Methods for evaluating oligonucleotide probes of variable length

• US 20040009484A1
• Filed: 07/11/2002
• Published: 01/15/2004
• Est. Priority Date: 07/11/2002
• Status: Abandoned Application

• Current Assignee: Renesas Technology Corporation (Renesas Electronics Corporation)
• Original Assignee: Renesas Technology Corporation (Renesas Electronics Corporation)
• Inventors: Chen, Chao, Cifuentes, Francisco J., Yoshikawa, Matthew C., Shannon, Karen W., Wolber, Paul K., Fulmer-Smentek, Stephanie B.
• Application Number:
  US10/195,053
• Publication Number:
  US 20040009484A1
• Time in Patent Office: Days
• US Class Current: 435/6
• CPC Class Codes: G16B 25/00 ICT specially adapted for hybridisation; ICT specially adapted for gene or protein expression
• CPC Class Codes: G16B 25/20 Polymerase chain reaction [PCR]; Primer or probe design; Probe optimisation

Abstract

Methods are disclosed for predicting the potential of a hybridization oligonucleotide of length greater than about 20 nucleotides to hybridize to a target nucleotide sequence. The method involves evaluating predictor oligonucleotides based on one or more parameters. A subset of oligonucleotides within the predetermined number of predictor oligonucleotides is selected based on an examination of the parameter and application of a rule that rejects some of the oligonucleotides identified above. Oligonucleotides are identified in the selected subset, viewed according to order of position along the nucleotide sequence, that are in clusters along a region of the nucleotide sequence. The clusters are ranked in order of number of oligonucleotides. A hybridization oligonucleotide is selected for each cluster, in descending order of cluster rank. The selected hybridization oligonucleotide has as its central nucleotide the central nucleotide of a region of the nucleotide sequence that corresponds to the cluster. The remaining nucleotides of the hybridization oligonucleotide are added, in correspondence to the nucleotides in the nucleotide sequence that extend in one or both directions from the central nucleotide, until a hybridization oligonucleotide of predetermined length is obtained. Cross-hybridization probes are obtained based on the hybridization oligonucleotides by deletion of at least one nucleotide from the hybridization oligonucleotide wherein the deletion(s) are evenly spaced with respect to the nucleotides of the hybridization oligonucleotide and are based on the number of nucleotides in the hybridization oligonucleotide.

Claims

1. A method for predicting the potential of a hybridization oligonucleotide of length greater than about 20 nucleotides to hybridize to a target nucleotide sequence, said method comprising:

(a) identifying a predetermined number of unique oligonucleotides of at least about 20 nucleotides in length within a nucleotide sequence of at least about 30 nucleotides in length that is hybridizable with said target nucleotide sequence, said oligonucleotides being chosen to sample a length of said nucleotide sequence,

(b) determining and evaluating for said oligonucleotides at least one parameter that is predictive of the ability of said oligonucleotides to hybridize to said target nucleotide sequence,

(c) selecting a subset of oligonucleotides within said predetermined number of unique oligonucleotides based on an examination of said parameter and application of a rule that rejects some of said oligonucleotides of step (b),

(d) identifying oligonucleotides in said selected subset, viewed according to order of position along said nucleotide sequence, that are in clusters along a region of said nucleotide sequence and that identify a contig in said nucleotide sequence,

(e) selecting for a cluster a hybridization oligonucleotide that comprises at least a portion of the nucleotide sequence of said contig wherein said hybridization oligonucleotide is different from any of the oligonucleotides in (d) which identify the contig.

2. A method according to claim 1 wherein in step (e) a hybridization oligonucleotide is selected for each cluster, in descending order of cluster rank, wherein said hybridization oligonucleotide has as its central nucleotide the central nucleotide of a region of said nucleotide sequence that corresponds to said cluster, the remaining nucleotides of said hybridization oligonucleotide being added, in correspondence to the nucleotides in said nucleotide sequence that extend in one or both directions from said central nucleotide, until a predetermined length of said hybridization oligonucleotide is obtained and a predetermined number of hybridization oligonucleotides are obtained, one from each cluster, wherein the higher the rank of said cluster, the higher the hybridization potential of said hybridization oligonucleotide for said target nucleotide sequence.

