A re-evaluation of chromatin organization in the Barr body by 3D-SIM

At the resolution level of 3D-SIM we compared the subchromosomal organization of the Barr body constituting a transcriptionally repressed CT with transcriptionally competent chromatin represented by autosomes and the Xa in female mouse C2C12 (Figure 1) and human RPE-1 cells (Additional file 1). In both cell types, the Barr body was highlighted by its intense DAPI staining and clearly demarcated from surrounding, less condensed chromatin. Moreover, a distinct folding substructure of DAPI-stained chromatin in the Barr body became evident with 3D-SIM, which could hardly be resolved by diffraction-limited wide-field microscopy even after deconvolution (Figure 1A, left panel). DNA-fluorescence in situ hybridization (FISH) painted Xi territories largely coincided with DAPI-delineated Barr bodies indicating that the Barr body comprises the entire Xi territory in these cell types (Figure 1B). Accordingly, painted X chromosome territories would allow a direct comparison between the 3D structure of the Barr body (Xi) and its Xa counterpart. 3D-FISH, however, typically requires heat denaturation of DNA, which might impede ultrastructural details of chromatin and proteins [44, 51]. Therefore, we avoided DNA denaturation and verified the Barr body/Xi by Xist RNA-FISH. Its chromatin landscape was compared against the entire nucleus reflecting the landscape of autosomal CTs and the active X.

Using a novel tailored 3D segmentation algorithm, DAPI-stained DNA signals were divided into seven intensity classes with equal intensity variance (Figure 1C). This classification was a deliberate simplification (compared to, for example, 65,536 grey levels in 16-bit images) but provided a clear visualization of nuclear landscapes shaped by different DAPI intensities and allowed for a statistical comparison between different nuclear areas or samples. Class 1 represented regions close to background intensities, suggesting a largely DNA-free compartment. Classes 2 and 3 represented chromatin of low staining intensity, which lined the more compacted CDCs represented by classes 4 to 6. Class 7 represented the highest DAPI intensities and mostly delineated the chromocenters in C2C12 nuclei. The respective DAPI classification in the Barr body also revealed a chromatin network of lower intensities pervading throughout the Xi territory (Figure 1C, inset 1). Note that in contrast to Barr body classifications carried out on SIM images, classifications based on wide-field microscopy images before and after deconvolution suggested highest DNA densities in the center of the Barr body gradually decreasing towards its periphery (inset magnifications in Figure 1C). This exemplifies an erroneous interpretation due to limits of microscopic resolution. DAPI intensity classifications of both entire nuclear volumes and of Barr body regions only confirmed the representation of all classes in the Barr body in both cell lines (Figure 1D). Compared with autosomal regions, low intensities, in particular classes 1 and 2 were, however, significantly underrepresented.

The suitability of DAPI as a marker for global chromatin representation despite its reported binding preference to AT-rich DNA [52] was verified by control stainings with SYTOX Green, a nucleic acid stain without sequence preference. This resulted in a similar classification profile of DNA intensities which was also seen with H2B-GFP-tagged nuclei (Additional file 2, see this file also for the applicability of SYTOX with different 3D-SIM microscope setups). The X chromosome is above average in its AT content [53], thus chromatin density classification for the Barr body based on DAPI intensities could be biased. These concerns were addressed by assessing DAPI intensity profiles of both Xi and Xa territories after 3D-FISH using X chromosome-specific painting probes (for a detailed explanation see Additional file 3).

We further substantiated the functional link between the topological chromatin density landscape and its biological relevance by quantitatively mapping the relative spatial distribution of immunodetected RNAP II, H3K4me3 and H3K27me3, markers for transcriptionally competent and repressed chromatin, respectively [54] on the seven DAPI intensity classes (Figure 2A,B,C,D). This approach was complemented by the measurement of minimal distances (nearest neighbor analysis) between the differently labeled fluorescent signals (Figure 2E). The average number and density of RNAP II sites (approximately 8,000 per nucleus in C2C12 cells and 14,000 in RPE-1 cells; approximately 9 sites/μm³ and 10 sites/μm³, respectively) were in the same range as estimated for HeLa and other cells from light and EM imaging of cryosections [55]. In line with their functional assignment, signals reflecting actively elongating RNAP II were distinctly overrepresented in the two lowest DAPI intensity classes 1 and 2 (Figure 2B). Notably, RNAP II sites were almost fully excluded from Barr bodies in C2C12 cells, while RPE-1 cells consistently retained a few RNAP II sites even in the interior of Barr bodies (Figure 2A), likely reflecting the higher fraction of escapees in Xi of human compared to mouse (15% versus 3%) [56].

Both in the Barr body and throughout the nucleus, H3K4me3 was found enriched at decondensed sites at the boundary of CDCs and IC channels, while H3K27me3 labeling sites were preferentially, although not exclusively, located in the more compacted interior of CDCs (Figure 2C). At the nuclear periphery, representing a transcriptionally largely but not completely repressed nuclear compartment [57], H3K4me3 was found closely associated with nuclear pores, recently defined as potential sites of transcriptional activity [58] (Figure 2C, right). H3K4me3 mapping to DAPI intensity classes revealed the most pronounced overrepresentation in the low intensity classes 2 and 3, while H3K27me3 overrepresentation was most evident in the intermediate classes 4 to 5 (Figure 2D). Notably, in contrast to RNAP II, H3K4me3 was underrepresented in class 1 (comprising the largely DNA-free IC), and both H3K4me3 and H3K27me3 were distinctly underrepresented in class 7 (chromocenters), illustrating their role as gene silencing/activation marks. The average minimal distance of around 200 nm between H3K4me3- and H3K27me3-marked chromatin signals in a nearest neighbor analysis confirmed their spatial separation (Figure 2E; see Additional file 4 for a comparative overview of all minimal distance measurements of this study).

The distinct nuclear landscapes shaped by different (DAPI-defined) chromatin density classes, their correlation with functionally distinct biological markers, together with previous experimental evidence as outlined in the introduction, justified the assignment of low intensity classes to the ANC comprising the functionally coherent IC and PR. Accordingly, we considered the underrepresentation of classes 1 to 3 in the Barr body, which exemplifies a globally transcriptionally repressed CT, as the result of a narrowing or even partial collapse of the ANC in the Xi.

