EP0948645A1 - Cleaved amplified rflp detection methods - Google Patents

Cleaved amplified rflp detection methods

Info

Publication number
EP0948645A1
EP0948645A1 EP97942525A EP97942525A EP0948645A1 EP 0948645 A1 EP0948645 A1 EP 0948645A1 EP 97942525 A EP97942525 A EP 97942525A EP 97942525 A EP97942525 A EP 97942525A EP 0948645 A1 EP0948645 A1 EP 0948645A1
Authority
EP
European Patent Office
Prior art keywords
sequence
primer
restriction site
strand
detectable label
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Withdrawn
Application number
EP97942525A
Other languages
German (de)
French (fr)
Other versions
EP0948645A4 (en
Inventor
Frederick Ausubel
Ronald W. Davis
Daphne Preuss
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
General Hospital Corp
Leland Stanford Junior University
Original Assignee
General Hospital Corp
Leland Stanford Junior University
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Priority claimed from US08/715,484 external-priority patent/US6004783A/en
Application filed by General Hospital Corp, Leland Stanford Junior University filed Critical General Hospital Corp
Publication of EP0948645A1 publication Critical patent/EP0948645A1/en
Publication of EP0948645A4 publication Critical patent/EP0948645A4/en
Withdrawn legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12Q—MEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEIC ACIDS OR MICROORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
    • C12Q1/00—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions
    • C12Q1/68—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving nucleic acids
    • C12Q1/6813—Hybridisation assays
    • C12Q1/6827—Hybridisation assays for detection of mutation or polymorphism
    • C12Q1/683—Hybridisation assays for detection of mutation or polymorphism involving restriction enzymes, e.g. restriction fragment length polymorphism [RFLP]
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12Q—MEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEIC ACIDS OR MICROORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
    • C12Q1/00—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions
    • C12Q1/68—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving nucleic acids
    • C12Q1/6844—Nucleic acid amplification reactions
    • C12Q1/6858—Allele-specific amplification

Definitions

  • This invention relates to the generation and detection of genetic polymorphisms .
  • RFLP restriction fragment length polymorphic
  • PCR-based approach involves the use of single short PCR primers of arbitrary sequence called RAPD primers (for random amplified polymorphic DNA; Reiter et al., Proc. Natl. Acad. Sci. USA 89: 1477-1481 , 1992; Williams et al., Theoret. Appl. Genet. 82:489-498, 1991).
  • RAPD primers for random amplified polymorphic DNA
  • SSLPs for simple sequence length polymorphism
  • the method employing SSLPs is based on amplification across tandem repeats of one or a few nucleotides known as "microsatellites.” Microsatellites occur frequently and randomly in most eukaryotic genomes and display a high degree of polymorphism due to variation in the numbers of repeated units.
  • a third category of PCR-based markers are called AFLPs (for amplified fragment length polymo ⁇ hisms).
  • DNA from two polymo ⁇ hic strains are cleaved with one or two restriction endonucleases, and adapters are ligated to the ends of the cleaved fragments.
  • the fragments are then amplified using primers complementary to the adapter(s).
  • the primers contain short stretches of random nucleotides at their 3' ends, which result in limiting the number of amplified fragments generated.
  • the invention features a method for detecting the presence or absence of a polymo ⁇ hic restriction site in a nucleic acid, involving the steps of (a) amplifying the nucleic acid by PCR using a first and a second primer flanking the polymo ⁇ hic restriction site, the first primer being tagged with the first member of a specific binding pair, the second primer being tagged with a detectable label; (b) digesting the PCR product of step (a) with the restriction endonuclease corresponding to the polymo ⁇ hic restriction site; (c) contacting the reaction product of step (b) with the second member of the specific binding pair, immobilized on a solid support; and (d) measuring the level of the detectable label bound to the solid support, the presence of the detectable label bound to the solid support being an indication of the absence of the polymo ⁇ hic restriction site in the nucleic acid.
