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The extent to which the three dimensional organization of the genome contributes to chromosomal translocations is an important question in cancer genomics. We now have generated a high resolution Hi-C spatial organization map of the G1-arrested mouse pro-B cell genome and mapped translocations from target DNA double strand breaks (DSBs) within it via high throughput genome-wide translocation sequencing. RAG endonuclease-cleaved antigen-receptor loci are dominant translocation partners for target DSBs regardless of genomic position, reflecting high frequency DSBs at these loci and their co-localization in a fraction of cells. To directly assess spatial proximity contributions, we normalized genomic DSBs via ionizing-radiation. Under these conditions, translocations were highly enriched in cis along single chromosomes containing target DSBs and within other chromosomes and sub-chromosomal domains in a manner directly related to pre-existing spatial proximity. Our studies reveal the power of combining two high-throughput genomic methods to address long-standing questions in cancer biology.
Recurrent chromosomal translocations are hallmarks of many cancers (Zhang et al., 2010; Gostissa et al., 2011). These translocations often represent rare events in tumor progenitors that are highly selected for contribution to oncogenicity. Thus, since cancer genome studies examine only the final outcome of a multi-step transformation, the complex genomic alterations observed are often difficult to fully interpret (Stratton, 2011). Notably, factors that mechanistically enhance translocations can promote recurrent non-oncogenic translocations in tumors and also promote particular oncogenic translocations (Wang et al., 2009; Gostissa et al., 2009a). Most translocations are formed by end-joining of two DSBs (Stephens et al., 2009). Thus, mechanistic factors that could influence translocations include DSB frequency at translocating loci, factors that promote physical juxtaposition ("synapsis") of DSBs, and factors that circumvent cellular DSB repair pathways that promote normal rejoining (Zhang et al., 2010)
DSBs are major drivers of translocations (Tsai and Lieber, 2010; Chiarle et al., 2011; Klein et al., 2011). Lymphoid malignancies commonly have recurrent translocations involving programmed DSBs in antigen receptor loci as one partner. In developing lymphocytes, such DSBs are introduced into both Immunoglobulin (Ig) and T cell receptor (TCR) loci by the RAG endonuclease during V(D)J recombination.(Schatz and Swanson, 2011). In mature B cells, assembled Ig loci can be broken downstream of activation induced cytidine deaminase (AID) activity during Ig heavy chain (IgH) class switch recombination (CSR) (Liu and Schatz, 2009b). Recurrent antigen receptor locus translocations in lymphoid malignancies reflects both high frequency programmed DSBs within these loci, as well as ability of their powerful enhancers to activate translocated oncogenes (Gostissa et al., 2009b).
Sources of DSBs in non-Ig translocation partners are less well-characterized (Tsai and Lieber, 2010). Mouse studies implicated AID-initiated c-myc DSBs in translocations (Robbiani et al., 2008); and human tumor analyses suggested that collaborations between AID and RAG generate DSBs leading to oncogene translocations (Tsai et al., 2008). High throughput genome wide translocation sequencing ("HTGTS") studies (Chiarle et al., 2011) and studies using a similar approach (Klein et al., 2011) showed that I-SceI DSBs within the IgH or c-myc translocate to other DSBs widely across the genome. In these studies, endogenous translocation hotspots were generated by AID-induced DSBs within off-target genes; while a broader set of genome wide translocations were associated with transcription start sites ("TSSs") (Chiarle et al., 2011; Klein et al., 2011). Beyond transcription, cell intrinsic factors, such as oxidative metabolism, replication stress, or cell extrinsic factors such as ionizing radiation (IR) or chemotherapeutics may generate DSBs (Tsai and Lieber, 2010). In general, DSBs outside of antigen receptor loci, for example in c-myc, are likely rate-limiting for translocations (Wang et al., 2009). In this regard, recurrent translocations in non-lymphoid tumors, for example in myeloid leukemias or prostate cancers, may be driven by oncogenic selection for rare events and/or reflect mechanistic drivers other than DSBs (Kurzrock et al., 2003; Lin et al., 2009; Mani et al., 2009).
