Detection of target nucleic acid sequence by PTO cleavage and extension-dependent signaling oligonucleotide hybridization assay

Patent metadata

Field	Value
Publication number	US-9868980-B2
Application number	US-201214374567-A
Country	US
Kind code	B2
Filing date	Jul 3, 2012
Priority date	Feb 2, 2012
Publication date	Jan 16, 2018
Grant date	Jan 16, 2018

Abstract

The present invention relates to the detection of a target nucleic acid sequence by a PCE-SH (PTO Cleavage and Extension-Dependent Signaling Oligonucleotide Hybridization) assay. The present invention does not use probes to be hybridized with target nucleic acid sequences for providing target signals. Interestingly, the present invention uses probes (signaling oligonucleotides) to be hybridized with the extended strand formed in a target-dependent manner in which the extended strand is synthesized using the CTO artificially selected as templates.

First claim

What is claimed is:

1. A method for detecting a target nucleic acid sequence from a DNA or a mixture of nucleic acids by a PCE-SH (PTO Cleavage and Extension-Dependent Signaling Oligonucleotide Hybridization) assay in a liquid phase, comprising:
(a) hybridizing the target nucleic acid sequence with an upstream oligonucleotide and a probing and targeting oligonucleotide (PTO); wherein the upstream oligonucleotide comprises a hybridizing nucleotide sequence complementary to the target nucleic acid sequence; the PTO comprises (i) a 3′-targeting portion comprising a hybridizing nucleotide sequence complementary to the target nucleic acid sequence and (ii) a 5′-tagging portion comprising a nucleotide sequence non-complementary to the target nucleic acid sequence; wherein the 3′-targeting portion of the PTO is hybridized with the target nucleic acid sequence and the 5′-tagging portion is not hybridized with the target nucleic acid sequence; the upstream oligonucleotide is located upstream of the PTO;
(b) contacting the resultant of the step (a) to an enzyme having a 5′ nuclease activity under conditions for cleavage of the PTO; wherein the upstream oligonucleotide or its extended strand induces cleavage of the PTO by the enzyme having the 5′ nuclease activity such that the cleavage releases a fragment comprising the 5′-tagging portion or a part of the 5′-tagging portion of the PTO;
(c) hybridizing the fragment released from the PTO with a capturing and templating oligonucleotide (CTO); wherein the CTO comprises in a 3′ to 5′ direction (i) a capturing portion comprising a nucleotide sequence complementary to the 5′-tagging portion or a part of the 5′-tagging portion of the PTO and (ii) a templating portion comprising a nucleotide sequence non-complementary to the 5′-tagging portion and the 3′-targeting portion of the PTO; wherein the fragment released from the PTO is hybridized with the capturing portion of the CTO;
wherein the CTO is not labeled;
(d) performing an extension reaction using the resultant of the step (c) and a template-dependent nucleic acid polymerase; wherein the fragment hybridized with the capturing portion of the CTO is extended to form an extended strand comprising an extended sequence complementary to the templating portion of the CTO, thereby forming an extended duplex;
(e) hybridizing the extended strand with a signaling oligonucleotide (SO); wherein the SO comprises a complementary sequence to the extended strand and at least one label; wherein the at least one label is located on the SO to provide a detectable signal directly by hybridization with the extended strand; and
(f) detecting the signal in said liquid phase; wherein the CTO and SO are not immobilized on a solid substrate; whereby the detection of the signal indicates the presence of the extended strand and the presence of the target nucleic acid sequence; wherein the detectable signal is provided by (i) the label linked to the SO, (ii) a combination of the label linked to the SO and a label linked to the fragment from the PTO, (iii) a combination of the label linked to the SO and a label to be incorporated into the extended strand during the extension reaction of the step (d), or (iv) a combination of the label linked to the SO and an intercalating dye.

2. The method according to claim 1 , wherein at least a portion of the SO comprises a complementary sequence to the extended sequence.

