IP Library Granted Patent US 9,297,006
Granted Patent B2
US 9,297,006 · App. 14/150,607 · Granted Mar 29, 2016

Methods of nucleic acid amplification and sequencing

Inventors: Celine Adessi (Ambilly, FR); Eric Kawashima (Nyon, CH); Pascal Mayer (Eloise, FR); Jean-Jaques Mermod (Geneva, CH); Gerardo Turcatti (Geneva, CH)
Assignee: Illumina, Inc.
C12N15/1068C12Q1/686C12Q1/6837C12Q1/6869
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Quick Facts
Patent No.
US 9,297,006
App. No.
14/150,607
Granted
Mar 29, 2016
Kind
B2
Abstract

Methods for amplification and sequencing of at least one nucleic acid comprising the following steps: (1) forming at least one nucleic acid template comprising the nucleic acid(s) to be amplified or sequenced, wherein said nucleic acid(s) contains at the 5′ end an oligonucleotide sequence Y and at the 3′ end an oligonucleotide sequence Z and, in addition, the nucleic acid(s) carry at the 5′ end a means for attaching the nucleic acid(s) to a solid support; (2) mixing said nucleic acid template(s) with one or more colony primers X, which can hybridize to the oligonucleotide sequence Z and carries at the 5′ end a means for attaching the colony primers to a solid support, in the presence of a solid support so that the 5′ ends of both the nucleic acid template and the colony primers bind to the solid support; (3) performing one or more nucleic acid amplification reactions on the bound template(s), so that nucleic acid colonies are generated and optionally, performing at least one step of sequence determination of one or more of the nucleic acid colonies generated. Solid supports, kits and apparatus for use in these methods.

Claims (22)

1. A method for parallel amplification of a collection of single nucleic acid molecules having different sequences comprising:

a) providing a vessel comprising the collection of single nucleic acid molecules,

b) treating the single nucleic acid molecules in the vessel by attaching a known, common sequence at the 5′ and 3′ ends of each nucleic acid molecule of the collection, thereby generating a collection of treated nucleic acid molecules wherein each of the collection of treated nucleic acid molecules contains a different sequence and the known, common sequence at its 5′ and 3′ ends,

c) separating the collection of treated nucleic molecules such that individual molecules from the collection of treated nucleic acid molecules are separated from each other, and

d) performing a single amplification reaction in the presence of forward colony primers and reverse colony primers complementary to and/or identical to the known common sequence, wherein at least one of the colony primers is immobilized on a solid support, thereby simultaneously amplifying the different sequence of each of the treated nucleic acid molecules separated in step c) under conditions such that a plurality of nucleic acid colonies is formed on the solid support and the collection of single nucleic acid molecules having different sequences is amplified.

2. The method according to claim 1 , wherein said forward colony primers and said reverse colony primers are immobilised on a solid support.

3. The method according to claim 1 , wherein said solid support is a bead or microparticle.

4. The method according to claim 1 , wherein said solid support is a planar surface.

5. A method for parallel amplification of a collection of single nucleic acid molecules having different sequences comprising:

a) treating the collection of nucleic acid molecules thereby generating a collection of treated nucleic acid molecules wherein each of the collection of treated nucleic acid molecules contains a different sequence and a known, common sequence at its 5′ and 3′ ends,

b) immobilizing the treated nucleic acid molecules on a solid support, thereby separating the collection of treated nucleic acid molecules such that individual treated nucleic acid molecules from the collection of treated nucleic acid molecules are separated from each other, and

c) performing an amplification reaction in the presence of forward colony primers and reverse colony primers complementary to and/or identical to the known common sequence, wherein at least one of the colony primers is immobilized directly to the solid support, thereby simultaneously amplifying the different sequence of each of the treated nucleic acid molecules separated in step b) under conditions such that a plurality of nucleic acid colonies is formed on the solid support and the collection of single nucleic acid molecules having different sequences is amplified.

6. The method according to claim 5 , wherein said forward colony primers and said reverse colony primers are immobilised on a solid support.

7. The method according to claim 5 , wherein said solid support is a bead or microparticle.

8. The method according to claim 5 , wherein said solid support is a planar surface.

9. A method for parallel amplification of a collection of single nucleic acid molecules having different sequences comprising:

a) treating the collection of nucleic acid molecules thereby generating a collection of treated nucleic acid molecules wherein each of the collection of treated nucleic acid molecules contains a different sequence and a known, common sequence at its 5′ and 3′ ends,

b) immobilizing the treated nucleic acid molecules on a solid support, the solid support comprising a lawn of immobilized colony primers comprising forward colony primers and/or reverse colony primers, the colony primers being complementary to and/or identical to the known common sequence, thereby separating the collection of treated nucleic acid molecules such that individual treated nucleic acid molecules from the collection of treated nucleic acid molecules are immobilized at intervals within the lawn of immobilized colony primers, and

c) performing an amplification reaction in the presence of the forward colony primers and/or the reverse colony primers thereby simultaneously amplifying the different sequence of each of the treated nucleic acid molecules separated in step b) under conditions such that a plurality of nucleic acid colonies is formed on the solid support and the collection of single nucleic acid molecules having different sequences is amplified.

10. The method of claim 9 , wherein the lawn of immobilized colony primers comprises forward colony primers and reverse colony primers.

11. The method of claim 9 , further comprising an additional step of performing at least one step of sequence determination of nucleic acids in one or more of the nucleic acid colonies.

12. The method of claim 9 , wherein the density of the nucleic acid colonies on the solid support is 10,000/mm 2 to 100,000/mm 2 .

Assignments (5)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 19, 2014
From: ADESSI, CELINE; KAWASHIMA, ERIC; MAYER, PASCAL; MERMOD, JEAN-JACQUES; TURCATTI, GERARDO
To: APPLIED RESEARCH SYSTEMS ARS HOLDING N.V.
Reel/Frame 033567/0271 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 19, 2014
From: APPLIED RESEARCH SYSTEMS ARS HOLDING N.V.
To: SOLEXA LIMITED; LYNX THERAPEUTICS, INC.
Reel/Frame 033567/0279 →
CHANGE OF NAME Recorded Aug 19, 2014
From: SOLEXA LIMITED
To: ILLUMINA CAMBRIDGE LIMITED
Reel/Frame 033567/0298 →
MERGER Recorded Aug 19, 2014
From: SOLEXA, INC.
To: ILLUMINA, INC.
Reel/Frame 033567/0308 →
CHANGE OF NAME Recorded Aug 19, 2014
From: LYNX THERAPEUTICS, INC.
To: SOLEXA, INC.
Reel/Frame 033568/0787 →
Priority Claims (1)
GB 98307985 · Sep 30, 1998 · national
Continuity (3)
Continuation 11506146 · Aug 17, 2006
Division 09806531
Related Publication 20140228254A1 · Aug 14, 2014