Fig. 4 O), and nuclei typically contain 16 ± 5 small foci (area of 6 ± 3 pixels). Few of these colocalize with polymerase II foci, and vice versa (Fig. 4, M–P). There are more polymerase II transcripts than polymerase I or III transcripts (Fig. 2 B), so it was possible that we might have missed some polymerase I or III foci. However, differential detection is unlikely to underlie the low colocalizations seen here, as the same values are obtained when we selected green foci and then determined how many also contain red foci, and vice versa (Fig. 4, values given at the bottom). These results are again consistent with possibility 3 in Fig. 1 A, and with the finding that some factories contain nascent RNA made by polymerase II (but not III), whereas others contain transcripts made by polymerase III (but not II; Pombo et al., 1999).
We now used 3C to compare the relative proximity of two plasmids when they encode similar or different promoters. Preliminary experiments (unpublished data) revealed that DsRed and EGFP lie closer (P < 0.05, Mann-Whitney test) in a II + II combination (i.e., IICMV,DsRed,pA + IICMV,EGFP,pA) than in a II + III combination (IICMV,DsRed,pA + III7SK,EGFP,pT). As inactive DNA (i.e., naked input and/or minichromosomes in the diffuse nuclear background) probably masks larger differences, we repeated the experiment after selecting the transcriptionally active fraction by ChIP using an antibody directed against trimethyl K4 in histone H3 (Barski et al., 2007). Then, DsRed–EGFP 3C products were seen in both the supernatant and pellet (Fig. 5 A, rows 1 and 3), which is consistent with the presence of inactive DNA in the supernatant. More such products were seen in the pellet (the active fraction) when promoters were similar (Fig. 5 A, row 3). In contrast, ALDOA is an active housekeeping gene on the host chromosome and no ALDOA–ALDOA 3C products are seen in the supernatant (Fig. 5 A, row 2); moreover, pellets from both combinations yield similar levels (Fig. 5 A, row 5). The mean of four independent experiments confirms that the II + II combination gives sixfold more DsRed–EGFP 3C product than the II + III combination (Fig. 5 A, row 7). We conclude that minichromosomes bearing similar promoters are more likely to be together, which confirms the FISH results.
Do active minichromosomes organize their own factories or share host factories? Plasmids encoding either the U2G or CMV unit, which are transcribed in different factories (Fig. 4, A–D), were transfected, and proximity between the common plasmid backbone and host U2 units was determined. Ninefold more plasmid–host 3C product was obtained with the U2G unit (Fig. 5 B). This is consistent with minichromosomal and host genes being transcribed in the same factory.
Using replicating minichromosomes as probes, we examined whether transcription occurs in factories and whether factories specialize in producing particular types of transcripts. Plasmids encoding the SV40 origin of replication are transfected into cos7 cells, where they are assembled into minichromosomes to be replicated and transcribed by the cellular machinery. By 24 h, there are at least 8,000 minichromosomes per cell (Fig. 2 A), and DNA FISH shows these to be concentrated in only ~20 foci (Fig. 2 C); this is in accord with results obtained with viruses (Pombo et al., 1994; Dean, 1997; Mearini et al., 2004). When two plasmids encoding different transcription units are cotransfected, RNA FISH reveals the two kinds of nascent RNA to be concentrated again in ~20 foci (Figs. 4 and S1); this is consistent with transcription of many templates in one factory. Moreover, the two different types of transcripts are generally found in distinct foci. For example, nascent transcripts produced from CMV and U2 promoters are seen in nonoverlapping foci (Fig. 4, A–D), as are most of those with and without an intron (even though they are produced from the same CMV promoter; Fig. 4 E–H). Similarly, nascent transcripts copied from polymerase I, II, and III units are all found in their own distinct foci (Fig. 4, I–P). 3C confirms that templates bearing similar promoters are more likely to be together than those with different promoters (Fig. 5 A). All these results are consistent with different templates being transcribed in different factories that specialize in transcribing particular types of gene.