3. The method according to claim 1 , wherein the SO is labeled with an interactive dual label comprising a reporter molecule and a quencher molecule and the hybridization between the SO and the extended strand in the step (e) induces change in signal from the interactive dual label to provide the detectable signal.

4. The method according to claim 1 , wherein the SO is labeled with a single label and the hybridization between the SO and the extended strand in the step (e) induces change in signal from the single label to provide the detectable signal.

5. The method according to claim 1 , wherein the method uses an additional SO comprising a complementary sequence to the extended strand, the two SOs are hybridized with the extended strand in an adjacent manner, the two SOs each comprises one label among a reporter molecule and a quencher molecule of an interactive dual label; and the hybridization between the two SOs and the extended strand induces change in signal from the interactive dual label to provide the detectable signal.

6. The method according to claim 1 , wherein the SO comprises one label among a reporter molecule and a quencher molecule of an interactive dual label, the fragment from the PTO comprises the other label among the reporter molecule and the quencher molecule; the extended strand comprises the label originated from the fragment from the PTO, and wherein the hybridization between the SO and the extended strand induces change in signal from the interactive dual label to provide the detectable signal.

7. The method according to claim 1 , wherein the SO comprises one label among a reporter molecule and a quencher molecule of an interactive dual label, and the templating portion of the CTO comprises a nucleotide having a first non-natural base; wherein the extension reaction in the step (d) is performed in the presence of a nucleotide having both a second non-natural base with a specific binding affinity to the first non-natural base and the other among the reporter molecule and the quencher molecule, thereby incorporating the label into the extended strand; wherein the hybridization between the SO and the extended strand induces change in signal from the interactive dual label to provide the detectable signal.

8. The method according to claim 1 , wherein the SO comprises one label among a reporter molecule and a quencher molecule of an interactive dual label, and the extension reaction in the step (d) is performed in the presence of a nucleotide having the other among the reporter molecule and the quencher molecule, thereby incorporating the label into the extended strand; wherein the hybridization between the SO and the extended strand induces change in signal from the interactive dual label to provide the detectable signal.

9. The method according to claim 1 , wherein the SO comprises an acceptor of a FRET (fluorescence resonance energy transfer) and the hybridization in the step (e) is preformed in the presence of an intercalating dye; wherein the hybridization between the SO and the extended strand induces change in signal from the acceptor of the SO to provide the detectable signal.

10. The method according to claim 1 , wherein the PTO, CTO and/or SO is blocked at its 3′-end to prohibit its extension.

11. The method according to claim 1 , wherein the upstream oligonucleotide is an upstream primer or an upstream probe.

12. The method according to claim 1 , wherein the method further comprises the step of providing a detectable signal between the steps (e) and (f) by melting the hybridization resultant of the step (e) or by melting and hybridizing the hybridization resultant of the step (e); wherein the step (f) is performed by detecting the signal to determine the presence of the extended strand.

13. The method according to claim 1 , wherein the method further comprises the step of providing and detecting a detectable signal after the step (f) by melting the hybridization resultant of the step (e) or by melting and hybridizing the hybridization resultant of the step (e), whereby the presence of the extended strand is determined one more time.

14. The method according to claim 13 , wherein the presence of the extended strand is determined by a melting curve analysis or a

Assignees

• Chun Jong Yoon
• Lee Young Jo
• Seegene Inc

Inventors

• Chun Jong Yoon
• Lee Young Jo

Classifications

• C12Q1/6844 Primary

  Nucleic acid amplification reactions · CPC title

• C12Q1/6818 Primary

  involving interaction of two or more labels, e.g. resonant energy transfer · CPC title

• C12Q1/6837

  using probe arrays or probe chips (C12Q1/6874 takes precedence) · CPC title

• C12Q1/6823 Primary

  Release of bound markers · CPC title

• C12Q2565/1015

  labels being on the same oligonucleotide · CPC title