Fusion of two DSBs to generate translocations requires their synapsis. Chromosomes occupy distinct nuclear territories (Cremer and Cremer, 2010) and are further organized into open and closed chromatin domains within different nuclear compartments (Gilbert et al., 2004; Lieberman-Aiden et al., 2009). Due to the substantial heterogeneity in spatial genome organization, most transcribed genes co-localize in at least a small subset of cells (Simonis et al., 2006; Lieberman-Aiden et al., 2009). The non-random nuclear position of genes and chromosomes has led to the notion that close spatial proximity of two genomic sequences will promote their preferential translocations (Meaburn et al., 2007). Accordingly, cytogenetic studies showed several genes that contribute to translocations were, on average, in relatively close proximity (e.g. Neves et al., 1999; Roix et al., 2003; Osborne et al., 2007; Wang et al., 2009), and live cell imaging studies showed DSBs to be relatively immobile (Soutoglou et al., 2007). However, analysis of the overall influence of genome organization on translocations requires a comprehensive characterization of 3D genome structure and measurement of the landscape of potential translocations in the same cellular system. We now directly assess the impact of DSB location within the 3D genome on translocation potential by mapping the genome structure of a G1-arrested mouse pro-B cell line with Hi-C and identifying the translocations that form with an induced DSB in these cells.
HTGTS and related studies of translocations in activated mouse B cells revealed enrichment of translocations along chromosome 15 on which the target I-SceI site in c-myc was located, suggesting, among other possibilities, potential effects related to chromosome organization (Chiarle et al., 2011; Klein et al., 2011). However, these studies did not determine whether enrichment was only on the true "cis" chromosome or on both chromosome 15 copies. Further studies to determine effects of chromosomal organization on translocations in such activated B cells are limited by potentially confounding factors. First, actively transcribed AID translocation hotspots, as well collectively abundant transcription-associated translocations, may be driven both by increased DSB frequency, as well as by propensity of actively transcribed genes to associate (Gilbert et al., 2004; Simonis et al., 2006; Lieberman-Aiden et al., 2009). Second, in activated cycling B cells, there are changes in genome organization and various cellular selections imposed as cells traverse the cell cycle. Finally, analysis of multiple I-SceI integration sites on different chromosomes is required to fully assess genome organization effects. Therefore, we developed a cell line system that overcomes these potential caveats.
We employed Bcl-2 transgenic Abelson Murine Leukemia Virus (A-MuLV) transformed pro-B cell lines that, in response to treatment with v-abl inhibitor STI571, arrest in the G1 cell cycle phase (Bredemeyer et al., 2006) (Fig. 1A). The STI571-mediated G1 arrest also induces RAG, which cleaves the endogenous Igκ, providing a positive control for frequent endogenous DSBs. For introduction of targeted DSBs at defined loci, we randomly integrated a retroviral substrate containing 26 I-SceI target sites (to increase cutting efficiency) and isolated different pro-B clones that each had a unique, single genomic substrate integration. To generate DSBs at these sites, we stably expressed an I-SceI-GR fusion protein (Chiarle et al., 2011), which allowed ligand-inducible cleavage of I-SceI substrates following G1-arrest (Fig. 1A).
Pro-B cells display little cytogenetic instability, even when deficient for non-homologous end-joining DSB repair (Sekiguchi et al., 2001). Correspondingly, when HTGTS libraries were prepared from wild type (WT) G1-arrested A-MuLV transformants with an I-SceI substrate in chromosome (chr) 15, we failed to observe translocations to Igκ (chr 6) and also found an increased background of artifactual junctions compared to what we found in activated B cells (Chiarle et al., 2011) (Fig. S1A and B). These findings suggested a low translocation frequency in WT pro-B lines that reduced our ability to generate large numbers of translocations junctions. DSBs activate the Ataxia-Telangiectasia mutated (ATM) kinase which then phosphorylates multiple substrates. We previously showed that ATM-deficiency results in dramatic cytogenetic instability in pro-B cells (Sekiguchi et al., 2001). In the absence of ATM, V(D)J recombination DSBs in A-MuLV transformants progress to chromosome breaks and translocations (Bredemeyer et al., 2006). Correspondingly, upon treating chr 15-integrated and chr 2-integrated WT pro-B lines, respectively, with ATM inhibitor (Ku55933 or "ATMi") before generation of HTGTS libraries, we found dramatic Igκ hotspots for both, as well as multiple translocations into other RAG targets including IgH, TCRγ and TCRα loci (Fig. S1A; Table S1). Therefore, we focused subsequent studies on genetically ATM-deficient (ATM−/−) pro-B cell lines.
