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CTCF establishes discrete functional chromatin domains at the Hox clusters during differentiation

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Science  27 Feb 2015:
Vol. 347, Issue 6225, pp. 1017-1021
DOI: 10.1126/science.1262088

Keeping repressed genes repressed

Hox genes confer positional identity to cells and tissues. Maintaining precise spatial patterns of Hox gene expression is vital during metazoan development. The transcriptional repressor CTCF is involved in the regulation of chromatin architecture. Narendra et al. show that a CTCF protein binding site insulates regions of active and repressed Hox gene expression from each other. This protects heterochromatin containing repressed Hox genes from the encroaching spread of active chromatin. The CTCF protein appears to organize the active and repressed chromatin regions into distinct architectural domains.

Science, this issue p. 1017

Abstract

Polycomb and Trithorax group proteins encode the epigenetic memory of cellular positional identity by establishing inheritable domains of repressive and active chromatin within the Hox clusters. Here we demonstrate that the CCCTC-binding factor (CTCF) functions to insulate these adjacent yet antagonistic chromatin domains during embryonic stem cell differentiation into cervical motor neurons. Deletion of CTCF binding sites within the Hox clusters results in the expansion of active chromatin into the repressive domain. CTCF functions as an insulator by organizing Hox clusters into spatially disjoint domains. Ablation of CTCF binding disrupts topological boundaries such that caudal Hox genes leave the repressed domain and become subject to transcriptional activation. Hence, CTCF is required to insulate facultative heterochromatin from impinging euchromatin to produce discrete positional identities.

Precise expression of Hox genes is required for cells to maintain their relative position within a developing embryo (14). For example, motor neurons (MNs) rely on Hox gene expression for the formation of position-dependent neural circuits that control voluntary movement (57). High concentration of retinoic acid (RA) signaling induces rostral Hox gene expression (Hox1 to Hox5) and, thus, cervical identity to differentiating MNs (8). The in vivo development of MNs with a cervical positional identity can be faithfully recapitulated in vitro by exposing differentiating embryonic stem cells (ESCs) to RA and a sonic hedgehog signaling agonist [smoothened agonist (SAG)] (fig. S1A) (see supplementary materials and methods) (9). ESC-derived MNs exposed to RA activate the rostral portion of the HoxA cluster (Hoxa1-6), whereas Hoxa7-13 remain repressed (Fig. 1A and table S1) (10, 11). The transcriptional partitioning of the HoxA cluster is mirrored at the level of chromatin. As previously described, H3K27me3—the catalytic product of Polycomb repressive complex 2 activity—decorates the entire HoxA cluster in ESCs (11) (Fig. 1B, top). Upon differentiation into MNs, H3K4me3 and RNA polymerase II (RNAPII) access the rostral segment of the cluster, whereas H3K27me3 becomes restricted to the caudal segment (11) (Fig. 1B). Within the HoxA cluster, MNs display two clear discontinuities in H3K4me3 and H3K27me3 density: at the intergenic region between Hoxa5 and Hoxa6 (C5|6) and between Hoxa6 and Hoxa7 (C6|7) (Fig. 1C). The DNA sequence underlying each of these discontinuities contains a highly conserved binding site for the CCCTC-binding factor (CTCF) (12) (Fig. 1C and fig. S1, B and C) that is constitutively occupied in both ESCs and differentiated MNs (Fig. 1B). CTCF-demarcated chromatin boundaries were observed at the HoxC and HoxD clusters as well (Fig. 1C and fig. S2) and have recently been identified in the orthologous bithorax complex in Drosophila melanogaster (13).

Fig. 1 CTCF localizes to a HoxA chromatin boundary in motor neurons.

(A) Heat map of HoxA relative expression (log2) between WT ESCs and MNs. (B) Normalized chromatin immunoprecipitation followed by deep sequencing (ChIP-seq) read densities for the indicated proteins and histone modifications in ESCs and MNs from two merged biological replicates. Genes that are activated during differentiation are annotated in green; repressed genes are shown in red. (C) Zoomed-in view of H3K4me3 and H3K27me3 boundaries, along with CTCF peaks and their underlying binding motifs. Blue highlights nucleotides that diverge from the consensus motif. The guide RNA used to target C5|6 is shown. (D) Sequencing chromatogram of the Δ5|6 line depicts a 9-bp deletion overlapping the CTCF core motif. (E) Normalized ChIP-seq read densities for CTCF in WT and Δ5|6 MNs from two merged biological replicates. The deleted CTCF binding site (C5|6) is boxed, as well as the neighboring site (C6|7).

