signature=ec60b45113de7d0987c1302a87f8f54b,Isothermal Strand Displacement Amplification Using Primer...

TECHNICAL FIELD

The present invention relates to methods for amplifying nucleic acid molecules without thermal cycling.

BACKGROUND ART

The most widely used method for amplification of specific sequences from within a population of nucleic acid sequences is that of polymerase chain reaction (PCR) (Dieffenbach C and Dveksler G eds. PCR Primer: A Laboratory Manual. Cold Spring Harbor Press, Plainview N.Y.). In this amplification method, oligonucleotides, generally 15 to 30 nucleotides in length on complementary strands and at either end of the region to be amplified, are used to prime DNA synthesis on denatured single-stranded DNA templates. Successive cycles of denaturation, primer hybridisation and DNA strand synthesis using thermostable DNA polymerases allows exponential amplification of the sequences between the primers. RNA sequences can be amplified by first copying using reverse transcriptase to produce a cDNA copy. Amplified DNA fragments can be detected by a variety of means including gel electrophoresis, hybridisation with labelled probes, use of tagged primers that allow subsequent identification (e.g. by an enzyme linked assay), use of fluorescently-tagged primers that give rise to a signal upon hybridisation with the target DNA (e.g. Beacon and TaqMan systems).

One disadvantage of PCR is the need of a thermocycler to heat and cool the amplification mixture to denature the DNA. This, amplification cannot be carried out in primitive sites or operated easily outside of a laboratory environment.

As well as PCR, a variety of other techniques have been developed for detection and amplification of specific sequences. One example is the ligase chain reaction (Barany F Genetic disease detection and DNA amplification using cloned thermostable ligase. Proc. Natl. Acad. Sci. USA 88:189-193 (1991)).

In addition to conventional methods of DNA amplification that rely on the thermal denaturation of the target during the amplification reaction, a number of methods have been described that do not require template denaturation during the amplification reaction and are thus termed isothermal amplification technologies.

Isothermal amplification was first described in 1992 (Walker G T, Little M C, Nadeau J G and Shank D. Isothermal in vitro amplification of DNA by a restriction enzyme/DNA polymerase system. PNAS 89: 392-396 (1992) and termed Strand Displacement Amplification (SDA). Since then, a number of other isothermal amplification technologies have been described including Transcription Mediated Amplification (TMA) and Nucleic Acid Sequence Based Amplification (NASBA) that use an RNA polymerase to copy RNA sequences but not corresponding genomic DNA (Guatelli J C, Whitfield K M, Kwoh D Y, Barringer K J, Richmann D D and Gingeras T R. Isothermal, in vitro amplification of nucleic acids by a multienzyme reaction modeled after retroviral replication. PNAS 87: 1874-1878 (1990): Kievits T, van Gemen B, van Strijp D, Schukkink R, Dircks M, Adriaanse H, Malek L, Sooknanan R, Lens P. NASBA isothermal enzymatic in vitro nucleic acid amplification optimized for the diagnosis of HIV-1 infection. J Virol Methods. 1991 December; 35(3):273-86).

Other DNA-based isothermal techniques include Rolling Circle Amplification (RCA) in which a DNA polymerase extends a primer directed to a circular template (Fire A and Xu SQ. Rolling replication of short circles. PNAS 92: 4641-4645 (1995), Ramification Amplification (RAM) that uses a circular probe for target detection (Zhang W, Cohenford M, Lentrichia B, Isenberg H D, Simson E, Li H, Yi J, Zhang D Y. Detection of Chlamydia trachomatisby isothermal ramification amplification method: a feasibility study. J Clin Microbiol. 2002 January; 40(1):128-32.) and more recently, Helicase-Dependent isothermal DNA amplification (HDA), that uses a helicase enzyme to unwind the DNA strands instead of heat (Vincent M, Xu Y, Kong H. Helicase-dependent isothermal DNA amplification. EMBO Rep. 2004 August; 5(8):795-800.)

Recently, isothermal methods of DNA amplification have been described (Walker G T, Little M C, Nadeau J G and Shank D. Isothermal in vitro amplification of DNA by a restriction enzyme/DNA polymerase system. PNAS 89: 392-396 (1992). Traditional amplification techniques rely on continuing cycles of denaturation and renaturation of the target molecules at each cycle of the amplification reaction. Heat treatment of DNA results in a certain degree of shearing of DNA molecules, thus when DNA is limiting such as in the isolation of DNA from a small number of cells from a developing blastocyst, or particularly in cases when the DNA is already in a fragmented form, such as in tissue sections, paraffin blocks and ancient DNA samples, this heating-cooling cycle could further damage the DNA and result in loss of amplification signals. Isothermal methods do not rely on the continuing denaturation of the template DNA to produce single stranded molecules to serve as templates from further amplification, but rely on enzymatic nicking of DNA molecules by specific restriction endonucleases at a constant temperature.

The technique termed Strand Displacement Amplification (SDA) relies on the ability of certain restriction enzymes to nick the unmodified strand of hemi-modified DNA and the ability of a 5′-3′ exonuclease-deficient polymerase to extend and displace the downstream strand. Exponential amplification is then achieved by coupling sense and antisense reactions in which strand displacement from the sense reaction serves as a template for the antisense reaction (Walker G T, Little M C, Nadeau J G and Shank D. Isothermal in vitro amplification of DNA by a restriction enzyme/DNA polymerase system. PNAS 89: 392-396 (1992). Such techniques have been used for the successful amplification of Mycobacterium tuberculosis(Walker G T, Little M C, Nadeau J G and Shank D. Isothermal in vitro amplification of DNA by a restriction enzyme/DNA polymerase system. PNAS 89: 392-396 (1992), HIV-1, Hepatitis C and HPV-16 Nuovo G. J., 2000), Chlamydia trachomatis(Spears P A, Linn P, Woodard D L and Walker G T. Simultaneous Strand Displacement Amplification and Fluorescence Polarization Detection of Chlamydia trachomatis. Anal. Biochem. 247: 130-137 (1997).

