J. Cell Biol.
© The Rockefeller University Press
0021-9525/97/12/1597/14 $2.00
Volume 139, Number 7, December 29, 1997 1597-1610

Spatial Organization of Large-Scale Chromatin Domains in the Nucleus: A Magnified View of Single Chromosome Territories

João Ferreira,^* Giovanni Paolella, Carlos Ramos,^* and Angus I. Lamond^§

^* Institute of Histology, Faculty of Medicine, 1699 Lisboa codex, Portugal;  Dipartimento di Biochimica e Mediche, via Sergio Pansini 5, 80131 Napoli, Italy; and ^§ Department of Biochemistry, University of Dundee, Dundee DD14HN, Scotland, UK.

Abstract

Materials and Methods

Results

Discussion

Footnotes

Acknowledgements

Abbreviations used in this paper

References

Abstract

ALTHOUGH considerable information is available about the primary structure of genes and sequence elements controlling their regulation, much less is understood about the higher order organization of DNA in the interphase nucleus. An understanding of chromosome organization is likely to be crucial for models of nuclear structure and function. Most studies of chromosome structure have focused on condensed metaphase chromosomes that can be readily identified as discrete units.

Metaphase chromosomes usually appear as thick fibers in which centromeres, but few other structural features, can be recognized. A major advance in analyzing chromosome structure emerged when techniques that produced differential staining showed metaphase chromosomes to have a characteristic pattern of alternating transverse bands (for review see Sumner, 1982). For example, staining with Giemsa dye after protein denaturation showed intensely stained bands (Giemsa dark) to alternate with pale staining (Giemsa light) bands along the chromosome length. Interestingly, the banding patterns produced by different techniques are related to each other (Bickmore and Sumner, 1989; Sumner, 1990). The banding patterns have been widely used to detect translocations and other chromosomal abnormalities in clinical cytogenetics, although insight into the structural basis for the banding has only recently emerged (Saitoh and Laemmli, 1994). According to this model, the light and dark bands, which differ in their content of AT base pairs, are reported to result from a differential folding path of the AT rich scaffold associated regions (SARs)¹ along the length of the chromosomes (Saitoh and Laemmli, 1994). Most widely expressed housekeeping genes in human cells map to the Giemsa light bands, suggesting that the banded structure is of functional significance (Holmquist, 1992; Craig and Bickmore, 1993). There is also a strong correlation between the presence of DNA in light or dark bands and the timing of its replication during S phase. Thus, most late replicating DNA occurs in dark bands, while most early replicating DNA occurs in light bands (for review see Bickmore and Sumner, 1989; Holmquist et al., 1982; Holmquist, 1992; Craig and Bickmore, 1993).

There is considerable evidence that a protein scaffold (Laemmli et al., 1977; Paulson and Laemmli, 1977) plays an important role in the organization of higher order chromosome structure (for review see Gasser and Laemmli, 1987; Saitoh et al., 1995; see also Bickmore and Oghene, 1996). In mammalian metaphase chromosomes, the scaffold defines the unit of higher order organization with chromatin arranged in tandem loops of ~50-100-kb pairs attached at their base to the protein scaffold. The scaffold interacts with chromatin at SARs also referred to as matrix attachment regions, MARs (for review see Gasser et al., 1989; Laemmli et al., 1992). Recently, SARs were shown to play a critical role in shape determination and maintenance of metaphase chromosomes (Strick and Laemmli, 1995). MARs (SARs) were also shown to bind to the nuclear scaffold (Mirkovitch et al., 1984), a substructure of complex and poorly defined composition believed to organize the chromatin in looped domains during interphase (for review see Jackson, 1991). At least two scaffold proteins have been characterized, called ScI and ScII. ScI, the major scaffold protein (Lewis and Laemmli, 1982), was later identified as topoisomerase II (Earnshaw and Heck, 1985; Gasser et al., 1986). More recently, ScII was cloned and sequenced and both ScI and ScII were shown to colocalize with the scaffold along the chromosome axis (Saitoh et al., 1994). An important issue for future studies will be to determine how the scaffold organization seen in metaphase relates to chromosome organization in interphase nuclei. We note that alternative models of chromosome organization, where chromatin compaction is achieved through successive levels of helical coiling (helical coiling models) have also been proposed (for example see Sedat and Manuelidis, 1978; Belmont et al., 1987; for review see Earnshaw, 1988).