We can envisage that these factories might form in two extreme ways from host components: either minichromosomes diffuse to preexisting host factories that then transcribe both host chromosomes and minichromosomes; or they recruit host factors, perhaps even complete assemblies (Mitchell and Fraser, 2008), to generate factories that transcribe only minichromosomes. Our results are most simply explained if both processes occur simultaneously. On the one hand, 3C results reveal that minichromosomal U2G genes lie near host U2 genes (Fig. 5 B); this suggests that a U2 promoter on a minichromosome must first diffuse to a host U2 factory before it can be transcribed (Fig. 6 A). On the other hand, nascent transcripts from polymerase I units are found in nucleoplasmic foci (Fig. 4, I–L; and Fig. S3) known as pseudonucleoli (Mais et al., 2005). As host (polymerase I) units are only active in the nucleolus, we must assume that nucleoplasmic minichromosomes recruit host factors to nucleate these pseudonucleoli, which then recruit additional minichromosomes (as in Fig. 6 A).
These results beg many other questions. For example, how many different types of factory are there? In this preliminary screen, we found five different kinds (Fig. 4), and we expect to find more. How might targeting be achieved? There is some evidence that certain factories contain high concentrations of particular factors (Bartlett et al., 2006). Then, as a promoter diffuses through the nucleus, it might only bind stably to a factory containing the appropriate factors. This might then increase the frequency of initiation. But how could a gene with an intron recruit (or be recruited to) a different factory from an intronless gene (Fig. 4, E–H), especially when binding to a factory inevitably precedes synthesis of a transcript with an intron? One possibility is that the β-globin intron used, which is known to contain binding sites for transcription factors (Jackson et al., 1995; Wen et al., 2005), stabilizes binding to a factory with the appropriate factors, as described above. Another possibility, which is consistent with both the imprecise targeting of a minority of plasmids to certain factories (Fig. 4, E–H) and of the majority to another set of factories that contain the splicing component SC35 (Fig. S2), is as follows. A newly replicated intron-containing gene might be “naïve,” and bind to and initiate (incorrectly) in a “nonsplicing” (polymerase II) factory. However, on binding to a “splicing” factory, it might acquire some mark (e.g., a histone modification) that now targets it to the appropriate factory (Fig. 6 B). We also note that just as transcriptionally active minichromosomes “pair” by binding to the appropriate factories, a similar process might underlie the pairing of homologous chromosomes in both somatic and meiotic cells (Fig. 6 C; Cook, 1997).
Oligonucleotides (MWG Biotech AG; or Sigma-Aldrich) are listed in Table S1 (available at http://www.jcb.org/cgi/content/full/jcb.200710053/DC1).
Plasmids with a common backbone but encoding transcription units with different promoters, introns, and 3′ ends (Fig. 1 B) were constructed as follows: plasmid 0,EGFP,pA from pEGFP-N1 (Clontech Laboratories, Inc.) by deleting bp 8–591 (using oligo pair 3); I45S,EGFP,pA by inserting the 250-bp truncated human polymerase I promoter (prepared using oligo pair 1; Pleschka et al., 1996) between the AseI and NheI sites of 0,EGFP,pA; III7SK,EGFP,pA by inserting the 234-bp human 7SK promoter (Boyd et al., 1995) between the PstI and KpnI sites of 0,EGFP,pA; IIU2,U2G,3′ box and IIU2p−,U2G,3′box from pEGPF-C1 (Clontech Laboratories, Inc.) by deleting bp 8–1,367 and inserting the 623-bp U2G fragment (Medlin et al., 2003) or the promoterless U2G fragment (both prepared using oligo pair 4; Cuello et al., 1999) between the AseI and PstI sites; and IICMV,EGFPV,pA by inserting 925 bp of the HBB intron 2 (chromosome 11 positions 5,203,482–5,204,406 in the National Center for Biotechnology Information 36 assembly; prepared by PCR amplification of human DNA using oligo pair 2) between the HindIII and PstI sites of pEGPF-C1. Analogous constructs encoding DsRed were made from pDsRed-N1 (Clontech Laboratories, Inc.). Appropriate construction was confirmed by sequencing (using oligo pair 13). S. Murphy and N.J. Proudfoot (University of Oxford, Oxford, UK) provided constructs containing the U2G, 7SK, and HBB fragments.
Cos7 cells (Mellon et al., 1981) were grown in DME + 10% fetal calf serum (Invitrogen). Cells in 90-mm Petri dishes were transfected using FuGene6 (Roche) with 1.2 μg of plasmid DNA plus sheared salmon sperm DNA (Sigma-Aldrich) added to 6 μg. After 8 h, cells were trypsinized, washed, and replated to reduce background of input DNA. For Fig. 5 B (where we wished to detect a few interactions between minichromosomes and host chromosomes against a high minichromosome–minichromosome background), transfected cells were grown for 6 h and washed before cross-linking. Transfection efficiencies were determined by measuring EGFP levels by microscopy and FACS. Polymerase II was inhibited by incubation (16 h at 37°C) in 50 μg/ml α-amanitin (Sigma-Aldrich).