Barr body structure maintains a contiguous, dense 3D chromatin network with a collapsed ANC channel system

We further aimed to validate whether the Barr body maintains a contiguous 3D ANC channel system, pervading the 3D chromatin network and leading to the nuclear pores (Figure 3). Optical sections of a DAPI-stained C2C12 nucleus denoting the position of the Barr body and a neighboring autosomal region showed irregularly shaped higher-density chromatin clusters pervaded by less intensely or unstained regions. The latter were remarkably wider in nuclear regions representing transcriptionally competent CTs, but also visible in the Barr body (Figure 3A,B) in line with DAPI intensity classifications. A higher-order 3D network of condensed CDCs and a low-density 3D channel system became obvious by 3D volume rendering (Figure 3C) and more evident by following-up these channels in respective movies (Additional files 5, 6 and 7). While nuclear areas harboring active CTs revealed wide-spaced channels and lacunae, the Barr body apparently retained only a rudimentary channel system representing the collapsed ANC. Yet, these channels could be followed from the Barr body interior through peripheral heterochromatin leading to Nup153-stained nuclear pores similar to nuclear regions with active CTs (Figure 3D and Additional file 7), further strengthening the maintenance of basic principles of CT organization in the Barr body.

To judge the potential impact of fixation artifacts on large-scale chromatin organization we performed 3D-SIM live-cell experiments with HeLa cells stably expressing histone H2B-GFP, a commonly used marker for the visualization of chromatin (Additional file 8). Live and fixed cells showed a high degree of similarity with regard to chromatin clusters, sites of decondensed chromatin, IC lacunae and ANC channels leading to nuclear pores. These observations largely ruled out that these features of higher-order chromatin organization, as seen at the level of 3D-SIM resolution, represent fixation artifacts.

Xist RNA foci are enriched at the boundaries of the collapsed ANC

We next explored in detail the topography of Xist RNA within the Barr body architecture of C2C12 and RPE-1 nuclei by 3D-SIM (Figure 4). Full-length Xist RNA is a 15 kb (mouse) to 17 kb (human) long, non-coding transcript (for reviews see Pontier and Gribnau [3] and Sengupta et al. [59]) with an estimated half-life of several hours, relying on a constant turnover of the transcript within the Xi territory [60, 61]. By 3D-SIM we identified Xist transcripts as distinct focal structures scattered throughout the Barr body (Figure 4A,B,C). Since our studies were done on fixed cells, these distributions may reflect snap-shots of dynamic positional changes of Xist foci possibly ongoing in living cells. Barr bodies of C2C12 nuclei harbored almost twice the amount of 3D-SIM discernible Xist RNA foci compared to RPE-1 nuclei (medians 95 and 54, respectively), while volumes of individual foci (medians 0.0195 μm³ and 0.0198 μm³) were almost identical in both cell types (Figure 4D). Xist RNA foci were preferentially found at low to intermediate intensity DAPI-stained chromatin sites, considered as a representation of the collapsed ANC (Figure 4A,B and Additional file 9). Further evidence for Xist RNA localization within this compartment was obtained in experiments that induce a re-opening of collapsed IC channels. For this purpose, we incubated living cells in hyperosmolar medium, which triggers a rapid hypercondensation of chromatin (HCC) concomitant with the widening of preformed IC channels [20, 62]. This effect is fully reversible when cells are exposed again to normotonic medium [20]. As expected, widening of the IC could be triggered also within the Barr body of HCC-treated nuclei. Xist RNA foci were observed in these Barr bodies nestling along the borders between compacted CDCs and the widened IC (Figure 4E). Notably, Xist RNA did not completely fill the widened IC suggesting its adhesion to chromatin bordering IC channels. The preferential localization of Xist RNA at lower intensity chromatin sites was confirmed by a quantitative mapping of Xist RNA signals to DAPI intensity classes, which demonstrated their overrepresentation in lower intensity classes both within normotonic and more pronounced within ‘HCC’ Barr bodies (Figure 4F).

Xist RNA and SAF-A partially overlap in chain-like structures

Previous studies hinted at a functional interaction between Xist RNA and the nuclear matrix protein SAF-A [63]. This prompted us to analyze the 3D nuclear topography of SAF-A in relation to Xist RNA in the Barr body of C2C12 cells by 3D-SIM (Figure 5). We found immunolabeled SAF-A signals abundantly distributed throughout the nucleus mostly localized at low DAPI intensity sites comprising the ANC (Figure 5A, inset 1). This localization became more obvious after induction of HCC (Figure 5B, inset 1). In the Barr body, immunodetected SAF-A signals were scarce. Yet, the few SAF-A foci typically showed a close spatial proximity or partial overlap with Xist RNA foci, occasionally forming chain-like structures that could weave through the narrow ANC of the Barr body (Figure 5A, insets 2 and 3). In Barr bodies of HCC-treated cells SAF-A was largely absent after immunodetection (Figure 5B, inset 2).

The apparent underrepresentation of SAF-A signals in the Barr body may be due to a Xi-specific conformational switch or post-translational modification on SAF-A leading to epitope masking or hindrance of SAF-A antibody binding and thus inadequate detection of SAF-A epitopes (discussed by Nakagawa and Prasanth [64]). To further investigate an antibody-borne effect and to verify the spatial proximity of SAF-A with Xist RNA, we transiently transfected C2C12 cells with mouse hrGFP-tagged SAF-A. In line with a previous observation [65], we found SAF-A-hrGFP enriched within the Barr body supporting a possible epitope masking of SAF-A in Barr bodies (Figure 5C). The close spatial proximity between Xist RNA and SAF-A was underpinned by their average minimal distance of approximately 110 to 125 nm in a nearest neighbor analysis (Figure 5D). Of note, control stainings using the same primary antibody simultaneously detected with red and green fluorescent secondary antibodies were measured in a parallel 3D-SIM study and yielded an average minimal distance of approximately 100 nm, which likely represents the collective offset associated with dual-color immunofluorescence detection with 3D-SIM [66] (see Additional file 4).

Xist RNA shows little spatial proximity with H3K27me3- and macroH2A1-enriched chromatin

Earlier observations described an embedding of Xist RNA in H3K27me3/macroH2A1-enriched chromatin sites along the Xi [67–69] and were recently supported for H3K27me3 by high-resolution molecular analyses [50, 68]. However, a direct and stable association of Xist RNA with H3K27me3 or the methylation conferring enzyme complex PRC2 was challenged by other studies (reviewed in Wutz [47], Sengupta et al. [59] and Jonkers et al. [70]) and further refuted by a recent study from Cerase and co-workers [66]. Here we compared the spatial relationship of Xist RNA with H3K27me3- and macroH2A1-enriched chromatin in the Barr bodies of C2C12 and RPE-1 cells by 3D-SIM after 3D immuno-RNA-FISH. Most Xist RNA foci appeared clearly separated from either H3K27me3- or macroH2A1-labeled chromatin (Additional file 10A,B, left panels) with average minimal distances >150 nm between Xist RNA and H3K27me3 or macroH2A1 signals, respectively (Additional file 10C). Co-immunodetection of macroH2A1- and H3K27me3-labelled chromatin, in contrast, showed a higher level of overlap (Additional file 10, right panels) in line with an average minimal distance of <140 nm between H3K27me3 and macroH2A1 (Additional file 10C; see Additional file 4 for a comparative overview of all assessed minimal distances from this study and Cerase et al. [66]). These different spatial proximities were corroborated by respective Manders’ and Pearson’s correlation coefficients (Additional file 11).