We generated large scale translocation libraries from three ATM−/− pro-B lines in which I-SceI substrates were integrated, respectively, into chr 18, chr 2, or chr 7 (Table S1). Consistent with ATMi-treated WT line results, predominant translocations in ATM−/− lines were within endogenous Igκ and other RAG target loci (Fig. 1B, Fig. 2, Fig. 3 and Fig. S2), with up to 25% of total junctions occurring within these loci. Junctions that were not to antigen receptor loci tended to be spread across the genome. In addition, we observed increased junctions near the I-SceI breaksite, which were substantially comprised of resections (Fig. S3B; Chiarle et al., 2011). Even when junctions within 2Mb of the breaksite were excluded, however, we observed a mild preference for junctions along the length of the same chromosome on which the I-SceI sequence was targeted (Fig. 1C, Fig. 2, Fig. 3 and Fig. S2). Finally, we observed dominant junctions to Igκ for two additional integrations on chr 2, as well as integrations on chr 3 and chr 13 (Table S1).
The finding that I-SceI DSBs in 8 different chromosomal sites form frequent translocations with 5 different antigen receptor loci indicates that high frequency DSBs can dominate translocation patterns. In this regard, we propose that the rate at which particular translocations are formed should be influenced by the product of at least three variables; namely the frequencies of DSBs at each partner site and the frequency at which these sites are synapsed. As illustrated by the extremes of such a model, highly frequent DSBs at one site would not drive translocations to a frequently synapsed site that was not broken; while frequent DSBs at two sites would not drive translocations between them if they were never proximal. Further tests of this model require normalization of DSB frequency across the genome so that proximity is an overall rate limiting factor. For this purpose, we γ-irradiated G1-arrested pro-B lines, a dosage that generates several hundred random DSBs per genome (Rothkamm and Lobrich, 2003). We reasoned that such ectopically introduced DSBs would obviate dominant endogenous DSBs as the main driving force for translocations. Accordingly, in IR-treated cells, the percentage of junctions within Ig and TCR loci decreased substantially (Fig. 1B and Table S1). However, Igκ still represented a weaker translocation hotspot after IR (Fig. 1B and Fig. S3A), suggesting that IR-introduced random DSB frequency remained lower than that of the endogenous Igκ DSBs. In addition, we did not observe enrichment of translocation junctions around TSSs in the γ-irradiated pro-B lines (Fig. 1D–F), supporting the notion that IR treatment helped normalize a broader distribution of DSBs.
IR-treatment generated a dramatic effect on the distribution of translocations across pro-B cell chromosomes. Thus, we observed a tremendous increase in the proportion of junctions along the full length of the (numerical) chromosome harboring the target I-SceI DSBs and not just in the area proximal to the breaksite (Fig. 1C, ,2,2, ,3,3, S2). Indeed, much of the chromosome harboring individual breaksites, in effect, became a translocation hotspot, with the overall level of junctions ranging from 25–40% of the total. This phenomenon was observed for all 8 separate I-SceI integrations. Based on studies of chromosome territories in cycling human cells (Bolzer et al., 2005; Lieberman-Aiden et al., 2009), we speculated that enriched breaksite chromosome translocations subsequent to IR may reflect spatial proximity of sequences along individual chromosomes.