In most cells, the compact structure of metaphase chromosomes decondenses during telophase, and in interphase it becomes difficult to distinguish individual chromosomes. Much of the data on chromosome structure in the interphase nucleus has come from studies on insect cells, particularly the polytene nuclei of salivary gland cells. This has shown that the chromosomes are folded in the nucleoplasm with focal attachments to the nuclear periphery (Agard and Sedat, 1983; Mathog et al., 1984; Hochstrasser et al., 1986; Hochstrasser and Sedat, 1987a, 1997b; for review see Hochstrasser et al., 1988). In some cases, chromosomes adopt a so-called Rabl configuration, with centromeres at one pole of the nucleus and telomeres at the other (Comings, 1980). A major advance in analyzing chromosome organization in mammalian cells has come with the recent development of fluorescence in situ hybridization methods, using both gene- and chromosome-specific probes (see for example Cremer et al., 1993; Lawrence et al., 1993). Using fluorescence in situ hybridization techniques, individual genes in the interphase nucleus are identified as foci with no obvious linkage between separate alleles. Analysis of entire chromosomes using chromosome-specific painting probes shows little or no overlap between separate chromosomes. Individual chromosomes appear to occupy defined territories but have irregular shapes and the homologues are not associated throughout interphase (for an overview, see Cremer et al., 1993 and references therein). It remains unclear whether the relative positions between different chromosomes is strictly specified or results from a more random assortment process (for example, Manuelidis, 1984, 1990; Nagele et al., 1995). It is also unclear whether all chromosomes in a given cell interact with the nuclear periphery or whether specific chromosomes selectively occupy defined positions in the nucleoplasm. Although it has been shown that certain chromosome regions, including telomeres and centromeres, can cluster at the nuclear periphery (for review see Spector, 1993 and references therein), it is not known whether other chromosome regions in mammalian nuclei specifically interact with the nuclear periphery. Another important question is to what extent the banded structure of mammalian metaphase chromosomes is reflected in their organization during interphase. The basic question of whether interphase chromosomes are ordered structures with specific sequences lying at particular sites (Cremer et al., 1993; Kurz et al., 1996), or conversely whether the folding of chromatin is a random event (Sachs et al., 1995), remains largely unanswered.

In this work, we have used a replication labeling method to follow the higher order organization of chromosomes in chinese hamster fibroblasts between metaphase and interphase. This approach has allowed us to follow the fate of specific collections of DNA sequences that replicate in a defined order during S phase. The data suggest a model for the organization of DNA in the mammalian cell nucleus based on the structure of interphase chromosomes.

Materials and Methods

Chemicals and Antibodies

Actinomycin D, 5,6-dichlorobenzimidazole riboside (DRB), emetine, a-amanitin, colcemid, nocodazole, 5-bromouridine-5-triphosphate (BrUTP), 5-chloro-2-deoxyuridine (CldU), 5-iodo-2-deoxyuridine (IdU), and 1,4-diazabicyclo(2.2.2)octane (DABCO), were purchased from Sigma Chemical Co. (St. Louis, MO). 5-bromo-2-deoxyuridine (BrdU) was obtained from Boehringer Mannheim (Mannheim, Germany). Three different commercially available monoclonal antibodies against BrdU were used in this study: mouse mAb (clone BMC 9318; Boehringer Mannheim); mouse mAb (clone B-44; Becton-Dickinson & Co., Mountain View, CA); rat mAb (clone BU 1/75, ICR 1; Harlan Sera-Lab, Ltd., Sussex, England). Rabbit polyclonal antiserum against lamin B (Drouin et al., 1991) was kindly given by S. Georgatos (European Molecular Biology Laboratory, Heidelberg, Germany); human anti-DNA (ref. L 70) and anti-kinetochore (refs. A76, A89 and A 188) autoimmune antisera were a kind gift of W. van Venrooij (Katholieke Universiteit, Nijmegen, The Netherlands); mouse mAb anti-hnRNP A1 protein (mAb 4B10) was a kind gift of G. Dreyfuss (University of Pennsylvania, Philadelphia, PA). FITC and Texas red-conjugated affinity purified secondary antibodies were purchased from Jackson ImmunoResearch Laboratories (West Grove, PA). Tissue culture reagents were supplied by GIBCO BRL (Gaithersburg, MD).

Cell Culture and Cell Synchronization

Diploid Chinese hamster fibroblasts (CHF; CCL-39 cells from American Type Culture Collection (ATCC), Rockville, MD, established from the lung of female Chinese hamster; chromosome number: 2n = 22) were cultured in DME supplemented with 2 mM glutamine, antibiotics (penicillin 100 µg/ml and streptomycin 100 µg/ml), and 10% FCS and maintained at 37°C with an atmosphere of 5% CO₂. To obtain cells at defined stages of S phase, the culture medium was supplemented with 20 mM Hepes, pH 7.4. IM-9 cells (CCL-159 cells from ATCC, a human lymphoblastic cell line; chromosome number: 2n = 46) and PtK2 cells (CCL-56 cells from ATCC, a marsupial epithelial cell line; 2n = 13) were cultured in RPMI-1640 medium supplemented with glutamine, antibiotics, and FCS as above.

For the synchronization of CHF cells at the G1/S border of the cell cycle, we routinely used two protocols. When protocol 1 was followed, mitotic cells were obtained from logarithmically growing cultures by mechanical shakeoff. Controls showed that this method isolated at least 95% of mitotic cells as judged by both phase contrast microscopy and staining with Hoechst 33342 (0.5-1 mM). The mitotic cells were centrifuged (700 g, 5 min), resuspended in culture medium, and replated at ~60% confluency. Hydroxyurea was then added to a final concentration of 1.5-2.0 mM. After 8-10 h of incubation, cells were released into fresh culture medium. Synchronization protocol 2 differs from protocol 1 only in that an enrichment in mitotic cells was achieved by adding nocodazole (100 ng/ml) to the cell cultures for 4 -5 h before mechanical shakeoff.

Synchronization of IM-9 cells was achieved using the double thymidine block as described (Johnson et al., 1993).

