- Research article
- Open Access
Motif oriented high-resolution analysis of ChIP-seq data reveals the topological order of CTCF and cohesin proteins on DNA
- Gergely Nagy†1, 5,
- Erik Czipa†1,
- László Steiner2,
- Tibor Nagy3, 6,
- Sándor Pongor4,
- László Nagy1, 5 and
- Endre Barta1, 3Email authorView ORCID ID profile
© The Author(s). 2016
- Received: 12 April 2016
- Accepted: 14 July 2016
- Published: 15 August 2016
ChIP-seq provides a wealth of information on the approximate location of DNA-binding proteins genome-wide. It is known that the targeted motifs in most cases can be found at the peak centers. A high resolution mapping of ChIP-seq peaks could in principle allow the fine mapping of the protein constituents within protein complexes, but the current ChIP-seq analysis pipelines do not target the basepair resolution strand specific mapping of peak summits.
The approach proposed here is based on i) locating regions that are bound by a sufficient number of proteins constituting a complex; ii) determining the position of the underlying motif using either a direct or a de novo motif search approach; and iii) determining the exact location of the peak summits with respect to the binding motif in a strand specific manner. We applied this method for analyzing the CTCF/cohesin complex, which holds together DNA loops. The relative positions of the constituents of the complex were determined with one-basepair estimated accuracy. Mapping the positions on a 3D model of DNA made it possible to deduce the approximate local topology of the complex that allowed us to predict how the CTCF/cohesin complex locks the DNA loops. As the positioning of the proteins was not compatible with previous models of loop closure, we proposed a plausible “double embrace” model in which the DNA loop is held together by two adjacent cohesin rings in such a way that the ring anchored by CTCF to one DNA duplex encircles the other DNA double helix and vice versa.
A motif-centered, strand specific analysis of ChIP-seq data improves the accuracy of determining peak positions. If a genome contains a large number of binding sites for a given protein complex, such as transcription factor heterodimers or transcription factor/cofactor complexes, the relative position of the constituent proteins on the DNA can be established with an accuracy that allow one to deduce the local topology of the protein complex. The proposed high resolution mapping approach of ChIP-seq data is applicable for detecting the contact topology of DNA-binding protein complexes.
- DNA loop
In chromatin immunoprecipitation combined with sequencing (ChIP-seq), DNA fragments represented by sequence reads correspond to those regions that can be chemically cross-linked with a protein in question. In case of transcription factors (TFs), the term “peak” is generally used to denote a loosely defined region to which an elevated number of reads can be mapped compared to the background, while the peak summit shows the highest coverage of the region. Peak summits are known to more-or-less coincide with the corresponding DNA elements . It is also known that due to possible protein-protein cross-linking events, components of a protein complex that are not directly involved in specific DNA binding can produce peaks that overlap with the peaks of TFs that anchor them to DNA .
The organization of interphase chromatin is mediated, among other mechanisms, by the dynamic formation of loop structures held together by cohesin, an evolutionarily conserved ring-like protein complex. The tripartite cohesin ring itself consists of RAD21, SMC1 and SMC3 proteins [3, 4] and is believed to anchor to DNA via STAG1/2 and CTCF [5–12]. CCCTC-binding factor (CTCF) is an 11-zinc finger protein, which binds to specific recognition sites (CTSs) on the DNA [13–15] that are supposed to serve as insulator elements [11, 16]. Parts of the cohesin complex are known in terms of atomic detail [17, 18], but most structural studies refer to cohesin being involved in sister-chromatid cohesion. The cohesin ring is large enough to embrace two sister chromatids, but this connection is believed to be topological rather than sequence specific, such as in the case of chromatin loop formation . It is hypothesized that the cohesin ring is similar both in interphase and in metaphase [9, 11, 19], but the chain topology of loop closure is not known in sufficient detail. Current models disagree even on fundamental points such as the number of DNA duplexes enclosed within a cohesin ring [4, 8, 9, 11, 12, 19–23]. The position of the ring relative to the CTCF molecules is also uncertain. For example, models suggested in current studies [22, 24] consistently depict the ring in a distal position with respect to the loop and the anchoring CTCF molecules. However, as far as we are aware, there are no experimental data available that directly support this view.