The use of SDA to date has depended on modified phosphorthioate nucleotides in order to produce a hemi-phosphorthioate DNA duplex that on the modified strand would be resistant to enzyme cleavage, resulting in enzymic nicking instead of digestion to drive the displacement reaction. Recently, however, several “nickase” enzyme have been engineered. These enzymes do not cut DNA in the traditional manner but produce a nick on one of the DNA strands. “Nickase” enzymes include N.Alw1 (Xu Y, Lunnen K D and Kong H. Engineering a nicking endonuclease N.Alw1 by domain swapping. PNAS 98: 12990-12995 (2001), N.BstNB1 (Morgan R D, Calvet C, Demeter M, Agra R, Kong H. Characterization of the specific DNA nicking activity of restriction endonuclease N.BstNBI. Biol. Chem. 2000 November; 381(11):1123-5.) and Mly1 (Besnier C E, Kong H. Converting MlyI endonuclease into a nicking enzyme by changing its oligomerization state. EMBO Rep. 2001 September; 2(9):782-6. Epub 2001 Aug. 23). The use of such enzymes would thus simplify the SDA procedure.

In addition, SDA has been improved by the use of a combination of a heat stable restriction enzyme (Ava1) and Heat stable Exo-polymerase (Bst polymerase). This combination has been shown to increase amplification efficiency of the reaction from a 108fold amplification to 1010fold amplification so that it is possible using this technique to amplify unique single copy molecules. The resultant amplification factor using the heat stable polymerase/enzyme combination is in the order of 109(Milla M. A., Spears P., A., Pearson R. E. and Walker G. T. Use of the Restriction Enzyme Ava1 and Exo-Bst Polymerase in Strand Displacement Amplification Biotechniques 1997 24:392-396.)

To date, all isothermal DNA amplification techniques require the initial double stranded template DNA molecule to be denatured prior to the initiation of amplification. In addition, amplification is only initiated once from each priming event.

The present inventors have now developed amplification methods which utilise enzymes and primers and do not require repeated temperature cycling.

DISCLOSURE OF INVENTION

In a first aspect, the present invention provides a method for isothermal DNA amplification comprising:providing to the DNA to be amplified an amplification mix comprising: a first primer at least partially complementary to a region of DNA and containing a non-regular base,

a second primer at least partially complementary to a region of DNA and containing a non-regular base,

a DNA polymerase,

an enzyme capable of strand displacement,

an enzyme that recognises a non-regular base in double-stranded DNA and causes a nick or excises a base in one DNA strand at or near the non-regular base; and

amplifying the DNA substantially without thermal cycling.

Optionally, the DNA can be denatured prior to, during, or at after addition of the amplification mix.

Preferably, the first primer is at least partially complementary to a region of a first strand of DNA, and the second primer is at least partially complementary to a region of DNA of the second strand of DNA.

The first and second primers can be oligonucleotides, oligonucleotide analogues, oligonucleotides of chimeric nature such as PNA/oligonucleotides or INA/oligonucleotides. Preferably, the primers are deoxyoligonucleotides.

Preferably, the oligonucleotide analogue is selected from intercalating nucleic acid (INA), peptide nucleic acid (PNA), hexitol nucleic acid (HNA), MNA, altritol nucleic acid (ANA), locked nucleic acid (LNA), cyclohexanyl nucleic acid (CAN), CeNA, TNA, (2′-NH)-TNA, nucleic acid based conjugates, (3′-NH)-TNA, α-L-Ribo-LNA, α-L-Xylo-LNA, β-D-Xylo-LNA, α-D-Ribo-LNA, [3.2.1]-LNA, Bicyclo-DNA, 6-Amino-Bicyclo-DNA, 5-epi-Bicyclo-DNA, α-Bicyclo-DNA, Tricyclo-DNA, Bicyclo[4.3.0]-DNA, Bicyclo[3.2.1]-DNA, Bicyclo[4.3.0]amide-DNA, β-D-Ribopyranosyl-NA, α-L-Lyxopyranosyl-NA, 2′—R-RNA, 2′-OR-RNA, α-L-RNA, and β-D-RNA, and mixtures thereof and hybrids thereof, as well as phosphorous atom modifications thereof, such as but not limited to phosphorothioates, methyl phospholates, phosphoramidites, phosphorodithiates, phosphoroselenoates, phosphotriesters and phosphoboranoates. In addition non-phosphorous containing compounds may be used for linking to nucleotides such as but not limited to methyliminomethyl, formacetate, thioformacetate and linking groups comprising amides. In particular nucleic acids and nucleic acid analogues may comprise one or more intercalator pseudonucleotides.

By INA is meant an intercalating nucleic acid in accordance with the teaching of WO 03/051901, WO 03/052132, WO 03/052133 and WO 03/052134 (Unest NS, assigned to Human Genetic Signatures Pty Ltd) incorporated herein by reference. An INA is an oligonucleotide or oligonucleotide analogue comprising one or more intercalator pseudonucleotide (IPN) molecules.

When a primer having the non-regular base binds to DNA it forms a site recognised by the enzyme.

The non-regular base (ie non-regular DNA base) is defined herein as a chemical entity other than adenine (A), thymine (T), guanine (G) and cytosine (C) capable of being inserted in a DNA backbone. Examples of non-regular bases include, but not limited, to deoxyinosine, 8 deoxyguanine, hydroxyuracil, 5-methyl-dC, 5 hydroxyuridine, 5 bromo-dU Inosine with C, ribonucleotides, and uracil. More preferably, the non-regular base is deoxyinosine.

It will be appreciated, however, that the non-regular base does not necessarily need to have the structure of a nucleotide.

The primers can have one or more non-regular bases. In some situations, two or more non-regular bases can improve the amplification process. The non-regular bases can be positioned close or spaced apart by at least several regular bases.