Incorporation of Halogenated Deoxynucleosides into Replicating DNA

Halogenated deoxynucleosides were added to exponentially growing cells to final concentrations of 5 or 10 µM for BrdU, 5 µM for CldU, and 2.5 µM for IdU. All manipulations were performed under minimal light.

Replication Pattern Progression. CHF cells growing on glass coverslips were synchronized as described above (protocol 1). After hydroxyurea removal (time point zero), the cells were pulse labeled for 25-30 min with BrdU (5 µM) before collection at hourly intervals. As a control experiment, BrdU was added for 20 min just before hydroxyurea release. Analyses were only performed on cells where the controls showed zero BrdU incorporation.

Labeling of DNA Sequences Replicating at Defined Stages of S Phase. To obtain CHF cell populations highly enriched for either replication patterns 1, 2, or 3, synchronized cells were pulse labeled with BrdU (10 µM final concentration, 15 min) beginning at 0-30 min (pattern 1), 80-90 min (pattern 2), or 150-160 min (pattern 3) after release from the hydroxyurea block. 7-8 h after entry into S phase, nocodazole was added for an additional 1-2 h to arrest cells in mitosis. To evaluate the percentage of cells labeled for a given pattern control, coverslips were removed at the end of the pulse and immediately fixed. Unsynchronized cell populations were used to specifically obtain cells that were labeled at either stages 4 or 5 of S phase. Stage 4 cells were obtained by pulse labeling the cultures with BrdU (10 µM, 15 min), followed by release in BrdU-free medium for 3.5-4 h. Nocodazole was then added for 40-60 min before harvesting mitotic cells. Cells at stage 5 were selected by adding BrdU (10 µM) to the cultures for 2.5 h. Without removing the BrdU-containing medium, nocodazole was added for an additional 40-60 min. Nocodazole-arrested mitotic cells were harvested by the mitotic "shake-off" method, as described. To control for the specificity of labeling of cells at either stage 4 or 5 (or 4 plus 5, see below), ~50% of the mitotics were replated back into culture and analyzed at different time points for up to 10 h. Only experiments where controls showed at least 80% of a given replication pattern were considered for further analysis.

Other Labeling Experiments. To follow the spatial distribution of late replicating chromatin in CHF cells during telophase and early G1, asynchronous cell populations were pulse labeled with BrdU (5 µM) for 20 min. After release into fresh culture medium (time point zero), the cells were harvested at hourly intervals. Only the first telophase/early G1 cells to appear labeled (i.e., at 2 and 3 h after BrdU release) were used for this purpose.

Quantitation of Labeling Patterns. We analyzed 50 or more nuclei for each of the five replication patterns, randomly selected from an asynchronous cell population pulse labeled with BrdU (10 µM final concentration, 30 min). For each nucleus, two coplanar equitorial confocal sections were obtained under standardized conditions. One image was from whole DNA immunostaining (anti-DNA antiserum) and the other from BrdU-DNA immunolabeling. The former was used to automatically select the nuclear boundary and the latter to select BrdU signal threshold (National Institutes of Health [NIH] Image 1.55 software). The proportion between the area occupied by the signal in the inner 80% of the nuclear profile and the total area of the signal was calculated and averages for each group (i.e., for each replication pattern) were compared using analysis of variance (ANOVA) followed by Scheffe's multicomparison tests. For the purposes of the present study, the inner 80% of the area of an equatorial nuclear profile will correspond to the internal compartment, whereas the outer rim, comprising the remaining 20% of this area, which runs parallel to the nuclear boundary, will be referred to as the peripheral compartment. We note that the inner 80% of the nuclear profile area corresponds to a normalized radius of 89.44% and, in volumetric terms, to 71.55% of the nuclear volume. Student's t test was used to compare, for each replication pattern, the actual proportion of the BrdU signal found in the internal compartment with the proportion expected for an homogeneous distribution of the signal.

Drug Treatments

CHF cells labeled for peripheral (late replicating) chromatin (see above) were replated at ~40-50% confluency in the presence of one of the following drugs: actinomycin D (10 µg/ml), DRB (150 µM), or emetine (40 µg/ml). Cells were then collected at 30 min and at 1, 3, and 6 h after replating. In control experiments, only drug solvents were added.

Immunolabeling Procedures

Cells growing on coverslips were fixed/extracted in 2.4% paraformaldehyde in HPEM buffer (30 mM Hepes, 65 mM Pipes, 10 mM EGTA, 2 mM MgCl₂, pH 6.9) plus 0.5% Triton X-100 for 15 min at room temperature; the cells were then washed in PBS containing 0.05% Tween 20 (PBS-Tw) 3 × 10 min and either immediately used or kept at 4°C in the dark for a maximum of 3 d. In some experiments, the cells were fixed in 70% ethanol, 50 mM glycine, pH 2.0, for 20-30 min at 20°C or fixed in 2% formaldehyde in PBS, pH 7.4 for 15 min at room temperature and permeabilized with 0.2% Triton X-100 in PBS for 5 min at 4°C (O'Keefe et al., 1992).

