4c

Abstract

The present invention relates in one aspect to a method for analysing the frequency of interaction of a target nucleotide sequence with one or more nucleotide sequences of interest (eg. one or more genomic loci) comprising the steps of: (a) providing a sample of cross-linked DNA; (b) digesting the cross-linked DNA with a primary restriction enzyme; (c) ligating the cross-linked nucleotide sequences; (d) reversing the cross linking; (e) digesting the nucleotide sequences with a secondary restriction enzyme; (f) ligating one or more DNA sequences of known nucleotide composition to the available secondary restriction enzyme digestion site(s) that flank the one or more nucleotide sequences of interest; (g) amplifying the one or more nucleotide sequences of interest using at least two oligonucleotide primers, wherein each primer hybridises to the DNA sequences that flank the nucleotide sequences of interest; (h) hybridising the amplified sequence(s) to an array or sequencing the amplified sequences; and (i) determining the frequency of interaction between the DNA sequences.

Description

REFERENCE TO RELATED APPLICATIONS [0001] This application is a continuation in part of international patent application PCT / IB2006 / 002268 filed Jul. 3, 2006, and published as WO 2007 / 004057 on Jan. 11, 2007, which claims priority from United Kingdom Patent Application Nos. 0605449.8 filed Mar. 17, 2006 and 0513676.7 filed Jul. 4, 2005.[0002] Each of the above referenced applications, and each document cited in this text (“application cited documents”) and each document cited or referenced in each of the application cited documents, and any manufacturer's specifications or instructions for any products mentioned in this text and in any document incorporated into this text, are hereby incorporated herein by reference; and, technology in each of the documents incorporated herein by reference can be used in the practice of this invention. [0003] It is noted that in this disclosure, terms such as “comprises”, “comprised”, “comprising”, “contains”, “containing” and the like can have the m...

AI Technical Summary

Benefits of technology

[0097] By way of example, the present invention is advantageous since it provides inter alia commercially useful nucleotides sequences, processes, probes and arrays.

[0098] By way of further example, the present invention is advantageous since it provides for the high throughput analysis of the frequency of interaction of two or more nucleotide sequences in the nuclear space.

[0099] By way of further example, the present invention is advantageous since using conventional 3C technology, each single DNA-DNA interaction must be analysed by a unique PCR reaction containing a unique pair of primers. High-throughput analysis is therefore only possible if PCR is automated, but the costs of so many primers will be too high. Accordingly, high-throughput (genome-wide) analysis of DNA-DNA interactions is not viable with conventional 3C technology. In contrast, the present invention now allows the simultaneous screening of thousands of DNA-DNA interactions. High-throughput analysis of DNA-DNA interactions according to the present invention will greatly increase the scale and resolution of analysis.

[0101] By way of further example, the present invention is advantageous because using conventional 3C technology only allows the selective amplification of a single DNA-DNA interaction. This is not informative when hybridised to an array. The technology has been improved such that all fragments that interact with a first (target) nucleotide sequence are now amplified eg. selectively amplified.

[0102] By way of further example, the present invention is advantageous because 4C technology can be used to detect balanced or unbalanced genetic aberrations—such as all types of translocations, deletions, inversions, duplications and other genomic rearrangements—in nucleic acid, for example, chromosomes. 4C technology (which measures proximity of DNA fragments) can even determine a subject's predisposition to acquire certain translocations, deletions, inversions, duplications and other genomic rearrangements (eg. balanced or unbalanced translocations, deletions, inversions, duplications and other genomic rearrangements). An advantage over current strategies is that it is not required to know the exact position of the change because the resolution of 4C technology is such that it can be used to detect rearrangements even when the ‘4C-bait’ (as defined by the primary and secondary restriction enzyme recognition sites that are analysed) is located away (eg. up to one megabase or even more) from the change. Another advantage over current strategies is that it allows for a simultaneous, unbiased genome-wide search for both balanced and unbalanced genomic rearrangements. Another advantage is that 4C technology allows the accurate mapping of changes since it can be used to define the two (primary) restriction sites between which changes occurred. Another advantage is that cells need not to be cultured before fixation. Thus, for example solid tumours can also be analysed for genomic rearrangements.

[0103] By way of further example, the present invention is advantageous because the 4C technology can also detect changes (eg. rearrangements) in a pre-malignant state, i.e. before all the cells contain these changes. Thus, the technology can be used not only in the diagnosis of disease but also in the prognosis of disease.

[0104] By way of further example, the array design according to the present invention is particularly advantageous as compared to existing genomic tiling arrays—such as Nimblegen genomic tiling arrays—since the design allows representation of a much larger part of the genome per single array. By way of example, for a restriction enzyme recognising a hexa-nucleotide sequence about 3 arrays with about 385,000 probes each will be sufficient to cover, for example, the complete human or mouse genome. For a restriction enzyme recognising more than 6 bp, a single array of about 385,000 probes can be used to cover, for example, the complete human or mouse genome. The advantages of the array design are that: (1) each probe is informative since each analyses an independent ligation event, greatly facilitating the interpretation of the results; and (2) a large representation of the genome can be spotted on a single array which is cost-effective.

[0105] 4C technology can advantageously be used for the fine-mapping of poorly characterised rearrangements originally detected by cytogenetic approaches (light microscopy, FISH, SKY, etc).

[0017] In a further embodiment, 4C technology can be multiplexed and used to screen for rearrangements in genomic DNA throughout the genome, at unknown positions.

Problems solved by technology

3C technology as currently applied only allows analysis of a limited number of selected DNA-DNA interactions owing to the limitations of the PCR amplification step, which requires knowledge of specific sequence information for each fragment to be analysed.

Moreover, selecting restriction fragments as candidates for long-range DNA interactions requires a substantial amount of prior knowledge (e.g. the location of hypersensitive sites) of the locus of interest, which is usually not available.

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