The DNA polymerase can be any suitable polymerase such as Taq polymerase Stoffel fragment, Taq polymerase, Advantage DNA polymerase, AmpliTaq, Amplitaq Gold, Titanium Taq polymerase, KlenTaq DNA polymerase, Platinum Taq polymersae, Accuprime Taq polymerase, Pfu polymerase, Pfu polymerase turbo, Vent polymerase, Vent exo- polymerase, Pwo polymerase, 9° N, DNA polymerase, Therminator, Pfx DNA polymerase, Expand DNA polymerase, rTth DNA polymerase, DyNAzyme™ EXT Polymerase, Klenow fragment, DNA polymerase 1, DNA polymerase, T7 polymerase, Sequenase™, T4 DNA polymerase, Bst B polymerase, phi-29 DNA polymerase and DNA polymerase Beta.

The strand displacement enzyme can be any suitable enzyme such as Helicases, AP endonucleases, mismatch repair enzymes capable of stand displacement or genetically (or otherwise) modified enzyme capable of stand displacement.

In a preferred form, the DNA polymerase also has strand displacement capability. The DNA polymerase can be any suitable polymerase having strand displacement capability. Examples include, but not limited to, Klenow exo- (New England Biolabs (NEB) catalogue number MO212S), Bst DNA polymerase large., fragment (NEB catalogue number MO275S), Vent exo- (NEB catalogue number MO257S), Deep Vent exo- (NEB catalogue number MO259S), M-MuLV reverse transcriptase (NEB catalogue number MO253S), 9° Nm DNA polymerase (NEB catalogue number MO260S) and Phi29 DNA polymerase (NEB catalogue number MO269S) ThermoPhi™ (Prokaria ehf). Preferably, the DNA polymerase is Klenow Exo-.

Preferably, the DNA polymerase is exonuclease deficient.

The enzyme can be any suitable enzyme that is capable of recognising non-regular base in double stranded DNA and can cause a nick or excise a base at or near the site of the non-regular base. Examples include, but not limited to, Endonuclease V (deoxyinosine 3′ endonuclease) (NEB catalogue number M0305S), Fpg (NEB catalogue number M0240S), hOGG1 (NEB catalogue number M0241S), RNase H (NEB catalogue number M0297S), APE1 (NEB catalogue number M0282S), Endonuclease III (NEB catalogue number MO268S), Endonuclease IV (NEB catalogue number M0304S), Endonuclease VIII (NEB catalogue number MO299S), T7 Endonuclease I (NEB catalogue number M0302S), USER Enzyme (NEB catalogue number M5505S), McrBC (NEB catalogue number M0272S) and Uracil DNA glycosylase (NEB catalogue number M0280S). Preferably, the enzyme is Endonuclease V.

It will be appreciated that other suitable enzymes can be made or obtained that recognise a non-regular base in double stranded DNA and act as required by nicking or causing base removal in the method according to the present invention.

The additives required for DNA amplification include nucleotides, buffers or diluents such as magnesium or manganese ions, co-factors, etc known to the art.

The amplification mix can also contain nucleotides, buffers or diluents such as magnesium or manganese ions, co-factors and suitable additives such as single stranded binding proteins such as T4gp32 or RecA.

Amplification can be carried out at any suitable temperature where the enzymes have desired activity. Typically, the temperature can be about 20° C. to about 75° C., about 25° C. to 60° C., or about 30° C. to 45° C. For the enzymes used in the current study, about 42° C. has been found to be particularly suitable. It will be appreciated that other temperatures, either higher or lower, can be used and would include ambient or room temperature. Importantly, the present invention does not require thermal cycling to amplify nucleic acids.

In one preferred from, the DNA is pre-treated with a modifying agent which modifies cytosine bases but does not modify 5′-methyl-cytosine bases under conditions to form single stranded modified DNA. Preferably, the modifying agent is selected from bisulphite, acetate or citrate and treatment does not result in substantial DNA fragmentation. More preferably, the agent is sodium bisulphite, a reagent, which in the presence of water, modifies cytosine into uracil.

Sodium bisulphite.(NaHSO3) reacts readily with the 5,6-double bond of cytosine to form a sulfonated cytosine reaction intermediate which is susceptible to deamination, and in the presence of water gives rise to a uracil sulfite. If necessary, the sulfite group can be removed under mild alkaline conditions, resulting in the formation of uracil. Thus, potentially all cytosines will be converted to uracils. Any methylated cytosines, however, cannot be converted by the modifying reagent due to protection by methylation.

Preferred methods for bisulphite treatment of nucleic acid can be found in WO 2004/096825 in the name of Human Genetic Signatures Pty Ltd (Australia), incorporated herein by reference.

If both strands of the treated DNA need to be amplified in the same amplification reaction, then four primers can be used (ie two primers for each of the modified strands of DNA).

In a second aspect, the present invention provides a kit for isothermal DNA amplification comprising:

a DNA polymerase;

an enzyme capable of strand displacement; and

an enzyme that recognises a non-regular base in double stranded DNA and causes a nick or excises a base in one DNA strand at or near the site of the non-regular base.

Preferably the kit further comprises:

additives required for DNA amplification.

Preferably the kit further comprises:

instructions to use the kit.

In a preferred form, the DNA polymerase and enzyme capable of strand displacement are the same enzyme.

In a third aspect, the present invention provides a primer for isothermal DNA amplification containing at least one internal non-regular base and when bound to a region of DNA forms a site recognised by an enzyme capable of causing a nick or excising a base in one DNA strand at or near the site of the non-regular base.

Preferably, the non-regular base is a chemical entity other than adenine (A), thymine (T), guanine (G) and cytosine (C) capable of being inserted in a DNA backbone. More preferably, the non-regular base is selected from the group consisting of deoxyinosine, 8 deoxyguanine, 5-methylCytosine, hydroxyuracil, ribonucleotides, and uracil. More preferably, the non-regular base is deoxyinosine.

