Changes in the organization of the genome during the mammalian cell cycle
© BioMed Central Ltd 2013
Published: 24 December 2013
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© BioMed Central Ltd 2013
Published: 24 December 2013
By using chromosome conformation capture technology, a recent study has revealed two alternative three-dimensional folding states of the human genome during the cell cycle.
Understanding the spatial organization of chromosomes represents a major quest, not only for our comprehension of how a length of 2 m of DNA can be packaged into a nucleus of just a few microns, but also because the physical interactions occurring within and between chromosomes are thought to play an important role in gene regulation, DNA replication and genome stability. Over recent years, the development of chromosome conformation capture (3C)-based techniques, together with the emergence of next-generation sequencing, have changed our view of nuclear organization. High-throughput conformation capture techniques have been developed to study the physical interactions of the chromatin fiber with or within genomic regions spanning from a few megabases (5C technique) to a whole-genome scale (4C and Hi-C techniques). In 2009, Eric Lander, Job Dekker and colleagues  described the first human chromosomal architecture at a resolution of 1 Mb. Then, four years later, owing to the rapid evolution of sequencing capabilities, Bing Ren and colleagues  published a high-resolution map of the ‘chromatin interactome’ in human fibroblasts at a resolution of 5 to 10 kb.
Despite the pace at which new details of mammalian chromosome organization are accumulating, many fundamental questions remain unanswered. For example, what is the cell-to-cell variability in the structures that give rise to compartments, TADs and promoter-enhancer interactions? How important is each of those structural layers for the regulation of transcription? What are the molecular mechanisms that determine the appearance of TADs and compartments? When are these layers established during development? Are these different levels of chromosome organization present throughout the cell cycle, or are they established at a particular phase? Finally, what is the structure of mitotic chromosomes? Are the hierarchical layers of folding maintained during mitosis, or do chromosomes acquire a different organization, as suggested by light and electron microscopy? A recent exciting study has shed light on these last questions .
Although DNA fluorescence in situ hybridization (FISH) coupled to super-resolution microscopy has previously been used in murine cells to investigate the presence of TADs within the X-inactivation center during the cell cycle from G1/S phase to mitotic prophase , a detailed molecular analysis of chromatin interactions throughout the cell cycle had not, until recently, been reported. Dekker and colleagues  now report the results of performing carbon-copy chromosome conformation capture (5C) and Hi-C experiments in synchronized human HeLa cells at different phases of the cell cycle. Using 5C technology spanning the whole of chromosome 21 at a resolution of 250 kb, the authors first studied the long-range chromatin interactions of early G1-, mid-G1-, S- and M-phase cells. Interaction maps of these different stages showed that the mitotic interaction pattern differs dramatically from that at all other stages, thus revealing two distinct chromosome folding states during the cell cycle. Using Hi-C (at a resolution of 40 kb) on mitotic and mid-G1-stage cells , the investigators further found that both compartments  and TADs [3, 4] appear to be absent throughout the entire genome in metaphase, becoming detectable only in early G1 phase and remaining unchanged throughout interphase. These observations on mitotic chromosomes were repeated and validated in another cell line and in primary human fibroblasts. Importantly, the authors showed that, apart from metaphase, compartments and TADs are not restricted to any specific cell cycle phase and they are easily detected in early G1, thus ruling out the possibility that the patterns observed in 5C or Hi-C could be due to a superposition of alternative cell-cycle phase-specific conformations.