Barr body formation at the onset of XCI in XX ESCs occurs after initial Xist RNA spreading together with RNAP II exclusion

We next studied the localization of Xist RNA at the onset of XCI in early differentiating XX ESCs and followed the process of chromatin compaction towards Barr body formation. Undifferentiated XX ESCs contain two active X chromosomes. Accumulation of Xist RNA at the designated Xi is considered the earliest visible event at the onset of XCI [71, 72], reviewed in Heard [1]. A previous study reporting on a gradual exclusion of RNAP II from the ‘Xist RNA domain’ following Xist RNA accumulation found no evidence for chromatin compaction in this domain within an observation time up to day 4 upon differentiation [35].

In the present study we extended the observation period in XX ESCs to identify the time point of Barr body formation during the XCI process. We re-investigated the temporal and spatial correlations between Xist RNA and RNAP II in relation to chromatin compaction in the designated Xi territory by 3D-SIM up to day 9 upon differentiation (Figure 6). In undifferentiated XX ESCs, the Xist probe detected a small RNA cluster on both Xa territories most likely representing Tsix RNA, a non-coding Xist antagonizing RNA, which fully overlaps with the Xist gene and is transcribed in the antisense orientation from both X chromosomes before onset of XCI [73]. These transcripts were found in close association with RNAP II sites, embedded in an overall decondensed chromatin environment and occasionally bridging across ANC channels (Figure 6A). A similar appearance was observed up to day 3 of differentiation. DAPI intensity profiles, recorded from a region with 200 nm radius around Tsix expression sites, were comparable to the profile of entire XX ESC nuclei. Between day 3 and 4 upon differentiation, a fraction of cells had started a pronounced focal spreading of transcripts within an extended though confined nuclear region most likely reflecting Xist RNA expressed from the designated Xi (Figure 6A, day 3). Notably, at this stage RNAP II was found abundant in the emerging ‘Xist RNA territories’ that did not show chromatin compaction. At day 4, when RNAP II sites appeared mostly at the edge of ‘Xist RNA territories’, a consistent chromatin reorganization characteristic for a typical Barr body had not yet occurred (Figure 6A, day 4). At day 5, that is, 1 to 2 days after initial Xist RNA spreading, a typical Barr body, largely depleted from RNAP II sites and clearly demarcated from surrounding less condensed chromatin was observed in the majority of cells. At this stage Xist RNA was distributed throughout, but confined to the newly formed Barr body (Figure 6A,B, day 5). The full level of chromatin compaction in the emerging Barr body, comparable to somatic C2C12 cells, was reached only at day 9 (Figure 6A,B, day 9; compare also Figure 1D). The number and volume measurements of individual Tsix/Xist RNA foci indicated a dynamic behavior during early differentiation (Figure 6C). The high variability between cells in the number of individual Xist RNA foci at day 5 and their consolidation towards smaller numbers and higher volumes at day 9 hint to a multimerization during this early stage of differentiation.

We further observed substantial changes in the H3K27me3 immunostaining pattern during XX ESC differentiation (Additional file 12). In undifferentiated XX ESCs, H3K27me3 was particularly enriched at chromocenters, as previously shown [68]. At an intermediate stage around day 4, the distinct staining of chromocenters became gradually diminished in a large fraction of cells and H3K27me3 signals were distributed over the entire nucleus, slightly enhanced at the nuclear periphery and around nucleoli. Around/after day 5 of differentiation a distinctive marking of the Barr body by a focal H3K27me3 enrichment appeared in a fraction of cells. At this time point these patterns co-existed in parallel within one sample, while the Xi-specific pattern was consistently observed in most cells only after day 7.

Xist induction in transgenic male ESCs: inconsistent Barr body consolidation and persistent spreading of Xist RNA into decondensed transcriptionally active chromatin

We utilized a male mouse ESC line (clone 36, described by Wutz and Jaenisch [49], here termed tr36 ESC) with a doxycycline-inducible Xist transgene stably integrated into chromosome 11 as a model system to study the formation of an ‘autosomal Barr body’. In male ESCs carrying an inducible autosomal Xist transgene, spreading of Xist RNA in cis and transcriptional repression of exemplarily examined genes from the respective autosome has been previously demonstrated [49, 74, 75]. Under our experimental conditions initial spreading of Xist RNA foci in tr36 ESCs occurred approximately 1.5 days after induction within an extended though confined nuclear region, similar to the pattern observed at initial Xist RNA spreading in XX ESCs (Figure 7A). In contrast to XX ESCs, where transformation of the designated Xi into a compacted Barr body, largely congruent with the painted ‘Xist territory’, was accomplished within one or two days after initial Xist spreading, tr36 ESCs failed to form an ‘autosomal Barr body’ fully consistent with an Xi correlated Barr body over an observation period extended up to 10 days. Xist RNA foci in most tr36 ESCs persisted within an expanded nuclear region with diameters up to approximately 4 μm pervading into decondensed chromatin regions. RNAP II signals, still observed within the autosomal ‘Xist territory’ at day 10 after Xist induction indicated the continued potential for transcriptional activity (Figure 7A,B). This phenotype, with variable manifestations of Xist RNA extension into decondensed chromatin marked by RNAP II, was also maintained after differentiation up to an observation period of 10 days (Figure 7C). The amount of discernible Xist RNA foci in tr36 ESCs was over two-fold increased and showed a wider distribution range compared to differentiating XX ESCs (Figure 7D). These features distinguished the ‘autosomal Barr body’ from its X chromosomal counterpart and illustrate its weaker potential for chromatin compaction and transcriptional silencing.

The large spatial expansion of the tr36 ESC ‘Xist territories’ and the high amount of Xist foci made their congruency with a single CT 11 questionable. Xist RNA-FISH combined with painting of CTs 11 showed in fact a wide expansion of Xist RNA beyond painted CTs 11 (Additional file 13A,B). To further clarify this observation we performed a karyotype analysis of tr36 ESCs. Multiplex (M)-FISH revealed a translocation t(11; 11) in 24% and a translocation t(11; autosome) in 5% of analyzed metaphases (Additional file 13C). The increased size of the ‘Xist territory’ and increased number of Xist RNA foci could thus in part be explained by these translocations where Xist RNA would spread onto a larger CT in cis represented by the translocation chromosome. The radial spreading of Xist RNA foci several μm beyond painted CTs 11 was, however, unlikely to be explained by the rare observation of a translocation t(11; autosome) and raised the suspicion of Xist RNA diffusing into neighboring CTs in this cell line.