A recent chromatin conformation capture (3C) based in situ Hi-C study pointed out that CTSs flanking the loops had a strand specific orientation, where generally the 5’ CTS was on the forward strand while the 3’ CTS was on the reverse strand . This orientation specificity was further confirmed experimentally by the inversion of an anchoring CTS . Earlier, we assigned the RXR-activated enhancers to induced genes in bone marrow derived macrophages through the use of regions bordered by active insulators that were bound both by CTCF and RAD21 . In some selected examples, we also showed by 3C-sequencing that these flanking CTSs could anchor DNA loops. By further scrutinizing our ChIP-seq data, we observed that there was a characteristic shift between the co-localizing CTCF and RAD21 peaks. These observations encouraged us to look for general patterns in the positions of cohesin-related ChIP-seq peaks in the hope of discovering further information about how the CTCF/cohesin complex closes the DNA loops. Here we use a novel high-resolution analysis of ChIP-seq data to build an approximate model of CTCF/cohesin driven chromatin loop formation.
In this work we study the contact positions of the CTCF and cohesin complex proteins relative to the CTCF transcription factor binding site. We apply a high-resolution, motif-centered analysis on the available human and mouse CTCF and cohesin ChIP-seq datasets and find a characteristic shift pattern between the peaks of CTCF and the components of the cohesin complex. Based on this pattern as well as the known biochemical and structural data about the DNA/CTCF/cohesin complex, we propose a new “double-embrace” model for DNA loop closure.
The summit-based high-resolution ChIP-seq analysis shows a characteristic shift pattern between the DNA contact points of CTCF, STAG1/2, RAD21 and SMC1/3 proteins
The high-resolution mapping approach proposed here seeks to extend the conventional analyses in two respects. Firstly we analyzed the fragment frequency distribution of the peaks and determined the most likely location of the genomic contact region of the DNA-protein interactions by using summit positions. Subsequently, we then represented the predicted contact points in terms of a genomic distance with respect to a reference point that we chose here as the center of the CTS. This had two important consequences: Since the CTS is a non-palindromic element, it has a strand specific orientation and thus the relative contact point positions can have both positive and negative values. Secondly, if we mapped the contact points of co-localizing DNA-binding proteins, we could then define an average distance (shift) between them. Underlying these considerations was the assumption that the fine positional shifts that may exist between the contact points of cohesin proteins (CTCF, RAD21, SMC1/3 and STAG1/2) may reflect the 3D position of the components within the complex. The genomic locations could thus be converted to approximate 3D distance constraints by projecting the shifts onto a 3D model of DNA.
The bottleneck of this analysis however is data quality. Researchers familiar with traditional ChIP-seq analysis are well aware of the quasi-chaotic uncertainty of peak positions. This is in part a natural consequence of the dynamic nature of DNA binding, which can be even more pronounced in the case of protein complexes. As a consequence, we needed a large number of co-occurring peaks (“co-peaks”) of distinct proteins from several cell types in order to derive peak shift values between the components of a protein complex. Preliminary experiments showed that we needed several hundred good quality (high coverage and well-resolved) co-peak data in order to determine a shift value within an accuracy of one base pair (Additional file 1: Figure S1). Producing such a large amount of ChIP-seq data can be a formidable task if a protein has few recognition sites within the genome. Fortunately, CTCF and cohesin have a large number of binding sites within the genome, and in addition, there are many ChIP-seq studies available in public databases. So in principle, the analysis could be carried out using the large body of data available on CTCF/cohesin. However there were a few conditions that had to be considered prior to conducting the analysis. First, we needed good quality ChIP-seq data for more than one cohesin protein that had been analyzed simultaneously in the same cell or tissue type (Additional file 2: Tables S1 and S2). Then, in order to decrease the number of non-relevant peaks, we selected those CTSs around which CTCF and at least one cohesin protein has been detected (see data collection). For this analysis we used the combination of an in-house developed computational pipeline  and custom-made scripts. Briefly, the analysis included the identification of CTCF/cohesin peaks, the building of a consensus CTS set and finally the determination of shifts between summits relative to the CTSs.