  • the invention features a method for detecting the presence or absence of a polymo ⁇ hic restriction site in a nucleic acid, involving the steps of: (a) amplifying the nucleic acid by PCR using a first and a second primer flanking the polymo ⁇ hic restriction site, the first primer being tagged with the first member of a specific binding pair, the second primer being tagged with a first detectable label; (b) digesting the PCR product of step (a) with the restriction endonuclease corresponding to the polymo ⁇ hic restriction site; (c) annealing and ligating to the single-stranded ends generated in the reaction of step (b) an oligonucleotide tagged with a second detectable label; (d) contacting the reaction product of step (c) with the second member of the specific binding pair, immobilized on a solid support; and (e) determining the levels of the first and second detectable labels bound to the solid support, the presence of only the first detect
  • the invention features a method for detecting the presence or absence of a polymo ⁇ hic restriction site in a nucleic acid, the method involving the steps of: (a) amplifying the nucleic acid by PCR using a first and a second primer flanking the polymo ⁇ hic restriction site, the first primer being tagged with a detectable label, the second primer being unlabeled; (b) digesting a portion of the reaction of step (a) with the restriction endonuclease corresponding to the polymo ⁇ hic restriction site, while leaving another portion of the reaction of step (a) undigested; (c) denaturing the digested and undigested portions from step (b); (d) contacting the product of step (c) with an oligonucleotide complementary to a sequence in the strand of the product of step (c) containing the detectable label, the sequence being between the polymo ⁇ hic restriction and the sequence complementary to the second primer, the oligonucleotide being
  • the invention features a method for detecting the presence or absence of a polymo ⁇ hic restriction site in a nucleic acid, involving the steps of: (a) amplifying the nucleic acid by PCR using a first and a second primer flanking the polymo ⁇ hic restriction site, the first primer being tagged with a first detectable label, the second primer being tagged with a second detectable label; (b) digesting the reaction product of step (a) with the restriction endonuclease corresponding to the polymo ⁇ hic restriction site; (c) denaturing the reaction product of step (b); (d) contacting the product of step (c) with a first and a second oligonucleotide, the first oligonucleotide being complementary to a first sequence in the strand of the product of step (c) containing the first detectable label, the first sequence being between the polymo ⁇ hic restriction site and the sequence corresponding to the first primer, the first oligonucleo
  • the invention features a method for detecting the presence or absence of a polymo ⁇ hic restriction site in a nucleic acid, involving the steps of: (a) amplifying the nucleic acid by PCR using a first and a second primer flanking the polymo ⁇ hic restriction site, the first primer being tagged with a first detectable label, the second primer being tagged with a second detectable label; (b) digesting the reaction product of step (a) with the restriction endonuclease corresponding to the polymo ⁇ hic restriction site; (c) denaturing the reaction product of step (b); (d) contacting the product of step (c) with a first and a second oligonucleotide, the first oligonucleotide being complementary to a first sequence in the strand of the product of step (c) containing the first detectable label, the first sequence being between the polymo ⁇ hic restriction site and the sequence complementary to the second primer, the first oligonucleot
  • the invention method for detecting the presence or absence of a polymo ⁇ hic restriction site in a nucleic acid involving the steps of: (a) amplifying the nucleic acid by PCR using a first and a second primer flanking the polymo ⁇ hic restriction site, the first primer being tagged with a first detectable label, the second primer being tagged with a second detectable label; (b) digesting the reaction product of step (a) with the restriction endonuclease corresponding to the polymo ⁇ hic restriction site; (c) denaturing the reaction product of step (b); (d) contacting the product of step (c) with a first and a second oligonucleotide, the first oligonucleotide being complementary to a first sequence in the strand of the product of step (c) containing the first detectable label, the first sequence being between the polymo ⁇ hic restriction site and the sequence corresponding to the first primer, the first oligonucleotide being
  • the invention features a method for detecting the presence or absence of a polymo ⁇ hic restriction site in a nucleic acid, involving the steps of: (a) amplifying the nucleic acid by PCR using a first and a second primer flanking the polymo ⁇ hic restriction site, the first primer being tagged with a first detectable label, the second primer being tagged with a second detectable label; (b) digesting the reaction product of step (a) with the restriction endonuclease corresponding to the polymo ⁇ hic restriction site; (c) denaturing the reaction product of step (b); (d) contacting the product of step (c) with a first and a second oligonucleotide, the first oligonucleotide being complementary to a first sequence in the strand of the product of step (c) containing the first detectable label, the first sequence being between the polymo ⁇ hic restriction site and the sequence complementary to the second primer, the first oligonucleot