BrdU-, CldU- or IdU-substituted DNA was denatured with 4 N HCl for 30 min at room temperature (O'Keefe et al., 1992) before immunolabeling. Less frequently, a nuclease-based detection sustem (cat. no. 1296736; Boehringer Mannheim) was used according to the instructions of the manufacturer. Chromosomes from metaphase spreads were denatured by incubation for 90 s in a mixture (2:5) of ethanol/0.1 M NaOH (Latos-Bielenska et al., 1987). Detection of substituted DNA was performed by indirect immunofluorescence. In double-labeling experiments with an anti- BrdU monoclonal antibody and antisera directed against other nuclear antigens (lamin B, DNA, or kinetochore antigens), detection of the halogenated deoxynucleoside preceded in general the labeling of the other antigen. Differential immunolabeling of CldU-DNA and IdU-DNA was performed essentially as described (Aten et al., 1994).

Where appropriate, total DNA was stained with either DAPI or YOYO as described (Saitoh and Laemmli, 1994). For microscopical analysis, the samples were mounted in PBS/glycerol (2:1) containing 10% DABCO as an antifading agent.

Microscopy and Image Analysis

For conventional microscopy, the samples were analyzed using 63 or 100× objectives on an Axiophot microscope (Carl Zeiss, Inc., Thornwood, NY) equipped with epifluorescence. Photographs were taken on Fujichrome 100 color film (Fuji Photo Film Co., Tokyo, Japan). Confocal microscopy was performed essentially as described (Ferreira et al., 1994) using the EMBL compact confocal microscope (Stelzer et al., 1991). Images were then transferred to a Macintosh personal computer and analyzed using standard software tools (NIH Image 1.5.4 and Adobe Photoshop 3.0). For three-dimensional (3D) reconstruction, serial optical sections were taken at 0.33-0.4-mm intervals. Series of confocal planes were analyzed using a new program, MacInsight, to optimize the processing of 3D information. 3D data sets were visualized and edited in the program (changes in levels were used to compensate for weak or unbalanced signals in the respective channels) and projected on the two-dimensional plane using a volume tracing algorithm. Lamin-stained voxels opacity was reduced to render the nuclear envelope semitransparent and allow visualization of internal nuclear structures.

Other Methods

Metaphase spreads were prepared as described (Earnshaw et al., 1989). To obtain nuclei with a small number of intact chromosomes, cells were induced to micronucleate with colcemid (0.5-1.0 µg/ml; Frackowiak et al., 1986; Geraud et al., 1989). To detect transcriptional activity in micronucleated cells, microinjection of Br-UTP, -amanitin controls and detection of Br-RNA were performed essentially as described (Jackson et al., 1993; Wansink et al., 1993). Poly(A) RNA was detected by in situ hybridization as previously described (Ferreira et al., 1994) using a biotinylated 2-O-methyl oligoribonucleotide probe (Sproat et al., 1989) containing 20 tandem uridine residues.

Results

Progression of Replication Patterns in Chinese Hamster Fibroblasts

A synchronized population of chinese hamster fibroblasts was prepared by collecting mitotic cells, which were then arrested at the G1/S transition by incubation in medium containing hydroxyurea (see Materials and Methods). To examine the patterns of replicating DNA at different stages of S phase, CHF cells were released from the hydroxyurea block and pulse labeled with bromodeoxyuridine (BrdU) at hourly intervals. Distinct replication patterns were observed that can be conveniently classified in five distinct stages (Fig. 1). During stages 1 and 2, predominantly internal DNA sequences are replicated forming a complex pattern comprising multiple nucleoplasmic foci. Stage 2 is distinguished from stage 1 by the more clumped appearance of the nucleoplasmic foci. At stage 3, fewer nucleoplasmic foci are observed, often located around the nucleolus, and extensive labeling of the nuclear periphery is evident. A striking feature of the late stages of replication (i.e., stages 4 and 5) is the predominant location of labeled DNA at the nuclear periphery (Fig. 1). Almost continuous labeling of the periphery is observed at stage 4, whereas at stage 5 the peripheral labeling is discontinuous.

The number of pulse-labeled cells displaying each of the five patterns was evaluated at each time point (Fig. 2 A). This shows a clear temporal separation between the early (stages 1 and 2) and late (stages 4 and 5) patterns. In contrast, the intermediate pattern (stage 3) overlaps extensively with both early and late stages and is consequently more difficult to characterize. Pulse labeling of asynchronously growing CHF cells with BrdU showed that ~40% of the labeled cells had a late pattern, 40% an early pattern, and 20% an intermediate pattern.

The proportion of the total fluorescence signal occupying the internal nucleoplasmic volume (i.e., the internal 71.55% of the nuclear volume; refer to Materials and Methods) was quantified from 50 or more nuclei at each of the five stages (Fig. 2 B). This shows that >80% of the signal is internal during stages 1 and 2, while only 7-12% is internal during stages 4 and 5. We conclude that there is a strong correlation between the localization of DNA and the timing of its replication within CHF nuclei.

Correlation between Replication Patterns and Chromosome Banding

We next examined which chromosome regions contributed DNA sequences to the subnuclear compartments revealed by the time-of replication experiments (Fig 3). CHF cells were pulse labeled with BrdU at defined time points during S phase, such that five populations were obtained, highly enriched, for each of the five separate replication patterns (refer to Materials and Methods for experimental details). Metaphase spreads were prepared from each population after nocodazole arrest of the cells in the subsequent mitosis (Fig. 3).