3. A method according to claim 1 wherein the hybridization oligonucleotide in (e) has a sequence overlapping multiple oligonucleotides in (d) which identify the contig.

4. A method according to claim 1 wherein said hybridization oligonucleotide is longer than any of the oligonucleotides in (d).

5. A method for predicting the potential of a hybridization oligonucleotide of length greater than about 20 nucleotides to hybridize to a target nucleotide sequence, said method comprising:

(a) identifying a predetermined number of unique oligonucleotides of at least about 20 nucleotides in length within a nucleotide sequence of at least about 30 nucleotides in length that is hybridizable with said target nucleotide sequence, said oligonucleotides being chosen to sample the entire length of said nucleotide sequence,

(b) determining and evaluating for each of said oligonucleotides at least one parameter that is independently predictive of the ability of each of said oligonucleotides to hybridize to said target nucleotide sequence,

(c) selecting a subset of oligonucleotides within said predetermined number of unique oligonucleotides based on an examination of said parameter and application of a rule that rejects some of said oligonucleotides of step (b),

(d) identifying oligonucleotides in said selected subset, viewed according to order of position along said nucleotide sequence, that are in clusters along a region of said nucleotide sequence,

(e) ranking said clusters in order of number of oligonucleotides in each cluster from greatest number to least number of oligonucleotides,

(f) selecting for each cluster, in descending order of cluster rank, a hybridization oligonucleotide of predetermined length that has as its central nucleotide the central nucleotide of a region of said nucleotide sequence that corresponds to said cluster, the remaining nucleotides of said hybridization oligonucleotide being added, in correspondence to the nucleotides in said nucleotide sequence that extend in one or both directions from said central nucleotide, until said hybridization oligonucleotide is obtained and a predetermined number of hybridization oligonucleotides are obtained, one from each cluster, wherein the higher the rank of said cluster, the higher the hybridization potential of said hybridization oligonucleotide for said target nucleotide sequence and wherein said hybridization oligonucleotide is different from any of said oligonucleotides in said cluster.

6. A method according to claim 5 wherein the length of a hybridization oligonucleotide is equal to, or greater than, the length of said region of said nucleotide sequence.

7. A method according to claim 5 wherein said unique oligonucleotides are of identical length N and wherein said unique oligonucleotides are spaced one nucleotide apart, said predetermined number comprising L−

N+1 oligonucleotides.

8. A method according to claim 5 wherein said parameter is selected from the group consisting of composition factors, thermodynamic factors, chemosynthetic efficiencies, kinetic factors and empirical factors.

9. A method according to claim 5 wherein said hybridization oligonucleotides are subsequently attached to a surface.

10. A method according to claim 5 wherein said target nucleotide sequence is DNA or RNA.

11. A method according to claim 5 wherein step (c) comprises identifying a subset of oligonucleotides within said predetermined number of unique oligonucleotides by establishing cut-off values for said parameter.

12. A method according to claim 5, which comprises determining the sizes of said clusters of step (d) by counting the number of contiguous oligonucleotides in said region of said hybridizable sequence.

13. A method according to claim 5 which comprises determining the sizes of said clusters of step (d) by counting the number of oligonucleotides in said subset that begin in a region of predetermined length in said hybridizable sequence.

14. A method according to claim 5 wherein the remaining nucleotides of said hybridization oligonucleotide are added (i) in correspondence to the nucleotides in said nucleotide sequence that extend equally or unequally in both directions from said central nucleotide, until a predetermined length of said hybridization oligonucleotide is obtained and a predetermined number of hybridization oligonucleotides are obtained or (ii) are added, in correspondence to the nucleotides in said nucleotide sequence that extend in only one direction from said central nucleotide, until a predetermined length of said hybridization oligonucleotide is obtained and a predetermined number of hybridization oligonucleotides are obtained.