The Barr body is characterized by a significant collapse of the ANC but maintains principle features of CT architecture

Despite major differences in compaction between transcriptionally competent CTs and the Xi territory, our data imply that both structures share a sponge-like organization, characterized by two spatially contiguous, interacting networks, a higher-order chromatin network built up from compact CDCs and an ANC channel network, which should both be considered as 3D networks with their own dynamic organization. A comparison of H2B-GFP-tagged chromatin in live and fixed cells demonstrated these basic principles of nuclear organization also in nuclei of living cells and ruled out fixation artifacts as a major issue. In addition, DAPI was verified as a suitable marker for global chromatin representation despite its binding preference to AT-rich DNA [52] by a comparison with the DNA sequence-independent dye SYTOX Green.

ANC channels characterized by their reduced DAPI intensities were further substantiated by their connectivity to nuclear pores and by linking topographical DAPI intensity mapping with functionally defined markers. This mapping analysis localized transcription competency markers (H3K4me3, RNAP II) and the nuclear matrix protein SAF-A within or at the boundaries of these channels, while the repressive marker H3K27me3 was strongly overrepresented within higher DAPI intensity classes remote from chromatin boundaries and assigned to interior parts of CDCs.

Our observations support predictions of an extended concept of the chromosome territory-interchromatin compartment (CT-IC) model [17, 20–22, 29, 76]. According to this model, CDCs are composed of approximately 1 Mb CDs carrying transcriptionally silent chromatin localized within the compact core and considered as the inactive nuclear compartment. This compartment is lined by a decondensed periphery of transcriptionally competent chromatin, the PR characterized by small chromatin loops, mostly constrained within a zone of approximately 100 nm, which borders IC channels. These loops are accessible for the assembly of transcription complexes [17, 22, 26] and represent sites for replication [77], which we show here also for Xi by 3D-SIM (for an experimental proof of principle see Additional file 14). The IC interacts functionally with the PR by providing factors for RNA processing, replication and facilitating nuclear transport. Accordingly, we consider the structurally complex IC/PR as a functionally interacting ANC channel system that can, depending on functional demands, expand or narrow. The figurative term ‘ANC channel’ may be illustrated by comparison with a creek lined by reed beds expanding into the water and not in the sense of a waterway clearly separated from the ‘mainland’ by a concrete embankment.

The concept of CDCs composed of approximately 1 Mb sized chromatin domains was supported by recent population-based Hi-C analyses, a molecular approach to define chromatin proximity patterns at high resolution [18, 45, 78]. The study of Dixon and co-workers [18] defined this compartmentalized structure as topological domains (TDs) with a median size of several hundred kb, while a small remaining fraction with a size of <50 kb was termed ‘boundary regions’. The similar length scale described for TDs and for microscopically observed 1 Mb chromatin domains suggests that both represent the same structures (reviewed in Gibcus and Dekker [19], Bickmore and van Steensel [79] and Dekker et al. [80]). Yet, the extent to which ‘genomic domains’ of a 2D plaid pattern obtained by Hi-C analyses of large cell populations match with the higher-order chromatin landscape perceived for single cells by 3D-SIM cannot be answered conclusively to date. ‘Boundary regions’, particularly enriched in housekeeping genes and active RNAP II [18] might largely represent decondensed chromatin loops in the PR, which may occasionally pervade deeply into the IC.

Our 3D-SIM study suggests that Barr body formation results from a partial collapse of the ANC depending on increased chromatin compaction within the PR and a closer proximity of approximately 1 Mb CDCs/TDs. The clear visualization of low DAPI intensity-defined ANC channels in Xi is compromised due to the small distances between CDCs, which are at or just below the resolution limit of 3D-SIM. Evidence for persisting channels even in the partially collapsed ANC of the Xi is provided by their connectivity to nuclear pores and their opening and expansion under hyperosmolaric conditions. A previous EM study [35] reporting evidence for distinct tunnels that pervade between 200 to 400 nm thick chromatin fibers of the Xi and end at nuclear pores is in line with our observations obtained under hyperosmolaric conditions. However, the width of the collapsed channel system within the Barr body of cells fixed under normotonic conditions seems to be smaller than reported in the EM study.

While the ANC of autosomal CTs is enriched with H3K4me3 and RNAP II, these hallmarks of transcriptionally competent chromatin are scarcely represented in the Barr body. Their occasional occurrence within the Barr body supports recent observations that genes escaping XCI are distributed throughout the Barr body [34, 36] and suggests that transcription can also occur within the Barr body. Still, it remains elusive whether the Barr body periphery maintains a more favorable environment for transcription than its interior as previously suggested [32].

Focal Xist RNA distribution throughout the Barr body at the collapsed ANC channels suggests its dynamic association with silenced genes

Conventional fluorescence microscopy implied the longstanding conception of a cloud of Xist transcripts and a uniform ‘coating’ of the Xi territory [70, 81–83]. The organization of Xist RNA as distinct foci distributed throughout the Xi, as revealed by 3D-SIM, may encourage some reconsideration. Notably, as a hypothetical model, a focal organization of Xist was already suggested in 1996 by Clemson and coworkers [84] and further considered in Xist RNA tagging experiments in living ESCs [85]. 3D-SIM also provides an informative basis for the comparative assessment of the number of Xist RNA foci. Our count of less than 100 foci per Barr body both in human and mouse somatic cells was significantly below the estimated 300 to 1,000 copies assessed by qPCR techniques [60, 86]. Since a labeled FISH probe bound to one Xist RNA molecule should yield sufficient fluorescence to be detected by 3D-SIM, this discrepancy likely reflects multimerization of Xist RNA molecules [70, 87, 88] and suggests the aggregation of three to ten Xist RNA transcripts on average for the formation of an individual focus.

Within the 3D chromatin environment of the Barr body, 3D-SIM analyses revealed the preferential localization of Xist RNA foci within and at the boundaries of the collapsed ANC channels. This localization was further elucidated after widening this compartment in the Barr body by induction of HCC. We hypothesize that both the collapsed ANC channels in Xi territories and the open ANC channels in transcriptionally competent CTs are enriched in coding and/or regulatory sequences. In line with this hypothesis RNA foci mark distinct sites of genes or regulatory sequences that become repressed during XCI. The clear spatial separation between most Xist RNA and H3K27me3 signals and a low degree of overlap at the resolution level of 3D-SIM additionally underlines the distinct localization of Xist RNA away from compacted CDCs that are enriched in H3K27me3. Spatial separation of Xist RNA and H3K27me3 is in agreement with our recent 3D-SIM study analyzing Polycomb proteins and Xist RNA [66]. Together, these findings support the recently proposed concept [10], that Xist RNA mediates recruitment of Polycomb proteins via an indirect rather than direct mechanism.