Since CTCF is the only known specific DNA binder among the components of the CTCF/cohesin complex, we expected that the corresponding ChIP-seq peaks will point to the same position with respect to CTS. In contrast, the fact that we found conserved shift values suggests that also the SMC proteins, STAG1/2 and RAD21 occupy conserved – relatively fixed – positions that are close enough to DNA so as to give rise to DNA-protein crosslinks during the ChIP-seq procedure.
The new “double-embrace” model explains both the biochemical and the shift pattern data
Although this model was derived from an observed peak shift pattern (Fig. 1a), it is in agreement both with the loop-closing function of the complex and with the subunit interactions suggested in previous studies [5, 7, 17–19]. At the same time it suggests novel subunit interactions that can be experimentally tested, for instance the CTCF/RAD21 interaction that follows from the shift pattern. In particular, our model supports the recent findings of Rao et al.  and Guo et al.  who showed that the two CTS anchor sites flanking a DNA loop must align in a convergent orientation. At the same time, our data also answer the important question of Bouwman and de Laat regarding the position of cohesin ring(s) with respect to CTSs . Namely, we found that the cohesin ring overlaps with the CTSs so that its center is slightly shifted towards the interior region of the loop.
The double embrace arrangement provides testable hypotheses that may help to clarify several, seemingly contradictory features of loop closure. Firstly, the loop has to be mechanically stable so as to fix the DNA molecule during transcription events. On the contrary, the loop has to be flexible so as to find its precise location on the DNA duplex. While the presence of two cohesin rings seemingly satisfies the stability criterion, the large number of intermolecular contacts of the double embrace structure may seem to contradict the need for flexibility. And yet, a sequential closure of the two rings might explain how a stable lock can form at a precise location of the DNA duplex. Namely, the ring formed first might glide along the DNA duplex and stop at a location where the SMC arms of the second ring lock the double ring structure. Such a scenario might in principle be deduced from a pattern of secondary peaks but the resolution of the current data does not allow this conclusion (data not shown). This semi-fixed or free gliding is also in accordance with the loop extrusion model in which cohesin ring(s) are moving along the loop until finding the anchor points .
Secondly, there is evidence that the hinge domain has DNA binding capability, and its opening and closing requires ATP-ase activity of the SMC head domain in both cohesin and condensin [31–33]. The hinge and head domains are separated by a relatively long rod like structure (approximately 45 nm in length), which in principle, should not favor interaction. In the double embrace structure, the SMC hinge domain of one ring is likely to be located in the vicinity of the head domain of the other ring, meaning that their apparent mean distance is only going to be a few nanometers, which may allow dynamic interactions. This effect only appears to happen when both rings are in the position of loop closure, with the consequence of the enzymatic reaction occurring only at the right place and the right time.
Third, the DNA duplex is known to form multiple loop structures [34, 35]. The double embrace model provides two clues regarding how this might happen. On the one hand, the double embrace can be easily extended to three (or more) DNA duplexes. Namely, in the double embrace structure, the ring anchored to duplex A encircles duplex B and vice versa. In a three duplex model, the ring anchored by CTCF to A encircles duplex B. The ring anchored to duplex B encircles duplex C, and the ring anchored to duplex C encircles duplex A. In other words, a triagonal structure can form in which the loops are connected by CTCF bound to a single cohesin ring. On the other hand, further loops can also form within a primary loop locked by a double embrace structure. In this structure, RAD21 and STAG1/2 proteins are facing the primary loop so they can interact with proteins bound to various sites within the original loop, forming multiple loop structures via protein/protein interactions.