15. A method according to claim 5 wherein step (b) comprises determining and evaluating for each of said oligonucleotides at least two parameters that are independently predictive of the ability of each of said oligonucleotides to hybridize to said target nucleotide sequence wherein said parameters are poorly correlated with respect to one another.

23. A method for selecting a cross-hybridization oligonucleotide probe for use in conjunction with a hybridization oligonucleotide of at least about 20 nucleotides for analyzing a target nucleotide sequence, said method comprising:

(a) identifying a hybridization oligonucleotide by a method according to claim 5,

(b) selecting a cross-hybridization oligonucleotide probe based on said hybridization oligonucleotide by a process comprising deletion of at least one nucleotide from said hybridization oligonucleotide wherein said deletion(s) are evenly spaced with respect to the nucleotides of said hybridization oligonucleotide and the number of deletions is based on the length of said cross-hybridization oligonucleotide probe.

24. A method according to claim 23 wherein said hybridization oligonucleotide is at least about 50 nucleotides in length and said deletions of step (b) are at a frequency of about one for every 20 to 25 nucleotides of said hybridization oligonucleotide.

25. A method according to claim 23 wherein said hybridization oligonucleotide is 60 nucleotides in length and said deletions are made at nucleotides 15, 30 and 45 of said hybridization oligonucleotide.

16. A method for predicting the potential of a hybridization oligonucleotide of at least about 20 nucleotides in length to hybridize to a complementary target nucleotide sequence, said method comprising:

(a) obtaining, from a nucleotide sequence at least about 30 nucleotides in length and complementary to said target nucleotide sequence, a set of overlapping oligonucleotides of at least about 20 nucleotides in length and of identical length N and spaced one nucleotide apart, said set comprising L−

N+1 oligonucleotides,

(b) determining and evaluating for each of said oligonucleotides the parameters;

(i) the predicted melt temperature of the duplex of said oligonucleotide and said target nucleotide sequence corrected for salt concentration and (ii) predicted free energy of the most stable intramolecular structure of the oligonucleotide at the temperature of hybridization of each of said oligonucleotides with said target nucleotide sequence,

(c) selecting a subset of oligonucleotides within said predetermined number of oligonucleotides based on an examination of said parameter and application of a rule that rejects some of said oligonucleotides of step (b),

(d) identifying oligonucleotides in said selected subset, viewed according to order of position along said nucleotide sequence, that are in clusters along a region of said nucleotide sequence,

(e) ranking said clusters in order of number of oligonucleotides in each cluster from greatest number to least number of oligonucleotides,

(f) selecting for each cluster, in descending order of cluster rank, a hybridization oligonucleotide of predetermined length that has as its central nucleotide the central nucleotide of a region of said nucleotide sequence that corresponds to said cluster, the remaining nucleotides of said hybridization oligonucleotide being added, in correspondence to the nucleotides in said nucleotide sequence that extend in one or both directions from said central nucleotide, until said hybridization oligonucleotide is obtained and a predetermined number of hybridization oligonucleotides are obtained, one from each cluster, wherein the higher the rank of said cluster, the higher the hybridization potential of said hybridization oligonucleotide for said target nucleotide sequence and wherein said predetermined length of said hybridization oligonucleotide is greater than the length of any of said oligonucleotides in said cluster.

17. A method according to claim 16 wherein the length of a hybridization oligonucleotide is equal to, or greater than, the length of said region of said nucleotide sequence.

18. A method according to claim 16 wherein said oligonucleotides are attached to a surface.

19. A method according to claim 16 wherein said hybridization oligonucleotide is at least 30 nucleotides in length.

20. A method according to claim 16 wherein the remaining nucleotides of said hybridization oligonucleotide are added (i) in correspondence to the nucleotides in said nucleotide sequence that extend equally or unequally in both directions from said central nucleotide, until a predetermined length of said hybridization oligonucleotide is obtained and a predetermined number of hybridization oligonucleotides are obtained or (ii) are added, in correspondence to the nucleotides in said nucleotide sequence that extend in only one direction from said central nucleotide, until a predetermined length of said hybridization oligonucleotide is obtained and a predetermined number of hybridization oligonucleotides are obtained.