  • the invention features a method for detecting the presence or absence of a polymo ⁇ hic restriction site in a nucleic acid, involving the steps of: (a) amplifying the nucleic acid by PCR using a first and a second primer flanking the polymo ⁇ hic restriction site, the first primer being tagged with the first member of a first specific binding pair, the second primer being tagged with a detectable label; (b) digesting the reaction product of step (a) with the restriction endonuclease corresponding to the polymo ⁇ hic restriction site; (c) contacting the reaction product of step (b) with the second member of the first specific binding pair, immobilized on a first solid support; (d) denaturing the reaction product of step (c) not bound to the first solid support; (e) contacting the product of step (d) with an oligonucleotide complementary to a sequence in the strand of the product of step (d) containing the detectable label, the sequence being between the polymo
  • the invention features a method for detecting the presence or absence of a polymo ⁇ hic restriction site in a nucleic acid, involving the steps of: (a) amplifying the nucleic acid by PCR using a first and a second primer flanking the polymo ⁇ hic restriction site, the first primer being tagged with a detectable label, the second primer being unlabeled; (b) digesting the reaction product of step (a) with the restriction endonuclease corresponding to the polymo ⁇ hic restriction site; (c) annealing and ligating to the single-stranded ends generated in the reaction of step (b) a first oligonucleotide tagged with the first member of a first specific binding pair; (d) contacting the reaction product of step (c) with the second member of the first specific binding pair, immobilized on a first solid support; (e) denaturing the reaction product of step (d) not bound to the first solid support; (f) contacting the product of step
  • the invention features a method for detecting the presence or absence of a polymo ⁇ hic restriction site in a nucleic acid, involving the steps of: (a) amplifying the nucleic acid by PCR using a first and a second primer flanking the polymo ⁇ hic restriction site, the first primer being tagged with the first member of a first specific binding pair, the second primer being tagged with a detectable label; (b) digesting the reaction product of step (a) with the restriction endonuclease corresponding to the polymo ⁇ hic restriction site; (c) contacting the reaction product of step (b) with the second member of the first specific binding pair, immobilized on a first solid support; (d) denaturing the reaction product from step (c) not bound to the first solid support; (e) contacting the product of step (d) with an oligonucleotide complementary to a sequence in the strand of the product of step (d) containing the detectable label, the sequence being between the
  • the invention features a method for detecting the presence or absence of a polymo ⁇ hic restriction site in a nucleic acid, involving the steps of: (a) amplifying the nucleic acid by PCR using a first and a second primer flanking the polymo ⁇ hic restriction site, the first primer being tagged with a detectable label, the second primer being unlabeled; (b) digesting the reaction product of step (a) with the restriction endonuclease corresponding to the polymo ⁇ hic restriction site; (c) annealing and ligating to the single-stranded ends generated in the reaction of step (b) a first oligonucleotide tagged with the first member of a first specific binding pair; (d) contacting the reaction product of step (c) with the second member of the first specific binding pair, immobilized on a first solid support; (e) denaturing the reaction product of step (d) not bound to the first solid support; (f) contacting the product of step
  • the invention features a method for detecting the presence or absence of a polymo ⁇ hic restriction site in a nucleic acid, involving the steps of: (a) amplifying the nucleic acid by PCR using a first and a second primer flanking the polymo ⁇ hic restriction site, the first primer containing a first sequence not complementary to or present in the nucleic acid, the second primer containing a second sequence not complementary to or present in the nucleic acid; (b) amplifying the product of step (a) by PCR using a third and a fourth primer, the third primer containing the first sequence or a sequence complementary to the first sequence, the third primer being tagged with the first member of a specific binding pair, the fourth primer containing the second sequence or a sequence complementary to the second sequence, the fourth primer being tagged with a detectable label; (c) digesting the product of step (b) with the restriction endonuclease corresponding to the polymo ⁇ hic restriction site; (d)
  • the invention features a method for detecting the presence or absence of a polymo ⁇ hic restriction site in a nucleic acid, involving the steps of: (a) amplifying the nucleic acid by PCR using a first and a second primer flanking the polymo ⁇ hic restriction site, the first primer containing a first sequence not complementary to or present in the nucleic acid, the second primer containing a second sequence not complementary to or present in the nucleic acid; (b) amplifying the product of step (a) by PCR using a third and a fourth primer, the third primer containing the first sequence or a sequence complementary to the first sequence, the third primer being tagged with the first member of a specific binding pair, the fourth primer containing the second sequence or a sequence complementary to the second sequence, the fourth primer being tagged with a detectable label; (c) digesting the PCR product of step (b) with the restriction endonuclease corresponding to the polymo ⁇ hic restriction site; (d)
