Methods for the amplification, quantitation and identification of nucleic
The invention relates to improved methods of amplifying and optionally quantifying and/or identifying a plurality of selected nucleic acid molecules from a pool of nucleic acid molecules. A first round of multiplex amplification used where the amplification reaction is allowed to proceed to a point prior to that at which significant competition between amplicons for reaction components has occurred. This is the followed by a second round of amplification that typically includes a fluorescent reporter to allow for each of the selected nucleic acid sequences to be quantified. The methods are useful for the amplification and quantification of nucleic acids from a variety of sources, such as gene expression products, whereby many such products may be amplified and quantified from very limited samples and from degraded archival samples.
1. A method of amplifying a plurality of selected nucleic acid molecules from a pool of nucleic acid molecules comprising:
(a) amplifying a plurality of selected nucleic acid molecules in a first round multiplex reaction including a plurality of outer primer pairs, each pair being specific for a selected nucleic acid sequence, present in the reaction in excess relative to amplicons synthesized with said outer primer pairs, and not exhausted after said first round multiplex reaction;
(b) diluting the amplicons and remaining reaction components from said first round multiplex reaction into a plurality of second round amplification reactions each including at least one pair of inner primers, each pair being specific for one of said selected nucleic acid sequences, wherein said dilution is at least a 20-fold dilution such that the amount of outer primers introduced into each of said second round amplification reactions is insufficient to impair the amplification of said selected nucleic acid molecules using said inner primers; and
(c) further amplifying said selected nucleic acid molecules in said plurality of second round amplification reactions whereby each second round reaction further amplifies a subset of said plurality of selected nucleic acid molecules respectively from said inner primers.
2. A method according to claim 1 wherein said nucleic acid molecules include DNA molecules.
3. A method of amplifying a plurality of selected nucleic acid molecules according to claim 1 wherein said primers included in said second round amplification reaction have a higher Tm than at least one of said outer primers included in said first round amplification reaction, such that said oligonucleotide priming in said second round amplification reaction is substantially biased in favour of said printers having said higher Tm.
4. A method of amplifying a-plurality of selected nucleic acid molecules according to claim 1 wherein at least one of said outer primers includes UTP nucleotides whereby said primer is amenable to digestion by a UNG enzyme.
5. A method of amplifying a plurality of selected nucleic acid molecules according to claim 4 wherein said outer primers are removed at the end of said first round of amplification by digestion with a UNG enzyme thereby substantially preventing contamination of said second round amplification reaction by said first round primers.
6. A method according to claim 1 wherein the first round multiplex reaction is allowed to proceed for up to about 20 cycles.
7. A method according to claim 1 wherein the multiplex amplification reaction amplifies more than about 4 selected nucleic acid molecules.
8. A method according to claim 7 wherein the multiplex amplification reaction amplifies between about 4 and 150 selected nucleic acid molecules.
9. A method according to claim 8 wherein the multiplex amplification reaction amplifies between about 10 and 150 selected nucleic acid molecules.
10. A method according to claim 9 wherein the multiplex amplification reaction amplifies between about 20 and 100 selected nucleic acid molecules.
11. A method of amplifying a plurality of selected nucleic acid molecules according to claim 1 , wherein the method is used in a method of detecting of polymorphisms, mutations, insertions and deletions.
12. A method of amplifying a plurality of selected nucleic acid molecules according to claim 1 , wherein the method is used in a method of diagnosis of diseases and disorders.
13. A method according to claim 12 , wherein the method is used for the diagnosis of a neoplasm.
14. A method according to claim 13 wherein said neoplasm is breast cancer.
15. A method according to claim 13 wherein said neoplasm is colorectal cancer.
16. A method according to claim 12 , wherein said method includes melt curve analysis.
17. A method according to claim 16 , wherein said melting curve is generated having a resolution in the range of about 0.05° C. to about 0.02° C.
18. A method according to claim 16 , wherein said melting curve is generated having a resolution of less than 0.02° C.
19. A method of amplifying a plurality of selected nucleic acid molecules according to claim 1 , wherein the method is used for the detection and identification of selected organisms.
20. A method according to claim 19 wherein said organisms are detected and identified by sequencing of said nucleic acid products.
21. A method according to claim 20 wherein said organisms are selected from the group of bacteria, viruses, fungi, mycoplasma, and parasites or combinations thereof.
22. A method according to claim 19 wherein said organisms are selected from the group of bacteria, viruses, fungi, mycoplasma, and parasites or combinations thereof.
23. A method according to claim 1 wherein the amplification reactions are automatically processed in a thermal cycling apparatus.
24. A method according to claim 23 wherein said thermal cycling apparatus is a multi-well real time thermal cycling apparatus.
