Method for controlling the extension of an oligonucleotide

• US 6,200,757 B1
• Filed: 01/19/1999
• Issued: 03/13/2001
• Est. Priority Date: 01/19/1999
• Status: Expired due to Term

• Current Assignee: Aventisub LLC (Sanofi )
• Original Assignee: Dade Behring, Inc. (Siemens AG)
• Inventors: Taylor, Marc, Kurn, Nurith, Lishanski, Alla, Liu, Yen Ping
• Primary Examiner(s): Horlick, Kenneth R.
• Assistant Examiner(s): Taylor, Janell E.
• Application Number:
  US09/233,413
• Time in Patent Office: 784 Days
• Field of Search: 435/91.1, 435/91.2, 435/6, 536/23.1, 536/24.3, 536/24.33, 536/25.3, 536/25.32, 536/26.71
• US Class Current: 435/6.11
• CPC Class Codes: C12Q 1/6848 characterised by the means for preventing contamination or increasing the specificity or sensitivity of an amplification reaction
• CPC Class Codes: C12Q 2525/186 incorporating a non-extendable or blocking moiety
• CPC Class Codes: C12Q 2527/101 Temperature

Abstract

The present invention relates to a method for selectively extending an oligonucleotide primer along a specific target polynucleotide sequence in a mixture of polynucleotides. A combination is provided comprising the mixture, an oligonucleotide primer having a modification, and a binding substance for the modification wherein the binding substance binds to the oligonucleotide and prevents the extension of the oligonucleotide along the target polynucleotide sequence. The temperature of the combination is adjusted to a level sufficient to irreversibly denature the binding substance and permit the extension of the oligonucleotide primer along the specific target polynucleotide sequence. The invention has particular application in the amplification of nucleic acids. Also disclosed are kits for carrying out a method in accordance with the present invention.

Claims

1. A method for selectively extending an oligonucleotide primer along a target polynucleotide sequence in a mixture of polynucleotides, said method comprising:

(a) providing in combination said mixture, an oligonucleotide primer having a modification, and a binding substance for said modification wherein said binding substance binds to said oligonucleotide and prevents the extension of said oligonucleotide along said target polynucleotide sequence and

(b) adjusting the temperature of said combination to a level sufficient to irreversibly denature said binding substance and permit the extension of said oligonucleotide primer along said specific target polynucleotide sequence.

2. A method for controlling the extension of an oligonucleotide along a template polynucleotide, said method comprising:

(a) providing in combination in a medium (i) a template polynucleotide (ii) an oligonucleotide at least a portion of which hybridizes to a portion of said template polynucleotide, said oligonucleotide comprising a modified moiety, (iii) all reagents required for extending said oligonucleotide along said template polynucleotide, and (iv) a binding substance for said modified moiety, said binding substance being capable of binding to said modified moiety and preventing said oligonucleotide from extending along said template polynucleotide, and

(b) subjecting said combination to conditions for releasing irreversibly said binding substance from said oligonucleotide and permitting said oligonucleotide to extend along said template polynucleotide.

3. A method according to claim 2 wherein said modified moiety is a modified nucleotide.

4. A method according to claim 3 wherein said modified nucleotide is an unnatural nucleotide or comprises a group that is unnatural.

5. A method according to claim 2 wherein said template polynucleotide is DNA or RNA.

6. A method according to claim 2 that is part of an amplification method.

7. A method according to claim 6 wherein said amplification method is selected from the group consisting of polymerase chain reaction, single primer amplification, and transcription-based nucleic acid amplification.

8. A method according to claim 2 wherein said binding substance is a protein.

9. A method according to claim 2 wherein said binding substance is an antibody.

10. A method for amplifying a target polynucleotide sequence, which comprises:

(a) providing in combination (i) a medium suspected of containing said target polynucleotide sequence, (ii) all reagents required for conducting an amplification of said target polynucleotide sequence, said reagents comprising a nucleotide polymerase, nucleoside triphosphates, and at least one primer extendable along said target polynucleotide sequence, and

(b) subjecting said combination to conditions for amplifying said target polynucleotide sequence,

wherein said primer comprises a modified moiety and wherein a binding substance for said modified moiety is included in said combination, said binding substance being capable of binding to said modified moiety and preventing said oligonucleotide from extending along said target polynucleotide sequence and wherein said binding substance is released irreversibly from said primer during said temperature cycling thereby permitting said primer to bind with and be extended along said target polynucleotide sequence.

11. A method according to claim 10 wherein said modified moiety is a modified nucleotide.

12. A method according to claim 11 wherein said modified nucleotide is an unnatural nucleotide or comprises a group that is unnatural.