  • the invention features a method for detecting the presence or absence of a polymo ⁇ hic restriction site in a nucleic acid, involving the steps of: (a) amplifying the nucleic acid by PCR using a first and a second primer flanking the polymo ⁇ hic restriction site, the first primer containing a first sequence not complementary to or present in the nucleic acid; (b) amplifying the product of step
  • step (a) by PCR using a third primer and the second primer, the third primer containing the first sequence, the third primer being tagged with a detectable label;
  • step (c) digesting a portion of the reaction of step (b) with the restriction endonuclease corresponding to the polymo ⁇ hic restriction site, while leaving another portion of the reaction of step (b) undigested;
  • step (d) denaturing the digested and undigested portions from step (c);
  • step (e) contacting the product of step (d) with an oligonucleotide complementary to a second sequence in the strand of the product of step (d) containing the detectable label, the second sequence being between the polymo ⁇ hic restriction site and the sequence complementary to the second primer, the oligonucleotide being tagged with a first member of a specific binding pair;
  • step (e) contacting the reaction product of step (e) with the second member of the specific binding pair, immobilized on a solid support; and (
  • the invention features a method for detecting the presence or absence of a polymo ⁇ hic restriction site in a nucleic acid, involving the steps of:
  • step (a) amplifying the nucleic acid by PCR using a first and a second primer flanking the polymo ⁇ hic restriction site, the first primer containing a first sequence not complementary to or present in the nucleic acid, the second primer containing a second sequence not complementary to or present in the nucleic acid;
  • step (b) amplifying the product of step (a) by PCR using a third and a fourth primer, the third primer containing the first sequence or a sequence complementary to the first sequence, the third primer being tagged with a first detectable label, the fourth primer containing the second sequence or a sequence complementary to the second sequence, the fourth primer being tagged with a second detectable label;
  • step (c) digesting the reaction product of step (b) with the restriction endonuclease corresponding to the polymo ⁇ hic restriction site;
  • step (e) contacting the product of step (d) with a first and a second oligonucle
  • the invention features a method for detecting the presence or absence of a polymo ⁇ hic restriction site in a nucleic acid, involving the steps of: (a) amplifying the nucleic acid by PCR using a first and a second primer flanking the polymo ⁇ hic restriction site, the first primer containing a first sequence not complementary to or present in the nucleic acid, the second primer containing a second sequence not complementary to or present in the nucleic acid; (b) amplifying the product of step (a) by PCR using a third and a fourth primer, the third primer containing the first sequence or a sequence complementary to the first sequence, the third primer being tagged with a first detectable label, the fourth primer containing the second sequence or a sequence complementary to the second sequence, the fourth primer being tagged with a second detectable label; (c) digesting the reaction product of step (b) with the restriction endonuclease corresponding to the polymo ⁇ hic restriction site; (d) denaturing the
  • the invention features a method for detecting the presence or absence of a polymo ⁇ hic restriction site in a nucleic acid, involving the steps of: (a) amplifying the nucleic acid by PCR using a first and a second primer flanking the polymo ⁇ hic restriction site, the first primer containing a first sequence not complementary to or present in the nucleic acid, the second primer containing a second sequence not complementary to or present in the nucleic acid; (b) amplifying the product of step (a) by PCR using a third and a fourth primer, the third primer containing the first sequence or a sequence complementary to the first sequence, the third primer being tagged with a first detectable label, the fourth primer containing the second sequence or a sequence complementary to the second sequence, the fourth primer being tagged with a second detectable label; (c) digesting the reaction product of step (b) with the restriction endonuclease corresponding to the polymo ⁇ hic restriction site; (d) denaturing the
  • the invention features a method for detecting the presence or absence of a polymo ⁇ hic restriction site in a nucleic acid, involving (a) amplifying the nucleic acid by PCR using a first and second primer flanking the polymo ⁇ hic restriction site, the first primer containing a first sequence not complementary to or present in the nucleic acid, the second primer containing a second sequence not complementary to or present in the nucleic acid; (b) amplifying the product of step (a) by PCR using a third and a fourth primer, the third primer containing the first sequence or a sequence complementary to the first sequence, the third primer being tagged with a first detectable label, the fourth primer containing the second sequence or a sequence complementary to the second sequence, the fourth primer being tagged with a second detectable label; (c) digesting the reaction product of step (b) with the restriction endonuclease corresponding to the polymo ⁇ hic restriction site; (d) denaturing the reaction product of step (
