Detection of hybridization on oligonucleotide microarray through covalently labeling microarray probe

• US 20030087298A1
• Filed: 11/01/2002
• Published: 05/08/2003
• Est. Priority Date: 11/02/2001
• Status: Abandoned Application

• Current Assignee: NimbleGen Systems, Inc. (Roche Holding AG)
• Original Assignee: NimbleGen Systems, Inc. (Roche Holding AG)
• Inventors: Green, Roland, Albert, Thomas
• Application Number:
  US10/287,722
• Publication Number:
  US 20030087298A1
• Time in Patent Office: Days
• US Class Current: 435/6
• CPC Class Codes: C12Q 1/6816 characterised by the detection means C12Q1/6804 takes precedence
• CPC Class Codes: C12Q 2565/537 characterised by the capture oligonucleotide acting as a primer

Abstract

A method for detecting hybridization between a probe with a free 3′ end on an oligonucleotide microarray and a polynucleotide from a sample is disclosed. The method involves contacting the sample with the probe under a hybridization condition under which desired hybridization events occur, performing an elongation reaction on the probe using at least one labeled nucleotide, removing unincorporated labeled nucleotides from the microarray, and determining whether the probe is labeled.

Claims

1. A method for detecting hybridization between a DNA probe on a microarray and a polynucleotide from a sample, the method comprising the steps of:

(a) providing a microarray with DNA probes having free 3′

ends;

(b) contacting the sample with the microarray under a hybridization conditions under which desired hybridization events occur;

(c) performing a template-dependent elongation reaction on the microarray in the presence of at least one labeled nucleotide;

(d) removing unincorporated labeled nucleotides from the microarray; and

(e) determining whether the probes in the microarray have been labeled.

2. The method of claim 1, wherein the probe is DNA.

3. The method of claim 1, wherein the polynucleotide is DNA.

4. The method of claim 1, wherein the polynucleotide is RNA.

5. The method of claim 1 further comprising the step of washing the oligonucleotide microarray.

6. A method for performing an assay of gene expression in a cell or tissue, the method comprising the steps of:

(a) providing a microarray with DNA probes having free 3′

ends and with probes designed to detect the expression of genes that might be expressed in the cell or tissue;

(b) extracting RNA from the cell or tissue;

(c) contacting the extracted RNA with the microarray under a hybridization conditions under which desired hybridization events occur without labeling the extracted RNA;

(d) performing a template-dependent elongation reaction on the microarray in the presence of at least one labeled nucleotide;

(e) removing unincorporated labeled nucleotides from the microarray; and

(f) determining whether the probes in the microarray have been labeled.

7. The method of claim 6, wherein the probe is DNA.

8. The method of claim 6, wherein the polynucleotide is DNA.

9. The method of claim 6, wherein the polynucleotide is RNA.

10. The method of claim 6 further comprising the step of washing the oligonucleotide microarray.