Expression monitoring by hybridization to high density oligonucleotide arrays

• US 6,040,138 A
• Filed: 09/15/1995
• Issued: 03/21/2000
• Est. Priority Date: 09/15/1995
• Status: Expired due to Term

• Current Assignee: Affymetrix, Inc. (Thermo Fisher Scientific Incorporated)
• Original Assignee: Affymetrix, Inc. (Thermo Fisher Scientific Incorporated)
• Inventors: Wong, Gordon G., Chee, Mark S., Lockhart, David J., Gingeras, Thomas R., Brown, Eugene L.
• Primary Examiner(s): Zitomer, Stephanie W.
• Application Number:
  US08/529,115
• Time in Patent Office: 1,649 Days
• Field of Search: 435/6, 435/5, 435/91.2, 435/91.1, 536/24.3-24.33, 536/23.1
• US Class Current: 435/6.11
• CPC Class Codes: C12Q 1/6809 Methods for determination or identification of nucleic acids involving differential detection
• CPC Class Codes: C12Q 1/6837 using probe arrays or probe chips C12Q1/6874 takes precedence
• CPC Class Codes: C12Q 2565/507 characterised by the density of the capture oligonucleotide
• CPC Class Codes: G01N 15/1433 using image recognition

Abstract

This invention provides methods of monitoring the expression levels of a multiplicity of genes. The methods involve hybridizing a nucleic acid sample to a high density array of oligonucleotide probes where the high density array contains oligonucleotide probes complementary to subsequences of target nucleic acids in the nucleic acid sample. In one embodiment, the method involves providing a pool of target nucleic acids comprising RNA transcripts of one or more target genes, or nucleic acids derived from the RNA transcripts, hybridizing said pool of nucleic acids to an array of oligonucleotide probes immobilized on surface, where the array comprising more than 100 different oligonucleotides and each different oligonucleotide is localized in a predetermined region of the surface, the density of the different oligonucleotides is greater than about 60 different oligonucleotides per 1 cm², and the olignucleotide probes are complementary to the RNA transcripts or nucleic acids derived from the RNA transcripts; and quantifying the hybridized nucleic acids in the array.

Claims

1. A method of analyzing the expression of one or more genes, said method comprising:

(a) providing a pool of target nucleic acids comprising RNA transcripts of one or more of said genes, or nucleic acids derived therefrom using said RNA transcripts as templates;

(b) hybridizing said pool of tarzet nucleic acids to an array of oligonucleotide probes immobilized on a surface, said array comprising more than 100 different oligonucleotides, at least some of which comprise control probes, wherein each different oligonucleotide is localized in a predetermined region of said surface, the density of said different oligonucleotides is greater than about 60 different oligonucleotides per 1 cm², and at least some of said oligonucleotide probes are complementary to said RNA transcripts or said nucleic acids derived therefrom using said RNA transcripts; and

(c) quantifying the hybridization of said nucleic acids to said array, wherein said quantification is proportional to the expression level of said genes.

2. The method of claim 1, wherein said array of oligonucleotides further comprises mismatch control probes.

3. The method of claim 2, wherein said quantifying comprises calculating the difference in hybridization signal intensity between each of said oligonucleotide probes and its corresponding mismatch control probe.

4. The method of claim 3, wherein said quantifying comprises calculating the average difference in hybridization signal intensity between each of said oligonucleotide probes and its corresponding mismatch control probe for each gene.

5. The method of claim 1, wherein hybridization and quantification is accomplished in under 48 hours.

6. The method of claim 1, wherein said multiplicity of genes is 100 genes or more.

7. The method of claim 1, wherein for each gene, said array comprises at least 10 different oligonucleotide probes complementary to subsequences of that gene.

8. The method of claim 1, wherein said hybridization is performed with a fluid volume of about 250 μ

l or less.

9. The method of claim 1, wherein said quantifying comprises detecting a hybridization signal that is proportional to the concentration of said RNA in said nucleic acid sample.

10. The method of claim 1, wherein said oligonucleotides are from 5 to about 50 nucleotides in length.

11. The method of claim 1, wherein said oligonucleotides are synthesized by light-directed polymer synthesis.

12. The method of claim 1, wherein said control probes comprise sequences from constitutively expressed control genes.

13. The method of claim 12, wherein said control genes are selected from the group consisting of β

-actin, GAPDH, and the transferrin receptor.

14. The method of claim 1, wherein said hybridization comprises a hybridization at low stringency of 30°

C. to 50°

C. and 6 X SSPE-T or lower and a wash at higher stringency.

15. The method of claim 1, wherein said pool of target nucleic acids is a pool of mRNAs.

16. The method of claim 1, wherein said pool of target nucleic acids is a pool of RNAs in vitro transcribed from a pool of cDNAs.

17. The method of claim 1, wherein said pool of target nucleic acids is amplified from a biological sample by an in vivo or an in vitro method.

18. The method of claim 1, wherein said pool of target nucleic acids comprises fluorescently labeled nucleic acids.

19. The method of claim 1, wherein said detecting comprises quantifying fluorescence of a label on said hybridized nucleic acids at a spatial resolution of 100 μ

m or higher.

20. The method of claim 19, wherein said quantification is by means of a scanning confocal fluorescence microscope.

21. The method of claim 1, wherein said providing comprises:

(i) hybridizing a pool of RNAs with a pool of oligonucleotides having the same sequences as said oligonucleotide probes to form a pool of hybridized nucleic acids;

(ii) treating said pool of hybridized nucleic acids with RNase A, thereby digesting single stranded nucleic acid sequences and leaving intact the hybridized double stranded regions;

(iii) denaturing the hybridized double-stranded regions and removing said oligonucleotides thereby leaving a pool of RNAs enhanced for those RNAs complementary to the oligonucleotide probes in said high density array.