The summit-based high-resolution ChIP-seq analysis can be applied to mapping other transcription factor complexes
In summary, the 3D organization of the chromatin and its role in global regulation of gene expression is one of the most important but still poorly understood mechanisms in molecular biology. Our results should therefore go some distance towards clarifying this issue. Through the meta-analyses of cistromic datasets we could show that the cohesin ring is in proximal position at the DNA loops. We are proposing a double embrace model that involves two cohesin rings that can now help explain the formation and the dynamic nature of these chromatin loops. Our model can also help to determine the structure of the DNA/CTCF/cohesin complexes at a higher resolution and should now help understanding of the molecular processes occurring during the closing and opening of the cohesin rings. Finally, the high resolution ChIP-seq analysis that we introduced here offers a novel way to better visualize the spatial organization of DNA bound protein complexes.
In the cases of CTCF and cohesin samples with common origin, the measurements were carried out under identical conditions.
Sequencing was carried out on Illumina platform.
The number of mapped reads was above 10 million. NCBI Build 37/hg19 and NCBI Build 38/mm10 were used as human and mouse reference genomes, respectively.
Raw data processing
Processing of raw data (including short read mapping, peak calling, the finding of enriched motifs and the creation of genome browser compatible files for data visualization) was carried out with an in-house developed ChIP-seq analysis pipeline  using the steps listed in Table S3 (Additional file 1). [38–41]. For peak calling and raw peak summit determination we used MACS2  and artifacts – based on the blacklisted genomic regions of ENCODE – were removed by intersectBed (BEDtools) .
Determination of the consensus binding sites of CTCF
As we expected a single shift or no shift between the CTCF and the cohesin complex, we differentiated these two groups of proteins. As the average resolution of the ChIP-seq coverage is about a few tens of base pairs, we calculated the average position of the sites bound by CTCF (consensus peak summits) based on the raw peak summits if these were present in at least two samples and were closer than 51 bps. Consensus peak summits for cohesin were determined in the same way. Finally, we collected those consensus CTCF peak summits that were closer to a consensus cohesin summit than 51 bps. Direction of the shift between the consensus peak summits of CTCF and cohesin was determined and showed that the cohesin is almost always downstream compared to the CTCF protein on the DNA.
Motif enrichments were determined by findMotifsGenome.pl  from the 100 bp regions of the most ubiquitous 5000 CTCF/cohesin bound sites, in two rounds. In the second motif enrichment search we used the top 5000 regions lacking the CTCF element (CTS) hits of the first search (which were mapped by annotatePeaks.pl, Homer). Score 6 was set for both CTCF motif matrices to ensure that as many CTSs were located as possible. The mapped CTSs were then filtered. ~90 % of the motifs were alone on the co-peaks and 76.8 % of them followed the shift both in human and mouse. In the case of overlaps, we chose those hits having the highest motif score. In the case of multiple elements under a co-peak, we chose that putative element following the shift and having the highest motif score. In the case of multiple elements in the opposite direction, we also selected the one with the highest motif score.
Determination of shifts between CTCF and cohesin bound sites
ChIP-fragment coverage of CTCF/cohesin samples were plotted on their own CTS set (where peaks of the individual sample overlap with the consensus CTS set) by annotatePeaks.pl using -hist 1 parameter . The maxima of each histogram and the position of these values relative to the CTS center are shown as scatter plots on Fig. 1a and Additional file 1: Figure S2 for human and mouse cells, respectively.
To further investigate the strand specific shift between CTCF and cohesin peak summits, we compared sample duos and trios that were derived from the same cell or tissue type with identical condition. In these cases, for each comparison, peaks were selected that overlapped with the consensus CTS set. Instead of the summit predictions of MACS2, we used the ones located with PeakSplitter, which was developed to discriminate subpeaks (in case of overlapping peaks) and thus gives more accurate local maxima. The distance of the summits relative to the reference points was established by closestBed (BEDtools) . Firstly, the reference point was the mathematical middle of the CTSs in the histograms and box plots showing the summit distribution of the CTCF and cohesin bound (Fig. 1b; Additional file 1: Figures S3B and S4-S7). Then, we set the CTCF summits as reference points (Fig. 1c; Additional file 1: Figures S3C and S8-S9).