13. A method according to claim 10 wherein said target polynucleotide is DNA or RNA.

14. A method according to claim 10 wherein only one primer is used and said target sequence contains at its 5′

-end at least a 10-base sequence hybridizable with a sequence at the 3′

-end of said target sequence to which said primer hybridizes.

15. A method according to claim 10 wherein first and second primers are employed and extended first primer is a template for said second primer and extended second primer is a template for said first primer.

16. A method according to claim 10 wherein said binding substance is a protein.

17. A method according to claim 10 wherein said binding substance is an antibody.

18. A method for amplifying a polynucleotide sequence of a target polynucleotide (“

target sequence”

), said method comprising;

(a) hybridizing to the 3′

-end of said target sequence a first oligonucleotide primer (“

first primer”

),

(b) extending, in the presence of a polymerase and nucleotide triphosphates, said first primer along at least said target sequence to produce an extended first primer, said first primer being capable of hybridizing to, and being extended along, (1) said extended first primer or (2) an extended second oligonucleotide primer (“

second primer”

) wherein said extended second primer results from the extension of a second primer capable of hybridizing to and extending along a polynucleotide that is complementary (complementary polynucleotide) to said target sequence,

(c) dissociating said extended first primer from said target sequence,

(d) hybridizing, to the 3′

-end of said extended first primer, said first or said second primer,

(e) extending said first or said second primer along said extended first primer,

(f) dissociating said extended first primer or said extended second primer from said extended first primer,

(g) hybridizing, to the 3′

-end of said extended first or said extended second primer, said first primer, and

(h) repeating steps (e)-(g) by repeated temperature cycling, wherein said primer comprises a modified nucleotide in the portion thereof that binds to said target polynucleotide and wherein an antibody for said modified nucleotide is included in said combination, said antibody being capable of binding to said modified nucleotide and preventing said primer from being extended along said target sequence and wherein said antibody is released irreversibly from said primer during said temperature cycling thereby permitting said primer to bind with and be extended along said target polynucleotide sequence.

19. A method according to claim 18 wherein said modified nucleotide is an unnatural nucleotide or comprises a group that is unnatural.

20. A method according to claim 18 wherein said target polynucleotide is DNA or RNA.

21. A method according to claim 18 wherein only said first primer is used and said target sequence contains at its 5′

-end at least a 10-base sequence hybridizable with a sequence at the 3′

-end of said target sequence to which said primer hybridizes.

22. A method according to claim 18 wherein said first and said second primers are different and said extended first primer is a template for said second primer and said extended second primer is a template for said first primer.

23. A method according to claim 18 wherein said modified nucleotide is at the 3′

-end portion of said oligonucleotide primer.

24. A method for detecting a target sequence of a target polynucleotide (“

target sequence”

), said method comprising;

(a) amplifying said target sequence by a method comprising;

(i) hybridizing to the 3′

-end of said target sequence a first oligonucleotide primer (“

first primer”

),

(ii) extending, in the presence of a polymerase and nucleotide triphosphates, said first primer along at least said target sequence to produce an extended first primer, said first primer being capable of hybridizing to, and being extended along, (1) said extended first primer or (2) an extended second oligonucleotide primer (“

second primer”

) wherein said extended second primer results from the extension of a second primer capable of hybridizing to and extending along a polynucleotide that is complementary (complementary polynucleotide) to said target sequence,

(iii) dissociating said extended first primer from said target sequence,

(iv) hybridizing, to the 3′

-end of said extended first primer, said first or said second primer,

(v) extending said first or said second primer along said extended first primer,

(vi) dissociating said extended first primer or said extended second primer from said extended first primer,

(vii) hybridizing, to the 3′

-end of said extended first or said extended second primer, said first primer, and

(viii) repeating steps (v)-(vii), and

(b) detecting said extended first primer and/or said extended second primer,

wherein said primer comprises a modified nucleotide in the portion thereof that binds to said target polynucleotide and wherein an antibody for said modified nucleotide is included in said combination, said antibody being capable of binding to said modified nucleotide and preventing said primer from being extended along said target sequence and wherein said antibody is released irreversibly from said primer during said temperature cycling thereby permitting said primer to bind with and be extended along said target polynucleotide sequence.

25. The method of claim 24 wherein the repeating of steps (v)-(vii) is achieved by repeated temperature cycling.

26. The method of claim 24 wherein said target polynucleotide is DNA or RNA.

27. The method of claim 24 wherein only said first primer is used and said target sequence contains at its 5′

-end at least a 10-base sequence hybridizable with a sequence at the 3′

-end of said target sequence to which said first primer hybridizes.

28. The method of claim 24 wherein said first and said second primers are different and said extended first primer is a template for said second primer and said extended second primer is a template for said first primer.