Nucleic acid target identification by structure based probe cleavage
The present invention provides for novel methods and compositions for nucleic acid sequence detection. Unique, identifying cleavage fragments from probes, bound to target nucleic acids, are produced during PCR by the 5′-nuclease activity of the polymerase. The identity of the targets can be determined by identifying the unique cleavage fragments.
1. A method of detecting the presence or absence of a target nucleic acid sequence in a sample, comprising the steps of:
(a) preparing a reaction mixture by contacting the sample comprising a target nucleic acid with
(i) a pair of oligonucleotide primers, wherein a first oligonucleotide primer comprises a sequence complementary to a region in one strand of the target nucleic acid sequence and primes the synthesis of a first extension product, and wherein a second oligonucleotide primer comprises a sequence complementary to a region in said first extension product and primes the synthesis of a nucleic acid strand complementary to said first extension product, and
(ii) an oligonucleotide probe comprising at least two distinct portions,
a first portion comprised of standard nucleotides with or without nucleotide analogs that comprises a sequence that is at least partially complementary to a region of the target nucleic acid sequence wherein said first portion anneals within the target nucleic acid sequence bounded by said pair of oligonucleotide primers, and wherein said first portion is blocked at the 3′ terminus to prohibit extension by a nucleic acid polymerase and to prevent cleavage by a 3′ to 5′ exonuclease; and a second portion attached to the 5′ end of the first portion comprised of either nucleotides or non-nucleotides or both nucleotides and non-nucleotides, and comprises a sequence that is non-complementary to the target nucleic acid sequence, wherein said second portion also comprises an exonuclease-resistant modification selected from propanediol spacer, or hexaethylene glycol (HEG) spacer;
(b) amplifying said target nucleic acid sequence with a nucleic acid polymerase having 5′ to 3′ nuclease activity under conditions that allows annealing of said pair of oligonucleotide primers and said oligonucleotide probe to the target nucleic acid sequence and synthesis of primer extension products from said pair of oligonucleotide primers while the 5′ to 3′ nuclease activity of said nucleic acid polymerase is able to cleave and release from the annealed oligonucleotide probe, fragments containing the second portion of the oligonucleotide probe with or without additional nucleotides from the first portion of the oligonucleotide probe;
(c) treating said released fragments containing the second portion of the oligonucleotide probe with a 3′ to 5′ exonuclease that cleaves said fragments up to the exonuclease-resistant modification thereby producing a single fragment having a unique mass-distinguishable size; and
(d) detecting the presence or absence of the single fragment by mass spectrometry, thereby detecting the presence or absence of the target nucleic acid sequence in the sample;
wherein the 3′ to 5′ exonuclease is selected from the group consisting of Exonuclease I from E. coli , Exonuclease IV from E. coli , Exonuclease V from E. coli , T4 Exonuclease IV from Phage T4, T4 DNA Polymerase from Phage T4, Exonuclease I from Yeast, DNA polymerase α from Drosophila , DNA polymerase γ from Drosophila , and Snake venom phosphodiesterase.
2. The method of claim 1 , wherein two or more target nucleic acids are detected in a single multiplexed reaction.
3. The method of claim 2 , wherein two or more oligonucleotide probes are used to detect the two or more target nucleic acids in the single multiplexed reaction.
4. The method of claim 1 , wherein the detecting step (d) is preceded by a step of purifying said reaction mixture for removing contaminants of mass spectrometry from said reaction mixture.
5. The method of claim 1 , wherein the detecting step (d) is done by a mass spectrometer, selected from the group consisting of Matrix-Assisted Laser Desorption Ionization-Time of Flight (MALDI-TOF) MS, Tandem MS, Electrospray Ionization-Time of Flight (ESI-TOF), ESI-iontrap, Liquid Chromatography (LC)-MS), Gas Chromatography (GC)-MS) and Ion Mobility (IM)-MS.
6. The method of claim 1 , wherein the nucleic acid polymerase is a thermostable DNA polymerase.
7. A method of detecting the presence or absence of a target nucleic acid sequence in a sample, comprising the steps of:
(a) preparing a reaction mixture by contacting the sample comprising a target nucleic acid with
(i) a pair of oligonucleotide primers, wherein a first oligonucleotide primer comprises a sequence complementary to a region in one strand of the target nucleic acid sequence and primes the synthesis of a first extension product, and wherein a second oligonucleotide primer comprises a sequence complementary to a region in said first extension product and primes the synthesis of a nucleic acid strand complementary to said first extension product, and
(ii) an oligonucleotide probe comprising at least two distinct portions,
a first portion comprised of standard nucleotides with or without nucleotide analogs that comprises a sequence that is at least partially complementary to a region of the target nucleic acid sequence wherein said first portion anneals within the target nucleic acid sequence bounded by said pair of oligonucleotide primers, wherein the first portion also comprises a modification at the 5′-end that renders it resistant to cleavage by a single strand-specific 5′-3′-exonuclease, and a second portion attached to the 3′ end of the first portion comprised of either nucleotides or non-nucleotides or both nucleotides and non-nucleotides, and comprises a sequence that is non-complementary to the target nucleic acid sequence, wherein said second portion also comprises a modification selected from propanediol spacer, or hexaethylene glycol (HEG) spacer that renders it resistant to cleavage by the single strand-specific 5′-3′ exonuclease;
(b) amplifying said target nucleic acid sequence with a nucleic acid polymerase having 5′ to 3′ nuclease activity under conditions that allows annealing of said pair of oligonucleotide primers and said oligonucleotide probe to the target nucleic acid sequence and synthesis of primer extension products from said pair of oligonucleotide primers while the 5′ to 3′ nuclease activity of said nucleic acid polymerase is able to cleave and release from the annealed oligonucleotide probe, fragments containing the second portion of the oligonucleotide probe with or without additional nucleotides from the first portion of the oligonucleotide probe;
(c) treating said released fragments containing the second portion of the oligonucleotide probe with the single strand-specific 5′-3′ exonuclease that cleaves said fragments up to the exonuclease-resistant modification thereby producing a single fragment having a unique mass-distinguishable size; and
(d) detecting the presence or absence of the single fragment by mass spectrometry, thereby detecting the presence or absence of the target nucleic acid sequence in the sample;
wherein the single strand-specific 5′-3′ exonuclease is selected from the group consisting of Exonuclease from B. subtilis , Exonuclease II from yeast, Exonuclease V from yeast, and Exonuclease from Neurospora crassa.
8. The method of claim 7 , wherein two or more target nucleic acids are detected in a single multiplexed reaction.
9. The method of claim 8 , wherein two or more oligonucleotide probes are used to detect the two or more target nucleic acids in the single multiplexed reaction.
10. The method of claim 7 , wherein the detecting step (d) is preceded by a step of purifying said reaction mixture for removing contaminants of mass spectrometry from said reaction mixture.
11. The method of claim 7 , wherein the detecting step (d) is done by a mass spectrometer, selected from the group consisting of Matrix-Assisted Laser Desorption Ionization-Time of Flight (MALDI-TOF) MS, Tandem MS, Electrospray Ionization-Time of Flight (ESI-TOF), ESI-iontrap, Liquid Chromatography (LC)-MS, Gas Chromatography (GC)-MS and Ion Mobility (IM)-MS.
12. The method of claim 7 , wherein the nucleic acid polymerase is a thermostable DNA polymerase.