Investigation of CTCF/cohesin co-occupied sites with ChIP-exo and DNase-seq data
To identify the genomic location and coverage of CTCF/cohesin proteins with near-single-nucleotide accuracy, we used publicly available HeLa DNase-seq and ChIP-exo data (SRX100899, SRX098243).
The single-nucleotide resolution border peak detection was executed with “model based analysis of ChIP-exo” (MACE) .
The DNase-seq bam files were downloaded directly from the ENCODE database . The raw sequence reads were then aligned to the hg19 human genome. The accurate prediction of CTCF/cohesin footprints were then done with the Wellington algorithm . This algorithm detects characteristic depletions of DNase I cuts and compares the result with a large number of cuts in the surrounding region of open chromatin that do not harbor bound proteins.
The identified ChIP-exo and DNase-seq borders were then compared with the processed ChIP-seq data and are shown in Additional file 1: Figures S3B and S3C.
Identification of CTSs involved in chromatin looping
ChIA-PET (Chromatin Interaction Analysis by Paired-End Tag Sequencing) data was used to collect CTSs that are involved in CTCF mediated chromatin looping. The CTCF ChIA-PET data were downloaded from the public database of ENCODE as a processed interaction set in “junction BED” format . We used the interaction sets of the MCF7 cell line in further analyses because it has biological replicates and good quality RAD21 (SRX190247) and CTCF (SRX190190) ChIP-seq data that are also derived from the ENCODE database.
The two sides of one interaction are actually two sections of the DNA (ChIA-PET DNA section with variable size). The ChIA-PET DNA sections contain CTSs, which are involved in CTCF-mediated DNA looping. To identify these we searched for the closest CTS to the midpoint of the ChIA-PET DNA sections that showed convergent motif orientation with the CTS of the other side if there was interaction .
We constructed a consensus interaction set from the replicas using intersectBed . 8482 interactions were selected and these showed 100 % overlap on both CTSs of the interaction (intersectBed -f 1 -r). A representative examples of the loops are shown in (Additional file 1: Figure S3A and Additional file 3: Table S11).
3C, Chromosome conformation capture; AR, androgen receptor; Bp, base pair; ChIA-PET, Chromatin Interaction Analysis with Paired-End-Tag sequencing; ChIP-exo, chomatin immunoprecipitation with exonuclease digestion and high-throughput sequencing; ChIP-seq, chromatin immunoprecipitation followed by sequencing; CTCF, CCCTC-binding factor; CTS, CTCF specific recognition sites; DHS, DNase I hypersensitivity sites; DNase-seq, deoxyribonuclease I digestion with high-throughput sequencing; ENCODE, ENCyclopedia Of DNA Elements; kb, kilobase; FOXA1, Forkhead box protein A1; MACE, model based analysis of ChIP-exo; MACS, Model-based Analysis of ChIP-Seq data; PET, paired-end tag; RAD21, Double-strand-break repair protein rad21 homolog; SMC, Structural Maintenance of Chromosomes; SMC1/3, constitutes the core subunits of the cohesin complexes involved in sister chromatid cohesion; STAG2, Cohesin subunit SA-2; TF, transcription factor; TFBS, transcription factor binding site
We thank Balázs Baksa (Al-Ba, Kecskemét, Hungary) for the artwork, János Juhász (Pázmány University, Budapest, Hungary) for his help with molecular modeling and Dr. Max Bingham (Freelance Editor, Rotterdam, The Netherlands) for the editorial assistance prior to submission. We thank M. Fuxreiter, and members of the L. Nagy lab for the helpful discussions. The authors thank the Genomic Medicine and Bioinformatic Core Facility at the University of Debrecen and The Hungarian National Information Infrastructure Development Institute for providing supercomputing facilities for data analysis.
This work has been supported by the Hungarian Ministry of Agriculture to EB and TN (grant number NAIK-MBK/M71411) and by the TÁMOP-4.2.2.C-11/1/KONV-2012-0010. We also acknowledge the support from COST action BM1006 (SEQAHEAD).
Availability of data and materials
The datasets supporting the conclusions of this article are included within the article and in Additional file 2. The scripts used during the analysis are available at the following web site: https://github.com/Raziel01/CTCF_Cohesin_shift_calculation.