Early studies found Xist RNA enrichment at G-light bands on the Xi in metaphase spreads, suggesting an association of Xist RNA with gene-dense chromatin [89], which was supported by later studies using high-throughput epigenomic mapping [36, 50, 68, 90]. The recent seminal study by Engreitz et al. [50] using an RNA antisense purification technology reported on Xist interactions with chromatin independent of sequence specificity. Here, Xist RNA was found to bind broadly across the X chromosome, though enriched at gene-dense sites, in particular at sites of silenced genes. This seeming discrepancy of a distinct focal distribution observed by our 3D-SIM analysis and a rather even Xist RNA distribution found by Engreitz et al. may be resolved by considering that the latter approach reflects observations obtained from averaging large cell populations, which may be consistent with a dynamic focal distribution seen at the single-cell level. Taken together this argues for a dynamic association of Xist RNA foci with stochastic binding to a subset of potential chromatin binding sites at a given point in time, rather than to a deterministic stable association at specific sites. These characteristics are evened out in population-based (Hi-C) analyses and our study exemplifies the importance of complementary high-resolution single-cell analyses. Xist RNA might thus contribute to the establishment of a silenced local chromatin environment by inactivating specific regulatory elements suggested by Calabrese et al. [36] or by blocking the access for the transcription machinery to the Xi at variable sites.

A structural role of Xist RNA for the maintenance of the specific Xi conformation was recently shown by chromosome conformation capturing and knock-down experiments [15, 16], which demonstrated the requirement of Xist RNA for a compacted Xi territory in somatic cells. The longstanding discussion of LINE-1 (L1) repeats as direct anchor points for Xist RNA (for review see Pontier and Gribnau [3]) was contradicted by the recent finding of a negative correlation between Xist RNA and L1 [50]. Yet L1 repeats, overall enriched in the X chromosome and considered to be concentrated in compacted chromatin domains [18, 50], may have an indirect impact on Xi compaction. L1 repeats may facilitate the formation of a repressive CC due to their reported tendency of large, repetitive stretches to form stable contacts [78].

Functional implications of Xist RNA’s spatial proximity to SAF-A

A previous study reported on the requirement of SAF-A for Xist RNA localization to the Barr body [63]. SAF-A has long been known as a nuclear matrix protein with specific DNA binding properties [91] and involvement in transcription, mRNA trafficking and splicing (for review see Han et al. [92]). Its potential role in nuclear architecture has remained elusive to date. Our finding of a particulate or fibrous-like SAF-A staining pattern in the ANC of both active CTs and the Barr body supports a function of SAF-A for the structural organization of chromatin within this functional compartment. Evidence for an interaction between Xist RNA and SAF-A was initially based on the dual binding properties of SAF-A to RNA and DNA [93]. RNA immunoprecipitation, enrichment of SAF-A:GFP fusion proteins at the Xi, dissociation of Xist RNA from Xi after SAF-A knock-down and a recently developed in silico protein RNA interaction prediction approach made this protein a strong candidate as a Xist RNA interaction factor [63, 65]. Yet, a direct spatial interaction between SAF-A and Xist RNA has not been proven so far (reviewed in Nakagawa and Prasanth [64] and Tattermusch and Brockdorff [94]). Our 3D-SIM single-cell analysis revealed a close spatial proximity between Xist RNA and SAF-A. Their functional interaction is further supported by the presumed Xi-specific post-translational modification or conformational switch of SAF-A upon interaction with Xist RNA (reviewed in Nakagawa and Prasanth [64]) resulting in an epitope masking within the Barr body. The resolution limit of 3D-SIM does not allow determination of whether the SAF-A pattern within the collapsed ANC of the Barr body is largely due to tight packing of protein molecules or to a true multimerization. The latter would further argue for a functional role for SAF-A in XCI, since SAF-A multimerization apparently requires interaction with nucleic acids [93]. A binding to Xist RNA could trigger SAF-A multimer formation, creating a scaffold that helps to maintain the integrity of the Barr body structure. Such a function might explain the enrichment of SAF-A within the Barr body.

Chromatin compaction in the committed Xi of early differentiating XX ESCs is accompanied by RNAP II exclusion at onset of inactivation

Time-resolved 3D-SIM analysis of XCI in XX ESCs revealed initial spreading of Xist RNA foci into a decondensed chromatin environment harboring numerous RNAP II sites around day 3 upon differentiation. Focal Xist RNA spreading was followed by RNAP II exclusion starting the day thereafter, in line with a previous study surveying an observation time up to day 4 [35]. This study showed major exclusion of RNAP II at day 4 but not yet evidence for chromatin compaction. Our extended observation period up to day 10 upon differentiation revealed the distinct global compaction of the Xist RNA-defined Xi territory towards a Barr body typically at day 5. This delay after initial Xist RNA spreading makes it unlikely that Xist RNA acts as an immediate mediator for chromatin compaction of the newly formed Xi. The close temporal occurrence of RNAP II exclusion and Barr body formation suggests a link between Barr body formation and transcriptional repression, but the time-resolution of our differentiation experiments does not allow statements about their temporal order and mutual interdependence, which likely includes other factors as well. It may be speculated that after RNAP II exclusion and/or the removal of H3K4me3 and other active chromatin marks as early events of gene repression during XCI [95], silenced genes in turn quickly undergo chromatin condensation. The higher level of chromatin compaction in the Barr body observed at day 9 may reflect a stable stage of chromatin arrangement in Xi mediated by repressive signatures such as DNA methylation that appear later during XCI in XX ESCs (for reviews see Heard et al. [12] and Nora and Heard [96]).

Structural features of an ‘autosomal Barr body’ differ from its Xi counterpart

Transgenic Xist induction from an autosome in tr36 ESCs failed to consolidate the respective CT into an ‘autosomal Barr body’ with features fully consistent with the Xi-derived Barr body. Spreading of Xist RNA beyond the compacted transgene carrier CT into decondensed, apparently transcriptionally active chromatin was observed up to day 10 upon Xist induction and another 10 days upon differentiation. Thus, this state does not reflect a specific feature of the non-differentiated state. The phenotypic inconsistencies between autosomal and X chromosomal Xist induction add on to the large body of evidence for an impaired silencing efficiency of autosomally transcribed Xist RNA and/or an impaired response of autosomes upon Xist induction, leaving room for different explanations: free Xist RNA may diffuse away from the transgenic autosome, as suggested in Jeon and Lee [83]. Our observation of a large radial expansion of Xist RNA beyond painted CTs 11 may reflect an impaired trapping and transmigration into neighboring CTs. The wide expansion could also reflect spreading in cis into abundant, highly extended chromatin loops that were not delineated by chromosome painting. Yet, previous studies found an extensive looping out from the bulk territory restricted to very few regions harboring particular gene-dense and transcriptionally active clusters [20, 97–99].

