ChIA-PET

Chromatin Interaction Analysis by Paired-End Tag Sequencing (ChIA-PET) is a technique that incorporates chromatin immunoprecipitation (ChIP)-based enrichment, chromatin proximity ligation, Paired-End Tags, and High-throughput sequencing to determine de novo long-range chromatin interactions genome-wide.^[1]
Genes can be regulated by regions far from the promoter such as regulatory elements, insulators and boundary elements, and transcription-factor binding sites (TFBS). Uncovering the interplay between regulatory regions and gene coding regions is essential for understanding the mechanisms governing gene regulation in health and disease (Maston et al., 2006). ChIA-PET can be used to identify unique, functional chromatin interactions between distal and proximal regulatory transcription-factor binding sites and the promoters of the genes they interact with.

ChIA-PET can also be used to unravel the mechanisms of genome control during processes such as cell differentiation, proliferation, and development. By creating ChIA-PET interactome maps for DNA-binding regulatory proteins and promoter regions, we can better identify unique targets for therapeutic intervention (Fullwood & Yijun, 2009).

Methodology

The ChIA-PET method combines ChIP-based methods (Kuo & Allis, 1999), and Chromosome conformation capture (3C), to extend the capabilities of both approaches. ChIP-Sequencing (ChIP-Seq) is a popular method used to identify TFBS while 3C has been used to identify long-range chromatin interactions (Dekker et al., 2002). However, both suffer from limitations when used independently to identify de-novo long-range interactions genome wide. While ChIP-Seq is typically used for genome-wide identification of TFBS (Barski et al., 2007; Wei et al., 2006), it provides only linear information of protein binding sites along the chromosomes (but not interactions between them), and can suffer from high genomic background noise (false positives).

While 3C is capable of analyzing long-range chromatin interactions, it cannot be used genome wide and, like ChIP-Seq, also suffers from high levels of background noise. Since the noise increases in relation to the distance between interacting regions (max 100kb), laborious and tedious controls are required for accurate characterization of chromatin interactions (Dekker et al., 2006).

The ChIA-PET method successfully resolves the issues of non-specific interaction noise found in ChIP-Seq by sonicating the chip fragments in order to separate random attachments from specific interaction complexes. The next step, which is referred to as enrichment, reduces complexity for genome-wide analysis and adds specificity to chromatin interactions bound by pre-determined TFs (transcription factors). The ability of 3C approaches to identify long-range interactions is based on the theory of proximity ligation. In regards to DNA inter-ligation, fragments that are tethered by common protein complexes have greater kinetic advantages under dilute conditions, than those freely diffusing in solution or anchored in different complexes. ChIA-PET takes advantage of this concept by incorporating linker sequences onto the free ends of the DNA fragments tethered to the protein complexes. In order to build connectivity of the fragments tethered by regulatory complexes, the linker sequences are ligated during nuclear proximity ligation. Therefore, the products of linker-connected ligation can be analyzed by ultra-high-throughput PET sequencing and mapped to the reference genome. Since ChIA-PET is not dependent on specific sites for detection as 3C and 4C are, it allows unbiased, genome-wide de-novo detection of chromatin interactions (Fullwood et al., 2009).

Workflow

Wet-lab portion of the workflow:

Figure 3. Biotinylated universal linkers with Mme1 restriction endonuclease sites are introduced.

Figure 4. Biotinylated universal linkers are ligated to the free DNA ends.

Figure 5. Ligation of linkers during proximity ligation.

Figure 6. Pull down of biotinylated linkers by streptavidin-beads, and amplification of DNA tags.

Figure 7. Conformations of universal linkers.

• Figure 1. Formaldehyde is used to cross-link the DNA-protein complexes. Sonication is used to break-up the chromatin and also to reduce non-specific interactions.
• Figure 2. A specific antibody of choice is used to enrich protein of interest bound chromatin fragments. ChIP material bound by the antibody are used to construct the ChIA-PET.
• Figure 3. Biotinylated oligonucleotide half-linkers containing flanking MmeI sites are used to connect proximity ligated DNA fragments. Two different linkers are designed (A and B) with specific nucleotide barcodes (CG or AT) for each of the two linker sequences (this will allow the identification of the chimeric ligation product as describe in Figure 7.).
• Figure 4. The linkers are ligated to the tethered DNA fragments.
• Figure 5. The linker fragments are ligated on the ChIP beads under dilute conditions. The purified DNA is then digested by MmeI, which cuts at a distance from its recognition site to release the tag-linker-tag structure.
• Figure 6. The biotinylated PETs are then immobilized on streptavidin-conjugated magnetic beads.
• Figure 7. PET sequences with AA (CG/CG) and BB (AT/AT) linker barcode composition are considered to be possible intra-complex ligation products, while the PET sequences with AB (CG/AT) linker composition are considered to be derived from chimeric ligation products between DNA fragments bounded in different chromatin complexes. #COMMENT: 3 blue-yellow chimeric product are missing (they are different!)