In a fourth aspect, the present invention provides use of the kit according to the second aspect of the present invention for DNA amplification substantially without thermal cycling.

In a fifth aspect, the present invention provides use of a primer according to the fourth aspect of the present invention for DNA amplification substantially without thermal cycling.

In a sixth aspect, the present invention provides use of a DNA polymerase having strand displacement capability for DNA amplification substantially without thermal cycling.

In a seventh aspect, the present invention provides use of an enzyme that recognises a non-regular base in double stranded DNA and causes a nick or excises a base in one DNA strand at or near the site of the non-regular base for DNA amplification substantially without thermal cycling.

In a eighth aspect, the present invention provides use of a DNA polymerase having strand displacement capability and an enzyme that recognises a non-regular base in double stranded DNA and causes a nick or excises a base in one DNA strand at or near the site of the non-regular base for DNA amplification substantially without thermal cycling.

The amplification method of the present invention can be used as a replacement for PCR or other known DNA amplification processes. Uses include, but not limited to, detection of disease, amplifying desired genes or segments of DNA or RNA, SNP detection, real time amplification procedures, amplifying bisulphite treated DNA, whole genome amplification methods, adjunct to cloning methods, in situ amplification of DNA on cytological specimens, such as detection of microbes in sections or smears, detection of microbes in food contamination, amplification of breakpoints in chromosomes such as BCR-ABL translocations in various cancers, amplification of sequences inserted into chromosomes that may be oncogenic and predictive of disease progression, such as HPV fragment insertion, detection of methylated versus unmethylated sequences in normal versus cancerous cells, and in in situ tests for methylation changes in IVF tests for the normalcy of blastocyst development.

A distinct advantage of the present invention is that it can be carried out directly on double stranded DNA. The invention can also used for RNA by carrying out reverse transcription of the RNA prior to isothermal amplification. Furthermore, the present invention does not require heating or cooling for amplification. It is contemplated that the method according to the present invention can be carried ‘in the field’ i.e. at room or ambient temperature without the need for powered laboratory equipment.

Throughout this specification, unless the context requires otherwise, the word “comprise”, or variations such as “comprises” or “comprising”, will be understood to imply the inclusion of a stated element, integer or step, or group of elements, integers or steps, but not the exclusion of any other element, integer or step, or group of elements, integers or steps.

Any discussion of documents, acts, materials, devices, articles or the like which has been included in the present specification is solely for the purpose of providing a Context for the present invention. It is not to be taken as an admission that any or all of these Matters form part of the prior art base or were common general knowledge in the field relevant to the present invention as it existed prior to development of the present invention.

In order that the present invention may be more clearly understood, preferred embodiments will be described with reference to the following drawings and examples.

DESCRIPTION OF THE DRAWINGS

FIG. 1 shows a schematic representation of a nucleic acid amplification method according to the present invention.

FIG. 2 shows an agarose gel analysis of the results of amplification of target sequences using a method according to the present invention.

FIG. 3 shows an agarose gel analysis of the results of amplification of target sequences using a method according to the present invention.

FIG. 4 shows an agarose gel analysis of a direct comparison of the isothermal method of DNA amplification with conventional Polymerase Chain Reaction (PCR).

FIG. 5 shows amplification of the 12S rDNA gene from human genomic DNA.

FIG. 6 shows results of isothermal amplification of various human papilloma virus (HPV) DNA.

FIG. 7 shows results of isothermal amplification of human papilloma virus (HPV) DNA testing effect of NO denaturation on the reaction.

FIG. 8 shows results of isothermal amplification using various placement of non-regular bases in primers

FIG. 9 shows results of isothermal amplification using oligonucleotide primers containing ribonucleotides in combination with RNase H and Klenow exo-.

FIG. 10 shows results of isothermal amplification using oligonucleotide primers containing 8-deoxyguanine in combination with fpg and Klenow exo-.

MODE(S) FOR CARRYING OUT THE INVENTION

Materials and Methods

Non-Regular Bases

A non-regular base is defined herein as a chemical entity other than adenine (A), thymine (T), guanine (G) and cytosine (C) capable of being inserted in a DNA backbone. Examples of non-regular bases include, but not limited, to deoxyinosine, 8 deokyguanine or hydroxyuracil, 5-methyl-dC, 5 bromo-dU Inosine with C ribonucleotides, and uracil.

The non-regular base deoxyinosine has been found to be useful by the present invention.

It should be noted that the non-regular base does not necessarily need to have the structure of a nucleotide to function in the present invention.

Primers

Primers can be synthesised using any commercially available DNA synthesis service or in-house DNA synthesisers. The non-regular bases can be incorporated into the primer at any position using standard phosphoamidite synthesis technology.

Enzymes

Several modes are available for carrying out this invention.I. Oligonucleotides containing deoxyinosine, a non-regular base which is recognised by the enzyme Endonuclease V

II. Oligonucleotides containing 8 deoxyguanine or hydroxyuracil, non-regular bases which are recognised by the enzyme Fpg.

III. Oligonucleotides containing 8 deoxyguanine or hydroxyuracil, non-regular bases which are recognised by the enzyme hOGG1

IV. Oligonucleotides containing ribonucleotides, non-regular bases which are recognised by the enzyme RNase H

V. Oligonucleotides containing uracil, a non-regular base which is recognised by the enzyme Uracil DNA glycosylase or USER enzyme.

VI. Oligonucleotides containing 5-methylCytosine, non-regular bases which are recognised by the enzyme McrBC.

Enzymes capable of strand displacement include Klenow exo-, Bst DNA polymerase large fragment, Vent exo-, Deep Vent exo-, M-MuLV reverse transcriptase, 9° Nm DNA polymerase and Phi29 DNA polymerase.