25. A method according to claim 23 wherein said thermal cycling apparatus is a continuous flow PCR device.
26. A method according to claim 23 wherein said thermal cycling apparatus is a rotary thermal cycling apparatus.
27. A method of amplifying a plurality of selected nucleic acid molecules from a pool of nucleic acid molecules comprising:
(a) amplifying a plurality of selected nucleic acid molecules in a first round multiplex reaction including a plurality of first round primer pairs comprising outer primers, each pair being specific for a selected nucleic acid sequence, present in the reaction in excess relative to amplicons synthesized with said outer primer pairs, and not exhausted after said first round multiplex reaction;
(b) diluting the amplicons and remaining reaction components from said first round multiplex reaction into a plurality of second round amplification reactions each including at least one pair of second round primers, each pair comprising an inner primer and one of said outer primers and being specific for one of said selected nucleic acid sequences, wherein said dilution is at least a 20-fold dilution such that the amount of outer primers introduced into each of said second round amplification reactions is insufficient to impair the amplification of said selected nucleic acid molecules using said second round primers; and
(c) further amplifying said selected nucleic acid molecules in said plurality of second round amplification reactions whereby each second round reaction further amplifies a subset of said plurality of selected nucleic acid molecules respectively from said second round primers.
28. A method of estimating the number of selected nucleic acid molecules from a pool of nucleic acid molecules comprising:
(a) amplifying a plurality of selected nucleic acid molecules in a first round multiplex reaction including a plurality of outer primer pairs, each pair being specific for a selected nucleic acid sequence, present in the reaction in excess relative to amplicons synthesized with said outer primer pairs, and not exhausted after said first round multiplex reaction;
(b) diluting the amplicons and remaining reaction components from said first round multiplex reaction into a plurality of second round amplification reactions each including a detectable reporter and at least one pair of inner primers, each pair being specific for one of said selected nucleic acid sequences, wherein said dilution is at least a 20-fold dilution such that the amount of outer primers introduced into each of said second round amplification reactions is insufficient to impair the amplification of said selected nucleic acid molecules using said inner primers; and
(c) further amplifying said selected nucleic acid molecules in said plurality of second round amplification reactions whereby each second round reaction further amplifies a subset of the plurality of selected nucleic acid molecules respectively from said inner primers; and
(d) monitoring each second round amplification reaction by means of said detectible reporter such that the number of selected nucleic acid molecules of each selected sequence is estimated.
29. A method of estimating the number of selected nucleic acid molecules from a pool of nucleic acid molecules according to claim 28 wherein said detectible reporter is a dye that intercalates double stranded DNA or interacts with single stranded DNA.
30. A method of estimating the number of selected nucleic acid molecules from a pool of nucleic acid molecules according to claim 28 wherein said second round amplification reaction includes a plurality of primer pairs and a plurality of fluorogenic probes such that a plurality of selected nucleic acid molecules of each selected sequence is amplified and quantified.
31. A method of estimating the number of selected nucleic acid molecules from a pool of nucleic acid molecules comprising:
(a) amplifying a plurality of selected nucleic acid molecules in a first round multiplex reaction including a plurality of outer primer pairs, each pair being specific for a selected nucleic acid sequence, present in the reaction in excess relative to amplicons synthesized with said outer primer pairs, and not exhausted after said first round multiplex reaction;
(b) diluting the amplicons and remaining reaction components from said first round multiplex reaction into a plurality of second round amplification reactions each including a detectable reporter and at least one pair of second round primers, each pair comprising an inner primer and one of said outer primers and being specific for one of said selected nucleic acid sequences, wherein said dilution is at least a 20-fold dilution such that the amount of outer primers introduced into each of said second round amplification reactions is insufficient to impair the amplification of said selected nucleic acid molecules using said second round primers; and
(c) further amplifying said selected nucleic acid molecules in said plurality of second round amplification reactions whereby each second round reaction further amplifies a subset of said plurality of selected nucleic acid molecules respectively; and
(d) monitoring each second round amplification reaction by means of said detectible reporter such that the number of selected nucleic acid molecules of each selected sequence is estimated.
32. A method of estimating the number of selected nucleic acid molecules from a pool of nucleic acid molecules according to claim 31 wherein said detectible reporter is a dye that intercalates double stranded DNA or interacts with single stranded DNA.
33. A method of estimating the number of selected nucleic acid molecules from a pool of nucleic acid molecules according to claim 31 wherein said second round amplification reaction includes a plurality of primer pairs and a plurality of fluorogenic probes such that a plurality of selected nucleic acid molecules of each selected sequence is amplified and quantified.