EB and LN initiated the project. EB and GN conceived and designed the overall project. EC and GN carried out the data collection and processing. EC, TN and LS performed the statistical and simulation analyses. EB, EC, GN and SP evaluated the results and wrote the manuscript. LN revised the manuscript. All authors reviewed the manuscript.
The authors declare they have no conflict of interest.
Consent for publication
Ethics approval and consent to participate
Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
- Park PJ. ChIP-seq: advantages and challenges of a maturing technology. Nat Rev Genet. 2009;10(10):669–80.View ArticlePubMedPubMed CentralGoogle Scholar
- Starick SR, Ibn-Salem J, Jurk M, Hernandez C, Love MI, Chung HR, Vingron M, Thomas-Chollier M, Meijsing SH. ChIP-exo signal associated with DNA-binding motifs provides insight into the genomic binding of the glucocorticoid receptor and cooperating transcription factors. Genome Res. 2015;25(6):825–35.View ArticlePubMedPubMed CentralGoogle Scholar
- Gruber S, Haering CH, Nasmyth K. Chromosomal cohesin forms a ring. Cell. 2003;112(6):765–77.View ArticlePubMedGoogle Scholar
- Nasmyth K, Haering CH. Cohesin: Its roles and mechanisms. Annu Rev Genet. 2009;43(1):525–58.View ArticlePubMedGoogle Scholar
- Rubio ED, Reiss DJ, Welcsh PL, Disteche CM, Filippova GN, Baliga NS, Aebersold R, Ranish JA, Krumm A. CTCF physically links cohesin to chromatin. Proc Natl Acad Sci USA. 2008;105(24):8309–14.View ArticlePubMedPubMed CentralGoogle Scholar
- Hadjur S, Williams LM, Ryan NK, Cobb BS, Sexton T, Fraser P, Fisher AG, Merkenschlager M. Cohesins form chromosomal cis-interactions at the developmentally regulated IFNG locus. Nature. 2009;460(7253):410–3.PubMedPubMed CentralGoogle Scholar
- Xiao T, Wallace J, Felsenfeld G. Specific sites in the C terminus of CTCF interact with the SA2 subunit of the cohesin complex and are required for cohesin-dependent insulation activity. Mol Cell Biol. 2011;31(11):2174–83.View ArticlePubMedPubMed CentralGoogle Scholar
- Feeney KM, Wasson CW, Parish JL. Cohesin: a regulator of genome integrity and gene expression. Biochem J. 2010;428(2):147–61.View ArticlePubMedGoogle Scholar
- Sofueva S, Hadjur S. Cohesin-mediated chromatin interactions--into the third dimension of gene regulation. Brief Funct Genomics. 2012;11(3):205–16.View ArticlePubMedGoogle Scholar
- Merkenschlager M, Odom DT. CTCF and cohesin: linking gene regulatory elements with their targets. Cell. 2013;152(6):1285–97.View ArticlePubMedGoogle Scholar
- Phillips-Cremins JE, Corces VG. Chromatin insulators: linking genome organization to cellular function. Mol Cell. 2013;50(4):461–74.View ArticlePubMedPubMed CentralGoogle Scholar
- Bouwman BA, de Laat W. Getting the genome in shape: the formation of loops, domains and compartments. Genome Biol. 2015;16:154.View ArticlePubMedPubMed CentralGoogle Scholar
- Ohlsson R, Renkawitz R, Lobanenkov V. CTCF is a uniquely versatile transcription regulator linked to epigenetics and disease. Trends Genet. 2001;17(9):520–7.View ArticlePubMedGoogle Scholar