It has been suggested that CTCF functions as a chromatin barrier insulator by restricting the spread of heterochromatin, though this remains in dispute (1416). Therefore, we tested whether CTCF can perform Hox gene barrier insulation during differentiation to produce functional MN circuits. We employed the clustered regularly interspaced short palindromic repeat (CRISPR) genome-editing tool (17, 18) in ESCs to disrupt CTCF binding sites that localize to chromatin boundaries within Hox clusters. We first generated a 9–base pair (bp) homozygous deletion within the core CTCF motif between Hoxa5 and Hoxa6 (Δ5|6) (Fig. 1D) and did not detect any mutations at potential off-target cleavage sites (table S2). The 9-bp deletion results in a total abrogation of CTCF occupancy (Fig. 1E). The neighboring CTCF binding site (C6|7) also shows a dramatic reduction in binding, suggesting an interdependence (Fig. 1E) (19, 20). Δ5|6 ESCs exhibit no defect in their ability to differentiate into MNs (fig. S3). To examine the transcriptional consequence of deleting CTCF binding sites within the HoxA cluster in response to patterning signals during cell differentiation, we performed RNA sequencing (RNA-seq) on wild-type (WT) and Δ5|6 cells at two stages: ESCs and differentiated MNs. In ESCs, all HoxA genes are repressed in both lines (Fig. 2A, left, and table S1). Upon differentiation, Hoxa1-6 are activated in the WT setting, whereas Hoxa7-13 remain repressed, mirroring the distribution of active and repressive chromatin across the cluster. Hoxa1-6 are equivalently activated in WT and Δ5|6 MNs. However, Hoxa7—the gene located immediately caudal to the affected C6|7 site—is up-regulated more than 25-fold relative to the WT control. Hoxa9 shows very modest expression in Δ5|6 MNs, whereas Hoxa10-13 remain fully repressed (Fig. 2A, right, and table S1). Furthermore, though Hoxa6—the gene located between the deleted C5|6 and C6|7 site—is equivalently expressed in terminally differentiated WT and Δ5|6 MNs, it is transcriptionally activated earlier in differentiating Δ5|6 cells than in WT cells, unlike the rostral Hoxa5 control (fig. S4). Thus, CTCF occupancy regulates the spatial and temporal activation of the HoxA cluster. Demonstrating that CTCF boundary activity is not restricted to a single Hox cluster, deletion of a 13-bp sequence within a binding site at the HoxC chromatin boundary results in the equivalent transcriptional activation of genes located caudal to the site of mutation (fig. S5).

Fig. 2 The chromatin boundary is disrupted upon deletion of the C5|6 CTCF motif.

(A) RNA-seq MA plot of WT versus Δ5|6 ESCs (left) and MNs (4 days after RA/SAG, right). MN data are representative of two biological replicate experiments; ESC data represent one experiment. Mean abundance is plotted on the x axis and enrichment is plotted on the y axis. Hb9 is a marker of motor neurons. (B) Normalized ChIP-seq read densities for the indicated protein and histone modifications along the HoxA cluster in ESCs and MNs (4 days after RA/SAG) from two biological replicates.

Fig. 3 Loss of CTCF alters topological architecture of the HoxA locus.

(A to C) Normalized ChIP-seq read densities for CTCF and 4C contact profiles in WT and Δ5|6 ESCs (A) and MNs [(B) and (C)] using a viewpoint (red) in either the rostral [(B), 4C.Hoxa5-A] or caudal [(A) and (C), 4C.Hoxa10] segment of the cluster. The ChIP signal is merged across two biological replicates and the 4C signal across three replicates. The median and 20th and 80th percentiles of sliding 5-kb windows determine the main trend line. Color scale represents enrichment relative to the maximum attainable 12-kb median value. Dotted lines highlight the region between C6|7 and C7|9.