Metaphase spreads from cells labeled at stages 1- 4 all showed a banded BrdU labeling pattern extending throughout each chromosome (Fig. 3, Stages 1- 4, and other data not shown). The BrdU banding pattern was also compared with DAPI labeling of the same chromosomes. For Stages 1 and 2, the most prominent BrdU bands correspond to R bands, which stain less strongly with DAPI (Fig. 3, Stages 1 and 2, large arrowheads). Some prominent R bands that incorporated BrdU during stage 1 may not appear labeled with BrdU during stage 2 (Fig. 3, Stage 2, small arrowheads and data not shown). We note that some bands stained strongly with DAPI (Q bands) were also labeled with BrdU in Stages 1 and 2. For Stages 3 and 4, the most prominent bands labeled with BrdU were the strongly DAPI stained Q bands (Fig. 3, Stages 3 and 4, large arrowheads). Stage 3 appears to mark a transition from having most BrdU label in DAPI pale bands (R bands) to having most BrdU label in DAPI bright bands (Q bands). At Stages 3 and 4, some BrdU incorporation was detected in the DAPI pale R bands. Since these chromosomes have a low resolution of banding obtained after nocodazole arrest, the finding of a subset of early replicating sequences (Stages 1 and 2) in Q band regions and a subset of late replicating sequences (Stage 4) in R band regions is not surprising and may arise through the progressive chromosome compaction that occurs between prophase and metaphase (Drouin et al., 1991). Chromosomes from cells labeled in Stage 5 show fewer BrdU bands than seen for Stages 1-4 and these bands are predominantly DAPI bright (Q) bands dispersed throughout the chromosomes (Fig. 3, Stage 5). The number of chromosomes labeled in each metaphase plate was highly variable for stage 5, consistent with the variable BrdU labeling intensity seen in interphase nuclei at stage 5, and likely due to the progressive shut-off of DNA replication at the end of S phase.

The previous results indicate that the peripheral compartment that replicates essentially (but not exclusively) during stages 4 and 5 is contributed by an extensive banded pattern present in every metaphase chromosome in CHF cells (Fig. 3 for Stage 4, larger panels). This finding is better demonstrated in metaphase spreads from cells that continuously incorporated BrdU during stages 4 and 5 of S phase (Fig. 4 C). In some of these stage 4 plus 5 experiments, while a fraction of the mitotics was used to obtain metaphase spreads, another fraction was replated into fresh BrdU-free culture medium. These cells progressed parasynchronously into the next cell cycle and harvesting at regular intervals showed that the BrdU-labeled chromatin remained peripheral during G1 and S phase (data not shown). Progression of these cells through G1 and reentry into S phase was judged in parallel immunostainings with an anti-PCNA antibody and checking for the emergence of replication-like patterns (Bravo and MacDonald-Bravo, 1987; Kill et al., 1991).

The difference in the banding pattern of early and late replicating DNA is illustrated by differential labeling of early (stages 1 plus 2) and late (stages 4 plus 5) replicating DNA using pulses of iododeoxyuridine (IdU) and chlorodeoxyuridine (CldU), respectively (Fig. 4, A and B). Parallel control experiments confirm the specificity of detecting incorporation of IdU and CldU (Fig. 4, D-F). These experiments show that early and late replicating DNA form distinct bands in an intercalated pattern extending along the metaphase chromosomes. At least for these sequences, accounting for ~80% of the total DNA content, the separate metaphase bands predominantly congregate during interphase into separate subnuclear compartments.

The Peripheral Compartment Is a Major Compartment in Other Cell Types

Having established that in CHF cells the peripheral compartment is a major one contributed extensively by most (or all) chromosomes, we next addressed whether a similar situation was observed in other cell types. We found that PtK2 cells pulse labeled with BrdU displayed spatial configurations of DNA replication similar to those seen in CHF cells (Fig. 5). In particular, one of the patterns (pattern C) shows replicating DNA concentrated at the nuclear periphery resembling pattern 4 of CHF cells (compare Fig. 5 C with Fig. 1 D). Quantitative analysis of the total fluorescence signal occupying the internal nucleoplasmic volume was performed in 44 nuclei that had a stage C pattern. This showed that only 5.37% of the signal was internal (SD, 0.0516). In PtK cells, it proved difficult to synchronize the temporal order of the replication patterns. The order of patterns was thus established by pulse labeling asynchronous cultures of PtK cells with CldU followed 3, 4, or 5 h later by a second pulse with IdU (Fig. 5, E and F, and data not shown). Using this approach, we could assign pattern C the third position among the four replication patterns seen in PtK cells. Pulse labeling of asynchronously growing cells with BrdU showed that this pattern accounted for ~30% of the labeled cells, indicating that stage C lasted for ~3 h (total S phase duration ~10 h as estimated from a standard cell cycle curve; Mitchison, 1971). To determine whether most chromosomes contributed to this long-lasting peripheral pattern, we pulse labeled asynchronously growing PtK cells with BrdU (10 µM; 30 min), and then estimated the proportion of stage C cells among the BrdU-labeled population at hourly intervals. This was done to delineate the time period during which stage C cells undergo mitosis. As these cells reach M phase and escape into the next cell cycle, their proportion will progressively decline in the premitotic group. We note that as the labelled cells emerge in the next cell cycle they appear as doublets with the two daughter cells displaying a similar, mirror-image-like BrdU labelling pattern. For the purposes of this analysis, we have only counted cells appearing as singlets, i.e., that are still in the premitotic group. The distinction between labeled singlets and doublets is easily established in PtK cells, since they have a very low mitotic index with few cells traversing S phase, and is further facilitated by replating the cells at low density (~15-20% confluency). In parallel, we also carefully analyzed the mitotics at each time point to determine the proportion of BrdU labeled vs. unlabeled cells and whether the labelling was present in all chromosomes ("complete" labelling) or in only a fraction of the chromosomes ("partial" labeling). Since PtK cells have a small number of chromosomes (2n = 13) that can be readily visualized as distinct particles during prophase, this stage was chosen for all the observations made on mitotics. The data were used to set up a graph that shows simultaneously the proportions of mitotics with complete chromosome labelling among the total mitotic population and of stage C singlets in the BrdU-labeled premitotic population (Fig. 6). The main result from this approach was that during the time period when stage C cells were undergoing mitosis, as shown by the decline in their proportion, the corresponding chromosomes displayed labelling scattered along their length (Fig. 6, and data not shown).

