Annealing control primer and its uses

• US 7,579,154 B2
• Filed: 01/10/2007
• Issued: 08/25/2009
• Est. Priority Date: 12/08/2001
• Status: Expired due to Term

• Current Assignee: Seegene, Inc.
• Original Assignee: Seegene, Inc.
• Inventors: Chun, Jong-Yoon
• Primary Examiner(s): Benzion; Gary
• Assistant Examiner(s): WOOLWINE, SAMUEL C
• Application Number:
  US11/651,605
• Publication Number:
  US 20070148683A1
• Time in Patent Office: 958 Days
• Field of Search: None
• US Class Current: 435/6.12
• CPC Class Codes: C12Q 1/6853 using modified primers or templates
• CPC Class Codes: C12Q 1/6876 Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes
• CPC Class Codes: C12Q 2525/101 incorporating non-naturally occurring nucleotides, e.g. inosine

Abstract

The present invention relates to an annealing control primer for improving annealing specificity in nucleic acid amplification and its applications to all fields of nucleic acid amplification-involved technology. The present primer comprises (a) a 3′-end portion having a hybridizing nucleotide sequence substantially complementary to a site on a template nucleic acid to hybridize therewith; (b) a 5′-end portion having a pre-selected arbitrary nucleotide sequence; and (c) a regulator portion positioned between said 3′-end portion and said 5′-end portion comprising at least one universal base or non-discriminatory base analog, whereby said regulator portion is capable of regulating an annealing portion of said primer in association with annealing temperature.

Claims

1. A method for improving the annealing specificity of a primer in nucleic acid amplification, comprising the steps of:

(a) preparing a 3′

-end portion of the primer having a hybridizing nucleotide sequence substantially complementary to a site on a template nucleic acid to hybridize therewith;

(b) forming at the 5′

-end of the 3′

-end portion a regulator portion comprising at least three contiguous universal bases to have the lowest Tm in the three portions of the primer, wherein the regulator portion restricts a primer annealing site to the 3′

-end portion to improve the annealing specificity of the 3′

-end portion; and

(c) forming at the 5′

-end of the regulator portion a 5′

-end portion having a pre-selected arbitrary nucleotide sequence substantially not complementary to any site on the template nucleic acid,

whereby the primer has three distinct portions and the annealing specificity of the primer is improved by the presence of the regulator portion and the 5′

-end portion, and

wherein the primer has a general formula of 5′

-X_p-Y_q-Z_r-3′

, wherein X_p represents said 5′

-end portion having said pre-selected arbitrary nucleotide sequence substantially not complementary to any site on the template nucleic acid;

Y_q represents said regulator portion comprising at least three contiguous universal base;

Z_r represents said 3′

-end portion having a hybridizing nucleotide sequence substantially complementary to a site on the template nucleic acid to hybridize therewith;

wherein p, q and r represent the number of nucleotides; and

wherein X, Y and Z is deoxyribonucleotide or ribonucleotide, and

wherein Z_r comprises at least 10 contiguous deoxythymidine nucleotides.

2. The method according to claim 1, wherein Z_r comprises at least 10 contiguous deoxythymidine nucleotides having 3′

-V at its 3′

-end;

in which V is one selected from the group consisting of deoxyadenosine, deoxycytidine and deoxyguanosine.

3. The method according to claim 2, wherein Z_r comprises at least 10 contiguous deoxythymidine nucleotides having 3′

-NV at its 3′

-end;

in which V is one selected from the group consisting of deoxyadenosine, deoxycytidine and deoxyguanosine, and N is one selected from the group consisting of deoxyadenosine, deoxythymidine, deoxycytidine and deoxyguanosine.

4. A method for improving the annealing specificity of a first primer in nucleic acid amplification, which comprises the steps of:

(a) preparing a 3′

-end portion of the first primer having a hybridizing nucleotide sequence substantially complementary to a site on a template nucleic acid to hybridize therewith at a first annealing temperature in said amplification;

(b) forming at the 5′

-end of the 3′

-end portion a regulator portion comprising at least three contiguous universal bases to have the lowest Tm in the three portions of the primer, wherein the regulator portion restricts a primer annealing site to the 3′

-end portion to improve the annealing specificity of the 3′

-end portion at a first annealing temperature in said amplification; and

(c) forming at the 5′

-end of the regulator portion a 5′

-end portion having a pre-selected arbitrary nucleotide sequence that serves as a priming site at a second annealing temperature in said amplification and is substantially not complementary to any site on the template nucleic acid,

(d) annealing the first primer to a target at the first annealing temperature and extending the first primer to form a first primer extension product;

(e) synthesizing a polynucleotide complementary to the first primer extension product;

(f) annealing a second primer to the portion of said complementary polynucleotide that is complementary to the pre-selected arbitrary nucleotide sequence at the second annealing temperature, and extending the second primer to form a second primer extension product;

whereby the first primer has three distinct portions and the annealing specificity of the first primer is improved by the presence of the regulator portion and the 5′

-end portion, and

wherein the first annealing temperature and the second annealing temperature are different.