21. A method according to claim 16, which is a computer based method wherein steps (a) through (f) are carried Out under computer control.

22. A computer system for conducting a method for predicting the potential of a hybridization oligonucleotide to hybridize to a target nucleotide sequence, said system comprising:

(a) input means for introducing a target nucleotide sequence into said computer system,

(b) means for determining a number of unique oligonucleotide sequences that are within a nucleotide sequence that is hybridizable with said target nucleotide sequence, said oligonucleotide sequences being chosen to sample the entire length of said nucleotide sequence,

(c) memory means for storing said oligonucleotide sequences,

(e) means for controlling said computer system to carry out a determination and evaluation for each of said oligonucleotide sequences a value for at least one parameter that is independently predictive of the ability of each of said oligonucleotide sequences to hybridize to said target nucleotide sequence,

(e) means for storing said parameter values,

(f) means for controlling said computer to carry out an identification from said stored parameter values a subset of oligonucleotide sequences within said number of unique oligonucleotide sequences based on said evaluation of said parameter,

(g) means for storing said subset of oligonucleotides,

(h) means for controlling said computer to carry out an identification of oligonucleotide sequences in said subset that are clustered along a region of said nucleotide sequence that is hybridizable to said target nucleotide sequence.

(i) means for storing said oligonucleotide sequences in said subset,

(j) means for outputting data relating to said oligonucleotide sequences in said subset,

(k) means for ranking said clusters in order of number of oligonucleotides in each cluster from greatest number to least number of oligonucleotides,

(l) means for selecting for each cluster, in descending order of cluster rank, a hybridization oligonucleotide of predetermined length that has as its central nucleotide the central nucleotide of a region of said nucleotide sequence that corresponds to said cluster, the remaining nucleotides of said hybridization oligonucleotide being added, in correspondence to the nucleotides in said nucleotide sequence that extend in one or both directions from said central nucleotide, until said hybridization oligonucleotide is obtained and a predetermined number of hybridization oligonucleotides are obtained, one from each cluster, wherein the higher the rank of said cluster, the higher the hybridization potential of said hybridization oligonucleotide for said target nucleotide sequence and wherein said predetermined length of said hybridization oligonucleotide is greater than the length of any of said oligonucleotides in said cluster, and

(m) means for outputting data relating to said hybridization oligonucleotides.

26. A method for selecting a cross-hybridization oligonucleotide probe for use in conjunction with a hybridization oligonucleotide of at least about 20 nucleotides in length for analyzing a target nucleotide sequence, said method comprising:

(a) identifying a hybridization oligonucleotide of at least 20 nucleotides in length that is specific for said target nucleotide sequence,

(b) selecting a cross-hybridization oligonucleotide probe based on said hybridization oligonucleotide of step (a) by a process comprising deletion of at least one nucleotide from said hybridization oligonucleotide wherein said deletion(s) are evenly spaced with respect to the nucleotides of said hybridization oligonucleotide.

27. A method according to claim 26 wherein said hybridization oligonucleotide is at least about 50 nucleotides in length and said deletions of step (b) are at a frequency of one for about every 20 to 25 nucleotides of said hybridization oligonucleotide.

28. A method according to claim 26 wherein said hybridization oligonucleotide is 60 nucleotides in length and said deletions are made at nucleotides 15, 30 and 45 of said hybridization oligonucleotide.