A- D

We have additionally addressed the same question using a different approach and human lymphoid cells growing in suspension (IM-9 cells). These cells were chosen because of their spherical nuclei, which should minimize geometrical constraints that might otherwise influence the spatial relationship between chromosome territories and the nuclear periphery in flat nuclei. After continuous BrdU labelling for a full S phase, the cells were released into BrdU-free medium and allowed to progress through several cell cycles before harvesting. This will produce cells with a progressively lower number of labelled chromosomes. After several days in culture (~7 d), a fraction of exponentially growing cells was harvested for the analysis of interphase chromosomes. Immediately after harvesting, colchicine was added to the remaining cells and metaphase spreads were prepared 30 min later. These spreads were used to estimate the average number of BrdU-labelled particles per cell. Two independent experiments were performed and for each experiment 50 metaphase plates were examined. In experiment I 84% of the cells had between one and seven particles labeled (average: 5.3 particles per cell) and in experiment II, 78% of the cells had between one and seven particles labeled (average: 5.7 particles per cell). We note that ~80% of the BrdU-labelled particles corresponded to fully labelled chromosomes and the remaining ~20% to partially labelled chromosome segments generated by sister chromatid exchange. For the analysis of interphase chromosomes, 100 cells double immunolabelled for BrdU and lamin B were analyzed per experimental group (Fig. 7). This showed that between ~97 (experiment I; 477 particles analyzed) and ~96% (experiment II; 498 particles analyzed) of the BrdU-labelled particles were in close contact with the peripheral lamina in these human lymphoid cells.

Compartmentalization of DNA in Interphase Is Independent of Chromosome Number

In the experiments described below, we made extensive use of micronucleated cells. Micronuclei originate from individual or small groups of chromosomes after induction of prolonged mitotic arrest (Frackowiak et al., 1986; Geraud et al., 1989). Before using this system in studies of chromatin compartmentalization, we asked whether micronuclei retain the functional characteristics of interphase chromatin. The results show that micronuclei are transcriptionally active as demonstrated by microinjection of bromo-UTP, concentrate an hnRNA binding protein (hnRNP A1) that is imported into the nucleus in a transcription-dependent fashion (Piñol-Roma and Dreyfuss, 1991), accumulate poly (A) RNA, which is known to accumulate in postmitotic nuclei depending on ongoing transcription (Moen et al., 1995) and replicate their DNA as assessed by pulse labelling with BrdU (Fig. 8).

Is the compartmentalization of DNA during interphase acting at the single chromosome level, independent of the number of chromosomes present? To address this question, we examined micronuclei generated from separate populations of CHF cells, enriched for cells pulse labelled with BrdU at each of the five stages of replication (Fig. 9). Treatment of CHF cells with colcemid typically gave rise to daughter cells containing 10-20 micronuclei. Many of the micronuclei contained only one or two chromosomes, as assessed by staining with anticentromere antibodies (data not shown). In every case, all the micronuclei display the same staining pattern as seen in intact cells, regardless of the number of chromosomes present or whether early or late replicating DNA had been labelled (Fig. 9). Furthermore, no micronucleus showed a different segregation pattern to its siblings. This demonstrates that compartmentalization of DNA sequences is independent of chromosome number. We conclude that the information required for segregation is an inherent property of each chromosome.

Interphase Compartmentalization of DNA Is Established during Telophase

To determine at what stage in the cell cycle the interphase compartmentalization of DNA is established, an asynchronous population of CHF cells was labelled with BrdU and analyzed at hourly intervals, with particular attention given to telophase and early G1 cells (Fig. 10). The first labelled cells correspond to those undergoing late replication when BrdU was first added. Typically, the first labelled mitotic cells were seen 2-3 h after the BrdU pulse. At the beginning of telophase, DNA that had been labelled during the late stages of S phase (i.e., replication stages 4 and 5) was not confined to the periphery of the nucleus, although lamin staining could be detected associated with the DNA (Fig. 10 A, stereo pair). At later stages of telophase, specifically at the telophase/G1 transition, the typical late pattern of peripheral nuclear labelling was observed (Fig. 10 B, stereo pair). Similar results were obtained when metaphase cells with BrdU-labelled late replicating chromatin (i.e., stages 4 and 5) were replated and the emerging telophase cells analyzed (data not shown). Addition of either transcription (Actinomycin D or DRB) or protein synthesis inhibitors (emetine) did not prevent segregation of late replicating chromatin to the periphery (data not shown). This indicates that activation of gene expression after mitosis is not required for DNA compartmentalization. We obtained further evidence that the spatial organization of DNA sequences typical of interphase is established during late telophase/G1 in CHF cells also for sequences replicating at other times during S phase. A culture of asynchronously growing cells was pulse labelled with BrdU and the cells collected at hourly intervals. For each time point, we have analyzed late telophase/early G1 cells and checked for the presence of BrdU-labelling patterns. This showed that each of the five patterns typical of CHF cells peaked at defined time points after BrdU release in a temporal order that is the reverse of that seen during S phase (Figs. 11 and 12). Since cells labelled at different stages of S phase reach the next cell cycle in a reversed order (i.e., late stages first), these results indicate that sequences replicating at other times during S phase also compartmentalize during late telophase/early G1.

