The invention relates to the field of molecular biology; more particularly, the invention relates to methods for single step, isothermal strand displacement amplification of target DNA. Even more particularly, the invention relates to methods for one-step strand displacement amplification of target DNA using a combination of a nicking agent and an exonuclease-deficient DNA polymerase.
Nucleic acid amplification methods are fundamental to a wide range of scientific activities from laboratory research to clinical diagnostics. A variety of in vitro nucleic acid amplification techniques have been developed and can be loosely categorized into those requiring temperature cycling, such as polymerase chain reaction (“PCR”) and those requiring no temperature cycling, such as strand displacement amplification (“SDA”). [1,2]. SDA is based on the ability of a restriction enzyme to nick one strand of double-stranded (ds) DNA and the ability of a 5′ to 3′ exonuclease-deficient (exo−) DNA polymerase to extend the 3′ end from the nick. New strands extending from the 3′ ends will displace the downstream strands, which dispatch from the dsDNA as amplification products. Exponential amplification is achieved by coupling both sense and antisense reactions in which strands displaced and dispatched from a sense reaction serve as new templates for an antisense reaction and vice versa [2].
Earlier studies suggested several advantages of SDA over PCR. First, SDA has a high amplification efficiency, reaching 1010-fold of amplification in as short as 15 min [3] while PCR typically requires as long as two hours to reach an equivalent amplification level. Second, SDA is a more reliable technique for generating high molecular weight (>12 kb) genomic DNA (“gDNA”). [4]. Third, SDA is more compatible with other techniques, such as real-time diagnostic analysis of infectious and genetics diseases. [1]. Finally SDA is an isothermal amplification that can be carried out on a heat block rather than requiring a thermalcycler for accurate temperature control.
Several drawbacks, however, have hindered the general applicability of traditional SDA. First, SDA requires a heat denaturation step prior to isothermal amplification. Not all SDA enzymes, however, are heat stable (like taq polymerase in PCR). Thus, SDA enzymes must be added stepwise to the reaction after target DNA heat denaturation, thereby converting what could be an automated, single-step workflow to a manual, two-step workflow: an initial preparation step prior to heat denaturation and subsequent step necessary for addition of enzymes after heat denaturation. Importantly, the second step requires opening the reaction vessel and exposing the sample to potential contamination. This stepwise procedure is unfavorable for high throughput applications, particularly in clinical diagnostic applications in which additional exposure of the sample to the environment increases the chance of contamination.
Second, traditional SDA applications employ restriction enzymes that typically cut both strands of a target nucleic acid rather than making a nick in only one strand. Indeed, previous studies used standard restriction enzymes such as HincII [2,7,8], B
The invention describes a single-step method for isothermal SDA that employs a nicking enzyme and a DNA polymerase. In preferred embodiments, the nicking enzyme is N.BbvClB and the DNA polymerase is Bst DNA polymerase. By regulating the interaction of these two enzymes, target SDA may be generated from non-denatured genomic DNA (“gDNA”) at amplification temperatures, i.e., without requiring a heat denaturation process. Thus, all reaction components, including the two enzymes, can be added simultaneously in a single step to a single reaction mixture, thereby facilitating high throughput applications. Furthermore, because reaction tubes are not opened mid-reaction, the possibility of contamination is minimized, thereby allowing SDA in clinical applications. Moreover, amplification costs are reduced due to smaller concentrations of requisite enzymes, as well as savings associated with elimination of costly dNTP[αS]. Greatly improved amplification efficiency and yields are attributable to the use of N.BbvClB.
In one embodiment, the method for isothermal strand displacement amplification of nucleic acids comprises a single step; particularly, combining, in a single reaction vessel, a mixture of: (i) double-stranded target nucleic acid; (ii) a nicking enzyme capable of nicking the double-stranded target nucleic acid; and (iii) a DNA polymerase lacking 5′-3′ exonuclease activity, under conditions sufficient to allow amplification of the target nucleic acid.
In another embodiment, the nicking enzyme is N.BbvClB and the DNA polymerase is Bst DNA polymerase, which may preferably be combined and present in the reaction mixture in equimolar concentrations. In yet another embodiment, conditions sufficient to allow amplification of the target nucleic acid include incubation at a temperature ranging from about 45° C. to about 55° C., and may preferably be conducted at a temperature of 45° C.