The DNA polymerase can be any suitable polymerase having strand displacement capability. Examples include, but not limited to, Klenow exo- (New England Biolabs (NEB) catalogue number M0212S), Bst DNA polymerase large fragment (NEB catalogue number M0275S), Vent exo- (NEB catalogue number M0257S), Deep Vent exo- (NEB catalogue number M0259S), M-MuLV reverse transcriptase (NEB catalogue number M0253S), 9° Nm DNA polymerase (NEB catalogue number M0260S) and Phi29 DNA polymerase (NEB catalogue number M0269S) ThermoPhi™ (Prokaria ehf). Preferably, the DNA polymerase is Klenow Exo-.

Amplification Mix

The non-regular base in primers was N=deoxyinosine.

DNA polymerase capable of strand displacement was Endonuclease V

Enzyme that recognises a non-regular base in double stranded DNA was Klenow Exo-

50 ng of primers

500 μM dNTPs,

1 mM MgCl2,

9 μl of X1 Stoffel buffer (Perkin Elmer-Applied Biosystems, Foster City, USA) in a reaction vessel.

Amplification

Amplification according to the present invention occurs in the following manner (see FIG. 1):

the first primer binds to one strand of DNA (A),

the DNA polymerase extends the first primer forming a double stranded molecule having a first newly synthesised strand containing a non-regular base (B),

the nicking enzyme causes a nick or base excision at or near the non-regular base of the extended DNA (C);

the strand displacing enzyme or DNA polymerase capable of strand displacement displaces the first newly synthesised strand (D),

the second primer binds to the displaced first newly synthesised strand (E),

the DNA polymerase extends the second primer forming a double stranded molecule having a second newly synthesised strand containing a non-regular base (F),

the nicking enzyme causes a nick or base excision at or near the non-regular base of the extended DNA (G),

the strand displacing enzyme or DNA polymerase capable of strand displacement displaces the second newly synthesised strand (H),

the first primer binds to the displaced second newly synthesised strand (I), and

the process continues forming repeated newly synthesised strands of DNA (J).

The polymerase should copy the first primer in a 5′-3′ direction as if this does not occur the reaction would stop after the third cycle of amplification as the nick site will be lost preventing further amplification. The above reaction will then continue cycling with repeated rounds of nicking, extension and displacement. The primer is usually regenerated by the polymerase to allow successive rounds of amplification.

Results

Specificity of Isothermal Amplification

In order to demonstrate the specificity of the present invention, amplification reaction was parried out on two artificial DNA molecules (target and non-target).

Target(SEQ ID NO 1)5′ AGGGAATTTTTTTTCGCGATGTTTCGGCGCGTTAGTTCGTTGCGTAT

ATTTCGTTGCGGTTTTTTTTTTGGTTTTTTCGGTTAGTTGCGCGGCGATT

TCGGGGATTTTAG 3′

Non-target(SEQ ID NO 2)5′ AGGGAATTTTTTTTTGTGATGTTTTGGTGTGTTAGTTTGTTGTGTAT

ATTTTGTTGTGGTTTTTTTTTTGGTTTTTTTGGTTAGTTGTGTGGTGATT

TTGGGGATTTTAG 3′

The difference between the two oligonucleotides was that in the non-target oligonucleotide all CpG doublets were replaced by TpG doublets.

Isothermal amplification was carried out using the following primer set directed to the detection of target DNA sequences;

Primer#1(SEQ ID NO 3)5′ AGGGAATTTTTTTTCGCNATGTTTCGGCGCGTTAGTTCGT 3′

Primer#2(SEQ ID NO 4)5′ CTAAAATCCCCGAAATCGCCGCNCAACTAACCGAAAAAAC 3′

non-regular base was N=deoxyinosine.

Primers were synthesised using standard phosphoamidite chemistry.

Amplification was carried out under the following conditions:

50 ng of each of the above oligonucleotide primers, 500 μM dNTPs, 1 mM MgCl2, 0.5U Endonuclease V, 2U Klenow Exo- in 9 μl of X1 Stoffel buffer (Perkin Elmer-Applied Biosystems, Foster City, USA).

Eight pmoles of both target and non-target oligonucleotides were diluted from 102to 10−4. One μl of the diluted DNA was then added to the above reaction mixture and incubated for 2 hours at 42° C.

Ten μl of the amplified product were mixed with 10 μl of water and the amplification products resolved on a E-Gel 48 4% agarose (HR) gel (Invitrogen Cat#G8080-04) and the gel run using the Powerbase™. Markers were the E-gel low range quantitative DNA ladder (Invitrogen cat#12373-031. Gels were visualised under UV irradiation using the Kodak UVIdoc EDAS 290 system.

FIG. 2 shows 4% agarose gel analysis of the amplification products produced after 2 hours incubation at 42° C. using a synthetic bisulphite methylated target sequences and a synthetic bisulphite unmethylated non-target sequences. The results demonstrate the specificity of the isothermal amplification reaction. Two synthetic 110 by oligonucleotides were synthesised (see below). Isothermal amplification was carried out using oligonucleotides containing a single internal inosine (I) base designed to be specific for the amplification of target synthetic bisulphite methylated DNA sequences. As can be seen, the reaction was specific for the amplification of target DNA molecules. No bands can be seen from the non-target even when an excess of non-target DNA was present. The reaction was specific for the detection of methylated sequences and did not amplify unmethylated sequences even when the template was in high abundance. Thus even at relatively low temperatures (42° C.) it was possible to discriminate between two sequences that are relatively similar.

Efficiency of Isothermal Amplification

In order to determine the efficiency of amplification, serially diluted target DNA was amplified by a method according to the present invention.

FIG. 3 shows 4% agarose gel analysis of the amplification products produced after 4 hours incubation at 42° C. The arrow indicates the correct amplification product. The doublet in FIG. 3A is a result of full length amplification products that contain intact primer sequences and strand displaced products that contain primer sequences 5′ of the inosine insertion.

Set A contained the following oligonucleotide primers

Primer#1(SEQ ID NO 5)5′ AGGNAATTTTTTTTCGCNATGTTTCGGCGCGTTAGTTCGT 3′

Primer#2(SEQ ID NO 4)5′ CTAAAATCCCCGAAATCGCCGCNCAACTAACCGAAAAAAC 3′

non-regular base was N=deoxyinosine.