- Kim TH, Abdullaev ZK, Smith AD, Ching KA, Loukinov DI, Green RD, Zhang MQ, Lobanenkov VV, Ren B. Analysis of the vertebrate insulator protein CTCF-binding sites in the human genome. Cell. 2007;128(6):1231–45.View ArticlePubMedPubMed CentralGoogle Scholar
- Ohlsson R, Lobanenkov V, Klenova E. Does CTCF mediate between nuclear organization and gene expression? Bioessays. 2010;32(1):37–50.View ArticlePubMedGoogle Scholar
- West AG, Gaszner M, Felsenfeld G. Insulators: many functions, many mechanisms. Genes Dev. 2002;16(3):271–88.View ArticlePubMedGoogle Scholar
- Haering CH, Löwe J, Hochwagen A, Nasmyth K. Molecular architecture of SMC proteins and the yeast cohesin complex. Mol Cell. 2002;9(4):773–88.View ArticlePubMedGoogle Scholar
- Gligoris TG, Scheinost JC, Burmann F, Petela N, Chan KL, Uluocak P, Beckouet F, Gruber S, Nasmyth K, Lowe J. Closing the cohesin ring: structure and function of its Smc3-kleisin interface. Science. 2014;346(6212):963–7.View ArticlePubMedPubMed CentralGoogle Scholar
- Remeseiro S, Losada A. Cohesin, a chromatin engagement ring. Curr Opin Cell Biol. 2013;25(1):63–71.View ArticlePubMedGoogle Scholar
- Haering CH, Farcas AM, Arumugam P, Metson J, Nasmyth K. The cohesin ring concatenates sister DNA molecules. Nature. 2008;454(7202):297–301.View ArticlePubMedGoogle Scholar
- DeMare LE, Leng J, Cotney J, Reilly SK, Yin J, Sarro R, Noonan JP. The genomic landscape of cohesin-associated chromatin interactions. Genome Res. 2013;23(8):1224–34.View ArticlePubMedPubMed CentralGoogle Scholar
- Rao SS, Huntley MH, Durand NC, Stamenova EK, Bochkov ID, Robinson JT, Sanborn AL, Machol I, Omer AD, Lander ES, et al. A 3D map of the human genome at kilobase resolution reveals principles of chromatin looping. Cell. 2014;159(7):1665–80.View ArticlePubMedGoogle Scholar
- Stigler J, Çamdere GO, Koshland DE, Greene EC. Single-Molecule Imaging Reveals a Collapsed Conformational State for DNA-Bound Cohesin. Cell Rep. 2016;15(5):988–998.Google Scholar
- Madabhushi R, Gao F, Pfenning AR, Pan L, Yamakawa S, Seo J, Rueda R, Phan TX, Yamakawa H, Pao PC, et al. Activity-induced DNA breaks govern the expression of neuronal early-response genes. Cell. 2015;161(7):1592–605.View ArticlePubMedPubMed CentralGoogle Scholar
- Guo Y, Xu Q, Canzio D, Shou J, Li J, Gorkin DU, Jung I, Wu H, Zhai Y, Tang Y, et al. CRISPR Inversion of CTCF Sites Alters Genome Topology and Enhancer/Promoter Function. Cell. 2015;162(4):900–10.View ArticlePubMedGoogle Scholar
- Daniel B, Nagy G, Hah N, Horvath A, Czimmerer Z, Poliska S, Gyuris T, Keirsse J, Gysemans C, Van Ginderachter JA, et al. The active enhancer network operated by liganded RXR supports angiogenic activity in macrophages. Genes Dev. 2014;28(14):1562–77.View ArticlePubMedPubMed CentralGoogle Scholar
- Barta E. Command line analysis of ChIP-seq results. Embnet Journal. 2011;17(1):13–17.Google Scholar
- Vlahovicek K, Kajan L, Pongor S. DNA analysis servers: plot.it, bend.it, model.it and IS. Nucleic Acids Res. 2003;31(13):3686–7.View ArticlePubMedPubMed CentralGoogle Scholar
- Zhang N, Kuznetsov SG, Sharan SK, Li K, Rao PH, Pati D. A handcuff model for the cohesin complex. J Cell Biol. 2008;183(6):1019–31.View ArticlePubMedPubMed CentralGoogle Scholar