In sum, these improvements will make isothermal SDA an ideal new assay for a clinical setting.
were added to reaction to convert non-biotin products to biotin-product. The biotin-nest primer, which does not contain N.BbvClB's recognition sequence, anneals to target (or non-biotin product) downstream of the 3′ end of AP
and is extended at 3′ end by Bst DNA polymerase to form a biotin-strand complementary to non-biotin product. The biotin-strands are eventually displaced by new strands that are extended from 3′ end of the upstream AP and dispatch as ss biotin-product. B) SDA products can be detected directly by real time probes, which remain quenched
in the absence of target product but emit signal
when hybridize to target product. Nicking enzyme N.BbvClB is show as
while Bst DNA polymerase is shown as
.
The terms “3′” and “5′” are used herein to describe the location of a particular site within a single strand of nucleic acid. When a location in a nucleic acid is “3′ to” or “3′ of” a reference nucleotide or a reference nucleotide sequence, this means that the location is between the 3′ terminus of the reference nucleotide or the reference nucleotide sequence and the 3′ hydroxyl of that strand of the nucleic acid. Likewise, when a location in a nucleic acid is “5′ to” or “5′ of” a reference nucleotide or a reference nucleotide sequence, this means that it is between the 5′ terminus of the reference nucleotide or the reference nucleotide sequence and the 5′ phosphate of that strand of the nucleic acid. Further, when a nucleotide sequence is “directly 3′ to” or “directly 3′ of” a reference nucleotide or a reference nucleotide sequence, this means that the nucleotide sequence is immediately next to the 3′ terminus of the reference nucleotide or the reference nucleotide sequence. Similarly, when a nucleotide sequence is “directly 5′ to” or “directly 5′ of” a reference nucleotide or a reference nucleotide sequence, this means that the nucleotide sequence is immediately next to the 5′ terminus of the reference nucleotide or the reference nucleotide sequence.
A “naturally occurring nucleic acid” refers to a nucleic acid molecule that occurs in nature, such as a full-length genomic DNA molecule or an mRNA molecule.
An “isolated nucleic acid molecule” refers to a nucleic acid molecule that is not identical to any naturally occurring nucleic acid or to that of any fragment of a naturally occurring genomic nucleic acid spanning more than three separate genes.
As used herein, “nicking” refers to the cleavage of only one strand of a fully double-stranded nucleic acid molecule or a double-stranded portion of a partially double-stranded nucleic acid molecule at a specific position relative to a nucleotide sequence that is recognized by the enzyme that performs the nicking. The specific position where the nucleic acid is nicked is referred to as the “nicking site.”
A “nicking agent” is an enzyme that recognizes a particular nucleotide sequence of a completely or partially double-stranded nucleic acid molecule and cleaves only one strand of the nucleic acid molecule at a specific position relative to the recognition sequence.
A “nicking endonuclease,” as used herein, refers to an endonuclease that recognizes a nucleotide sequence of a completely or partially double-stranded nucleic acid molecule and cleaves only one strand of the nucleic acid molecule at a specific location relative to the recognition sequence. Unlike a restriction endonuclease, which requires its recognition sequence to be modified by containing at least one derivatized nucleotide to prevent cleavage of the derivatized nucleotide-containing strand of a fully or partially double-stranded nucleic acid molecule, a nicking endonuclease typically recognizes a nucleotide sequence composed of only native nucleotides and cleaves only one strand of a fully or partially double-stranded nucleic acid molecule that contains the nucleotide sequence.
An “amplification primer,” as used herein, is an oligonucleotide that anneals to a template nucleic acid comprising a sequence of an antisense strand nucleic acid and functions as a primer for an initial primer extension. The resulting extension product from the initial primer extension, that is, the strand containing the nucleotide of the amplification primer, is then nicked and the fragment in the same strand containing the 3′ terminus at the nicking site serves as a primer for subsequent primer extensions.
The present invention describes a novel method that enables SDA reactions to be conducted without disrupting workflow and without heat denaturation of target neucleic acid. Indeed, this single-step, isothermal SDA reaction method does not require any sophisticated treatment, but instead utilizes reactants already and otherwise present in a typical SDA reaction mixture. While not wishing to be bound by a particular theory, the method appears to operate based on interactions of two SDA enzymes in conjunction with the naturally present CCTCAGC sequence in human gDNA. When added to reaction, the CCTCAGC sites in non-denatured gDNA are recognized and nicked by N.BbvClB. New strands are then extended from 3′ ends of the nicks by Bst polymerase present in reaction to displace the downstream strands that form ssDNA which immediately serve as templates for SDA primers that are also present in the system leading to initiation of specific target amplification, all occurring simultaneously.
