Methods and compositions for ordering restriction fragments

• US 8,288,095 B2
• Filed: 09/11/2009
• Issued: 10/16/2012
• Est. Priority Date: 02/23/1998
• Status: Expired due to Fees

• Current Assignee: Illumina Incorporated
• Original Assignee: Illumina Incorporated
• Inventors: Macevicz, Stephen C.
• Primary Examiner(s): Lu, Frank W
• Application Number:
  US12/558,396
• Publication Number:
  US 20100136548A1
• Time in Patent Office: 1,131 Days
• Field of Search: 435/6, 435/91.1, 435/91.2, 435/183, 435/6.11, 435/6.12, 435/320.1, 435/6.1, 436/94, 436/501, 536/23.1, 536/24.3, 536/24.33, 536/25.3
• US Class Current: 435/6.1
• 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 15/64 General methods for preparing the vector, for introducing it into the cell or for selecting the vector-containing host
• CPC Class Codes: C12N 15/66 General methods for inserting a gene into a vector to form a recombinant vector using cleavage and ligation; Use of non-functional linkers or adaptors, e.g. linkers containing the sequence for a restriction endonuclease
• CPC Class Codes: C12Q 1/6809 Methods for determination or identification of nucleic acids involving differential detection
• CPC Class Codes: C12Q 1/683 involving restriction enzymes, e.g. restriction fragment length polymorphism [RFLP]
• CPC Class Codes: C12Q 1/6841 In situ hybridisation
• CPC Class Codes: C12Q 1/6869 Methods for sequencing
• CPC Class Codes: C12Q 1/6872 involving mass spectrometry
• CPC Class Codes: C12Q 1/6874 involving nucleic acid arrays, e.g. sequencing by hybridisation
• CPC Class Codes: C12Q 2521/301 Endonuclease
• CPC Class Codes: C12Q 2521/501 Ligase
• CPC Class Codes: G16B 30/00 ICT specially adapted for sequence analysis involving nucleotides or amino acids

Abstract

The invention relates to methods and systems for sequencing and constructing a high resolution physical map of a polynucleotide. In accordance with the invention, nucleotide sequences are determined at the ends of restriction fragments produced by a plurality of digestions with a plurality of combinations of restriction endonucleases so that a pair of nucleotide sequences is obtained for each restriction fragment. A physical map of the polynucleotide is constructed by ordering the pairs of sequences by matching the identical sequences among the pairs.

Claims

1. A method of polynucleotide sequencing, comprising:

(a) providing a mixture of circular polynucleotides, wherein each of said circular polynucleotides comprises;

(i) a first Type IIs restriction endonuclease recognition site;

(ii) a target polynucleotide fragment; and

(iii) a second Type IIs restriction endonuclease recognition site,

wherein the first Type IIs restriction endonuclease recognition site is flanking a 5′

end of the target polynucleotide fragment, the second Type IIs restriction endonuclease recognition site is flanking a 3′

end of the target polynucleotide fragment, and the cleavage sites of the first and second Type IIs restriction endonucleases are within the interior of the target polynucleotide fragment, wherein the first and second Type IIs restriction endonuclease recognition sites are arranged such that a first Type IIs restriction endonuclease recognizing said first Type II restriction endonuclease recognition site and a second Type IIs restriction endonuclease recognizing said second Type II restriction endonuclease recognition site cleave the target polynucleotide fragment, and wherein said circular polynucleotides comprise different target polynucleotide fragments;

(b) cleaving the different target polynucleotide fragments contained in said mixture of the circular polynucleotides with said first Type IIs restriction endonuclease and said second Type IIs restriction endonuclease, thereby producing restriction fragments comprising segments from the ends of the different target polynucleotide fragments; and

(c) determining sequences of the segments from the ends of the different target polynucleotide fragments after the cleaving step.

2. The method of claim 1, wherein the first Type IIs restriction endonuclease recognition site and the second Type IIs restriction endonuclease recognition site are different.

3. The method of claim 1, wherein the first Type IIs restriction endonuclease recognition site and the second Type IIs restriction endonuclease recognition site are the same.

4. The method of claim 1, wherein each of the first Type IIs restriction endonuclease and the second Type IIs restriction endonuclease has a 16/14 reach between its recognition site and its cleavage site.

5. The method of claim 4, wherein step (c) comprises determining a nine base sequence located on the end of each of the segments from the ends of the different target polynucleotide fragments.

6. The method of claim 1, wherein the target polynucleotide fragments comprise genomic DNA sequences.

7. The method of claim 1, wherein the target polynucleotide fragments comprise cDNAs.

8. The method of claim 7, further comprising determining the frequency of expression of the cDNAs.

9. The method of claim 1, further comprising determining an ordering of the segments from the ends of the different target polynucleotide fragments.

10. The method of claim 1, wherein said determining sequences of the segments from the ends of the different target polynucleotide fragments comprises performing a sequencing reaction on a DNA sequencer.

11. The method of claim 1, wherein the target polynucleotide fragments are fragments resulting from a restriction endonuclease digest of a target polynucleotide.

12. The method of claim 1, further comprising concatenating the segments from the ends of the different target polynucleotide fragments prior to said determining sequences of the segments from the ends of the different target polynucleotide fragments.

13. The method of claim 1, wherein the circular polynucleotides comprise circular vectors.

14. The method of claim 13, wherein the circular polynucleotides are formed by ligating the different target polynucleotide fragments into a circular vector.

15. The method of claim 1, further comprising amplifying the segments from the ends of the different target polynucleotide fragments by polymerase chain reaction after the cleaving step.