5. The method according to claim 4, wherein said universal base is selected from the group consisting of deoxyinosine, inosine, 7-deaza-2′

-deoxyinosine, 2-aza-2′

-deoxyinosine, 2′

-OMe inosine, 2′

-F inosine, deoxy 3-nitropyrrole, 3-nitropyrrole, 2′

-OMe 3-nitropyrrole, 2′

-F 3-nitropyrrole, 1-(2′

-deoxy-beta-D-nbofuranosyl)-3-nitropyrrole, deoxy 5-nitroindole, 5-nitroindole, 2′

-OMe 5-nitroindole, 2′

-F 5-nitroindole, deoxy 4-nitrobenzimidazole, 4-nitrobenzimidazole, deoxy 4-aminobenzimidazole, 4-nitrobenzimidazole, 4-nitrobenzimidazole, deoxy 4-aminobenzimidazole, 4-aminobenzimidazole, deoxy nebularine, 2′

-F nebularine, 2′

-F 4-nitrobenzimidazole, PNA-5-introindole, PNA-nebularine, PNA-inosine, PNA-4-nitrobenzimidazole, PNA-3-nitropyrrole, morpholino-5-nitroindole, morpholino-nebularine, morpholino-inosine, morpholino-4-nitrobenzimidazole, morpholino-3-nitropyrrole, phosphoramidate-5-nitroindole, phosphoramidate-nebularine, phosphoramidate-inosine, phosphoramidate-4-nitrobenzimidazole, phosphoramidate-3-nitropyrrole, 2′

-0-methoxyethyl inosine, 2′

0-methoxyethyl nebularine, 2′

-0-methoxyethyl 5-nitroindole, 2′

-0-methoxyethyl 4-nitrobenzimidazole, 2′

-0-methoxyethyl 3-nitropyrrole, and combinations thereof.

6. The method according to claim 5, wherein said universal base is deoxyinosine, 1-(2′

-deoxy-beta-D-ribofuranosyl)-3-nitropyrrole or 5-nitroindole.

7. The method according to claim 6, wherein said universal base is deoxyinosine.

8. The method according to claim 4, wherein said regulator portion comprises more than three contiguous nucleotides having universal base or non-discriminatory base analog.

9. The method according to claim 4, wherein the second annealing temperature is higher than the first annealing temperature.

10. The method according to claim 4, wherein said first annealing temperature is approximately equal to the Tm of said 3′

-end portion of said primer.

11. The method according to claim 4, wherein said second annealing temperature is approximately equal to the Tm of said 5′

-end portion of said primer.

12. The method according to claim 4, wherein the primer has a general formula of 5′

-X_p-Y_q-Z_r-3′

, wherein X_p represents said 5′

-end portion having said pre-selected arbitrary nucleotide sequence substantially not complementary to any site on the template nucleic acid;

Y_q represents said regulator portion comprising at least three contiguous universal base;

Z_r represents said 3′

-end portion having a hybridizing nucleotide sequence substantially complementary to a site on the template nucleic acid to hybridize therewith;

wherein p, q and r represent the number of nucleotides; and

wherein X, Y and Z is deoxynbonucleotide or ribonucleotide.

13. The method according to claim 12, wherein Z_r comprises at least 10 contiguous deoxythymidine nucleotides.

14. The method according to claim 13, wherein Z_r comprises at least 10 contiguous deoxythymidine nucleotides having 3′

-V at its 3′

-end;

in which V is one selected from the group consisting of deoxyadenosine, deoxycytidine and deoxyguanosine.

15. The method according to claim 14, wherein Z_r comprises at least 10 contiguous deoxythymidine nucleotides having 3′

-NV at its 3′

-end;

in which V is one selected from the group consisting of deoxyadenosine, deoxycytidine and deoxyguanosine, and N is one selected from the group consisting of deoxyadenosine, deoxythymidine, deoxycytidine and deoxyguanosine.

16. The method according to claim 12, wherein p represents an integer of 15 to 60.

17. The method according to claim 12, wherein q represents an integer of 3 to 15.

18. The method according to claim 12, wherein r represents an integer of 6 to 50.

19. The method according to claim 12, wherein p is an integer of 15 to 60, q is an integer of3 to 15 and r is an integer of 6to 30.