Set B contained the same primers but the reaction was supplemented by the addition of 1 mM DTT.

Primer#2(SEQ ID NO 6)5′ CTAAAATCCCCGAAATCGCCNCGCAACTAACCGAAAAAAC 3′

non-regular base was N=deoxyinosine.

Primers were synthesised using standard phosphoamidite chemistry.

Amplification was carried out under the following conditions:

50 ng of each of the above oligonucleotide primers, 500 μM dNTPs, 1 mM MgCl2, 0.5U Endonuclease V, 2U Klenow Exo- in 9 μl of X1 Stoffel buffer (Perkin Elmer-Applied Biosystems, Foster City, USA).

The target DNA was a synthetic 110 by oligonucleotide

(SEQ ID NO 1)5′ AGGGAATTTTTTTTCGCGATGTTTCGGCGCGTTAGTTCGTTGCGTAT

ATTTCGTTGCGGTTTTTTTTTTGGTTTTTTCGGTTAGTTGCGCGGCGATT

TCGGGGATTTTAG 3′

Eight pmoles of target DNA were serially diluted from 10−3to 10−7. One μl of the diluted DNA was then added to the above reaction mixture and incubated for 4 hours at 42° C.

Ten μl of the amplified product were mixed with 10 μl of water and the amplified products resolved on a E-Gel 48 4% agarose (HR) gel (Invitrogen Cat# G8080-04) and the gel run using the Powerbase™. Markers were the E-gel low range quantitative DNA ladder (Invitrogen cat#12373-031. Gels were visualised under UV irradiation using the Kodak UVIdoc EDAS 290 system.

As can be seen from FIG. 3 the method was capable of DNA amplification from target DNA sequences using a 105dilution of the template DNA. In addition, as can be seen from FIG. 3B by adding DTT to a final concentration of 1 mM improved the amplification as compared to FIG. 3A. This means that it was possible to have multiple displacement events from the same correctly hybridised oligonucleotide, unlike conventional PCR where only one new copy can be made from each correct priming event. This means that in theory the isothermal technique according to the present invention could be even more sensitive than PCR at amplifying DNA sequences as multiple copies of the target can be made from each correct priming event.

PCR Amplification Comparison

In order to compare the efficiency of the present invention with the market amplification standard, PCR was carried out using the same primers and target DNA.

PCR was carried out using the following primers

Primer#1(SEQ ID NO 3)5′ AGGGAATTTTTTTTCGCNATGTTTCGGCGCGTTAGTTCGT 3′

Primer#2(SEQ ID NO 4)5′ CTAAAATCCCCGAAATCGCCGCNCAACTAACCGAAAAAAC 3′

non-regular base was N=deoxyinosine.

PCR reaction mixes were prepared using 100 ng of each of the above primers in X1 Promega master mix in a total reaction volume of 25 μl. Samples of PCR products were amplified in a ThermoHybaid PX2 thermal cycler under the following conditions; 25, cycles of amplification at 95° C. for 30 seconds, 50° C. for 45 seconds, 68° C. for 45 seconds.

The target DNA was a synthetic 110, by oligonucleotide:

(SEQ ID NO 1)5′ AGGGAATTTTTTTTCGCGATGTTTCGGCGCGTTAGTTCGTTGCGTAT

ATTTCGTTGCGGTTTTTTTTTTGGTTTTTTCGGTTAGTTGCGCGGCGATT

TCGGGGATTTTAG 3′

Eight pmoles of target DNA were serially diluted from 10−2to 10−8. One μl of the diluted DNA was then added to the above reaction mixture.

Ten μl of the PCR derived product were mixed with 10 μl of water and the PCR products resolved on a 4% agarose gels (Invitrogen Cat# G6000-04) and the gel run using the Powerbase™: Markers were the E-gel low range quantitative DNA ladder (Invitrogen cat#12373-031. Gels were visualised under UV irradiation using the Kodak UVIdoc EDAS 290 system.

FIG. 4 shows a direct comparison of the isothermal method of DNA amplification with conventional Polymerase Chain Reaction (PCR). Using PCR, it was just possible to see an amplified band using a 106dilution of the template DNA. The use of 25 cycles of amplification is usually sufficient to successfully amplify multi-copy targets such as 12S ribosomal DNA sequences.

From the results it can be seen that the isothermal method of DNA amplification is a rapid, sensitive and specific method for DNA amplification. The method requires no expensive cycling equipment therefore could be carried out in any routine lab or even doctors surgery.

Direct Amplification of Double Stranded DNA

FIG. 5 shows amplification of the 12S rDNA gene from human genomic DNA. Amplification was carried out under the following conditions:

50 ng of each of the oligonucleotide primers(SEQ ID NO 7)F15′ AACAAAACTGCTCNCCAGAACACTACNAGCCACAGCTTAA-3′

and

(SEQ ID NO 8)R15′ TGGTGAGGTTGATCNGGGTTTATCNATTACAGAACAGGCT-3′,

500 μM dNTPs, 1 mM MgCl2in 9 μl of X0.5 Stoffel buffer (Perkin Elmer-Applied Biosystems, Foster City, USA) and 1 μl of genomic of human genomic (Promega Cat#G147A) at concentrations of 150 ng, 15 ng, 1.5 ng and 0.15 ng. The reaction mixes were heated at 95° C. for 2 minutes then snap-chilled on ice. The reaction mixes were then supplemented with 0.5U Endonuclease V, 2U Klenow Exo- and 1 mM DTT in 10 μl of X0.5 Stoffel buffer (Perkin Elmer-Applied Biosystems, Foster City, USA).