29. A method according to claim 26 wherein said hybridization 30 oligonucleotide of at least about 20 nucleotides in length is selected by a method comprising:

(a) identifying a predetermined number of unique oligonucleotides of at least about 20 nucleotides in length within a nucleotide sequence of at least about 30 nucleotides in length that is hybridizable with said target nucleotide sequence, said oligonucleotides being chosen to sample the entire length of said nucleotide sequence,

(b) determining and evaluating for each of said oligonucleotides at least one parameter that is independently predictive of the ability of each of said oligonucleotides to hybridize to said target nucleotide sequence,

(c) selecting a subset of oligonucleotides within said predetermined number of unique oligonucleotides based on an examination of said parameter and application of a rule that rejects some of said oligonucleotides of step (b),

(d) identifying oligonucleotides in said selected subset, viewed according to order of position along said nucleotide sequence, that are in clusters along a region of said nucleotide sequence,

(e) ranking said clusters in order of number of oligonucleotides in each cluster from greatest number to least number of oligonucleotides, and

(f) selecting for each cluster, in descending order of cluster rank, a hybridization oligonucleotide of predetermined length that has as its central nucleotide the central nucleotide of a region of said nucleotide sequence that corresponds to said cluster, the remaining nucleotides of said hybridization oligonucleotide being added, in correspondence to the nucleotides in said nucleotide sequence that extend in one or both directions from said central nucleotide, until said hybridization oligonucleotide is obtained and a predetermined number of hybridization oligonucleotides are obtained, one from each cluster, wherein the higher the rank of said cluster, the higher the hybridization potential of said hybridization oligonucleotide for said target nucleotide sequence and wherein said predetermined length of said hybridization oligonucleotide is greater than the length of any of said oligonucleotides in said cluster.

30. A method according to claim 29 wherein said parameter is selected from the group consisting of composition factors, thermodynamic factors, chemosynthetic efficiencies and kinetic factors.

31. A method according to claim 29 wherein said hybridization oligonucleotides are subsequently attached to a surface.

32. A method according to claim 29, which is a computer based method wherein each of said steps is carried out under computer control.

42. An addressable array comprising:

(a) a support having a surface,

(b) a spot on said surface having bound thereto an oligonucleotide probe specific for a target nucleic acid sequence and

(c) at least one spot on said surface having bound thereto a cross-hybridization oligonucleotide probe wherein said cross-hybridization oligonucleotide probe measures the extent of the occurrence of a cross-hybridization event of a predetermined probability between an interfering nucleic acid sequence and said oligonucleotide probe specific for a target nucleic acid sequence wherein said cross-hybridization oligonucleotide probe is selected by a method according to claim 26.

43. A method for detecting a target nucleic acid sequence, said method comprising:

(a) contacting a medium suspected of containing said target nucleic acid sequence with the array of claim 42 and

(b) determining a result of said contacting, said result indicating the presence or absence of said target nucleic acid sequence in said medium.

44. An assay result determined by a method according to claim 43.

45. A method comprising forwarding to a remote location a result according to claim 44.

33. A method for selecting a set of target-specific oligonucleotide probes of at least about 20 nucleotides in length for use in analyzing a target nucleotide sequence, said method comprising:

(a) identifying a cross-hybridization oligonucleotide probe based on said target nucleic acid sequence by a process comprising deletion of at least one nucleotide from a single hybridization oligonucleotide wherein said deletion(s) are evenly spaced with respect to the nucleotides of said hybridization oligonucleotide and the number of deletions is based on the length of said cross-hybridization oligonucleotide probe,

(b) determining cross-hybridization results employing said cross-hybridization oligonucleotide probe and target-specific oligonucleotide probe and

(c) selecting or rejecting said target-specific oligonucleotide probe for said set based on said cross-hybridization results.

34. A method according to claim 33 wherein said cross-hybridization oligonucleotide probe is at least about 50 nucleotides in length and said deletions of step (a) are at a frequency of one for about every 20 to 25 nucleotides of said hybridization oligonucleotide.

35. A method according to claim 33, which is a computer based method wherein steps (a)-(c) are carried out under computer control.

