Efficient arrays of amplified polynucleotides

• US 7,910,302 B2
• Filed: 10/29/2007
• Issued: 03/22/2011
• Est. Priority Date: 10/27/2006
• Status: Active Grant

• Current Assignee: Complete Genomics Incorporated (BGI Genomics Co., Ltd.)
• Original Assignee: Complete Genomics Incorporated (BGI Genomics Co., Ltd.)
• Inventors: Drmanac, Radoje T, Callow, Matthew
• Primary Examiner(s): Horlick; Kenneth R.
• Assistant Examiner(s): Thomas; David C
• Application Number:
  US11/927,388
• Publication Number:
  US 20090143235A1
• Time in Patent Office: 1,240 Days
• Field of Search: None
• US Class Current: 435/6.11
• CPC Class Codes: C12Q 1/6809 Methods for determination or identification of nucleic acids involving differential detection
• CPC Class Codes: C12Q 1/686 Polymerase chain reaction [PCR]
• CPC Class Codes: C12Q 1/6874 involving nucleic acid arrays, e.g. sequencing by hybridisation
• CPC Class Codes: C12Q 2531/119 Strand displacement amplification [SDA]
• CPC Class Codes: C12Q 2539/103 Serial analysis of gene expression [SAGE]
• CPC Class Codes: C12Q 2565/501 being an array of oligonucleotides

Abstract

The present invention is related generally to analysis of polynucleotides, particularly polynucleotides derived from genomic DNA. The invention provides methods, compositions and systems for such analysis. Encompassed by the invention are arrays of polynucleotides in which the polynucleotides have undergone multiple rounds of amplification in order to increase the strength of signals associated with single polynucleotide molecules.

Claims

1. A method of making a random array of amplified polynucleotides, said method comprising the steps of:

a) providing;

i) a surface, which comprises capture probes, wherein said capture probes have free 3′

ends, and

ii) a plurality of concatemers disposed on said surface, wherein each concatemer is bound to capture probes at a specific position on said surface and wherein each concatemer comprises multiple copies of a monomer, and said monomer comprises a first interspersed adaptor that is located between a first and second target sequence of a target polynucleotide, wherein said first and second target sequences are contiguous segments of said target polynucleotide; and

b) extending said capture probes such that said concatemers disposed on said surface are amplified;

wherein the amplification products of said concatemers are attached to the surface at or near the specific position of the concatemer amplified, thereby making said random array of amplified polynucleotides.

2. The method of claim 1, wherein said amplification products are attached to said surface through duplexes formed between said amplification products and said capture probes.

3. The method of claim 1, wherein for a number of said plurality of concatemers, different concatemers comprise first and second target sequences from different target polynucleotides.

4. The method of claim 1, wherein said first interspersed adaptor comprises a recognition site for a nicking endonuclease, and wherein said recognition site is oriented such that a cleavage site for said nicking endonuclease is located substantially near one end of said adaptor.

5. The method of claim 1, wherein the capture probes are extended using a strand displacement polymerase.

6. The method of claim 1, wherein said surface is a planar surface that comprises discrete regions, wherein each discrete region comprises said capture probes attached thereto, and wherein at least a majority of said discrete regions have amplification products of a single concatemer attached.

7. The method of claim 6, wherein each of said discrete regions has an area less than 1 μ

m².

8. The method of claim 6, wherein said discrete regions have a nearest neighbor distance such that a majority of said discrete regions is optically resolvable.

9. The method of claim 6, wherein each of said discrete regions is surrounded by an inter-regional space that does not bind said concatemers or said amplification products.

10. A method of making a random array of target polynucleotides, said method comprising the steps of:

a) providing a plurality of concatemers on a surface, wherein;

i) said surface comprises capture probes,

ii) each of said plurality of concatemers comprises multiple copies of a target polynucleotide and an adaptor; and

iii) each concatemer is attached to a specific position on said surface through duplexes formed between said capture probes and said adaptors in the concatemer, wherein said duplexes comprise a recognition site for a nicking endonuclease;

b) cleaving at least a portion of the plurality of concatemers with a nicking endonuclease to form cleavage products, wherein said cleavage products remain attached to said capture probes;

c) circularizing said cleavage products on said capture probes; and

d) extending said capture probes by rolling circle replication to create at least one copy of each circularized cleavage product;

thereby making said random array of target polynucleotides.

11. An array made according to the method of claim 10.

12. A kit containing the array of claim 11.

13. A method of making a random array of amplified target polynucleotides, said method comprising the steps of:

a) providing a plurality of tailed concatemers, wherein each of said tailed concatemers comprises multiple copies of a monomer, and said monomer comprises a first interspersed adaptor that is located between a first and second target sequence of a target polynucleotide, wherein said first and second target sequences are contiguous segments of said target polynucleotide;

b) extending said tailed concatemers with a strand-displacing polymerase to form concatemer-extension product complexes; and

c) disposing said concatemer-extension product complexes on a surface, wherein;

i) said surface comprises capture probes,

ii) a majority of said concatemer-extension product complexes from a single concatemer occupy a single region of said surface, and

iii) said majority of said concatemer-extension product complexes is attached to said surface by one or more duplexes formed between said capture probes and said tail portions,

thereby forming said random array of target polynucleotides.

14. The method of claim 13, wherein said tailed concatemers are formed by a method comprising combining a plurality of tailed primers with a plurality of concatemers under annealing conditions, wherein:

a) each of said plurality of concatemers comprises multiple copies of said monomer;

b) at least a portion of said tailed primers anneal to at least a portion of said first interspersed adaptor; and

c) each of said plurality of tailed primers comprise a tail portion which is not complementary to said concatemers.