An incomplete Xist RNA-induced gene silencing in the autosomal part of a translocation chromosome t(X; 4) in an XX ESC line was explained by an attenuated spreading of Xist RNA into the autosomal part of the translocation chromosome [100]. The high abundance of Xist RNA foci observed here in tr36 ESCs, however, does not support this assumption. Incomplete inactivation of autosomes has also been considered as a lack of evolutionary adaptation in autosomes, making X chromosomal DNA particularly susceptible for Xist RNA-induced gene silencing possibly by its high enrichment of L1 repeat sequences. Mouse chromosome 11 is an overall L1-poor chromosome, though with a relative enrichment in segments A1 to A5 [53]. One may speculate that compacted chromatin segments largely void of RNAP II seen after transgenic Xist induction in tr36 ESCs might represent chromosome 11 segments enriched in L1 repeats and thus susceptible for gene silencing, while the remaining part of the chromosome may undergo only an incomplete inactivation process.

Model views of Barr body architecture and general CT architecture shed light on structure-function conundrums of nuclear organization

Model views of the Barr body architecture as the structural hallmark for a transcriptionally repressed CT in comparison to active CTs are presented as virtual 2D sections at different levels of resolution in Figure 8, with the objective to draw them to scale. They integrate our findings on the topographical relationships between chromatin or specific chromatin marks (H3K4me3, H3K27me3) with Xist RNA, SAF-A and RNAP II. The contiguous 3D chromatin network compartment typically consists of CDCs (marked red in Figure 8B), which hamper the identification of individual CDs. Thus, this view argues for a higher-order integration of distinct individual CDs in the order of 500 kb to approximately 1 Mb (encircled in Figure 8B, right) visualized during S-phase as replication foci [101, 102] or even smaller subunits reflecting replicons of approximately 150 kb [101]. CD networks also connect neighboring CTs with each other [20, 23]. Accordingly, individual CTs are typically not separated by a distinct interchromosome domain as was initially predicted [103]. However, such a margin still holds for nuclei of senescent fibroblasts [104, 105] and of bovine embryos [106] emphasizing that there is no one-size-fits-all model of structural interactions or separations of neighboring CTs.

In autosomal CTs (Figure 8B, right), the transcriptionally competent periphery of CDCs, that is the PR (colored in green), signifies its enrichment in active histone marks confined within a zone of approximately 100 nm around segmented chromatin borders. Chromatin domains may co-exist, which either represent transcriptionally competent or silent chromatin [18, 45]. The local shape and width of both CDCs and the IC are highly variable, with larger IC lacunae harboring nuclear bodies [29] (not shown here). The IC channel system carries SAF-A, indicating a nuclear matrix expanding within the IC. Whether the interior of the IC is actually free of chromatin cannot conclusively be assessed on DAPI-stained 3D-SIM images, since they do not provide the resolution to detect individual DNA molecules within the context of a bulk DNA/chromatin staining. EM evidence based on the specific display of DNA, however, provide strong substantiation for a general absence of many chromatin loops expanding into the interior of wider IC channels and lacunae [23].

Compared to autosomal CTs, H3K27me3-enriched CDCs within the Barr body are moved closer together. A higher compaction of individual CDs can be assumed but is, again, beyond the resolution limit of 3D-SIM. ANC channels appear significantly collapsed to the extent that only a few non-collapsed sites are detectable that may harbor active chromatin marks (Figure 8B, left). Xist RNA foci are found along the collapsed ANC.

Figure 8C provides speculative model views at nucleosomal resolution, co-existing within a Barr body (boxes 1, 2 and 3) and within a transcriptionally active region typical for an autosomal CT (box 4). They are drawn as experimentally testable predictions for future studies considering the potential 3D organization of chromatin at the resolution level of the approximate 10 nm nucleosome fiber. Box 1 illustrates transcriptional activity of escaped genes in the Barr body interior, supported by the finding of escaped genes throughout the Barr body [34]. In line with the structural organization of transcriptionally competent sites in autosomal CTs (box 4), we propose that transcriptional activity requires small extended 10 nm thick chromatin loops. These loops are enriched in active histone marks and expand from the compacted core chromatin into the ANC facilitating biochemical interactions with nuclear bodies, recruitment of factors required for transcription and for co-transcriptional splicing. Of note, extended chromatin loops comprise only a few kb, much below the size of many genes and thus require a highly dynamic organization of chromatin domains for the transcription of an entire gene since only a small part of it is actually presented as an expanded loop where transcription initiation complexes and chromatin remodeling factors can bind. A transcribed part of a gene is rapidly re-compacted. Similar scenarios can be envisaged for chromatin replication and DNA repair implicating the requirement for a dynamic organization also at transcriptionally silent locations. Pulse DNA replication labeling experiments with varying chase times after incorporation of labeled nucleotides demonstrate the location of nascent DNA at boundaries of CDCs, whereas with increasing chase time post-replicative DNA is progressively shifted into the cluster interior (see Additional file 14 and Fakan and van Driel [26] for previous TEM data). Boxes 2 and 3 exemplify hypothetical scenarios for transcriptionally silent regions within the Barr body. Less condensed chromatin is present in the collapsed ANC in the form of ‘closed’ configurations of 10 nm thick chromatin fibers, possibly enriched with repressive histone marks. At some sites a narrow, chromatin-free IC channel may exist, while other sites are filled completely with ‘closed’ or ‘open’ chromatin loops needed for replication or repair tasks. Box 3 illustrates the possibility of fully compacted neighboring CDCs without any chromatin looping into the narrow IC channel. Xist RNAs accumulate at specific yet DNA sequence-independent sites, where they may dynamically interact with XCI-susceptible genes/regulatory sequences, clogging the IC channel at this site and using Xi-specific SAF-A as an anchor which may also be essential for a structural separation of CDCs.

Even in a transcriptionally fully silent part of a CT, it is essential that the space-time organization of CDs/TDs is compatible with their ‘opening’ and ‘closure’ to fulfill the demands of chromatin replication and DNA repair. Maintenance of a compartmentalization in the Barr body may be important to avoid chromatin entanglement, which could interfere with necessary chromatin movements during chromatin replication and the structural transformation into a mitotic chromosome [107].

Cells and culture conditions

Human retina epithelial-derived, hTERT-RPE-1 cells were grown in DMEM/HF-12 (1:1) supplemented with 10% FCS. They were characterized as tetraploid with few chromosomal rearrangements (M-FISH data upon request). Female mouse C2C12 myoblast cells, cultured in DMEM/20% FCS, are near tetraploid, including four copies of the X chromosome [108]. Both cell lines contain two inactive X chromosomes. HeLa cells stably transfected with histone H2B-GFP [109] were grown in RPMI 1640/10% FCS.