Hoxa7-specific transcriptional activation in Δ5|6 MNs suggests that the intact C7|9 peak serves as a new boundary. To study if there is a relocation of the chromatin boundary during MN differentiation in the mutant line, we investigated the chromatin state of ESCs and differentiated MNs. Site-specific ablation of CTCF does not affect the chromatin state of undifferentiated cells, as WT and Δ5|6 ESCs possess H3K27me3 distributed across the entire HoxA cluster (Fig. 2B, top). However, after differentiation, Δ5|6 MNs exhibit a 50% reduction in H3K27me3 levels, specifically within the region delimited by C5|6 and C7|9 (Fig. 2B and fig. S6, A and C). In agreement with C7|9 serving as the new boundary element in Δ5|6 MNs, H3K27me3 density recovers to WT levels immediately caudal to the C7|9 peak. Moreover, deletion of C5|6 results in a complementary expansion of H3K4me3 and RNAPII up to the C7|9 boundary (Fig. 2B and fig. S6, B and D). The Δ5|6 mutation does not produce pleiotropic effects, as chromatin boundaries are not disrupted in trans within the HoxC and HoxD clusters (fig. S6, C to E). Likewise, ablation of the C5|6 CTCF binding event within the HoxC cluster (Δ5|6HoxC) results in an equivalent chromatin boundary relocation (fig. S5). Thus, CTCF does not function within the Hox clusters according to the traditional definition of a chromatin insulator—to restrict the spread of repressive chromatin into adjacent euchromatin—but rather serves to restrict in cis the exposure of Polycomb repressed genes to Trithorax activity.

CTCF-dependent insulation occurs via its ability to mediate looping interactions between nonadjacent segments of DNA (21). Accordingly, CTCF is enriched at boundaries between topologically associated domains (TADs) (15, 22, 23). To test how CTCF-mediated looping may regulate the dynamic spatial reorganization of the HoxA cluster during differentiation, we performed 4C-seq in WT and Δ5|6 cells using viewpoints located within either the transcriptionally active (4C.Hoxa5-A) or repressive (4C.Hoxa10) domains of the HoxA cluster (Fig. 3). In WT and Δ5|6 ESCs, the strong interaction signal of both 4C-seq viewpoints extends to the perimeter of the HoxA cluster, suggesting an organization of the locus as a single architectural domain that the C5|6 binding site does not alter (Fig. 3A and fig. S7, A and B). As expected, in WT cells this domain partitions during differentiation into two at roughly the C6|7 position, mirroring the distribution of H3K4me3 in the rostral domain and H3K27me3 in the caudal domain (24, 25). This is demonstrated by the strong interactions with the 4C.Hoxa5-A viewpoint that occur almost exclusively within the rostral domain (Fig. 3B) and interactions with the 4C.Hoxa10 viewpoint that are restricted to the caudal domain (Fig. 3C). Unlike the case in ESCs, deletion of the C5|6 CTCF binding site affects the spatial organization of the HoxA cluster in MNs. The Δ5|6 mutation repositions the topological boundary in MNs to the intact C7|9 site, matching the de novo chromatin boundary and thereby evicting Hoxa7 from the caudal repressed domain and into the rostral active domain (Fig. 3, B and C, and fig. S8, A and B). Thus, the elimination of a CTCF binding site causes a structural reorganization of the HoxA cluster that results in an aberrant chromatin boundary and altered gene expression.