To test whether or not the high level of translocations on the breaksite-containing chromosome represented true cis-translocations, we generated A-MuLV transformed pro-B cell lines from 129/BALB/c F1 mice and introduced into them a single-copy retroviral construct containing a V(D)J recombination substrate (Bredemeyer et al., 2006). We used this substrate because of its high efficiency of generating DSBs and translocations in the ATM-deficient pro-B lines (Mahowald et al., 2009). We treated two cell lines which, respectively, contained a substrate integrated into the BALB/c-derived chr 7 and into the 129-derived chr 9 with STI571 and ATMi to promote unrepaired DSBs within integrated V(D)J substrates and also with IR to generate genome-wide DSBs (Fig. 4). Translocation patterns of RAG-generated construct DSBs strongly resembled those generated from I-SceI-initiated DSBs after IR treatment, with libraries from both chr7 and chr9 integrations being enriched for junctions at antigen receptor loci and all along the breaksite chromosome (Fig S4A,B). Thus, our general findings with I-SceI DSBs can be generalized to more than one type of target DSB and, more specifically, to a known class of physiological DSBs. We extracted and plotted 129 versus BALB/c allele-specific translocations based on available SNPs (Yalcin et al., 2011) (Fig. 4A,B and Fig. S4C,D). After removal of junctions lying within 2Mb of the breaksite to remove resections, we observed enriched breaksite chromosome translocations only on the BALB/c allele for the chr. 7 integration and only on the 129 allele for chr. 9 integration, indicating that they were, indeed, enriched only on the cis chromosome (Fig. 4 and Fig. S4E–J). Translocations to other chromosomes showed no allele-specific bias.
To determine whether the spectrum of translocations observed by HTGTS was related to pre-existing spatial juxtaposition frequencies of translocation partners, we performed Hi-C (Lieberman-Aiden et al. 2009) to map the spatial organization of the complete genome in G1-arrested ATM−/− and WT pro-B cells prior to induction of DSBs and irradiation. Hi-C combines Chromosome Conformation Capture (3C, Dekker et al., 2002) with purification of ligation junctions followed by deep sequencing to detect and quantify chromosomal interactions throughout the genome. The resulting Hi-C data provide insights into the folding of the mouse genome in the ATM−/− cells that were used for analysis of translocations (Fig. 5) as well as in WT pro-B cells (Supp. Fig. S5). A two-dimensional heat map of interactions throughout the genome, where each pixel represents all interactions between two 10 Mb regions, shows that intra-chromosomal interactions are much more frequent than inter-chromosomal interactions (Fig. 5A), reflecting “chromosome territories” that have been observed previously by Hi-C and cell imaging (Lieberman-Aiden, 2009; Mayer et al. 2005). When we analyzed interactions within single chromosomes at higher resolution (1 Mb), we found a decreasing interaction frequency with increasing genomic distance (Fig. 5B,D), which is characteristic of the flexible polymer nature of the chromatin fiber (Dekker et al., 2002).
The intra-chromosomal interaction maps are also characterized by reproducible "plaid" patterns of alternating regions with high and low interaction frequency (Fig. 5B and S5D). This pattern becomes even more obvious upon normalizing Hi-C signals for genomic distance and displaying the correlations between interaction profiles of loci (Fig. 5C). Previous work showed that the first principle component of this correlation map captures this plaid pattern, with positive values corresponding to open and transcriptionally active domains (A-domains), and negative values corresponding to closed and inactive chromatin (B-domains) (Lieberman-Aiden et al., 2009). In these G1-arrested ATM−/− and WT cells, we found that this domain structure correlated with gene density, showing that the G1 mouse genome is compartmentalized in A- and B-domains, similar to human (Fig. 5C, S5E).
In cycling human cells, intra-chromosomal contact probability (P(s)) has been shown to decay rapidly as a function of genomic distance (s), following a power law with exponent −1 (P(s)~s−1) for loci separated by 0.5–7 Mb. This represents a fractal globule conformation, a polymer state characterized by dense packing in the absence of topological entanglements (Lieberman-Aiden, 2009, Mirny 2011). When we plotted the Hi-C data for mouse G1-arrested cells in a similar fashion we find a power law scaling with exponent −1 for loci separated by 0.5 up to at least 5 Mb, indicating that mouse chromatin in G1 cells also folds according to a fractal globule (Fig. 5D).