  • the invention features a method for detecting the presence or absence of a polymo ⁇ hic restriction site in a nucleic acid, involving the steps of (a) amplifying the nucleic acid by PCR using a first and a second primer flanking the polymo ⁇ hic restriction site, the first primer containing a first sequence not complementary to or present in the nucleic acid, the second primer containing a second sequence not complementary to or present in the nucleic acid; (b) amplifying the product of step (a) by PCR using a third and a fourth primer, the third primer containing the first sequence or a sequence complementary to the first sequence, the third primer being tagged with the first member of a first specific binding pair, the fourth primer containing the second sequence or a sequence complementary to the second sequence, the fourth primer being tagged with a detectable label; (c) digesting the reaction product of step (b) with the restriction endonuclease corresponding to the polymo ⁇ hic restriction site; (d) contacting the
  • the invention features a method for detecting the presence or absence of a polymo ⁇ hic restriction site in a nucleic acid, involving the steps of: (a) amplifying the nucleic acid by PCR using a first and a second primer flanking the polymo ⁇ hic restriction site, the first primer containing a first sequence not complementary to or present in the nucleic acid; (b) amplifying the product of step (a) by PCR using a third primer and the second primer, the third primer containing the first sequence, the third primer being tagged with a detectable label; (c) digesting the reaction product of step (b) with the restriction endonuclease corresponding to the polymo ⁇ hic restriction site; (d) annealing and ligating to the single-stranded ends generated in the reaction of step (c) a first oligonucleotide tagged with the first member of a first specific binding pair; (e) contacting the reaction product of step (d) with the second member of the
  • the invention features a method for detecting the presence or absence of a polymo ⁇ hic restriction site in a nucleic acid, involving the steps of: (a) amplifying the nucleic acid by PCR using a first and a second primer flanking the polymo ⁇ hic restriction site, the first primer containing a first sequence not complementary to or present in the nucleic acid, the second primer containing a second sequence not complementary to or present in the nucleic acid; (b) amplifying the product of step (a) by PCR using a third and a fourth primer, the third primer containing the first sequence or a sequence complementary to the first sequence, the third primer being tagged with the first member of a first specific binding pair, the fourth primer containing the second sequence or a sequence complementary to the second sequence, the fourth primer being tagged with a detectable label; (c) digesting the reaction product of step (b) with the restriction endonuclease corresponding to the polymo ⁇ hic restriction site; (d)
  • step (e) denaturing the reaction product from step (d) not bound to the first solid support
  • step (f) contacting the product of step (e) with an oligonucleotide complementary to a third sequence in the strand of the product of step (e) containing the detectable label, the third sequence being between the polymo ⁇ hic restriction site and the sequence corresponding to or complementary to the second primer, the oligonucleotide being immobilized on a second solid support; and (g) determining the ratio of the level of the detectable label bound to the first solid support to the level of the detectable label bound to the second solid support, a ratio of 0:1 being an indication of a homozygote containing the polymo ⁇ hic restriction site, in a case where the total amount of the reaction product from step (d) not bound to the first solid support was used in steps (e) and (f); a ratio of 1 :0 being an indication of a homozygote lacking the polymo ⁇ hic restriction site, in a case where the total amount of the reaction product from step (d) not bound to the first solid support was used in steps
  • the invention features a method for detecting the presence or absence of a polymo ⁇ hic restriction site in a nucleic acid, the method involving the steps of: (a) amplifying the nucleic acid by PCR using a first and a second primer flanking the polymo ⁇ hic restriction site, the first primer containing a first sequence not complementary to or present in the nucleic acid; (b) amplifying the product of step (a) by PCR using a third primer and the second primer, the third primer containing the first sequence, the third primer being tagged with a detectable label; (c) digesting the reaction product of step (b) with the restriction endonuclease corresponding to the polymo ⁇ hic restriction site; (d) annealing and ligating to the single- stranded ends generated in the reaction of step (c) a first oligonucleotide tagged with the first member of a first specific binding pair; (e) contacting the reaction product of step (d)
  • the invention features a kit for detecting the presence or absence of a polymo ⁇ hic restriction site in a nucleic acid, the kit containing one or more sets of a first and a second primer flanking the polymo ⁇ hic restriction site, the first primer being tagged with the first member of a specific binding pair, the second primer being tagged with a detectable label.