2 × 105 cells were washed in PBS, resuspended in 2 ml PBS, and analyzed on a flow cytometer (FACScan; Becton Dickinson). Cell debris/clusters were differentiated from single cells using forward and side scattering and eliminated from the analysis. Backgrounds were determined using mock-transfected cells and those transfected with IICMV,EGFP,pA or IICMV,DsRed,pA (Fig. 3 B). Data on 10,000 cells were analyzed using CellQuest software (Becton Dickinson), and the fractions of cells expressing red fluorescence (from the reference plasmid) and green fluorescence (from the test plasmid) were calculated.
Plasmid DNA from a “Hirt” extract (Hirt, 1967) of ~107 cells was digested with the appropriate restriction enzyme, separated on an agarose gel, and blotted onto nylon. Probes were labeled with DIG (digoxigenin) using a DIG labeling kit (Roche) by random priming and hybridized at 65°C for 16 h in “Church” buffer (0.5 M sodium phosphate buffer, 1 mM EDTA, 1% bovine serum albumin, and 7% SDS, pH 7.2), then bound targets were detected using a DIG detection kit (Roche).
Total DNA from ~107 cells was purified using Trizol (Invitrogen), and the EGFP copy number was determined by qPCR using a thermal cycler (Roter-Gene 3000; Corbett Life Science); signals were normalized relative to those given by GAPDH. In brief, each 25-μl reaction contained Platinum SYBR Green qPCR SuperMix-UDG with ROX (Invitrogen) and 5 pmol of each primer (oligo pairs 11 and 12). Cycling conditions were: 50°C for 30 min and 95°C for 10 min followed by 40 cycles at 94°C for 15 s and 57.5°C for 30 s. Samples were run in triplicate and each experiment was repeated three times.
Absolute copy numbers were obtained by reference to the known numbers of pure plasmids. Concentration and purity was determined from the absorbance using a spectrometer (Nanodrop ND-100; Thermo Fisher Scientific).
Total RNA was purified using Trizol, and cDNA was prepared using the SuperScript III Platinum one-step system for RT-PCR (Invitrogen) and normalized to GAPDH mRNA levels in the same sample. qRT-PCR was conducted similarly to qPCR.
Absolute copy numbers were obtained by reference to known numbers of EGFP transcripts prepared by in vitro transcription using T7 RNA polymerase (Roche). The template (pcDNA-EGFP-N1) was constructed by inserting EGFP (from pEGFP-N1) between the HindIII and BamHI sites into pcDNA3 (Invitrogen). The integrity and size of RNA were verified by gel electrophoresis, and concentration and purity were determined from the absorbance (see DNA copy number...).
Plasmid DNA was detected using DNA FISH (Brown, 2002). Cells were rinsed in PBS, fixed (17 min at 20°C) in 4% paraformaldehyde and 0.05% acetic acid in 0.15 M NaCl, washed three times (5 min at 20°C) in PBS, incubated (30 min at 37°C) with 50 μg/ml RNase (which removes all detectable EGFP RNA; Fig. 3 C), permeabilized (5 min at 37°C) in 0.01% pepsin, pH 2.0, rinsed in water treated with diethylpyrocarbonate, postfixed (5 min at 20°C) in 4% paraformaldehyde in PBS, washed (10 min at 20°C) in PBS, denatured (2 min at 70°C) in 70% deionized formamide and 2× SSC (0.03 M sodium citrate and 0.3 M NaCl, pH 7.0), and immediately dehydrated (for 3 min) by passage through 70, 90, and then 100% ice-cold ethanol before hybridization (16 h at 37°C) in a moist chamber. Hybridization mix contained 50 ng of DIG- and/or biotin-tagged probe, 25% deionized formamide, 2× SSC, 200 ng/μl of sheared salmon sperm DNA, 5× “Denhardt's” solution (0.1% Ficoll 400, 0.1% polyvinylpyrolidone, and 0.1% bovine serum albumin), 50 mM phosphate buffer (20 mM KH2PO4, and 30 mM KHPO4 × 2 H2O, pH 7.0), and 1 mM EDTA. Probes were prepared by DIG random priming (Roche) of pure plasmid DNA, purified using Sephadex G-50 spin columns (GE Healthcare), and denatured (10 min at 94°C) before hybridization. Cells were then washed three times in 2× SSC (15 min at 37°C) and twice (5 min at 20°C) in TST (0.15 M NaCl, 0.1 M Tris-HCl, and 0.05% Tween 20, pH 7.5), and incubated in 1.4% blocking reagent (Roche) in TS (0.15 M NaCl and 0.1 M Tris-HCl, pH 7.5). Immunodetection was performed either using sheep anti-DIG (60 min at 20°C; 1:250; Roche) followed by donkey anti–sheep Cy3 (30 min at 20°C; 1:250; Jackson ImmunoResearch Laboratories) or using mouse anti-biotin (30 min at 20°C; 1:250; Jackson ImmunoResearch Laboratories) followed by donkey anti–mouse Alexa 488 (30 min at 20°C; 1:200; Invitrogen) or donkey anti–mouse Cy5 (30 min at 20°C; 1:150; Jackson ImmunoResearch Laboratories). Cells were washed three times (5 min at 20°C) in PBS after incubation with each antibody and mounted in Vectashield (Vector Laboratories) containing 1 μg/ml DAPI (Sigma-Aldrich).