Dry-lab portion of the workflow:

PET extraction, mapping, and statistical analyses

The PET tags are extracted and mapped to the reference human genome in-silico.

Identification of ChIP enriched peaks (binding sites)

Self-ligated PET are used for identifying ChIP enriched sites because they provide the most reliable mapping (20 + 20 bit/s) to the reference genome.

ChIP enrichment peak-finding algorithm

A called peak is considered a binding site if there are multiple overlapping self-ligated PETs. The false discovery rate (FDR) is determined using statistical simulations to estimate the random background of PET-derived virtual DNA overlaps, and the estimated background noise.

Filtering of repetitive DNA (affects non-specific binding)

Satellite regions and binding sites present in regions with severe structural variations are removed.

ChIP enrichment count

The numbers of self-ligation and inter-ligation PETs (within + 250 bp window) are reported at each site. The total number of self-ligated and inter-ligated PETs at a specific site is called the ChIP enrichment count.

Figure 8. PET Classification: Uniquely aligned PET sequences can be classified by whether they are derived from one DNA fragment or two DNA fragments.

Figure 8. Intra and inter-ligated PETs are clustered around TFBS when mapped to the reference human genome.

• Self-ligation PETs

If the two tags of a PET are mapped on the same chromosome with the genomic span in the range of ChIP DNA fragments (less than 3 Kb), with expected self-ligation orientation and on the same strand, they are considered to be derived from a self-ligation of a single ChIP DNA fragment, and considered a self-ligation PET.

• Inter-ligation PETs

If a PET does not fit into these criteria, then the PET most likely resulted from a ligation product between two DNA fragments and referred to as an inter-ligation PET. The two tags of an inter-ligation PETs do not have fixed tag orientations, might not be found on the same strands, might have any genomic span, and might not map to the same chromosome.

• Intrachromosomal inter-ligation PETs

If the two tags of an inter-ligation PET are mapped in the same chromosome but with a span > 3 Kb in any orientation, then these PETs are called intrachromosomal inter-ligation PETs.

• Interchromosomal inter-ligation PETs

PETs which are mapped to different chromosomes are called interchromosomal inter-ligation PETs.

Figure 9. Proposed mechanism showing how distal regulatory elements can initiate long-range chromatin interactions involving promoter regions of target genes.

Figure 9. Proposed DNA looping mechanism between distal regulatory proteins and the promoter region

The interactions form DNA loop structures with multiple TFBS at the anchoring center. Small loops might package genes near the anchoring center in a tight sub-compartment, which could increase the local concentration of regulatory proteins for enhanced transcriptional activation. This mechanism might also enhance transcription efficiency, allowing RNA pol II to cycle the tight circular gene templates. The large interaction loops are more likely to link together distant genes at either end of the loop residing near anchor sites for coordinated regulation, or could separate genes in long loops to prevent their activation. Adapted from Fullwood et al. (2009).

Strengths and weaknesses

Advantages of the ChIA-PET method

• ChIA-PET is an unbiased, whole-genome and de-novo approach for long-range chromatin interaction analysis.
• A ChIA-PET experiment is capable of providing two global datasets: The protein factor binding sites (self-ligated PETs); and The interactions between the binding sites (inter-ligated PETs).
• ChIA-PET involves ChIP to reduce the complexity for genome-wide analysis and adds specificity to chromatin interactions bound by specific factors of interest.
• ChIA-PET is compatible with tag-based next-generation sequencing approaches such as Roche 454 pyrosequencing, Illumina GA, ABI SOLiD, and Helicos.
• ChIA-PET is applicable to many different protein factors involved in transcriptional regulation or chromatin structural conformation.
• ChIA-PET analysis can be applied to chromatin interactions involved in a particular nuclear process. By using general TFs such as RNA Polymerase II, it may be possible to identify all chromatin interactions involved in transcription regulation. Further, the use of protein factors involved in DNA replication or chromatin structure would allow identification of all interactions due to DNA replication and chromatin structural modification (Fullwood et al., 2009).

