Fluorescence polarization in nucleic acid analysis

• US 6,440,707 B1
• Filed: 11/07/2000
• Issued: 08/27/2002
• Est. Priority Date: 08/21/1998
• Status: Expired due to Fees

• Current Assignee: Washington University In St Louis
• Original Assignee: Washington University In St Louis
• Inventors: Kwok, Pui-Yan, Chen, Xiangning, Levine, Leanna
• Primary Examiner(s): Siew, Jeffrey
• Application Number:
  US09/708,346
• Time in Patent Office: 658 Days
• Field of Search: 435/6, 435/91.1, 435/91.2, 435/91.41, 536/22.1, 536/23.1, 536/24.3, 536/24.37, 536/24.33, 536/25.32
• US Class Current: 435/91.2
• CPC Class Codes: C12Q 1/6816 characterised by the detection means C12Q1/6804 takes precedence
• CPC Class Codes: C12Q 1/6827 for detection of mutation or polymorphism
• CPC Class Codes: C12Q 2522/101 Single or double stranded nucleic acid binding proteins
• CPC Class Codes: C12Q 2527/125 Specific component of sample, medium or buffer
• CPC Class Codes: C12Q 2535/131 Allele specific probes
• CPC Class Codes: C12Q 2561/119 Fluorescence polarisation
• CPC Class Codes: C12Q 2563/107 fluorescence

Abstract

A new method for DNA diagnostics based on template-directed primer extension and detection by fluorescence polarization is described. In this method, amplified genomic DNA fragments containing polymorphic sites are incubated with a oligonucleotide primer designed to hybridize to the DNA template adjacent to the polymorphic site in the presence of allelic dye-labeled dideoxyribonucleoside triphosphates and a modified Taq DNA polymerase. The primer is extended by the dye-terminator specific for the allele present on the template. At the end of the reaction, the fluorescence polarization of the two dye-terminators in the reaction mixture are analyzed directly without separation or purification. This homogeneous DNA diagnostic method is shown to be highly sensitive and specific and is suitable for automated genotyping of large number or samples.

Claims

1. A method for detecting the presence of a target site, if present, of at least one nucleotide in a template nucleic acid comprising:

(a) forming an oligonucleotide bound to the target site wherein the oligonucleotide comprises a fluorophore linked to a terminator contained therein; and

(b) detecting fluorescence polarization of the fluorophore of the fluorescently-labeled oligonucleotide,

wherein the oligonucleotide is formed from a primer bound to the template immediately 3′

to the target site and a terminator covalently linked to a fluorophore, and wherein said terminator-linked fluorophore binds to the target site and reacts with the primer to produce an extended primer which is said fluorescently labeled oligonucleotide,

wherein an increase in fluorescence polarization indicates the presence of the target site

thereby detecting the presence of the target site by said increase in fluorescence polarization.

2. The method of claim 1, wherein said fluorophore is selected from the group consisting of:

5-carboxyfluorescein (FAM-ddNTPs);

6-carboxy-X-rhodamine (ROX-ddNTPs);

N,N,N′

,N′

-tetramethyl-6-carboxyrhodamine (TMR-ddNTPs); and

BODIPY-Texas Red (BTR-ddNTPs).

3. The method of claim 1 wherein step (b) is conducted in the presence of a single stranded DNA binding (SSB) protein.

4. The method of claim 1 wherein step (b) is conducted in the presence of an organic solvent.

5. The method of claim 4, wherein the organic solvent is methanol.

6. A method of diagnosing the presence of a genetic polymorphism characterized by the presence of a single nucleotide target site in a subject, comprising:

(a) isolating genomic DNA or RNA from a sample of biological material, wherein template genomic DNA or template DNA prepared from the RNA comprises one or more target sites, and wherein each target site comprises a genetic polymorphism;

(b) forming a fluorescently labeled oligonucleotide bound to the target site if present wherein the oligonucleotide comprises a fluorophore linked to a terminator contained therein;

(c) detecting fluorescence polarization of the fluorophore of the fluorescently-labeled oligonucleotide;

wherein the oligonucleotide is formed from a primer bound to the template immediately 3′

to the target site and a terminator covalently linked to a fluorophore, and wherein said terminator-linked fluorophore binds to the target side and reacts with the primer to produce an extended primer which is said fluorescently labeled oligonucleotide,

wherein an increase in fluorescence polarization indicates the presence of the target site

thereby detecting the presence of the target site which comprises a genetic polymorphism by said increase in fluorescence polarization.

7. The method of claim 6, wherein said fluorophore is selected from the group consisting of:

5-carboxyfluorescein (FAM-ddNTPs);

6-carboxy-X-rhodamine (ROX-ddNTPs);

N,N,N′

,N′

-tetramethyl-6-carboxyrhodamine (TMR-ddNTPs); and

BODIPY-Texas Red (BTR-ddNTPs).

8. A method for detecting the presence of specified nucleotides at a first and second target single nucleotide site in each of two alleles in templates which comprise amplified genomic DNA which method comprises

(a) forming a first fluorescently labeled oligonucleotide from a first primer bound to a first template allele immediately 3′

to the target site and a first terminator covalently linked to a first fluorophore, and wherein said terminator linked fluorophore binds to a first target site if present and reacts with the primer to produce an extended primer which is said first fluorescently labeled oligonucleotide, and

forming a second fluorescently labeled oligonucleotide from said primer bound to a second template allele immediately 3′

to the target site and a second terminator covalently linked to a second fluorophore, and wherein said terminator linked fluorophore binds to a second target site if present and reacts with the primer to produce an extended primer which is said second fluorescently labeled oligonucleotide, and

(b) detecting fluorescence polarization of the fluorophores of each of said first and second differently fluorescently labeled oligonucleotides

whereby an increase in fluorescence polarization of said first fluorophore indicates the presence of the first target site, and

whereby an increase in fluorescence polarization of said second fluorophore indicates the presence of the second target site.

9. The method of claim 8 wherein step (b) is conducted in the presence of a single stranded DNA binding (SSB) protein.

10. The method of claim 8 wherein step (b) is conducted in the presence of an organic solvent.

11. A method for detecting the presence of a target site of at least one nucleotide in a template nucleic acid comprising detecting fluorescence polarization of a fluorescently labeled oligonucleotide which is bound to the target site

wherein an increase in fluorescence polarization indicates the presence of the target site, thereby detecting the presence of the target site by said increase in fluorescence polarization;

and

wherein the fluorescently labeled oligonucleotide comprises a fluorophore linked to a terminator therein; and

wherein the fluorescently labeled oligonucleotide has been formed from a primer bound to the template immediately 3′

to the target site and terminator covalently linked to a fluorophore, and wherein said terminator-linked fluorophore binds to the target site and reacts with the primer to produce an extended primer which is said fluorescently labeled oligonucleotide.

12. The method of claim 11 wherein the template nucleic acid is amplified from the genome of an organism.