36. A method for detecting differences between an individual sequence and a known reference sequence, said method comprising:

(a) combining under hybridization conditions labeled individual sequence, a surface bound reference oligonucleotide probe based on said known reference sequence and a set of surface bound deletion oligonucleotide probes of at least about 20 nucleotides in length wherein said set of deletion oligonucleotide probes is prepared by a process comprising deletion of at least one nucleotide from a single hybridization oligonucleotide wherein said deletion(s) are evenly spaced with respect to the nucleotides of said hybridization oligonucleotide and the number of deletions is based on the length of said cross-hybridization oligonucleotide probe,

(b) determining hybridization ratios for said set of deletion oligonucleotide probes with respect to said reference oligonucleotide probe and

(c) relating said hybridization ratios to the presence or absence of differences between said individual sequence and said reference sequence.

37. An addressable array comprising:

(a) a support having a surface,

(b) a spot on said surface having bound thereto an oligonucleotide probe specific for a target nucleic acid sequence and

(c) at least one spot on said surface having bound thereto a cross-hybridization oligonucleotide probe wherein said cross-hybridization oligonucleotide probe measures the extent of the occurrence of a cross-hybridization event of a predetermined probability between an interfering nucleic acid sequence and said oligonucleotide probe specific for a target nucleic acid sequence wherein said cross-hybridization oligonucleotide probe is selected by a process comprising deletion of at least one nucleotide from a single hybridization oligonucleotide wherein said deletion(s) are evenly spaced with respect to the nucleotides of said hybridization oligonucleotide and the number of deletions is based on the length of said cross-hybridization oligonucleotide probe.

38. A method for detecting a target nucleic acid sequence, said method comprising:

(a) contacting a medium suspected of containing said target nucleic acid sequence with the array of claim 37 and

(b) determining a result of said contacting, said result indicating the presence or absence of said target nucleic acid sequence in said medium.

39. A method according to claim 38 wherein said determining of said result comprises examining said array for the presence of a hybrid of said target nucleic acid sequence and said oligonucleotide probe specific for said target nucleic acid sequence, the presence thereof indicating the presence of said target nucleic acid sequence in said medium.

40. An assay result determined by a method according to claim 38.

41. A method comprising forwarding to a remote location a result according to claim 40.

46. A method for predicting the potential of a hybridization oligonucleotide of at least about 20 nucleotides in length to hybridize to a complementary target nucleotide sequence, said method comprising:

(a) obtaining, from a nucleotide sequence at least about 30 nucleotides in length L and complementary to said target nucleotide sequence, a set of overlapping oligonucleotides of at least about 20 nucleotides in length and of identical length N and spaced S nucleotides apart, said set comprising 1+Int[(L−

N)/S] oligonucleotides, wherein “

Int”

is the integer part of the indicated quotient,

(b) determining experimentally and evaluating for each of said oligonucleotides the hybridization of said oligonucleotides with said target nucleotide sequence,

(c) selecting a subset of oligonucleotides within said predetermined number of oligonucleotides based on said evaluation and application of a rule that rejects some of said oligonucleotides of step (b),

(d) identifying oligonucleotides in said selected subset, viewed according to order of position along said nucleotide sequence, that are in clusters along a region of said nucleotide sequence,

(e) ranking said clusters in order of number of oligonucleotides in each cluster from greatest number to least number of oligonucleotides,

(f) selecting for each cluster, in descending order of cluster rank, a hybridization oligonucleotide of predetermined length that has as its central nucleotide the central nucleotide of a region of said nucleotide sequence that corresponds to said cluster, the remaining nucleotides of said hybridization oligonucleotide being added, in correspondence to the nucleotides in said nucleotide sequence that extend in one or both directions from said central nucleotide, until said hybridization oligonucleotide is obtained and a predetermined number of hybridization oligonucleotides are obtained, one from each cluster, wherein the higher the rank of said cluster, the higher the hybridization potential of said hybridization oligonucleotide for said target nucleotide sequence and wherein said predetermined length of said hybridization oligonucleotide is greater than the length of any of said oligonucleotides in said cluster.