Weaknesses

• It is well established that cis and trans-regulatory complexes contain unique combinations of proteins based on cell and tissue specific conditions (Dekker et al., 2006). While identification of single, functional TFBS is a significant advancement, the use of ChIA-PET to identify individual proteins in a complex would require guess work and multiple experiments to identify each interacting protein. This would be a costly and time consuming endeavour.
• ChIA-PET is limited by the quality, purity, and specificity of the antibodies used (Fullwood et al., 2009).
• ChIA-PET is dependent on identification of sequences that can be mapped to the reference sequence (ref).
• ChIA-PET requires the use of peak-calling computer algorithms to organize and map PET reads to the reference genome. Because of variations between software platforms, results can vary depending on which program is used.
• Although repetitive DNA regions can be associated with gene regulation (Polak & Domany, 2006), they need to be removed as they can affect the data (Fullwood et al., 2009).

History

Fullwood et al. (2009), used ChIA-PET to detect and map the chromatin interaction network mediated by estrogen receptor alpha (ER-alpha) in human cancer cells. The resulting global chromatin interactome map revealed that remote ER-alpha-binding sites were also anchored to gene promoters through long-range chromatin interactions suggesting that ER-alpha functions by extensive chromatin looping in order to bring genes together for coordinated transcriptional regulation.

Analysis and software

Software typically used in a ChIA-PET experiment

ELAND

Maps ChIP enriched DNA fragments to the reference human genome.

RepeatMasker

In-silico masking of repetitive elements.

Monte Carlo simulation

Used to estimate the false discovery rates.^[2]

PET-Tool

A software suite for processing and managing of Paired-End di-Tag sequence data.

ChIA-PET Tool

A software suite for processing ChIA-PET data.ChIA-PET Tool web site ChIA-PET Tool paper

Alternatives

Chromatin immunoprecipitation:

ChIP-Seq, ChIP-PET, ChIP-SAGE, ChIP-CHIP.

Chromosome conformation capture:

2-C, 3-C, 4-C, 5-C.

Paired-end tags:

PET.

See also

• Chia pet

References

• Barski et al., (2007). High-resolution profiling of histone methylations in the human genome. Cell. (129); 823–37.
• Dekker, (2002). Capturing chromosome conformation. Science. (295); 1306–1311.
• Dekker, (2006). The three ‘C’ s of chromosome conformation capture: controls, controls, controls. Nat. Methods. (3); 17–21.
• Fullwood et al., (2009). An oestrogen-receptor-α bound human chromatin interactome. Nature. (462); 58-64.
• Fullwood & Yijun, (2009). ChIP-based methods for the identification of long-range chromatin interactions. J Cell Biochem. 107(1); 30–39.
• Johnson et al., (2007). Genome-wide mapping of in vivo protein-DNA interactions. Science. (316); 1497–502.
• Kuo & Allis, (1999). In-vivo cross-linking and immunoprecipitation for studying dynamic Protein: DNA associations in a chromatin environment. Methods. (19); 425–33.
• Li, G., Fullwood, M.J., Xu, H., Mulawadi, F.H., Velkov, S., Vega, V., Ariyaratne, P.N., Mohamed, Y.B., Ooi, H.S., Tennakoon, C., Wei, C.L., Ruan, Y. and Sung, W.K. ChIA-PET tool for comprehensive chromatin interaction analysis with paired-end tag sequencing. Genome Biol, 11 (2). R22.
• Maston et al., (2006). Transcriptional Regulatory Elements in the Human Genome. Annu. Rev: Genomics. Hum Genet. (7); 29–59.
• Polak & Domany, (2006). Alu elements contain many binding sites for transcription factors and may play a role in regulation of developmental processes. BMC Genomics. (7); 133.
• Wei et al., (2006). A global map of p53 transcription-factor binding sites in the human genome. Cell. (124); 207–19.

External links

• ChIA-PET Genome Browser - This browser is for viewing the data from Fullwood et al. (2009), and includes a custom Whole Genome Interaction Viewer which provides a macroscopic picture of binding sites and interactions along with a whole genome landscape.