Differential enzymatic fragmentation

• US 8,163,485 B2
• Filed: 06/01/2010
• Issued: 04/24/2012
• Est. Priority Date: 10/21/2003
• Status: Active Grant

• Current Assignee: Orion Genomics LLC
• Original Assignee: Orion Genomics LLC
• Inventors: Jeddeloh, Jeffrey A., Lakey, Nathan D.
• Primary Examiner(s): Bausch, Sarae
• Application Number:
  US12/791,625
• Publication Number:
  US 20100240064A1
• Time in Patent Office: 693 Days
• Field of Search: None
• US Class Current: 435/6.1
• CPC Class Codes: C12Q 1/683 involving restriction enzymes, e.g. restriction fragment length polymorphism [RFLP]
• CPC Class Codes: C12Q 1/6858 Allele-specific amplification
• CPC Class Codes: C12Q 2521/331 Methylation site specific nuclease
• CPC Class Codes: C12Q 2545/101 with an internal standard/control

Abstract

The present invention provides methods for detecting the presence of methylation at a locus within a population of nucleic acids.

Claims

1. A method of detecting the quantity of methylation at a locus within a population of nucleic acids, the method comprising

(a) dividing the population of nucleic acids into at least two physically distinct portions, thereby generating at least a first portion and a second portion,

(b) after step (a), contacting the first portion with a methylation-sensitive restriction enzyme to obtain a first portion of nucleic acids with fragmented unmethylated copies of the locus and intact methylated copies of the locus;

(c) after step (b), quantifying the number of intact copies of the locus in the first portion;

(d) after step (a), contacting the second portion with a methylation-dependent restriction enzyme to obtain a second portion of nucleic acids with fragmented methylated copies of the locus and intact unmethylated copies of the locus, wherein the methylation-dependent restriction enzyme is contacted to the second portion under conditions that allow for at least some copies of potential restriction enzyme cleavage sites for the methylation-dependent restriction enzyme in the locus to remain uncleaved;

(e) after step (d), quantifying the number of intact copies of the locus in the second portion; and

(f) determining the quantity of methylation at the locus within the population of nucleic acids by comparing the number of intact copies of the locus in the first portion and number of intact copies of the locus in the second portion.

2. The method of claim 1, further comprising quantifying the number of intact copies of the locus in a third portion of the nucleic acids;

and comparing the number of intact copies of the locus in the third portion to the number of intact copies of the locus in the first portion and/or intact copies of the locus in the second portion.

3. The method of claim 1, further comprising contacting a third portion of the nucleic acids with a methylation-dependent restriction enzyme and a methylation-sensitive restriction enzyme;

and quantifying the number of intact copies of the locus in the third portion;

wherein step (f) comprises determining the quantity of methylation at the locus within the population of nucleic acids by comparing the number of the intact copies of the locus in the third portion to the number of intact copies of the locus in the first portion and/or the number of intact copies of the locus in the second portion.

4. The method of claim 2, further comprising contacting a fourth portion of the nucleic acids with a methylation-dependent restriction enzyme and a methylation-sensitive restriction enzyme;

and quantifying the number of intact copies of the locus in the fourth portion;

wherein step (f) comprises determining the quantity presence of methylation at the locus within the population of nucleic acids by comparing the number of intact copies of the locus in the fourth portion to the number(s) of intact copies of the locus in the third portion and/or intact copies of the locus in the first portion and/or intact copies of the locus in the second portion.

5. The method of claim 4, further comprising determining the presence of a mutation within the population of nucleic acids at the locus.

6. The method of claim 5, comprising contacting a fifth portion of the nucleic acids with a methylation-insensitive restriction enzyme;

and quantifying the number of intact copies of the locus in the fifth portion after the contacting with the methylation-insensitive restriction enzyme;

wherein determining the presence of a mutation at the locus comprises comparing the number of the intact copies of the locus in the fifth portion to the number(s) of intact copies of the locus in the fourth portion and/or intact copies of the locus in the third portion and/or intact copies of the locus in the first portion and/or intact copies of the locus in the second portion.

7. The method of claim 1, wherein the nucleic acids are contacted with an agent that modifies unmethylated cytosines before the quantifying (steps (c) and (e));

and the intact copies of the locus are amplified with a pair of oligonucleotide primers comprising at least one primer that distinguishes between methylated and unmethylated DNA contacted with the agent.

8. The method of claim 7, wherein the agent is sodium bisulfite.

9. The method of claim 3, wherein the methylation-dependent restriction enzyme is contacted to the third portion under conditions that allow for at least some copies of potential restriction enzyme cleavage sites for the methylation-dependent restriction enzyme in the locus to remain uncleaved.

10. The method of claim 4, wherein the methylation-dependent restriction enzyme is contacted to the fourth portion under conditions that allow for at least some copies of potential restriction enzyme cleavage sites for the methylation-dependent restriction enzyme in the locus to remain uncleaved.

11. The method of claim 1, wherein the locus has a density of methylation and the density of methylation at the locus is determined by comparing the number of quantified in step (e) with a control value representing the quantity of methylation in a control DNA.

12. The method of claim 1, wherein the methylation-sensitive restriction enzyme is contacted to the first portion under conditions that allow for at least some copies of potential restriction enzyme cleavage sites for the methylation-sensitive restriction enzyme in the locus to remain uncleaved.

13. The method of claim 2, wherein the methylation-sensitive restriction enzyme is contacted to the first portion under conditions that allow for at least some copies of potential restriction enzyme cleavage sites for the methylation-sensitive restriction enzyme in the locus to remain uncleaved.

14. The method of claim 3, wherein the methylation-sensitive restriction enzyme is contacted to the third portion under conditions that allow for at least some copies of potential restriction enzyme cleavage sites for the methylation-sensitive restriction enzyme in the locus to remain uncleaved.

15. The method of claim 4, wherein the methylation-sensitive restriction enzyme is contacted to the fourth portion under conditions that allow for at least some copies of potential restriction enzyme cleavage sites for the methylation-sensitive restriction enzyme in the locus to remain uncleaved.

16. The method of claim 1, wherein the methylation is at the C5 position of a cytosine within the locus.

17. The method of claim 1, wherein the nucleic acids are DNA.

18. The method of claim 17, wherein the DNA is genomic DNA.

19. The method of claim 1, wherein the methylation-sensitive restriction enzyme is selected from the group consisting of:

Aat II, Aci I, Acl I, Age I, Alu I, Asc I, Ase I, AsiS I, Bbe I, BsaA I, BsaH I, BsiE I, BsiW I, BsrF I, BssH II, BssK I, BstB BstN I, BstU I, Cla I, Eae I, Eag I, Fau I, Fse I, Hha I, HinP1 I, HinC II, Hpa II, Hpy99 I, HpyCH4 IV, Kas I, Mlu I, MapAl I, Msp I, Nae I, Nar I, Not I, Pml I, Pst I, Pvu I, Rsr II, Sac II, Sap I, Sau3A I, Sfl I, Sfo I, SgrA I, Sma I, SnaB I, Tsc I, Xma I, and Zra I.

20. The method of claim 1, wherein the methylation-dependent restriction enzyme is McrBC.