Method for producing circular DNA formed from single-molecule DNA

• US 8,962,245 B2
• Filed: 08/22/2011
• Issued: 02/24/2015
• Est. Priority Date: 09/02/2010
• Status: Expired due to Fees

• Current Assignee: Kurume University
• Original Assignee: Kurume University
• Inventors: Mizuno, Shinichi, Nagafuji, Koji, Okamura, Takashi
• Primary Examiner(s): Horlick, Kenneth R.
• Assistant Examiner(s): THOMAS, DAVID C
• Application Number:
  US13/819,396
• Publication Number:
  US 20130164757A1
• Time in Patent Office: 1,282 Days
• Field of Search: None
• US Class Current: 435/6.1
• CPC Class Codes: C07H 21/04 with deoxyribosyl as saccharide radical
• CPC Class Codes: C12N 15/10 Processes for the isolation, preparation or purification of DNA or RNA chemical preparation of DNA or RNA C07H21/00; preparation of non-structural polynucleotides from microorganisms or with enzymes C12P19/34
• CPC Class Codes: C12N 15/1096 cDNA Synthesis; Subtracted cDNA library construction, e.g. RT, RT-PCR
• CPC Class Codes: C12N 15/64 General methods for preparing the vector, for introducing it into the cell or for selecting the vector-containing host
• CPC Class Codes: C12Q 1/6806 Preparing nucleic acids for analysis, e.g. for polymerase chain reaction [PCR] assay C12Q1/6804 takes precedence
• CPC Class Codes: C12Q 2525/307 Circular oligonucleotides

Abstract

There is provided a method for producing a circular DNA which consists of a circular DNA formed from a single-molecule DNA and which does not comprise circular DNA formed from multiple-molecule DNA. According to the method of the present invention, a circular DNA molecule formed only from a single-molecule DNA can be reliably produced.

Claims

1. A method for producing a circular DNA, the method comprising the following steps:

1) providing a DNA molecule;

2) a step of covalently binding an adapter (A) to one end of the DNA molecule, and covalently binding to the other end of the DNA molecule an adapter (B) comprising an adapter (b) and the adapter (A), wherein;

the adapter (B) binds to the DNA molecule via the adapter (b) and not the adapter (A),

the adapter (A) comprises a cleavage site capable of generating a cleavage end which can non-specifically bind to any cleavage end of the adapter (A), and

the adapter (b) comprises a cleavage site capable of generating a cleavage end which can specifically bind only to the cleavage end from the same adapter (b);

3) a first cleavage step of cleaving the DNA molecule obtained in step

     2) at the cleavage site of each of the adapters (A);

4) a first circularization step of binding both ends of the DNA molecule obtained in step

     3) to circularize the DNA molecule;

5) a step of eliminating uncircularized linear DNA molecules obtained in step

     4);

6) a second cleavage step of cleaving the circular DNA molecules from step

     5) at the cleavage site of the adapter (b); and

7) a second circularization step of binding both ends of the DNA molecule obtained in step

     6) to circularize the DNA molecule and obtain a circular DNA.

6. A method for producing a cDNA library, comprising performing the method according to claim 1 to produce the cDNA library.

7. A method for identifying a gene by subjecting a circular DNA molecule obtained by using the method according to claim 1 to a mate-pair method, the method comprising the following steps:

1) a step of reading nucleotide sequences, each consisting of 15 to 600 nucleotides, flanking to both sides of an adapter (B) in a circular DNA molecule obtained by using the method according to claim 1; and

2) a step of identifying a gene contained in the circular DNA molecule by comparing the read nucleotide sequences with the sequences of both ends of a known gene.

8. A method for detecting a fusion gene by subjecting a circular DNA molecule obtained by using the method according to claim 1 to a mate-pair method, the method comprising the following steps:

1) a step of reading nucleotide sequences each consisting of 15 nucleotides or more and 600 nucleotides or less that are flanking to both sides of an adapter (B) in a circular DNA molecule obtained by using the method according to claim 1; and

2) a step of comparing the read nucleotide sequences with the sequences of both ends of a known gene, wherein if the genes of both ends correspond to known different genes, the gene comprised in the circular DNA molecule is identified to be a fusion gene.

9. The method for detecting a fusion gene according to claim 8, wherein the sequences of both sides flanking to both sides of the adapter (B) correspond to both ends of a known fusion gene.

10. A method for detecting a disease characterized by the expression of the fusion gene detected by the method according to claim 8, wherein the fusion gene is used as a marker.

11. The method according to claim 8, wherein if the sequences flanking to both sides of the adapter (B) correspond to the terminal sequences of different genes and do not correspond to both ends of a known fusion gene, the gene comprised in the circular DNA molecule is identified to be a novel fusion gene.

2. A method for producing a circular DNA, the method comprising the following steps:

1) providing a DNA molecule;

1) providing a DNA molecule consisting of the single gene;

2) a step of covalently binding an adapter (A) to one end of the DNA molecule, and covalently binding to the other end of the DNA molecule an adapter (B) comprising an adapter (b) and the adapter (A), wherein;

the adapter (B) binds to the DNA molecule via the adapter (b) and not the adapter (A),

the adapter (A) is a double-stranded DNA comprising a restriction enzyme recognition site comprising a palindromic sequence, and

the adapter (B) comprises the adapter (b) and the adapter (A), wherein;

the adapter (b) is a double-stranded DNA comprising identical nick-generating enzyme recognition sites being reversely oriented to each other, wherein the adapter (b) is a double-stranded DNA comprising a double-stranded DNA sequence having a unique sequence for each adapter (b) between the identical nick-generating enzyme recognition sites being reversely oriented to each other, said unique sequence consisting of 4 to 15 nucleotides, and if the adapter (b) is cleaved at the identical nick-generating enzyme recognition sites being reversely oriented to each other, the cleavage site rebinds only to the cleavage site from the same adapter (b);

3) a first cleavage step of cleaving the DNA molecule obtained in step

     2) with the restriction enzyme which recognizes the restriction enzyme recognition site comprised in the adapter (A);

4) a first circularization step of ligating both ends of the DNA molecule obtained in step

     3) to circularize the DNA molecule;

5) a step of eliminating uncircularized linear DNA molecules obtained in step

     4);

6) a second cleavage step of cleaving the circular DNA molecules from step

     5) with a nick-generating enzyme recognizing the nick-generating enzyme recognition sites or restriction enzyme sites of the adapter (b); and

7) a second circularization step of binding both ends of the DNA molecule obtained in step

     6) to circularize the DNA molecule and obtain a circular DNA.

3. The method according to claim 2, which further comprises a step of digesting with endonuclease a circularized DNA formed by binding the adapters (b) via cleavage sequence sites being partially different from each other and circularization in step 7) of claim 2.

4. The method according to claim 2, wherein

the adapter (A) is a double-stranded DNA comprising a restriction enzyme recognition site X comprising a palindromic sequence, and

the adapter (B) is a double-stranded DNA consisting of two DNA strands complementary to each other having the following structure y₁-Y-y₂-X:

5. The method according to claim 4, wherein the nick-generating enzyme is Nb.BtsI or Nt.BsqQI.