Comparative fluorescence hybridization to nucleic acid arrays

• US 5,830,645 A
• Filed: 12/09/1994
• Issued: 11/03/1998
• Est. Priority Date: 12/09/1994
• Status: Expired due to Term

• Current Assignee: Medical Research Council (Government of United Kingdom), Regents of the University of California (University of California)
• Original Assignee: Medical Research Council (Government of United Kingdom), Regents of the University of California (University of California)
• Inventors: Pinkel, Daniel, Gray, Joe W., Albertson, Donna
• Primary Examiner(s): Jones, W. Gary
• Assistant Examiner(s): MARSCHEL, ARDIN H
• Application Number:
  US08/353,018
• Time in Patent Office: 1,425 Days
• Field of Search: 435/6, 435/91.2, 427/213.1, 382/128, 382/129, 536/24.3, 536/24.33, 536/26.6
• US Class Current: 435/6.11
• CPC Class Codes: C12Q 1/6816 characterised by the detection means C12Q1/6804 takes precedence
• CPC Class Codes: C12Q 1/6837 using probe arrays or probe chips C12Q1/6874 takes precedence
• CPC Class Codes: C12Q 2545/101 with an internal standard/control
• CPC Class Codes: G16B 25/00 ICT specially adapted for hybridisation; ICT specially adapted for gene or protein expression

Abstract

The present invention provides methods of determining relative copy number of target nucleic acids and precise mapping of chromosomal abnormalities associated with disease. The methods of the invention use target nucleic acids immobilized on a solid surface, to which a sample comprising two sets of differentially labeled nucleic acids are hybridized. The hybridization of the labeled nucleic acids to the solid surface is then detected using standard techniques.

Claims

1. A method for comparing relative copy number of nucleic acid sequences in a two or more collections of nucleic acid molecules, the method comprising:

(a) providing a plurality of target elements bound to a solid surface, each target element comprising a target nucleic acid, wherein the target nucleic acid is isolated from a cell nucleus and lacks superstructure of a condensed chromosome;

(b) contacting the target elements with;

(I) a first collection of labeled nucleic acid molecules comprising a plurality of first nucleic acid sequences each substantially complementary to a different target nucleic acid, such that the first nucleic acid sequences specifically hybridize to the target nucleic acids under pre-selected hybridization conditions, and

(ii) at least a second labeled collection of nucleic acid molecules comprising a plurality of second nucleic acid sequences each substantially complementary to a different target nucleic acid, such that the second nucleic acid sequences specifically hybridize to the target nucleic acids under pre-selected hybridization conditions;

wherein the first and second labels are distinguishable from each other; and

(c) comparing the amount of binding of the first and second collections of labeled nucleic acid molecules to same target nucleic acid, thereby determining the copy number of at least one of the first nucleic acid sequences relative to the copy number of at least one of the second nucleic acid sequences.

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

3. The method of claim 1, wherein the target nucleic acids are cDNA.

4. The method of claim 1, wherein the first and second collections of labeled nucleic acids comprise human DNA.

5. The method of claim 1, wherein the target nucleic acids are about 1000 to about 1,000,000 nucleotides in complexity.

6. The method of claim 1, wherein the complexity of the sequence in the first collection of nucleic acids for which relative copy number is determined is less than 1 % of the total complexity of the collection.

7. The method of claim 1, wherein the solid support is a plurality of beads.

8. The method of claim 1, wherein the solid support is glass.

9. The method of claim 1, wherein the first and second labels are fluorescent labels.

10. The method of claim 1, further comprising the step of blocking the hybridization capacity of repetitive sequences in the first and second collections of nucleic acids.

11. The method of claim 10, wherein the first and second collections of nucleic acids are mixed with unlabeled blocking nucleic acids comprising repetitive sequences.

12. The method of claim 11, wherein the unlabeled blocking nucleic acids are Cot-1 DNA.

13. The method of claim 1, wherein the first collection of labeled nucleic acids comprises mRNA or cDNA from a test cell and the second collection of labeled nucleic acids comprises mRNA or cDNA from a reference cell.

14. The method of claim 1, wherein the first collection of labeled nucleic acids is from a test genome and the second collection of labeled nucleic acids is from a normal reference genome.

15. The method of claim 14, wherein the test genome comprises nucleic acids from fetal tissue.

16. The method of claim 14, wherein the test genome comprises nucleic acids from a tumor.