Ten μl of the amplified product were mixed with 10 μl of water and the amplification products resolved on a E-Gel 48 4% agarose (HR) gel (Invitrogen Cat#G8080-04) and the gel run using the Powerbase™. Markers were the E-gel low range quantitative DNA ladder (Invitrogen cat#12373-031. Gels were visualised under UV irradiation using the Kodak UVIdoc EDAS 290 system.

Viral DNA Amplification

Plasmids containing full-length human papilloma virus (HPV) viral genomes HPV 1a (45021), HPV 16 (45113D) and HPV 18 (45152D) were obtained from the ATCC. Plasmids preparations were prepared as indicated by the supplier's recommendations. After plasmid purification using the Qiagen Plasmid midi kit (Cat# 12143) plasmids were linearised with Hind III (NEB Cat# R0104S) for HPV-1a and HPV-16 or with ClaI (NEB Cat# R0197S) according to the manufacturers instructions. Ten fold serial dilutions of the plasmids were prepared in sterile water to serve as templates for isothermal amplification.

Isothermal amplification was carried out using the following primer set directed to the detection of target HPV DNA sequences:

HPV-1a primers

Primer#1(SEQ ID NO 9)5′ GGAGGAGTTAGTGTCNCCTCAGCAACCTTATGCTGTCNTT 3′

Primer#2(SEQ ID NO 10)5′ GCACAGTGGGCACACNATGTTCAAAGATCNCAGAAGGAG 3′

HPV-16

Primer#1(SEQ ID NO 11)5′ CCAGCTGGACAAGCAGAACCNGACAGAGCCCATTAC 3′

Primer#2(SEQ ID NO 12)5′ CCAAAGTACGAATGTCTACNTGTGTGCTTTGTACNCACAAC 3′

HPV-18

Primer#1(SEQ ID NO 13)5′ GCTGCAACCGAGCACNACAGGAACGACTCCAACGACNCAGAG 3′

Primer#2(SEQ ID NO 14)5′ ACAACATTGTGTGACNTTGTGGTTCGGCTCNTCGGGCTGG 3′

non-regular base was N=deoxyinosine.

Primers were synthesised using standard phosphoamidite chemistry.

Amplification was carried out under the following conditions:

50 ng of each of the above oligonucleotide primers, 500 μM dNTPs, 1 mM MgCl2, 0.5U Endonuclease V, 2U Klenow Exo- in 9 μl of X1 Stoffel buffer (Perkin Elmer-Applied Biosystems, Foster City, USA).

Ten-fold serial dilutions of purified plasmid DNA were prepared ranging from 100 ng/μl to 100 fg/μl. Plasmid dilutions were heated at 95° C. for 2 minutes then snap-chilled on ice until required. One μl of the diluted DNA was then added to the above reaction mixture and incubated for 4 hours at 42° C.

Ten μl of the amplified product were mixed with 10 μl of water and the amplification products resolved on a E-Gel 48 4% agarose (HR) gel (Invitrogen Cat# G8080-04) and the gel run using the Powerbase™, Markers (M) were the E-gel low range quantitative DNA ladder (Invitrogen cat#12373-031. Gels were visualised under UV irradiation using the Kodak UVidoc EDAS 290 system. The results are shown in FIG. 6.

The HPV 18 (45152D) was ten fold serially diluted to determine if pre-heat treatment was required for amplification using the isothermal system.

Isothermal amplification was carried out using the following primer set directed to the detection of target HPV DNA sequences:

HPV-18

Primer#1(SEQ ID NO 13)5′ GCTGCAACCGAGCACNACAGGAACGACTCCAACGACNCAGAG 3′

Primer#2(SEQ ID NO 15)5′ AAATTCCNGTTGACCTTCTATGTCACNAGCAATTAAGCGAC 3′

non-regular base was N=deoxyinosine.

Primers were synthesised using standard phosphoamidite chemistry.

Amplification was carried out under the following conditions:

50 ng of each of the above oligonucleotide primers, 500 μM dNTPs, 1 mM MgCl2, 0.5U Endonuclease V, 2U Klenow Exo- in 9 μl of X1 Stoffel buffer (Perkin Elmer-Applied Biosystems, Foster City, USA).

Ten-fold serial dilutions of purified plasmid DNA were prepared ranging from 100 ng/μl to 1 ng/μl. One μl of the diluted DNA without pre-denaturation was then added to the above reaction mixture and incubated for 4 hours at 42° C.

Ten μl of the amplified product were mixed with 10 μl of water and the amplification products resolved on a E-Gel 48 4% agarose (HR) gel (Invitrogen Cat# G8080-04) and the gel run using the Powerbase™. Markers (M) were the E-gel low range quantitative DNA ladder (Invitrogen cat#12373-031. Gels were visualised under UV irradiation using the Kodak UVidoc EDAS 290 system. Results are shown in FIG. 7.

The results suggest that in certain instances there is no requirement for initial denaturation of double stranded DNA templates prior to isothermal amplification.

Placement of Non-Regular Base

Isothermal amplification was carried out using the following primer set directed to the detection of the following target sequence:

(SEQ ID NO 1)5′ AGGGAATTTTTTTTCGCGATGTTTCGGCGCGTTAGTTCGTTGCGTAT

ATTTCGTTGCGGTTTTTTTTTTGGTTTTTTCGGTTAGTTGCGCGGCGATT

TCGGGGATTTTAG 3′

Wild type forward primer(SEQ ID NO 16)5′-AGGGAATTTTTTTTCGCGATGTTTCGGCGCGTTAGTTCGT

(SEQ ID NO 3)G5′-AGGGAATTTTTTTTCGCNATGTTTCGGCGCGTTAGTTCGT

(SEQ ID NO 17)C5′-AGGGAATTTTTTTTCGNGATGTTTCGGCGCGTTAGTTCGT

(SEQ ID NO 18)A5′-AGGGAATTTTTTTTCGCGNTGTTTCGGCGCGTTAGTTCGT

(SEQ ID NO 19)T5′-AGGGAATTTTTTTTCGCGANGTTTCGGCGCGTTAGTTCGT

Wild type reverse primer(SEQ ID NO 20)5′-CTAAAATCCCCGAAATCGCCGCGCAACTAACCGAAAAAAC

(SEQ ID NO 4)G5′-CTAAAATCCCCGAAATCGCCGCNCAACTAACCGAAAAAAC

(SEQ ID NO 21)C5′-CTAAAATCCCCGAAATNGCCGCGCAACTAACCGAAAAAAC

(SEQ ID NO 22)A5′-CTAAAATCCCCGAANTCGCCGCGCAACTAACCGAAAAAAC

(SEQ ID NO 23)T5′-CTAAAATCCCCGAAANCGCCGCGCAACTAACCGAAAAAAC

non-regular base was N=deoxyinosine.