The finding that TADs and compartments apparently disappear during metaphase, and reappear in early G1, raises the questions of why they are lost and also what mechanism ensures their prompt re-establishment upon exit from mitosis. It is known that certain transcription factors and histone modifications or associated factors can act as ‘bookmarking’ factors on mitotic chromosomes  by remaining bound to the condensed chromatin polymer in order to ensure the propagation of transcriptional states to daughter cells. It is therefore tempting to speculate that structural bookmarking factors that propagate organizational information to daughter cells might similarly exist. Although the molecular bases of compartments and TADs remain elusive, accumulating evidence suggests that long-range interactions between genomic sites bound by the proteins CTCF and cohesin contribute to the organization of chromatin architecture at the TAD scale, either by associating with TAD boundaries  or by supervising a network of long-range interactions inside single TADs that might stabilize the structure within TADs . Interestingly, both CTCF and cohesin have been shown to associate with mitotic chromosomes , suggesting that mutual interactions between CTCF and/or cohesin binding sites might readily occur upon exit from mitosis, thus enabling TADs to be established immediately at the beginning of G1 phase. Other factors that might remain bound during mitosis to the positions of TAD or compartment boundaries include Polycomb group proteins, which have been shown to significantly overlap with TAD boundaries  on mitotic chromosomes in Drosophila
The apparent loss of partitioning into TADs and compartments observed in mitotic chromosomes by Dekker and colleagues  suggests that they contain unusually few structural details compared with those of their interphase counterparts. However, the authors cleverly exploited the quantitative information present in the Hi-C mitotic chromosome data to build a structural model. The foundation of their approach is that Hi-C or 5C interaction maps represent the frequency at which every pair of genomic loci along the chromatin polymer encounter each other, averaged over millions of cells. It is therefore possible to use models from polymer physics to simulate virtual Hi-C (or 5C) data and compare them with data from experiments. Using such an approach, the thermodynamic ensemble of configurations of a model chromosome can be generated by computer simulations, and a contact map is retrieved by averaging the contacts of each pair of loci over all simulated polymer conformations, allowing a straightforward comparison with experimental data.
In the case of mitotic chromosome data, the Hi-C or 5C contact maps are homogeneous, with no sign of the regular patterning due to TADs and compartments that characterize the interphase contact maps . Dekker and colleagues also noted that the contact probability between two loci gradually decreases with increasing genomic distance (albeit significantly more slowly than on interphase chromosomes), and then suddenly falls off to zero at approximately 10 Mb. This unusual behavior cannot be explained by any simple polymer models. Building on the well-established experimental evidence describing the quantitative properties of mitotic chromosomes (such as cylindrical symmetry, linear organization of chromatids and chromatin packing density), the authors thus set out to build various alternative models for the chromatin organization within mitotic chromosomes, simulated all of them and tested each model’s predictions. In order to reproduce the unexpected fall-off in contact probabilities for loci that are separated by >10 Mb, they had to impose that the chromatin fiber is linearly organized, so that genomic loci belonging to distal parts of the chromosome (that is, separated by >10 Mb) cannot be brought into close spatial proximity. Furthermore, they had to impose that the chromatin fiber is arranged in an array of consecutive loops, each spanning approximately 80 kb, in order for their simulations to account correctly for the gentle decrease in contact frequencies in the genomic length range between 0 and 10 Mb. Thus, amongst all possible models tested, it was this combination of linear organization and consecutive looping that best accounted for the behavior of the contact probability of mitotic chromosomes over all genomic length scales. Interestingly, the authors further discovered that they could simultaneously reproduce the scaling of contact probabilities and the homogeneity of the mitotic contact maps only when they allowed the size of the loops to be different (and stochastic) in each of the polymer configurations.
The study by Dekker and colleagues represents a powerful combination of biochemical investigation and polymer modeling . The prowess of such an approach is that it can provide insights into structure that would not have been obtained without modeling. The picture that emerges, thanks to their study, is that of a mitotic chromosome composed of consecutive loops of chromatin, the size of which is on average 80 kb, although this varies from cell to cell, which are arranged in a linear fashion eventually resulting in an effective cylindrical chromosomal volume (Figure 1, right panel). This picture is both qualitatively and quantitatively in agreement with previously proposed ‘loops-on-a-scaffold’ models of mitotic chromosomes based on microscopy and biochemical assays.
Although the molecular mechanisms that could mediate this pervasive local looping remain elusive, the model predicts that cell-to-cell variability of looping events has a sizeable effect in organizing the structure of mitotic chromatin. Indeed, the potential importance of fluctuations in interphase chromosome structure was also recently revealed by an adaptation of the Hi-C technique to single cells . In the future, this type of single-cell approach, together with physical modeling and quantitative analysis, could allow the exploration of chromosome structure in situations where cell-to-cell variability might be crucial, such as during early development.
Chromosome conformation capture
Circularized chromosome conformation capture
Carbon-copy chromosome conformation capture
High-throughput conformation capture
Topologically associating domain
LG was supported by an EMBO Fellowship (ALTF 1559–2011); work in the lab of EH is supported by the “Ligue Nationale contre le cancer”, the EpiGeneSys FP7 257082 Network of Excellence, ERC Advanced Investigator award 250367 and EU FP7 MODHEP EU grant no. 259743.