Whole chromosomes within the mammalian nucleus often occupy preferred positions relative to one another (Boyle et al., 2001; Lieberman-Aiden, 2009; Sengupta et al., 2008). Indeed, in the G1-arrested mouse pro-B cells, we also find that the longest chromosomes (chr 1, 2, 3, etc.) interact with each other more frequently than with the shortest chromosomes (chr 17, 18, 19 etc.) and vice versa (Fig. 5E). However, intermediate length chromosomes have a less well-defined position relative to other chromosomes (Suppl. Fig. 5E; see below).
Overall, G1-arrested WT cells and ATM−/− cells showed similar folding principles (Pearson correlation between WT and ATM−/− around 0.98), indicating that, as judged at the current resolution of Hi-C, ATM deficiency by itself does not affect formation and relative positioning of chromosome territories, chromosome compartmentalization in A- and B-domains, and folding of chromatin according to a fractal globule (Supp. Fig. S5). We observed changes in the precise genomic locations of A- and B-compartments in 8% of the genome of WT as compared to ATM−/− cells; as expected given that these cells may display some differences in gene expression (Bredemeyer et al., 2008), which impacts the localization of genes in the A- or B-compartment (Lieberman-Aiden et al. 2009).
We compared the features of 3D spatial genome organization in the ATM−/− G1-arrested pro-B lines before translocations with the patterns of translocations after I-SceI induction and IR treatment. The most obvious similarity between spatial organization and translocation frequency is the enrichment of both chromatin interactions and translocations within the chromosome harboring the I-SceI DSBs (Figs. 2,,33,,5).5). This finding suggests that enrichment for translocations on the breaksite chromosome is driven by spatial proximity of regions of the same chromosome. To investigate whether translocations correlate with spatial proximity at a finer scale within the breaksite chromosome, we compared translocation frequency with interaction frequency between the chromosomal region containing the I-SceI site and 1 Mb bins along the rest of the breaksite chromosome (Fig. 6A, 6B). The translocation profile looks strikingly similar to and correlates strongly with the Hi-C interaction frequency between the I-SceI site and other regions along the breaksite chromosome for I-SceI sites on chr18, chr2, and chr7 (Fig 6, Supp. Fig. 6D–E). Thus, when acceptor DSBs are widely available along all chromosomes (e.g. after IR), our findings show that the spatial conformation of the chromosome containing the breaksite is a strong predictor of translocation frequency along that chromosome.
To examine whether the correlation between translocations and spatial interactions extends to inter-chromosomal events genome-wide, we compared the frequency of interaction between trans chromosomal regions and the I-SceI breaksite to their frequency of forming translocations. We excluded bins that contained translocation hotspots related to Ig and TCR loci. We then calculated the frequency of interaction between 5 Mb bins on trans chromosomes and the I-SceI site to their frequency of forming translocations with the I-SceI break. We found that bins with higher translocation counts (>=2 translocations per 1,000 in the dataset) also had a significantly higher distribution of Hi-C interaction scores with the induced breaksite than bins with few or no translocations (< 2 translocations per 1,000 in the dataset; Fig. 7A). This result is statistically significant over a broad range of translocation thresholds (Suppl. Fig. S7A). Thus, even though interchromosomal interactions are weaker than intrachromosomal interactions, these weak preferences affect the likelihood of translocations between interchromosomal regions. This significant correlation between translocation frequency and Hi-C score is also evident when the average Hi-C profile is plotted around bins that display frequent and infrequent inter-chromosomal translocations with I-SceI sites (Suppl. Fig. S7B).
