Methods for rapid production of double-stranded target DNA

• US 9,206,473 B2
• Filed: 11/01/2011
• Issued: 12/08/2015
• Est. Priority Date: 06/09/2004
• Status: Active Grant

• Current Assignee: Wisconsin Alumni Research Foundation (University of Wisconsin System)
• Original Assignee: Wisconsin Alumni Research Foundation (University of Wisconsin System)
• Inventors: Sussman, Michael R., Richmond, Kathryn E., Rodesch, Matt J.
• Primary Examiner(s): MUMMERT, STEPHANIE KANE
• Application Number:
  US13/286,932
• Publication Number:
  US 20150284767A1
• Time in Patent Office: 1,498 Days
• Field of Search: None
• US Class Current: 1/1
• CPC Class Codes: C12Q 1/686 Polymerase chain reaction [PCR]
• CPC Class Codes: C12Q 2533/107 Probe or oligonucleotide ligation

Abstract

A method of rapidly producing a double-stranded target DNA is disclosed. The method includes the step of producing multiple single stranded primary DNA constructs having (a) partially overlapping and complementary internal regions that together define the target DNA, and (b) flanking regions on either side of the internal regions containing a PCR primer recognition site and a restriction enzyme recognition site. The primary DNA constructs are amplified to form a pool of double-stranded primary constructs, and a restriction enzyme is used to cleave off the flanking regions. The target double-stranded DNA is then assembled from the cleaved fragments. Hundreds of thousands of oligonucleotides can be synthesized and quickly and efficiently assembled into many different individual double-stranded DNA target sequences using this method.

Claims

1. A method for making a double-stranded DNA target sequence, the method comprising the following steps in the order set forth below:

(a) synthesizing in parallel a plurality of single-stranded oligonucleotide primary constructs, each oligonucleotide primary construct comprising;

(i) an internal region, wherein each internal region has at least one portion overlapping and complementary to a portion of an internal region of at least one different primary construct, and wherein the internal regions of the plurality of oligonucleotide primary constructs together define the double-stranded DNA target sequence, and

(ii) a 5′ and

a 3′

flanking region flanking the 5′ and

the 3′

end of the internal region, each of the flanking regions including both a primer recognition site and a recognition site for a restriction enzyme capable of cleaving the oligonucleotide primary construct at each of the junctions of the internal region and the flanking regions;

(b) performing polymerase chain reaction (PCR) on the single-stranded primary constructs using a set of PCR primers that target the primer recognition site(s) in the flanking regions to amplify at least a subset of the plurality of the single-stranded oligonucleotide primary constructs of step (a) to generate an amplified pool of double-stranded primary constructs;

(c) cleaving the flanking regions from the double-stranded primary constructs of step (b) by digesting said constructs with the restriction enzyme, thereby generating a plurality of double-stranded internal regions;

(d) denaturing the plurality of double-stranded internal regions of step (c) to form a plurality of single-stranded internal regions;

(e) annealing the complementary portions of two or more different single-stranded internal regions of step (d), thereby producing a plurality of hybridized DNA constructs that include both single-stranded and double stranded segments;

(f) extending the double-stranded segments of the hybridized DNA constructs using a polymerase and dNTPs in the absence of primers, thereby generating a plurality of double-stranded secondary DNA constructs comprising the sequences of two or more of the internal regions of the single-stranded oligonucleotide primary constructs of step (a);

(g) repeating the denaturing, annealing, and extending steps one or more times with the double-stranded secondary DNA constructs produced in the extending step to generate increasingly long double-stranded secondary DNA constructs, whereby the double-stranded DNA target sequence is generated.

2. The method of claim 1 wherein step (a) is performed by using an automated gene synthesizer instrument to construct the primary constructs as single stranded DNA probes in a microarray on a common substrate and by then detaching the primary constructs from the substrate.

3. The method of claim 1 wherein the flanking regions at the ends of all of the primary constructs are the same and wherein in step (b) a single set of PCR primers is used to amplify all of the primary constructs.

4. The method of claim 1 wherein the restriction enzyme used in step (c) is Mly I.

5. The method of claim 1 where step (b) is performed multiple times using multiple different sets of primers.

6. The method of claim 1 wherein the step (c) is performed multiple times using multiple different restriction enzymes.

7. The method of claim 1 wherein for each of the primary constructs except for the two primary constructs corresponding to the two ends of the double-stranded DNA target sequence, each half of the sequence of the internal region of the primary construct is complementary to the sequence of a half of the internal region of another primary construct.

8. The method of claim 1 further comprising the step of isolating from the products of step (g) the longest double-stranded DNA construct produced.

9. The method of claim 1, wherein step (a) of synthesizing in parallel a plurality of single-stranded oligonucleotide primary constructs is performed on a microarray;

and wherein for each oligonucleotide primary construct, the oligonucleotide primary construct is at least 70 nucleotides in length, the internal region is at least 40 nucleotides in length, and the flanking regions are at least 15 nucleotides in length.

10. The method of claim 9 wherein step (a) is performed by using an automated gene synthesizer instrument to construct the primary constructs as single stranded DNA probes in a microarray on a common substrate and by then detaching the primary constructs from the substrate.

11. The method of claim 9 wherein the flanking regions at the ends of all of the primary constructs are the same and wherein in step (b) a single set of PCR primers is used to amplify all of the primary constructs.

12. The method of claim 9 wherein the restriction enzyme used in step (c) is Mly I.

13. The method of claim 9 where step (b) is performed multiple times using multiple different sets of primers.

14. The method of claim 9 wherein the step (c) is performed multiple times using multiple different restriction enzymes.

15. The method of claim 9 wherein for each of the primary constructs except for the two primary constructs corresponding to the two ends of the double-stranded DNA target sequence, each half of the sequence of the internal region of the primary construct is complementary to the sequence of a half of the internal region of another primary construct.

16. The method of claim 9 further comprising the step of isolating from the products of step (g) the longest double stranded DNA construct produced.