These data argue that in response to RA signaling, the most rostral CTCF binding event forges a topological boundary within the HoxA cluster that can insulate active from repressive chromatin and thus maintain proper gene expression. This model predicts that eliminating the C7|9 CTCF binding site in Δ5|6 MNs would cause aberrant activation of Hoxa7-10 and caudal regression of the topological boundary to the C10|11 position. Using the CRISPR genome-editing tool in Δ5|6 ESCs, we mutated the C7|9 CTCF binding site. Δ5|6:7|9 ESCs harbor a 21-bp deletion spanning the C7|9 motif on one allele. The other allele contains a 20-bp insertion that disrupts the motif (fig. S9). Hoxa7-10 are highly up-regulated in the double-mutant MNs relative to the WT control (Fig. 4, A and B, fig. S4, and table S1). Hoxa9-10 are the most up-regulated genes in the polyA-selected transcriptome, whereas Hoxa11-13 remain transcriptionally silent. This phenotype is specific to CTCF ablation, as deletion of a YY1 binding motif adjacent to the C7|9 site does not result in the transcriptional activation of caudal genes (fig. S10) (26). The transcriptional profile of Δ5|6:7|9 MNs suggests an underlying caudal boundary shift. Accordingly, 4C-seq using the active 4C.Hoxa5-B viewpoint shows a shift of the topological boundary from C6|7 to the intact C10|11 position in Δ5|6:7|9 MNs (Fig. 4C and fig. S8C), allowing for a parallel expansion of H3K4me3 onto the Hoxa10 gene (Fig. 4D). Conversely, H3K27me3 density progressively decreases relative to the WT control in a rostral direction from the C10|11 CTCF site.

Fig. 4 Compound C5|6:7|9 deletion causes a further caudal spread of active transcription within the HoxA locus.

(A) RNA-seq MA plot of WT versus ∆5|6:7|9 MNs. Mean abundance is plotted on the x axis, and enrichment is plotted on the y axis. (B) Heat map of HoxA relative expression in MNs (day 4) versus EBs (embryoid bodies) (day 0) across two biological replicates (single replicate in the ∆5|6:7|9 line). (C) Normalized ChIP-seq read densities for CTCF and 4C contact profiles in WT and Δ5|6:7|9 MNs using the 4C.Hoxa5-B viewpoint (red) from two biological replicates. The median and 20th and 80th percentiles of sliding 5-kb windows determine the main trend line. The color scale represents enrichment relative to the maximum attainable 12-kb median value. Dotted lines highlight the region between C6|7 and C10|11. (D) Normalized ChIP-seq read densities for the indicated proteins and histone modifications along the HoxA cluster in MNs (4 days after RA/SAG). A magnified view of the boxed region is presented on the right.

These results indicate that in response to patterning signals during differentiation, CTCF partitions the Hox clusters into insulated architectural domains, upon which Trithorax and Polycomb activities are superimposed in a mutually exclusive fashion to establish discrete Hox transcriptional programs. In agreement with our findings, deletion of a CTCF binding site at the boundary of a Polycomb domain containing the Tcfap2e locus resulted in its transcriptional activation (27). Whether the expansion of H3K4me3 activity that we observe in the Hox clusters is the result of aberrant enhancer contacts with caudal genes or an alternative local mechanism of Trithorax expansion remains to be tested. Our 4C-seq results agree with previous studies, which have shown that the caudal and rostral domains of the HoxA cluster in differentiated cells are incorporated into separate adjacent TADs, the borders of which align with the chromatin boundary. Our findings thus imply that CTCF is functionally required to delimit TAD boundaries, though a high-resolution all-versus-all (Hi-C) approach will be required to confirm this claim.

Supplementary Materials

www.sciencemag.org/content/347/6225/1017/suppl/DC1

Materials and Methods

Figs. S1 to S10

Tables S1 to S3

References (28, 29)

References and Notes

  1. Acknowledgments: All sequencing data have been deposited to the Gene Expression Omnibus as series GSE60240 and will be made immediately available upon publication. We thank L. A. Rojas, C. Leek, A. Singhal, S. Tu, R. Bonasio, and L. Vales for thoughtful discussions and revision of the manuscript. We also thank the New York University Genome Technology Center for help with sequencing. This work was supported by grants from the NIH (R37-37120 and GM-64844 to D.R., T32 GM007238 to V.N., R01HD079682 to E.O.M., and GM086852 and GM112192 to J.A.S.). D.A. was supported by the Project A.L.S. foundation. P.P.R. is a National Cancer Center postdoctoral fellow. J.A.S. is a Leukemia and Lymphoma Society scholar. V.N., E.O.M., and D.R. conceived the project, designed the experiments, and wrote the paper; V.N. performed most of the experiments and the bioinformatic analysis; D.A. performed the immunocytochemistry; and P.P.R., R.R., and J.A.S. advised on the 4C-seq procedure and analysis.
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