Transcripts were detected using RNA FISH (Osborne et al., 2004). Cells were rinsed in PBS, fixed (17 min at 20°C) in 4% paraformaldehyde and 0.05% acetic acid in 0.15 M NaCl, rinsed three times (5 min at 20°C) in PBS, permeabilized (5 min at 37°C) in 0.01% pepsin, pH 2.0, rinsed in diethylpyrocarbonate-treated H2O, postfixed (5 min at 20°C) in 4% paraformaldehyde in PBS, and washed (10 min at 20°C) in PBS before hybridization (16 h at 37°C) in a moist chamber. Probes for EGFP, Neor, and DsRed were prepared by PCR followed by nick-translation (Roche) or asymmetrical PCR using oligo pairs 5–9. In some cases, three probes for each target were mixed. Biotinylated oligonucleotide probes (oligo 10) complementary to the preU2 sequence were used for U2G (Smith and Lawrence, 2000). Hybridization, subsequent washes, and immunodetection were performed as described for DNA FISH.
In analogous experiments using nonreplicating plasmids and different fixation conditions, two patterns of nuclear signal were seen (Binnie et al., 2006). Some transfected nuclei contained plasmid transcripts concentrated in foci (as we found), but others contained diffusely spread transcripts; as plasmid input increased, the fraction with the diffuse pattern increased. We also observed two patterns in preliminary experiments and were concerned that a diffuse pool might obscure some foci and/or artifactually aggregate to create foci. But as we used progressively harsher fixation, progressively more nuclear signal was detected (up to 1.5-fold), and the cell fraction with foci increased. Therefore, we used harsh conditions where detection is optimized, >85% nuclear signal was in the foci (see Results), and it is unlikely that much diffuse pool is extracted or aggregates (as nuclear signal does not fall or remain constant).
Cells were fixed (17 min at 20°C) in 4% paraformaldehyde and 250 mM Hepes, pH 8.0, permeabilized (5 min at 37°C) in 0.5% Triton X-100 and 0.5% saponin, postfixed and hybridized as with RNA FISH, and UBF or SC-35 were detected using mouse monoclonal anti-UBF (2 h at 20°C; 1:150; Santa Cruz Biotechnology, Inc.) or anti-SC-35 (2 h at 20°C; 1:200; Sigma-Aldrich) followed by donkey anti−mouse Alexa 647 (2 h at 20°C; 1:200; Invitrogen). Alternatively, RNA polymerase II was detected using a rabbit antibody directed against phospho-Ser2 in the heptads of the C-terminal domain of the largest catalytic subunit (2 h at 20°C; 1:250; Abcam) followed by donkey anti–rabbit Alexa 488 (2h at 20°C; 1:250; Invitrogen).
2.5 μm of orange or green intensity calibration beads (0.1% intensity; Invitrogen) were added to the mounting medium at 6 × 104/ml. Images were collected on a microscope (Axioplan 2; Carl Zeiss, Inc.) with a charge-coupled device camera (MicroMax 1024B; Princeton Instruments) using an exposure that gave a signal intensity of the beads of 200–255 on the grayscale. Signal intensities were measured using ImageJ (W.S. Rasband, National Institutes of Health, Bethesda, MD; http://rsb.info.nih.gov/ij/) and normalized relative to the intensity of the reference beads.