For transient transfection, RPE-1 and C2C12 cells were grown in six-well dishes up to 70% confluency and transfected with 1 μg of pBOS_H2B-GFP, pCAGGS_SAF-Ah:hrGFP or pCAGGS_SAF-Am:hrGFP (human and mouse SAF-A, respectively). Transfections were done with Lipofectamine 2000 (Invitrogen, Carlsbad, CA, USA) following the supplier’s instructions. Cells were fixed 24 h post-transfection. For induction of HCC, cells were incubated for 5 min in hyperosmolaric (approximately 750 mOsm) medium before fixation as previously described [20, 62]. For pulse replication labeling by incorporation of the thymidine analogue 5-ethynyl-2-deoxyuridine (EdU), EdU was added at a final concentration of 10 μM to the medium for 5 min.

Undifferentiated mouse ESC lines, the female wild type ESC (clone E16.7, XX ESCs) [110] and the male Xist-transgenic ESC (J1 ESC, clone 36, tr36 ESCs) [49] containing one copy of full-length mouse Xist cDNA under the control of a doxycycline inducible promoter on chromosome 11 were cultivated under feeder-free conditions on gelatinized cover slips in KO-DMEM (Invitrogen) supplemented with 16% FBS (stem cell tested; GE-Healthcare, Little Chalfont, UK), 1% non-essential amino acids (100 × stock; PAA), 2 mM GlutaMAX (Invitrogen) and 0.1 mM β-mercaptoethanol (Roth, Karlsruhe; Germany). To maintain the undifferentiated state, culture media were supplemented with 1,000 U/ml LIF (PAA), 1 μM PD 0325901 (MEK inhibitor; Axon Medchem, Groningen, The Netherlands) and 3 μM CHIR 99021 (CSK3 inhibitor; Axon Medchem). Medium was changed daily and cells were split every second day. The undifferentiated state was monitored by the typical morphology of ESC colonies as well as by immunodetection of SSEA-1 (Millipore, Billerica, MA, USA). After differentiation, induced by withdrawal of LIF, PD 0325901 and CHIR 99021, cells were cultivated for up to 10 days.

Xist transcription in tr36 ESCs was induced by adding 1 μg/ml doxycycline to the medium. XX ESCs have a diploid karyotype 42,XX,+6,+8 (M-FISH data on request).

3D DNA/RNA-FISH, immunodetection and immuno-FISH

Chromosome painting probes delineating human chromosome X or mouse chromosomes 11 and X, generated from flow sorted chromosomes (gift of M Ferguson-Smith, University of Cambridge, Cambridge, UK) were amplified and hapten-labeled by degenerate oligonucleotide-primed (DOP)-PCR using the 6 MW primer as previously described in detail [111]. Next, 40 ng of labeled probe was used per μl of hybridization mix. Fixation and pretreatment steps of cells for DNA-FISH were performed as previously described [48]. For delineation of human Xist transcripts, a full-length cDNA (OriGene, Rockville, MD, USA) was used and amplified by a whole genome amplification kit (Genomi-Phi; GE Healthcare, Fairfield, CT, USA). Mouse Xist RNA probes were generated by specific amplification of exons 1a and 6. Xist RNA probes were labeled with biotin by nick translation. Then, 20 ng of labeled Xist RNA probe and 100 ng salmon sperm DNA were dissolved per μl of hybridization solution (50% formamide/2 × SSC/10% dextran sulfate). Ribonucleoside vanadyl complex (New England Biolabs, Ipswich, MA, USA) was added to the permeabilization buffer and to the probe at 2 mM final concentration to prevent RNase activity.

The following antibodies were used for immunodetection: antibodies against RNAP II Ser2P, detecting the actively elongating form of RNAP II [112], (rat monoclonal; kindly provided by D Eick, Ludwig Maximilians University (LMU) Munich, Munich, Germany), H3K27me3 (mouse monoclonal; Active Motif, Carlsbad, CA, USA), macroH2A1 (rabbit polyclonal; Active Motif), PCNA (rat monoclonal; Heinrich Leonhardt Lab, Martinsried, Germany), murine SAF-A (rabbit polyclonal; Brockdorff Lab, Oxford, UK) and hrGFP (polyclonal; Agilent Technologies, Santa Clara, CA, USA). Prior to using the SAF-A antibodies in the experiments described here they were tested by immunofluorescence on a variety of cell lines, antibody-antigen competition assays and immunoprecipitation followed by either Western blotting or mass spectrometry.

For immunofluorescence (IF) detection, cells were seeded on 18 × 18 mm borosilicate glass coverslips, number 1.5H (170 μm ± 5 μm thickness; Marienfeld Superior, Lauda-Königshofen, Germany). Cells were washed two times with PBS and fixed with 2% formaldehyde/PBS for 10 min following a stepwise replacement with 0.05% PBS/Tween (PBST). For permeabilization, cells were incubated in 0.5% Triton X-100/PBS for 10 min and subsequently washed twice in PBST.

For combined immuno-RNA-FISH, cells were equilibrated in 2 × SSC and incubated in 50% formamide/2 × SSC at 4°C for 2 to 4 h. Labeled and denatured RNA-FISH probe was added, cells were mounted on slides, sealed with removable rubber cement and samples were allowed to hybridize at 37°C overnight. Unbound probes were removed with 3 × washing in 2 × SCC and 3 × washing with 4 × SSCT at 37°C and probe detection was carried out in 2% BSA/0.5% FSG/4 × SSCT for 1 h at room temperature.

For subsequent IF, cells were equilibrated in 1 × PBST and blocked with 2% BSA/0.5% FSG/PBST for 1 h. Antibodies were diluted in blocking solution and incubated for 1 h followed by thorough washing with PBST. For detailed description of the immuno-RNA-FISH procedure for super-resolution microscopy see Markaki et al. [48]. After the IF procedure, cells were post-fixed for 10 min in 4% formaldehyde/PBS. DNA was counterstained with 1 μg/ml DAPI or 0.25 μM SYTOX Green (Molecular Probes, Eugene, OR, USA) in PBS for 10 min. Samples were mounted in Vectashield antifade mounting medium (Vector Laboratories, Burlingame, CA, USA) and sealed with nail varnish. In case of a combined RNA-/DNA-FISH approach, positions of individual cells were stored and imaged subsequently as described in detail by Markaki et al. [48].