15. The method of claim 13, further comprising subsequent to step (c) a step of:

d) extending said majority of said concatemer-extension product complexes with a strand-displacing polymerase.

16. The method of claim 13, wherein the extension products are additionally attached to the surface using chemical attachment.

17. The method of claim 13, wherein the extension products are additionally attached to the surface using hybridization to other capture probe.

18. An array made according to the method of claim 13.

19. A kit containing the array of claim 18.

20. A method of making a random array of target polynucleotides, said method comprising the steps of:

a) combining under annealing conditions a plurality of dendrimers and a plurality of single stranded DNA circles, wherein;

i) each of said plurality of single stranded DNA circles comprises a monomer, and said monomer comprises a first interspersed adaptor that is located between a first and second target sequence of a target polynucleotide, wherein said first and second target sequences are contiguous segments of said target polynucleotide, and

ii) each of said plurality of dendrimers comprises a primer capable of annealing to said first interspersed adaptors of said plurality of single stranded DNA circles,

b) annealing said first interspersed adaptors of said single stranded DNA circles to said primers of said plurality of dendrimers;

c) extending said primers annealed with said first interspersed adaptors with a strand-displacing polymerase to form a plurality of dendrimer-extension product complexes, wherein said dendrimer-extension product complexes comprise multiple copies of said single stranded DNA circles; and

d) disposing said dendrimer-extension product complexes on a surface such that each of at least a majority of said plurality of dendrimer-extension product complexes occupies a separate region of said surface,

thereby forming said random array of target polynucleotides.

21. The method of claim 20, wherein said first interspersed adaptors of different single stranded DNA circles are different.

22. The method of claim 20, wherein each dendrimer-extension product complex comprises first and second target sequences of multiple different target polynucleotides.

23. The method of claim 20, wherein:

a) said surface comprises capture probes;

b) each of said plurality of dendrimers further comprises at least one probe complementary to said capture probes; and

c) said disposing comprises attaching said dendrimer-extension product complexes to said surface by forming duplexes between said capture probes and said complementary probes of said dendrimers.

24. An array made according to the method of claim 20.

25. A kit containing the array of claim 24.

26. A method of forming a spatially-compact single stranded amplicon, said method comprising the steps of:

a) combining under annealing conditions a dendrimer and a single stranded DNA circle, wherein;

i) said single stranded DNA circle comprises a target polynucleotide and an adaptor, and

ii) said dendrimer comprises a primer capable of annealing to said adaptor and at least one capture sequence identical to a portion of said single stranded DNA circle,

b) extending said primer annealed to said adaptor with a strand-displacing polymerase to form a single-stranded amplicon, wherein said at least one capture sequence forms a duplex with a complementary portion of said single stranded amplicon,

thereby forming said spatially-compact single stranded amplicon.

27. The method of claim 26, wherein said at least one primer has a free 3′

end.

28. The method of claim 26, wherein the single-stranded amplicon comprises a concatemer of the concatemer of said target polynucleotide and adapter is generated in step b).

29. The method of claim 26, further comprising the step:

c) extending said at least one capture sequence.

30. A plurality of amplicons made from different target polynucleotides according to claim 26.

31. A method of forming a single-stranded amplicon comprising multiple target polynucleotide sequences, said method comprising the steps of:

a) combining under annealing conditions a dendrimer and a plurality of single stranded DNA circles, wherein;

i) each single stranded DNA circle comprises a target polynucleotide and an adaptor, and

ii) said dendrimer comprises multiple primer sites complementary to adaptors on different DNA circles,

b) extending said primer sites annealed to said adaptor with a strand-displacing polymerase to form a single stranded amplicon, wherein portions of each amplicon are complementary to target polynucleotides of different DNA circles,

thereby forming said single stranded amplicon comprising multiple target polynucleotide sequences.

32. A plurality of amplicons made from different target polynucleotides according to claim 31.

33. A method of forming a double stranded amplicon, the method comprising the steps of:

a) providing a single stranded amplicon comprising a concatemer having multiple copies of a monomer, and said monomer comprises a first interspersed adaptor that is located between a first and second target sequence of a target polynucleotide, wherein said first and second target sequences are contiguous segments of said target polynucleotide;

b) annealing primers to the adaptors of the single stranded amplicon; and

c) extending the primers with a non-strand displacing polymerase so that substantially every annealed primer is extended to form an extension product that abuts the next annealed primer, thereby forming a double stranded amplicon.

34. The method of claim 33, further including the step of ligating said extension products to said abutting annealed primers.

35. A method of making a random array of target polynucleotides, said method comprising the steps of:

a) providing a support having a surface;

b) combining in a reaction mixture first primer probes, beads comprising second primer probes on their surfaces, and a plurality of concatemers each comprising multiple copies of a monomer, and said monomer comprises a first interspersed adaptor that is located between a first and second target sequence of a target polynucleotide, wherein said first and second target sequences are contiguous segments of said target polynucleotide, said first primer and second primer probes being capable of amplifying in a polymerase chain reaction a portion of said concatemers;

c) forming an emulsion with said reaction mixture so that aqueous compartments are formed that contain second primers, and no more than one bead and no more than one concatemer;

d) conducting a polymerase chain reaction in said aqueous compartments so that portions of said concatemer are amplified on said beads; and

e) disposing said beads from said emulsion onto said surface such that substantially every bead occupies a separate region of said surface,

thereby forming said random array of target polynucleotides.

36. The method of claim 35, wherein said surface of said support has capture probes attached thereto and wherein said bead further comprises at least one probe complementary to the capture probes and wherein said step of disposing further includes attaching said beads to said surface by one or more duplexes formed between capture probes and complements thereof on said beads.