Although ssDNA can be produced from non-denatured gDNA in SDA reactions, production of ssDNA is correlated to the concentration of SDA enzymes present in the reaction tube. In the one-step, isothermal SDA, amplification occurred primarily in tubes containing 4 U of N.BbvClB (#4, 7 and 10) and not in tubes that had less N.BbvClB enzyme. The decreased SDA amplification in these reactions may be due to a failure in generating ssDNA from gDNA, as opposed to target amplification from the ssDNA because all those enzyme mixes with less N.BbvClB were able to produce strong SDA when ssDNA had been already generated, e.g., through heat denaturation as demonstrated in bi-thermal SDA. The best results were achieved when the N.BbvClB:Bst polymerase enzymes were in an activity ratio of about 1:1 to about 1:2.
Unlike PCR which typically produces a single species of product, SDA results in amplification products of differing lengths. This makes analysis on agarose gel to pinpoint specific SDA products difficult. [12]. Thus, choosing the best technique to accurately identify correct product from a product mix is important for SDA reactions. Two techniques have proven useful with the single-step, isothermal SDA method of the present invention.
The first technique incorporates the NanoChip® electronic microarray, which has been previously described. [5,6,13,14]. Because analysis on NanoChip® electronic microarrays requires biotin-product, while SDA typically produces non-biotin product, biotin-nest primers have been used with the one-step, isothermal SDA reaction to “catch” and “convert” the non-biotin SDA products to biotin-products. Successful demonstration of this conversion is demonstrated herein and has been described previously. [11].
The second technique incorporates real-time product analysis. Real-time SDA was developed to accommodate two ubiquitous fluorescence-labeled FV probes that were primarily designed for a real-time PCR. Both probes demonstrated low backgrounds in the absence of target but high specificity and affinity to their targets due to the incorporation of an Eclipse™ Dark Quencher, the MGB™ technology, and modified bases, such as Super A and Super T. With the single-step, isothermal, real-time SDA developed with these two probes, rapid analysis of SNP clinical samples was demonstrated. It is worthy of note that incubating at 45° C. is preferred for the presently claimed single-step, isothermal real-time SDA. The real-time data confirm that single-step, isothermal SDA amplification is very efficient, allowing real-time SNP analysis to occur in as few as 10 min, greatly surpassing both bi-thermal, real-time SDA described previously [9,15,16] and all real-time PCR analyses known to the inventors.
Methods and Compositions for Isothermal SDA
SNP analysis of the Factor V Leiden (“FV”) gene was used as a test model to demonstrate feasibility of the single-step, isothermal SDA method of the present invention for clinical applications. Those of skill in the art will appreciate that the presently claimed method is generally applicable for genomic target amplification. Indeed, because the recognition sequence for N.BbvClB, CCTCAGC, is present in all genes throughout the entire genome, the reaction should generate a pool of ssDNA products from every gene. Once generated, this pool of ssDNA will serve as templates for designated targets whose primers are present in reaction. Moreover, experiments using the single-step, isothermal SDA method of the present invention to amplify the prothrombin gene, either in monoplex or biplex amplification with the FV gene have been successful. The combination of 4 U N.BbvClB nicking enzyme and 4 U Bst DNA polymerase also produced the best result.
Genomic DNA (“gDNA”) was prepared from human whole blood from San Diego Blood Bank (San Diego, Calif., USA) using Qiagen Midi DNA Kit (Qiagen, Valencia, Calif., USA) and stored at −20° C. until use. Genotypes of the DNA samples used in this study were determined by SNP analysis on a Nanogen Molecular Biology Workstation.
Nicking endonuclease N.BbvClB and Bst DNA polymerase (Large Fragment) were purchased from New England Bio-labs (Beverly, Mass., USA). Sequences of oligonucleotides useful in the practice of the invention are described in Table 1.