3D-SIM

Super-resolution imaging on fixed samples was performed on a DeltaVision OMX V3 system (Applied Precision, GE Healthcare) equipped with a 100 ×/1.40 NA Plan Apo oil immersion objective (Olympus, Tokyo, Japan), Cascade II:512 EMCCD cameras (Photometrics, Tucson, AZ, USA) and 405, 488 and 593 nm diode lasers [113]. Live-cell super-resolution imaging was performed with a DeltaVision OMX V3 Blaze system (Applied Precision), equipped with a 60 ×/1.42 NA Plan Apo oil objective and Olympus and sCMOS cameras (PCO, Kelheim, Germany) for high-speed stack acquisition. In both cases, 3D-SIM image stacks were acquired with a z-distance of 125 nm and with 15 raw images per plane (five phases, three angles). The raw data was then computationally reconstructed using Wiener filter settings 0.002 and channel-specifically measured optical transfer functions (OTFs) using the softWoRx 6.0 software package (Applied Precision) to obtain a super-resolution 3D image stack with a lateral (x-y) resolution of approximately 120 nm and an axial (z) resolution of approximately 300 nm [31, 43]. The level of spherical aberration was minimized and matched to the respective OTFs using immersion oil different refractive indices (RIs). Best results were typically obtained with OTFs measured on 110 nm diameter red and green fluorescent FluoSpheres (Invitrogen) and 170 nm diameter blue fluorescent FluoSpheres (Invitrogen), respectively, using RI 1.512, and sample acquisition with RI 1.514 for depth adjustment in the region of optimal reconstruction a few μm into the sample. Images from the different color channels were registered with alignment parameters obtained from calibration measurements with 0.2 μm diameter TetraSpeck beads (Invitrogen). The reconstruction process generates 32-bit data sets with the pixel number doubled in the lateral axes, and the lateral pixel size halved from 80 nm to 40 nm in order to meet the Nyquist sampling criterion.

To normalize all image stacks for subsequent image processing and data analysis, the stack-specific mode grey value (representing the peak of the background noise) was subtracted, negative values discarded and finally the format converted to 16-bit composite TIFF stacks using an in-house script in ImageJ (http://rsbweb.nih.gov/ij). In some cases 32-bit images were first shifted to positive values, prior to 16-bit transformation and subsequent mode subtraction, leading to identical results.

Conventional wide-field (deconvolution) image stacks were generated from 3D-SIM raw data by average projection of five consecutive phase-shifted images from each plane (only of the first angle) and, in case, subjected it to an iterative 3D deconvolution using softWoRx 6.0. For direct comparison with 3D-SIM images, the pixel numbers were doubled in x and y using a bicubic interpolation in ImageJ to unify voxel sizes in all cases to 40 × 40 × 125 nm.

Chromatin density classification by 3D assessment of DAPI/SYTOX Green intensity classes

For chromatin density quantification, a hidden Markov random field model classification, combining a finite Gaussian mixture model with a spatial model (Potts model) was used, implemented in the open-source statistics software R [114]. Fluorescently stained DNA was segmented into seven classes with equal intensity variance. This approach allows threshold-independent signal intensity classification at the voxel level, not only based on the intensity of an individual voxel but also considering the classification of surrounding voxels (for a detailed description see Zhang et al. [115]). Class 1 represents voxels with intensities close to background level, while class 7 assigns highest chromatin ‘density’. This approach compensates for DNA/chromatin staining intensity variations between individual cells, cell types and experiments. Prior to segmentation, a 3D mask was generated in ImageJ to define the nuclear space according to the DAPI signal. Nucleoli contributed with <5% to the total nuclear volume in both C2C12 and RPE-1 cells (data not shown) and were included in DAPI intensity classifications. 3D masks for Barr bodies, defined as volumes with an enrichment of Xist RNA, were generated by Otsu thresholding of the Xist RNA signals followed by transformation into a binary mask file and dilation by several pixels.

Quantification of 3D-SIM discernible segmented Xist RNA objects and colocalization analyses

Number and volumes of Xist RNA foci were quantified using Volocity (Perkin Elmer, Waltham, MA, USA). Objects were defined by the ‘separate touching objects’ function after setting an intensity threshold monitored by visual inspection of the signals’ intensity histogram. 3D renderings were performed with Amira 5.2.2 (Visualization Sciences Group, Burlington, MA, USA). In order to make DAPI signals comparable between different nuclei, the DAPI intensities were leveled to the same mean value.

Colocalization analyses were based on Manders’ coefficients M1 and M2, quantifying the amount of overlapping pixels, and Pearson’s correlation (PC) coefficient, assessing the correlation of data sets in a voxel-by-voxel intensity-based analysis. Pearson’s coefficients were calculated on non-thresholded images from the fraction of the stack containing the Barr body volume (approximately 15 z stacks) and its surroundings, or similar sized volumes of the controls, respectively. Barr bodies were defined as volumes with an enrichment of Xist RNA including their close surroundings. The ‘Barr body’ 3D mask was obtained by applying a Gaussian filter, thresholding to remove low intensity signals and converting the obtained stack into a binary file which mapped all voxels of interest for coefficient calculation. Manders’ coefficients were calculated for the signal intensities of voxels in a similar way. To estimate the threshold, for every image stack for both channels a separate small 3D volume from the area outside the cell or nucleus was selected. Average intensity of this ‘background sub-stack’ was calculated and served as a base to calculate the threshold for Manders’ coefficient calculation.

Nearest neighbor analysis and quantitative localization of specific nuclear targets correlated to DAPI intensity classes

Nearest neighbor/minimal distance measurements were performed using the TANGO Plugin for ImageJ/Fiji [116]. Mode subtracted, 16-bit transformed 3D-SIM image stacks were imported into TANGO. Nuclear masks were generated from the DAPI channel using a watershed algorithm to segment the signals from background and morphological filters to transform the signals to coherent binary mask, covering the entire nuclear space. Barr body masks were generated as described above by dilating the Xist signals covering the Barr body region. For spot centroid determination, the signals in the red and green channels were pre-filtered and segmented as follows: 1) top hat filter with one pixel radius in x-y and z; 2) Laplacian of Gauss filter with one pixel radius in x-y and z; and 3) spot detector 3D with Otsu auto-thresholding. The segmented objects were discarded if their signal intensity was less than twice the mean intensity of the image and if their volume was smaller than two voxels. Finally the minimal distances of intensity weighted centroid xyz-positions of all segmented green and red signals/spots within the masked nuclear or Barr body region were determined. Statistical differences in colocalization coefficients as well as nearest neighbor distances of different experiments were analyzed by pairwise t-test comparison with Bonferroni correction of level of significance. To determine the distribution of defined nuclear targets with regard to chromatin intensity classes the centroid xyz-coordinates of TANGO-segmented objects were mapped on the segmented chromatin classes obtained as described above. For calculating the over/underrepresentation of target signals in each chromatin class, the respective fraction sizes were subtracted for each nucleus/Barr body, and the mean values and standard deviations determined. Alternatively, over/underrepresentation was normalized for the chromatin class size by calculating the ratio between target signal fraction and chromatin class fraction and subtracting the value 1 (for a workflow see Additional file 15).