Methods for producing a single stranded polydeoxynucleotide having two different defined sequences and kits

• US 5,683,879 A
• Filed: 06/07/1995
• Issued: 11/04/1997
• Est. Priority Date: 07/31/1992
• Status: Expired due to Fees

• Current Assignee: DADE Behring Beteiligungs GmbH (Siemens AG)
• Original Assignee: Behringwerke Aktiengesellschaft (Sanofi )
• Inventors: Chen, Yan, Ullman, Edwin F., Hahnenberger, Karen M., Laney, Maureen
• Primary Examiner(s): Campbell, Eggerton A.
• Application Number:
  US08/475,236
• Time in Patent Office: 881 Days
• Field of Search: 435/5, 435/6, 435/91.2, 935/77, 935/78, 536/23.1, 536/24.33
• US Class Current: 435/6.12
• CPC Class Codes: C12Q 1/6844 Nucleic acid amplification reactions
• CPC Class Codes: C12Q 1/6853 using modified primers or templates
• CPC Class Codes: C12Q 1/686 Polymerase chain reaction [PCR]
• CPC Class Codes: C12Q 2525/186 incorporating a non-extendable or blocking moiety
• CPC Class Codes: C12Q 2537/163 blocking probe

Abstract

A method is disclosed for extending a primer to produce a single stranded polydeoxynucleotide that has two or more defined sequences. A combination is provided which comprises a template polynucleotide, a blocker polynucleotide, a primer polynucleotide and a polynucleotide Q. The template polynucleotide has three sequences T1, T2 and T3 wherein T1 is non-contiguous and 3'"'"' of T3 and wherein the 5'"'"' end of T3 is 5'"'"' of the 5'"'"' end of T2. The primer polynucleotide has a second defined sequence at its 3'"'"' end that is hybridizable with T1. The blocker polynucleotide has sequence B1 that is hybridizable with T3. Polynucleotide Q has sequences S1 and S2 wherein S1 is 3'"'"' of S2 and homologous with T2 and S2 is complementary to a first defined sequence that is to be introduced at the 3'"'"' end of the polynucleotide primer, when it is extended during the method of the invention. Polynucleotide Q is either attached to the 5'"'"' end of the blocker polynucleotide or present as a separate reagent. The primer is extended along the template polynucleotide and along at least a portion of sequence T2 and thereafter along the polynucleotide Q to give a single stranded polynucleotide having two or more defined sequences.

Claims

1. A method for producing from a polynucleotide primer a single stranded polydeoxynucleotide having two different defined sequences P1 and P'"'"'2, said method comprising the steps of:

(a) providing in combination (1) a template polynucleotide (template) having three sequences T1, T2 and T3 wherein T1 is non-contiguous with and 3'"'"' of said T2 and T3 and the 3'"'"' end of said T3 is contiguous with or lies within said T2, (2) a polynucleotide primer (primer) P1 whose 3'"'"' end is hybridizable with said T1, (3) a blocker polynucleotide with sequence B1, said B1 being hybridizable with said T3, and (4) polynucleotide Q having a sequence S1 and a sequence S2 wherein said Q is either attached at its 3'"'"'-end to the 5'"'"' end of said blocker polynucleotide or present as a separate reagent and wherein said S1 is 3'"'"' of said S2 and substantially identical to said T2 and wherein said S2 is complementary to said P'"'"'2, and

(b) subjecting said combination to conditions for extending said primer, by means of a polymerase, P1 along the template and along at least a portion of said T2 and thereafter along said polynucleotide Q, wherein said polymerase has little or no 5'"'"'-3'"'"' exonuclease activity under said conditions for extending and wherein the 3'"'"'-end of said polynucleotide Q is not extended by said polymerase.

2. The method of claim 1 comprising the steps of dissociating said extended primer from it duplex, hybridizing a primer P2 to said P'"'"'2 and extending said primer along said extended primer to give a second extended primer characterized by a sequence P'"'"'1 that is 3'"'"' of said P2 and capable of hybridizing to said primer P1.

3. The method of claim 1 which comprises amplifying said extended primers by a polymerase chain reaction.

4. The method of claim 1 wherein said polynucleotide Q is attached to the 5'"'"' end of said blocker polynucleotide.

5. An isolated polynucleotide primer comprising a single strand of DNA comprised of a sequence T3 and a sequence T2 wherein the 3'"'"' end of said T3 is contiguous with the 5'"'"' end of T2, said single strand being complexed to a blocker DNA sequence comprised of a sequence B1 complementary to said T3 and a sequence S1 which is 5'"'"' of B1 and substantially identical to said T2.

6. The a primer polynucleotide of claim 5 having a sequence at its 3'"'"' end complexed with a sequence T1 in said single strand of DNA.

7. A kit comprising in packaged combination:

(a) a primer polynucleotide having a sequence at its 3'"'"' end hybridizable with a first sequence T1 in a target polynucleotide

(b) a blocker polynucleotide having a sequence B1, said B1 being hybridizable with a sequence T3 in said target polynucleotide wherein said T3 is 3'"'"' of said T1 and the 5'"'"' end of said T3 is 5'"'"' of the 5'"'"' end of a sequence T2, and

(c) a polynucleotide Q having sequences S1 and S2 wherein S1 is 3'"'"' of said S2 and substantially identical to said T2 in said template polynucleotide and wherein said S2 is a sequence that is substantially identical to at least the 3'"'"' end portion of a second polynucleotide primer, the 3'"'"'end of said polynucleotide Q being incapable of chain extension in the presence of a polymerase.

8. The kit of claim 7 wherein said polynucleotide Q is a part of said blocker polynucleotide.

9. The kit of claim 7 wherein said polynucleotide Q is separate from said blocker polynucleotide.

10. The kit of claim 7 which comprises template dependent DNA polymerase.

11. The kit of claim 7 which comprises deoxynucleoside triphosphates.

12. The kit of claim 7 wherein one of said primers is labeled with a reporter molecule.