#Synthesized at Nanogen North (Bothell, WA, USA);
*indicates superbase structure in oligonucleotide;
Bold and underlined letter indicates SNP base
Both forward and reverse amplification primers contain a recognition sequence CCTCAGC (underlined) for N.BbvClB. Because these two primers, when fully matched to complementary strands, are nicked by N.BbvClB at the recognition site to allow generation of multiple copies of product from a single primer (i.e., “amplifiable”), they are termed amplification primers (AP). The bumper primer does not contain the recognition sequence (thus “non-amplifiable”). Other oligonucleotides in Table 1 are useful for converting SDA product to biotinylated (biotin-) product (FV nest primer), for real-time product detection and for preparing product detection reporters. Unless specified separately, all oligonucleotides in Table 1 were synthesized in the Integrated DNA Technologies (IDT, Coralville, Iowa, USA).
For analysis on NanoChip® electronic microarrays, reactions were performed in a 10 μL final volume containing 50 ng human gDNA, 250 nM forward and reverse AP, 25 nM reverse bumper and 500 nM nest primer, 3.75 mM MgCl2, 36 mM K2HPO4 (pH7.6), 0.25 mM each dNTPs, 4 U N.BbvClB and 4 U Bst DNA polymerase diluted in Diluent A (New England Biolabs, Beverly, Mass., USA). All components, including the two enzymes, were added to a 200-μL microcentrifuge tube at room temperature. The tube subsequently proceeded directly to incubation on a 50° C. heat block for 30 min (no initial target heat denaturation step was involved). Addition of nest primers converts non-biotin product to biotin-products as shown in
A real-time assay was developed to confirm product amplification resulting from the improved one-step SDA of the present invention. The real-time reaction was also run in a 10 μL final volume having a similar composition to that described above (50 ng gDNA, 250 nM FV forward and reverse AP, 25 nM FV reverse bumper, 3.75 mM MgCl2, 50 mM K2HPO4, pH7.6, 0.10 mM each dNTPs, 4 U N.BbvClB and 4 U Bst DNA polymerase) plus 0.5 μL of a 20 fold concentrated probe solution that contains two fluorescence labeled probes specific to wild type and mutant Factor V Leiden (“FV”) products, respectively (Table 1). No nest primer was used in this assay. Fluorescence on the probes is quenched in the absence of target products but is emitted when the probes hybridize to their targets, as shown in
Additional embodiments of the invention are described in the Examples below.
The nicking enzyme, N.BbvClB, and Bst DNA polymerase are useful to exemplify the one-step, isothermal SDA method of the present invention. Skilled artisans, however, will recognize that other combinations of nicking enzymes and exonuclease-deficient DNA polymerases can be used to practice the claimed invention. Accordingly, the invention should not be understood to be limited to nicking enzyme, N.BbvClB, and Bst DNA polymerase.
To understand the role of each enzyme and their interactions in SDA, twelve combinations were prepared of the two enzymes as shown in Table 2.
*all enzyme levels were determined in 2 μL of Diluent A from New England Bio-labs (Beverly, MA, USA).
A master mix containing all SDA reaction components, except the two enzymes, was prepared and aliquoted (8 μL each) to individual reaction tubes. The first set of 12 tubes was subjected to a bi-thermal amplification procedure, i.e., reaction tubes were first heated to 95° C. for 5 min and returned to 50° C. Then, after reaching 50° C., 2 μL of enzyme mix from Table 2 was added to each tube and incubated at 50° C. for 30 min. As shown in
The second set of tubes was not subjected to heat denaturation at 95° C. To each tube, 2 μL of enzyme mix from Table 2 was added at room temperature. All tubes were incubated at 50° C. for 30 min. As shown in
To determine the amplification time required for SDA, reactions were prepared and incubated at 50° C. for 25, 30, 35, 40 and 45 min, respectively.
SNP Analysis
Because the improved, single-step, isothermal SDA resulted in strong target amplifications, the feasibility of using the method for SNP analysis was investigated. SNP analysis was tested using 9 human genomic samples, consisting of three known FV wild type (WT), three FV mutant (Mut) and three FV heterozygotes (Het) samples. The single-step reactions were prepared as described and incubated at 50° C. for 30 min (without the initial heat denaturation step).
Real-Time One-Step, Isothermal SDA Reactions
Although the foregoing invention has been described in some detail by way of illustration and example for purposes of clarity and understanding, it may be readily apparent to those of ordinary skill in the art in light of the teachings of this invention that certain changes and modifications may be made thereto without departing from the spirit or scope of the appended claims.
This patent application claims the priority benefit of U.S. Provisional Application Ser. No. 60/837,712, filed Aug. 15, 2006, the specification of which is incorporated herein by reference in its entirety.
Number | Date | Country | |
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60837712 | Aug 2006 | US |