Discussion

In this study, we have used a pulse-labelling protocol at defined stages of S phase to analyze the organization of large scale chromatin domains. In both CHF and PtK cells, we observe a similar close correlation between the spatial organization of chromatin domains and the timing of their replication during S phase. In mitosis, all metaphase chromosomes show a pattern of intercalated early and late replicating DNA bands extending along their entire length. During late telophase, most, if not all, of these DNA bands become compartmentalized, with multiple chromatin domains from each chromosome separating into two principal nuclear compartments; i.e., the peripheral and internal nucleoplasmic compartments. The peripheral compartment predominantly contains late replicating G/Q bands, whereas the internal compartment predominantly contains early replicating R bands. These data thus show a correlation between the G/Q banding pattern of metaphase chromosomes and the subsequent separation of these chromosome bands between distinct nuclear compartments during interphase.

The present analysis of chromatin organization involves experiments requiring nuclear permeabilization and DNA denaturation steps. Although we cannot formally exclude that the DNA denaturation or other experimental techniques used in our analyses have induced some rearrangement of chromatin, we consider it most unlikely that this has had any significant influence on the results presented. We observe similar results when alternative protocols were used to avoid acidic denaturation of DNA and when permeabilization followed fixation (for a detailed discussion of the effects of fixation and permeabilization procedures on higher order chromatin structure, see Belmont et al., 1989).

One of the main conclusions from this study is that DNA compartmentalization is a phenomenon acting at the level of individual chromosomes and is independent of the total number of chromosomes present in the nucleus. This conclusion stems largely from the analysis of micronucleated CHF cells, which exhibit many typical features of intact interphase cells, including transcriptional activity, replication, and progression through the cell cycle. Correct separation of late replicating DNA to the nuclear periphery and early replicating DNA to the internal nucleoplasm was always observed, regardless of chromosome number, even in micronuclei containing only a single chromosome. In every case, the micronuclei resembled Lilliputian replicas of the whole nuclei from which they were derived. Clearly, chromosomes in CHF cells are not organized like "marbles in a bag," with some exclusively located at either the nuclear periphery or within the nucleoplasm, and they also do not show the Rabl orientation seen in insect nuclei (for example see Comings, 1980; Marshall et al., 1996). Instead, most chromosomes contribute multiple regions to both the peripheral and internal nucleoplasmic compartments. Our analyses here of marsupial kidney epithelial and human lymphoid cells also strongly support this notion.

We propose that the higher order organization of most DNA in CHF nuclei is best described by an autonomous chromosome compartment model. A key feature of the compartment model is that multiple regions from each chromosome reassort during interphase to cluster in a common subnuclear location. The CHF cells provide a particularly clear example of chromosome compartmentalization, with most DNA sequences partitioning between the two major compartments; i.e., peripheral and internal nucleoplasmic. PtK cells, although less extensively studied due to difficulties in obtaining finely synchronized populations, also have a prominent peripheral compartment contributed by most chromosomes. It should be noted, however, that at least one other minor chromatin region (i.e., nucleolar peripheral) is seen at stage 3 of replication, although in CHF cells this contains a small proportion of the total DNA. There is evidence that chromosomes that do not contain rDNA may also contribute to this chromatin region at least through their centromeres (Pluta et al., 1995; Carmo-Fonseca et al., 1996), but whether all chromosomes contribute DNA to the perinucleolar chromatin region remains to be determined. In other cell types, the number of compartments may vary, as may the proportion of total DNA in each. Previous labelling studies in other mammalian cell lines have shown a degree of separation of early and late replicating sequences during interphase, with clusters of late replicating sequences sometimes present in the nucleoplasm as well as at the nuclear periphery (Nakamura et al., 1986; Nakayasu and Berezney, 1989; Fox et al., 1991; Kill et al., 1991; O'Keefe et al., 1992; Hozák et al., 1994). Although less dramatic than in CHF cells, clear spatial separation between significant amounts of early and late replicating DNA is evident in these cell types. This is consistent with the chromosome compartment model, although it does not exclude that different modes of chromosome organization may also occur in other cell types. For example, in vitro studies using synchronously replicating Xenopus sperm nuclei showed that incorporation of labelled nucleotides occurred at several hundred evenly spaced foci and showed no preferential association with the nuclear membrane (Mills et al., 1989). Comparing the data from Diptera and CHF cells, it is clear that there can be differences in how cells organize chromatin in the nucleus. In the future, it will be interesting to extend these analyses to compare other cell types, including plant and insect cells as well as other mammalian cell types, which will help to determine the generality of the autonomous chromosome compartment model.