Relative proximity between templates was assessed using 3C (Dekker et al., 2002; de Laat, 2007; Ohlsson and Gondor, 2007). 4 × 107 cells were fixed (10 min at 20°C) in 50 ml DME + 10% FCS supplemented with 2% formaldehyde before glycine was added to 0.125 M. Cells were pelleted; lysed (90 min at 4°C) with vigorous stirring in 50 ml of 10 mM Tris-HCl, pH 8, 10 mM NaCl, 0.2% NP-40, and protease inhibitors (Sigma-Aldrich); repelleted; incubated (1 h at 37°C) with shaking in NEB buffer for BamHI (New England Biolabs, Inc.) + 0.3% SDS; and subsequently incubated in 1.8% Triton-X (1 h at 37°C). 106 nuclei were digested (16 h at 37°C) with 600 U BamHI and incubated (20 min at 65°C) in a final concentration of 1.6% SDS. Samples containing 2 μg DNA were incubated (1 h at 37°C) in 1% Triton X-100 and the volume was adjusted to 2 ml, then incubated (4 h at 16°C) in 2,000 U T4 DNA ligase (New England Biolabs, Inc.), incubated (16 h at 65°C) with 100 μg/ml proteinase K (Sigma-Aldrich), and treated (30 min at 37°C) with 0.4 μg/ml RNase A (Roche). DNA was then purified by phenol extraction and ethanol precipitation. PCR (30 cycles; controls showed this was in the linear range) was performed with serially diluted samples using oligo pairs 14–17, and PCR products were sized by gel electrophoresis. Expected ligation products were generally prepared in vitro from each pair of templates and used to confirm that amplification efficiencies were equivalent. Plasmid pTP18 (Pavelitz et al., 1995) and a BAC (RP-11-114A14; BACPAC Resources Center) were used as sources of host U2 and host ALDOA DNA, respectively. The relative cross-linking frequency is the intensity of the DsRed–EGFP or plasmid–host U2 band divided by the product of the intensities of the ALDOA–ALDOA and PCR control bands, normalized relative to equivalent values given by the reference experiment (i.e., II + III or CMV in Fig. 5).
For Fig. 5, transcriptionally active chromatin fractions were selected before 3C by incubation (16 h at 4°C) with antibodies against trimethyl K4 in histone H3 (Abcam). After immunoselection (Cai et al., 2006) on protein G–Sepharose beads, beads were washed once (at 4°C for 5 min) with low-stringency buffer (10 mM Tris-HCl, 150 mM NaCl, and 10 mM MgCl2, pH 7.5), twice (at 4°C for 5 min) with high-stringency buffer (10 mM Tris-HCl, 500 mM NaCl, and 10 mM MgCl2, pH 7.5), and once (at 4°C for 5 min) with low-stringency buffer. Beads were then incubated (37°C for 16 h) with 600 U of BamHI or PstI and the 3C ligation was performed. Plasmid copy numbers in experimental and reference samples were shown to be equivalent by PCR amplification of Neor using oligo pair 18 (Fig. 5 B, row 5).
The Mann-Whitney test, one-way analysis of variance (ANOVA) and Student's t tests were performed using GraphPad Prism version 4.00 for Windows (GraphPad Software, Inc.). Sample sizes were such that the last five samples analyzed yielded values that lay within 5% of the progressive mean.
Fig. S1 shows that nuclear foci containing high concentrations of minichromosomal transcripts colocalize with the active form of RNA polymerase II. Fig. S2 shows that intron-containing RNA colocalizes with faint SC-35 foci. Fig. S3 shows that transcripts made from a polymerase I promoter colocalize with UBF. Table S1 lists oligonucleotide sequences of primers, linkers, and probes. Online supplemental material is available at http://www.jcb.org/cgi/content/full/jcb.200710053/DC1.
We thank S. Murphy and N.J. Proudfoot for constructs.
We thank the University of Oxford (Clarendon Award), the UK Government (Overseas Research Student Award), and the E.P. Abraham Research Fund for support.
Abbreviations used in this paper: 3C, chromosome conformation capture; ChIP, chromatin immunoprecipitation; CMV, cytomegalovirus; DIG, digoxigenin; LCR, locus control region; qRT-PCR, quantitative RT-PCR; UBF, upstream binding factor.