Four sets of primers were then compared to determine the effect of inosine placement in the oligonucleotide.

Primers were synthesised using standard phosphoamidite chemistry.

Amplification was carried out under the following conditions:

50 ng of each of the above oligOnucleotide primers, 500 μM dNTPs, 1 mM MgCl2, 0.5U Endonuclease V, 2U Klenow Exo- in 9 μl of X1 Stoffel buffer (Perkin Elmer-Applied Biosystems, Foster City, USA).

Ten-fold serial dilutions of target DNA were prepared ranging from 10−2dilution to 10−6. One μl of the diluted target DNA was then added to the above reaction mixture and incubated for 4 hours at 42° C.

Ten μl of the amplified product were mixed with 10 μl of water and the amplification products resolved on a E-Gel 48 4% agarose (HR) gel (Invitrogen Cat# G8080-04) and the gel run using the Powerbase™. Markers (M) were the E-gel low range quantitative DNA ladder (Invitrogen cat#12373-031. Gels were visualised under UV irradiation using the Kodak UVIdoc EDAS 290 system and results shown in FIG. 8. The results for the DNA being amplified suggested that for the reaction worked more efficiently when the inosine substituted a G in the sequence. Further experiments indicated that a preferred placement of the inosine for this DNA amplification test was CI where the inosine replaced a G in a CpG dinucleotide.

Amplification Using Ribonucleotide

Isothermal amplifications were carried out using a primer set directed to the detection of the following target DNA sequences;

(SEQ ID NO 1)5′ AGGGAATTTTTTTTCGCGATGTTTCGGCGCGTTAGTTCGTTGCGTAT

ATTTCGTTGCGGTTTTTTTTTTGGTTTTTTCGGTTAGTTGCGCGGCGATT

TCGGGGATTTTAG 3′

Primer#1(SEQ ID NO 24)5′ AGGGAATTTTTTTTCGrCrGrAUrGTTTCGGCGCGTTAGTTCGT

Primer#2(SEQ ID NO 25)5′ CTAAAATCCCCGAAAUrCrGrCrCGCGCAACTAACCGAAAAAAC

non-regular base was r=ribonucleotide.

Primers were synthesised using standard phosphoamidite chemistry.

Amplification was carried out under the following conditions:

50 ng of each of the above oligonucleotide primers, 500 μM dNTPs, 1 mM MgCl2, 0.1U RNaseH, 2.5U Klenow Exo- in 9 μl of X10 reaction buffer (either NEB buffer 1, Klenow Buffer or Stoffel buffer).

Ten-fold serial dilutions of target DNA were prepared ranging from 10−1to 10−3. One μl of the diluted DNA was then added to the above reaction mixture and incubated for 4 hours at 42° C.

Ten μl of the amplified product were mixed with 10 μl of water and the amplification products resolved on a E-Gel 48 4% agarose (HR) gel (Invitrogen Cat# G8080-04) and the gel run using the Powerbase™. Markers (M) were the E-gel low range quantitative DNA ladder (Invitrogen cat#12373-031. Gels were visualised under UV irradiation using the Kodak UVIdoc EDAS 290 system and results shown in FIG. 9.

Amplification Using 8-Deoxyguanine

Isothermal amplifications were carried out using a primer set directed to the detection of the following target DNA sequences;

(SEQ ID NO 1)5′ AGGGAATTTTTTTTCGCGATGTTTCGGCGCGTTAGTTCGTTGCGTAT

ATTTCGTTGCGGTTTTTTTTTTGGTTTTTTCGGTTAGTTGCGCGGCGATT

TCGGGGATTTTAG 3′

P#1(SEQ ID NO 26)5′ AGGGAATTTTTTTTCGCNNNGATGTTTCGGCGCGTTAGTTCGT

P#2(SEQ ID NO 27)5′ CTAAAATCCCCGAAATCGGCCNNNGCGCAACTAACCGAAAAAAC

non-Regular Base was NNNG=8-deoxyguanine.

Primers were synthesised using standard phosphoamidite chemistry.

Amplification was carried out under the following conditions:

50 ng of each of the above oligonucleotide primers, 500 μM dNTPs, 1 mM MgCl2, 1U Fpg, 2.5U Klenow Exo- in 9 μl of X10 reaction buffer X1 Stoffel buffer (Perkin Elmer-Applied Biosystems, Foster City, USA).

Ten-fold serial dilutions of target DNA were prepared ranging from 10−1to 10−3. One μl of the diluted DNA was then added to the above reaction mixture and incubated for 4 hours at 42° C.

Ten μl of the amplified product were mixed with 10 μl of water and the amplification products resolved on a E-Gel 48 4% agarose (HR) gel (Invitrogen Cat# G8080-04) and the gel run using the Powerbase™. Markers (M) were the E-gel low range quantitative DNA ladder (Invitrogen cat#12373-031. Gels were visualised under UV irradiation using the Kodak UVIdoc EDAS 290 system and results are shown in FIG. 10.

It will be appreciated by persons skilled in the art that numerous variations and/or modifications may be made to the invention as shown in the specific embodiments without departing from the spirit or scope of the invention as broadly described. The present embodiments are, therefore, to be considered in all respects as illustrative and not restrictive.