What is the mechanism that promotes the segregation of DNA into compartments? Since the pattern is established before G1, it is clear that the process of replication itself cannot be primarily responsible. The interphase pattern is not dependent upon activation of gene expression in daughter nuclei, since it is correctly established in the presence of transcription or translation inhibitors. Thus, it is not an indirect effect of differential DNA transcription, causing some sequences to be pushed out to the periphery. It is interesting that at early stages of telophase, when late replicating DNA sequences have not yet moved to the nuclear periphery, extensive lamin staining on the DNA is evident (see Fig. 10). Although most of these internal projections of lamin staining are resolved by late telophase/ early G1 (see Fig. 10), some may persist throughout interphase and remain associated with the minor fraction of internally located late replicating DNA during stages 4 and 5 (data not shown). These projections may correspond to tubular invaginations of the nuclear envelope that associate with lamins (Fricker et al., 1997, and references therein). The binding of lamins, or lamina-associated polypeptides (Gerace and Foisner, 1994), to specific chromosomal regions may play a role in establishing compartments. Consistent with this idea, B type lamin foci bind to late replicating DNA sequences in mouse 3T3 cells (Moir et al., 1994). In addition, there is also biochemical evidence for the binding of lamins and lamina-associated polypeptides to chromatin and associated proteins (Hoger et al., 1991; Yuan et al., 1991; Taniura et al., 1995; Pyrpasopoulou et al., 1996). The direct binding of lamin B1 to DNA, via SARs, was also reported (Luderus et al., 1992). There also appears to be a close structural association of the lamina with chromatin (see Belmont et al., 1993, and references therein) possibly involving discrete chromosomal regions (Hochstrasser and Sedat, 1987; Paddy et al., 1990; Belmont et al., 1993; Marshall et al., 1996). The binding of one of the lamina-associated polypeptides, termed LBR (lamin B receptor), to the heterochromatin-specific protein HP-1 (Ye and Worman, 1996) and to native chromatin fragments (Pyrpasopoulou et al., 1996) was recently reported. Importantly, the binding of purified LBR to intact chromosomes is not homogeneous, but rather follows a distinctive banding pattern present throughout the chromosomes that is reminiscent of Q banding (Pyrpasopoulou et al., 1996). These results are in good agreement with our finding that the peripheral/lamina-facing compartment is extensively represented in the Q bands of most chromosomes. Clearly, more experiments are needed to resolve whether this binding has implications in the compartmentalization of large scale chromatin domains during interphase. Our results show that the interphase compartmentalization of chromatin may occur in single chromosomes independently of physical interactions with other chromosomes (micronucleation experiments) and in the absence of ongoing transcriptional activity. The autonomous feature of the model does not, however, exclude that chromosomes may influence the chromatin organization of each other through their gene products, e.g., long-lived proteins that can withstand short-term protein synthesis inhibition. The nuclear lamins and lamina-associated polypeptides are well positioned to play this role since these molecules are recycled in subsequent cell cycles (for review see Georgatos et al., 1994; Marshall and Wilson, 1997).

We note that an important role for the nuclear periphery, involving either the nuclear lamina, the nuclear pores, or both, in the 3D organization of the genome has previously been discussed (Blobel, 1985; Gerace, 1985).

CHF cells segregate most of their DNA into two major compartments during interphase. It will be important now to analyze exactly which DNA sequences are present in each compartment and to understand what significance this may have for the organization of genes and relevant nongene sequences. For example, preferential assortment of specific genes within the nucleus (see for example Lawrence et al., 1993), of centromeric sequences to the nuclear or nucleolar periphery (Pluta et al., 1995), of telomeric repeats to the close proximity of the nuclear envelope in some cell types (Rawlins et al., 1991), or to the internal nucleoplasm in human cells (where telomeres correspond mostly to R bands; Ludérus et al., 1996) and the recent finding that some genes occupy a preferential position in their chromosome territory (Kurz et al., 1996) might reflect the compartmental organization of chromosomes.

Another important question is whether the compartments might be to some extent functionally distinct. The fact that they contain DNA sequences that are replicated at different times during S phase is consistent with the idea that DNA binding factors are differentially distributed between them. Future studies will therefore address the possible relation between gene expression and DNA compartments.

Footnotes

Received for publication 21 August 1997 and in revised form 17 October 1997.

The authors are grateful to R. Saffrich for help with the microinjection experiments. We also thank our colleagues M. Carmo-Fonseca, I. Mattaj, F. Stewart, K. Weis, K. Bohmann, E. Izaurralde, J. Lewis, and C. Lyon for helpful comments on the manuscript. T. Cremer and P. Lichter are also thanked for helpful suggestions. We also thank the following laboratories for generously providing antibodies used in this study: W. van Venrooij for human autoimmune antibodies against kinetochore antigens and DNA, G. Dreyfuss for the 4B10 monoclonal antibody, and S. Georgatos for the rabbit polyclonal antibody against lamin B.

Abbreviations used in this paper

3D; three-dimensional CHF, chinese hamster fibroblast; PtK, marsupial kidney epithelial; SAR, scaffold associated region.

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