To evaluate the impact of whole chromosome nuclear positioning on translocation frequency, we compared interaction patterns of whole chromosomes (Fig. 5E) with translocation frequency across whole chromosomes. We observed a high correlation between inter-chromosomal translocation frequencies and whole chromosome nuclear position for both the chr18 and the chr2 I-SceI target sites (Fig. 7B). Strikingly, the chr2 and chr18 I-SceI target sites showed completely different inter-chromosomal translocation distributions, which correlated with their own specific inter-chromosomal nuclear interaction profiles (Fig 7B). Thus, while DSB frequency is presumably similar across all chromosomes in these two experiments, the frequency of translocations differs dramatically depending on the relative proximity of other chromosomes to the I-SceI breaksite chromosome. While we noted an occasional discordance between whole chromosome Hi-C interaction levels and translocation frequency (such as the chr2 I-SceI site with chr9), the correlation in these cases between translocation frequency and spatial proximity was still significant at a 5 Mb resolution (Supp. Fig. S7D). Finally, like other medium-length chromosomes, chr 7 did not exhibit a strong positioning relative to other whole chromosomes (Supp Fig. S7C). Correspondingly, while we did not find a significant correlation between chr7 I-SceI DSB translocations and whole chromosome position (Supp. Fig. S7E), we did find a positive correlation (R=0.53) when inter-chromosomal translocation frequency was compared to the nuclear position of a smaller region of chr 7 (1Mb) around the I-SceI target site (Supp. Fig. S7E).
Our combined Hi-C and HTGTS analyses show definitively that the 3D genome organization and spatial proximity among loci strongly influence patterns of chromosomal rearrangements and translocations genome wide. Nuclear organization and chromosome conformation have been implicated in gene regulation (Cremer and Cremer, 2010), and also have been shown to influence translocations based on cytogenetic studies (Neves et al., 1999; Roix et al., 2003; Meaburn et al., 2007; Wang et al., 2009). However, such cytogenetic studies have certain limitations, including only being done for a single pair of genomic loci and in a limited number of cells. In addition, the actual definition of two proximal loci in cytogenetic studies has been somewhat arbitrary (Neves et al., 1999; Mathas et al., 2009; Mani et al., 2009; Lin et al., 2009; Wang et al., 2009). Our approach avoids such caveats, allowing clear demonstration that spatial proximity can guide joining of DSBs genome wide to form translocations. Thus, in IR-treated G1-arrested pro-B lines, where DSBs are not limiting, the position of a DSB can vastly change the landscape of its predominant translocation partners (Fig. 7B). In addition, our study further shows that cellular heterogeneity in the spatial conformation of the genome allows high frequency DSBs to dominate the translocation landscape, even if they are not proximal in a large proportion of the cells.
Our studies reveal the power of combining two high-throughput genomic methods to answer long-standing questions regarding the influence of nuclear organization on important biological processes. The only previous mammalian Hi-C dataset studied genome organization in cycling human cells (Lieberman-Aiden et al., 2009). Our current study demonstrates the broad applicability of Hi-C by applying it to analyze the genome organization of G1-arrested mouse pro-B lines. Application of HTGTS and related methods to activated primary B cells previously demonstrated that AID-initiated DSBs are the major endogenous sources of translocations to c-myc and IgH target I-SceI DSBs in that cell type (Chiarle et al., 2011; Klein et al., 2011). Our current studies show an even stronger contribution of RAG-initiated DSBs in generating high frequency translocations with target I-SceI DSBs in multiple different chromosomal locations in ATM−/− A-MuLV transformed pro-B lines. Therefore, endogenous DSBs generated in the context of antigen receptor locus diversification dominate the translocation landscape in both pro-B cells and mature B cells. Notably, we found frequent translocations to multiple known RAG targets including various T cell receptor loci in the pro-B lines, even though some of these loci are not thought to be highly accessible to RAG in pro-B cells, demonstrating the sensitivity of HTGTS for revealing "off-target" RAG-initiated DSBs.