- Sanborn AL, Rao SS, Huang SC, Durand NC, Huntley MH, Jewett AI, Bochkov ID, Chinnappan D, Cutkosky A, Li J, et al. Chromatin extrusion explains key features of loop and domain formation in wild-type and engineered genomes. Proc Natl Acad Sci U S A. 2015;112(47):E6456–6465.View ArticlePubMedPubMed CentralGoogle Scholar
- Gruber S, Arumugam P, Katou Y, Kuglitsch D, Helmhart W, Shirahige K, Nasmyth K. Evidence that loading of cohesin onto chromosomes involves opening of its SMC hinge. Cell. 2006;127(3):523–37.View ArticlePubMedGoogle Scholar
- Shintomi K, Hirano T. How are cohesin rings opened and closed? Trends Biochem Sci. 2007;32(4):154–7.View ArticlePubMedGoogle Scholar
- Akai Y, Kanai R, Nakazawa N, Ebe M, Toyoshima C, Yanagida M. ATPase-dependent auto-phosphorylation of the open condensin hinge diminishes DNA binding. Open Biol. 2014;4(12):140193.Google Scholar
- Fudenberg G, Imakaev M, Lu C, Goloborodko A, Abdennur N, Mirny LA. Formation of Chromosomal Domains by Loop Extrusion. Cell Rep. 2016;15(9):2038–2049.Google Scholar
- Tang Z, Luo OJ, Li X, Zheng M, Zhu JJ, Szalaj P, Trzaskoma P, Magalska A, Wlodarczyk J, Ruszczycki B, et al. CTCF-Mediated Human 3D genome architecture reveals chromatin topology for transcription. Cell. 2015;163(7):1611–27.View ArticlePubMedGoogle Scholar
- Wheeler DL, Barrett T, Benson DA, Bryant SH, Canese K, Chetvernin V, Church DM, Dicuccio M, Edgar R, Federhen S, et al. Database resources of the national center for biotechnology information. Nucleic Acids Res. 2008;36(Database issue):D13–21.PubMedGoogle Scholar
- The EPC. An integrated encyclopedia of DNA elements in the human genome. Nature. 2012;489(7414):57–74.View ArticleGoogle Scholar
- Li H, Durbin R. Fast and accurate long-read alignment with Burrows–Wheeler transform. Bioinformatics. 2010;26(5):589–95.View ArticlePubMedPubMed CentralGoogle Scholar
- Zhang Y, Liu T, Meyer CA, Eeckhoute J, Johnson DS, Bernstein BE, Nusbaum C, Myers RM, Brown M, Li W, et al. Model-based Analysis of ChIP-Seq (MACS). Genome Biol. 2008;9(9):R137–7.View ArticlePubMedPubMed CentralGoogle Scholar
- Heinz S, Benner C, Spann N, Bertolino E, Lin YC, Laslo P, Cheng JX, Murre C, Singh H, Glass CK. Simple combinations of lineage-determining transcription factors prime cis-regulatory elements required for macrophage and B cell identities. Mol Cell. 2010;38(4):576–89.View ArticlePubMedPubMed CentralGoogle Scholar
- Robinson JT, Thorvaldsdóttir H, Winckler W, Guttman M, Lander ES, Getz G, Mesirov JP. Integrative genomics viewer. Nat Biotechnol. 2011;29(1):24–6.View ArticlePubMedPubMed CentralGoogle Scholar
- Quinlan AR, Hall IM. BEDTools: a flexible suite of utilities for comparing genomic features. Bioinformatics (Oxford, England). 2010;26(6):841–2.View ArticleGoogle Scholar
- Wang L, Chen J, Wang C, Uusküla-Reimand L, Chen K, Medina-Rivera A, Young EJ, Zimmermann MT, Yan H, Sun Z, et al. MACE: model based analysis of ChIP-exo. Nucleic Acids Res. 2014;42(20):e156–6.View ArticlePubMedPubMed CentralGoogle Scholar
- Piper J, Elze MC, Cauchy P, Cockerill PN, Bonifer C, Ott S. Wellington: a novel method for the accurate identification of digital genomic footprints from DNase-seq data. Nucleic Acids Res. 2013;41(21):e201–1.View ArticlePubMedPubMed CentralGoogle Scholar