22. The method of claim 1, wherein said providing comprises:

(a) hybridizing a pool of RNAs with paired target specific oligonucleotides wherein said paired target specific oligonucleotides are complementary to regions on either side of a subsequence, said subsequence being complementary to at least one of said oligonucleotide probes in said array;

(b) treating said pool of nucleic acids with RNase H to digest the hybridized (double stranded) nucleic acid sequences;

(c) isolating the remaining nucleic acid sequences having a length about equivalent to said subsequence.

23. The method of claim 1, wherein said providing comprises:

(a) hybridizing a pool of poly A⁺ mRNAs with oligonucleotides that hybridize specifically with preselected mRNA target messages;

(b) treatng said pool of nucleic acids with RNase H to digest the hybridized (double stranded) nucleic acid sequences thereby separating the coding sequence from the polyA⁺ tail;

(c) isolating or ampifying the re polyA⁺ RNA in said pool.

37. The method of claim 2, wherein said oligonucleotide probes present in said array are oligonucleotide probes identified by the steps comprising:

providing a high density array of oligonucleotide probes, said array comprising a multiplicity of oligonucleotide probes, wherein each probe is complementary to a subsequence of said target nucleic acid and for each probe there is a corresponding mismatch control probe;

hybridizing said target nucleic acid to said array of oligonucleotide probes; and

identifying those probes for which the difference in hybridization signal intensity between each probe and its mismatch control is detectable.

38. The method of claim 2, wherein said oligonucleotide probes analyzed in said quantifying step are identified by the steps comprising:

providing a high density array of oligonucleotide probes, said array comprising a multiplicity of oligonucleotide probes, wherein each probe is complementary to a subsequence of said target nucleic acid and for each probe there is a corresponding mismatch control probe;

hybridizing said target nucleic acid to said array of oligonucleotide probes; and

identifying those probes for which the difference in hybridization signal intensity between each probe and its mismatch control is detectable.

41. The method of claim 1, wherein at least some of said oligonucleotide probes are from about 10 to about 40 nucleotides in length.

42. The method of claim 1, wherein at least some of said oligonucleotide probes are from about 15 to 40 nucleotides in length.

43. The method of claim 1, wherein at least some of said oligonucleotides are up to about 500 nucleotides in length.

44. The method of claim 1, wherein at least some of said oligonucleotides are greater than 10 nucleotides in length.

45. The method of claim 1, wherein at least some of said oligonucleotides are greater than 15 nucleotides in length.

24. A method of identifying oligonucleotide probes to quantify the expression of a target nucleic acid, comprising:

providing a high density array of oligonucleotide probes, said array comprising a multiplicity of oligonucleotide probes, wherein each probe is complementary to a subsequence of said target nucleic acid and for each probe there is a corresponding mismatch control probe;

hybridizing said target nucleic acid to said array of oligonucleotide probes; and

identifying those probes for which the difference in hybridization signal intensity between each probe and its mismatch control is detectable.

25. The method of claim 24, further comprising:

hybridizing said probes identified for which the difference in hybridization signal intensity between each probe and its mismatch control is detectable to a pool of nucleic acids comprising nucleic acids other than said target nucleic acids; and

identifying probes having the lowest hybridization signal, wherein both the probe and its mismatch control have a hybridization intensity equal to or less than 10 times background.

26. The method of claim 24, wherein said oligonucleotide probes ranges in length from about 10 to about 50.

27. The method of claim 24, wherein said oligonucleotide probes are all the same length.

28. The method of claim 24, wherein said difference in hybridization intensity between each probe and its mismatch control is at least 10% of a background signal.

29. The method of claim 24, wherein said multiplicity of probes includes all the probes of a single length that are exactly complementary to a subsequence of said target nucleic acid, and wherein said probes have a length between about 5 and 50 nucleotides.

30. The method of claim 24, wherein said array comprises more than 100 different oligonucleotides wherein each different oligonucleotide is localized in a predetermined region of said surface and the density of said different oligonucleotides is greater than about 60 different oligonucleotides per 1 cm² of said surface.

31. The method of claim 24, wherein hybridization is performed with a fluid volume of about 250 μ

l or less.

32. The method of claim 24, wherein said target nucleic acid is a nucleic acid comprising at least a partial sequence or complementary sequence of a gene.

33. The method of claim 24, wherein said oligonucleotide probes are synthesi zed by light-directed polymer synthesis.

34. The method of claim 24, wherein said mismatch control probes have a centrally l ocated 1 base mismatch.

35. The method of claim 24, wherein said hybridization comprises hybridization at low stringency of 30°

C. to 50°

C. and 6 X SSPE-T or lower followed by one or more washes at progressively increasing stringency until a desired level of hybridization specificity is obtained.

36. The method of claim 25, wherein the sequences of the nucleic acids in said pool comprise the sequences of said probes.

39. A method of identifg polynucleotide probes to quantify the expression of a target nucleic acid, comprising:

providing a high density array comprising polynucleotide probes complementary to a subsequence of said target nucleic acid, wherein for each of said probes there is a corresponding mismatch control probe on said array;

hybridizing said array to a pool of nucleic acids comprising nucleic acids other than said target nucleic acids; and

identifying probes having a hybridization intensity equal to or less than a background intensity, wherein at least one of said probes chosen is used to quantify said expression of said target nucleic acid.

40. The method of claim 39, further comprising after said identifying step:

hybridizing said probes identified to said target nucleic acid; and

identifiing those probes for which the difference in hybridization signal intensity between each probe and its mismatch control is detectable.