Our Hi-C data show that basic features of chromosome and nuclear organization previously described for human cells can be extended to mouse cells. As in human cells, mouse chromosomes are compartmentalized in A- and B-compartments and chromatin at the Mb scale folds according to a fractal globule. In addition, chromosomes display preferred relative positions, with longer chromosomes preferentially associating with each other, as do the shorter chromosomes. These similarities are striking, given that mouse chromosomes are fewer in number than human chromosomes and differ in their centromere placement (acrocentric). Together with the recent characterization of Drosophila genome organization (Sexton et al. 2012), this mouse Hi-C dataset reveals functional organization of chromatin that is common across species. In addition, whereas previous Hi-C analyses were complicated by the use of cycling cells, resulting in interaction maps representing the average of all chromosome conformations throughout the cell cycle (Lieberman-Aiden et al., 2009), our current Hi-C map of G1-arrested cells represents a far more homogeneous interphase organization. Similar features between G1 arrested cells and cycling cells likely arise from the large fraction of cells being in G1 in a population of cycling cells. Though cell type specific differences in genome organization are expected, the mouse Hi-C data generated here can inform a broad range of future studies of the implications of genome folding in cell function in this important model organism.
Our Hi-C data provide the highest-resolution analysis of the spatial organization of a mammalian genome to date. The Hi-C libraries were sequenced approximately 5–10 times more deeply than in previous studies (Supp. Fig. S6; Supp. Table 2). We estimate that the resolution of intra-chromosomal interaction detection is around 100 Kb, whereas inter-chromosomal interactions can be assessed at about 1 Mb resolution (Supp. Fig. S6). Previous Hi-C maps for human cells allowed a resolution of about 1 Mb in cis, and 5 Mb in trans. In our study we find strong correlations between intra-chromosomal translocation frequencies and Hi-C interaction frequencies when we compare these phenomena at 1 Mb resolution.
Interestingly, when we analyze our Hi-C data at the highest level of resolution (i.e. 100 Kb), we find the correlation between spatial proximity with translocation frequency is reduced, though it remains high (Fig S6C). This somewhat lower correlation at a very local level may reflect the local movement of DSBs within a distance of a few hundred Kb, consistent with previously described Brownian motion of chromatin over distances up to 0.5–1 µm (Marshall et al.,1997). This DSB movement on a very local scale may also contribute to synapsis of sequences that are spatially proximal.
The view of genome organization provided by Hi-C reflects cellular heterogeneity. Thus, the observed number of molecules in a Hi-C experiment that represents a certain interaction corresponds to the fraction of cells in the experiment in which those genomic regions were proximal. Our Hi-C studies show that 5 antigen receptor locus translocation "hotspots" (Igh, Igκ, Igλ, TCRα/δ, TCRγ) have a finite probability of contacting 8 different randomly integrated I-SceI loci, indicating that these 40 different pairs of loci are in close spatial proximity in a sub-population of cells (Supp. Fig. S3C). Thus, this genomic spatial heterogeneity in the G1-arrested pro-B cells allows high frequency antigen receptor locus DSBs and frequent I-SceI DSBs to translocate in the fraction of cells where their contact occurs. Thus, our findings support the proposed model in which translocation frequency is a function of DSB frequency at two sites and the fraction of individual cells in a population in which the sites are juxtaposed. The latter will in part reflect known heterogeneity in the genomic spatial organization, as well as known factors that cause certain classes of genes, (e.g. genes that are actively transcribed or existing on similar sized chromosomes) to have an increased chance of being proximal (Gilbert et al., 2004; Lieberman-Aiden et al., 2009).
By saturating the genome with DSBs, we generated a situation in which high frequency DSBs in a limited number of locations no longer totally dominates translocations. Under these conditions, spatial proximity of two DSBs is a dominant factor in determining the landscape of translocations genome wide. By extension, our findings on the ability of spatial proximity to guide translocations indicates that if a gene was broken very infrequently, it would translocate to a potential target DSB, whether it occurred at high or low frequency, and at a rate that would be strongly influenced by spatial proximity. This finding has great relevance to translocations in cancer; since it is likely that, other than major RAG- or AID-initiated DSBs in antigen receptor loci, DSBs in many partner translocation targets in lymphoid cells and translocation-initiating DSBs in other cell types likely occur at low frequency. Indeed, in many non-lymphoid cancers, factors other than DSB generation, such as spatial proximity, may play a much more important role than in lymphoid cancers (Lin et al., 2009; Mani et al., 2009). In addition, formation of translocations between randomly generated DSBs, such as those induced by chemotherapies and radiotherapies, will likely reflect a strong influence of spatial proximity like that we observe upon IR-treatment of pro-B lines. Our findings also suggest that spatial proximity may be a major driving force for the activation of certain oncogenes via translocation to a wide range of recurrent partners (Ohno et al., 2006; Barreca et al., 2011; Liu et al., 2009a).
We show that spatial proximity leads to a tremendous preference for DSBs to translocate to sites all along the true cis chromosome on which they reside and not just near the breaksite. Such notions have been speculated (Chiarle et al., 2011; Klein et al., 2011 and Mahowald et al., 2009), but never before tested. This finding should facilitate interpretation of cancer genomes and the evolution of increasingly complex karyotypes. As one example, preferential joining of cis DSBs along a chromosome might have mechanistic relevance for chromothripsis, a chromosome catastrophe phenomenon that results in extensive intra-chromosomal rearrangements in various cancer genomes (Stephens et al, 2011; Liu et al., 2011; Rausch et al. Cell 2012). Thus, chromothripsis may be promoted by the intrinsic spatial organization of given chromosomes such that DSBs within them are highly likely to be re-ligated to another DSB on the same chromosome. Cis-translocation preferences may also contribute to the predisposition of DSBs to be fused intra-chromosomally by C-NHEJ (Ferguson et al., 2000). Finally, spatial organization of chromosomes in cancer progenitors may contribute to particular initial oncogenic rearrangements, with changes in spatial organization during subsequent stages of cancer progression influencing accumulation of additional genomic rearrangements.
A-MuLV transformed cell lines were generated as described (Bredemeyer et al., 2006: Li et al., 2008). A retroviral construct containing 26X I-SceI sites was randomly integrated in the genome. F1 mice were generated by crossing BABL/cJ and 129S6.For F1 cells, a retroviral construct containing DEL-CJ substrate was used (Bredemeyer et al., 2006). Integration sites were cloned as described (Mahowald et al., 2009).
Cells were treated with 3µM STI571 (Novartis) and 100nM TA (Sigma) for 4 days. In some experiments, 5Gy IR was applied at day 2. ATM inhibitor (Ku55933, Tocris) was used at 15µM. HTGTS was performed as described (Chiarle et al., 2011). (see Extended Experimental Procedures). Data are available from NCBI/SRA (SRA049021).
Hi-C was performed on A-MuLV transformants after 2 days of treatment with 3µM STI571 as described (Lieberman-Aiden et al., 2009) with some modifications. Hi-C data were coverage-corrected (to account for restriction fragment size and mappability) according to the total number of sequence reads in each bin. (see Extended Experimental Procedures). Data are available at GEO accession no. GSEXXXXX and can be interactively visualized at http://hic.umassmed.edu.
SNP data were downloaded from the Wellcome Trust Sanger Institute (Yalcin et al., 2011). We further extracted translocation coordinates that have SNPs with “Above Threshold Genotype” tags (ATG) between the 129S5 and BALB/cJ strains. Translocations from six individual F1 libraries that contain those SNPs were further analyzed and plotted.
A high resolution Hi-C spatial organization map of the G1-arrested mouse cell genome
Genomic spatial heterogeneity contributes to recurrent chromosomal translocations
Spatial organization of chromosomes promotes dominant translocations in cis
Translocations are guided genome-wide by pre-existing spatial genome organization
This work was supported by NIH grant ARRA Supplement 3P01CA092625-09S1 and a Leukemia and Lymphoma Society of America (LLS) SCOR grant to F.W.A and by NIH grant R01 HG003143 and a W.M. Keck Foundation Distinguished Young Scholar Award to J.D. Y.Z. was supported by CRI postdoctoral fellowship. D.G.H., A.C.S., and M.G.B. were supported by the German National Merit Foundation. F.W.A. is an Investigator of the Howard Hughes Medical Institute.
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