  • the kit further contains the second member of the specific binding pair, immobilized on a solid support.
  • the kit further contains an oligonucleotide complementary to the single-stranded ends generated in the nucleic acid upon digestion of the nucleic acid with the restriction enzyme corresponding to the polymo ⁇ hic restriction site, the oligonucleotide being tagged with a second detectable label.
  • the invention features a kit for detecting the presence or absence of a polymo ⁇ hic restriction site in a nucleic acid, the kit containing: (a) a first and a second primer flanking the polymo ⁇ hic restriction site, the first primer being tagged with a detectable label, the second primer being unlabeled; (b) an oligonucleotide complementary to a sequence in the strand of the nucleic acid complementary to the second primer, the sequence being between the polymo ⁇ hic restriction site and the sequence complementary to the second primer, the oligonucleotide being tagged with a first member of a specific binding pair; and (c) the second member of the specific binding pair, immobilized on a solid support.
  • the invention features a kit for detecting the presence or absence of a polymo ⁇ hic restriction site in a nucleic acid, the kit containing: (a) a first and a second primer flanking the polymo ⁇ hic restriction site, the first primer being tagged with a first detectable label, the second primer being tagged with a second detectable label; (b) a first oligonucleotide, the first oligonucleotide being complementary to a first sequence in the strand of the nucleic acid complementary to the second primer, the first sequence being between the polymo ⁇ hic restriction site and either the sequence corresponding to the first primer or the sequence complementary to the second primer, the first oligonucleotide being tagged with the first member of a first specific binding pair; (c) a second oligonucleotide, the second oligonucleotide being complementary to a second sequence in the strand of the nucleic acid complementary to the first primer, the second sequence
  • the invention features a kit for detecting the presence or absence of a polymo ⁇ hic restriction site in a nucleic acid, the kit containing: (a) a first and a second primer flanking the polymo ⁇ hic restriction site, the first primer being tagged with the first member of a first specific binding pair, the second primer being tagged with a detectable label; (b) the second member of the first specific binding pair, immobilized on a first solid support; (c) an oligonucleotide complementary to a first sequence in the strand of the nucleic acid containing the sequence corresponding to the second primer, the first sequence being between the polymo ⁇ hic restriction site and the sequence corresponding to the second primer, the oligonucleotide being tagged with the first member of a second specific binding pair; and (d) the second member of the second specific binding pair, immobilized on a second solid support.
  • the invention features a kit for detecting the presence or absence of a polymo ⁇ hic restriction site in a nucleic acid, the kit containing: (a) a first and a second primer flanking the polymo ⁇ hic restriction site, the first primer being tagged with a detectable label, the second primer being unlabeled; (b) a first oligonucleotide complementary to the single-stranded ends generated in the nucleic acid upon digestion of the nucleic acid with the restriction enzyme corresponding to the polymo ⁇ hic restriction site, the oligonucleotide being tagged with the first member of a first specific binding pair; (c) the second member of the first specific binding pair, immobilized on a first solid support; (d) a second oligonucleotide complementary to a sequence in the strand of the nucleic acid complementary to the second primer, the sequence being between the polymo ⁇ hic restriction site and either the sequence corresponding to the first primer or the sequence
  • the invention features a kit for detecting the presence or absence of a polymo ⁇ hic restriction site in a nucleic acid, the kit containing: (a) a first and a second primer flanking the polymo ⁇ hic restriction site, the first primer being tagged with the first member of a first specific binding pair, the second primer being tagged with a detectable label; (b) the second member of the first specific binding pair, immobilized on a first solid support; and (c) an oligonucleotide complementary to a first sequence in the strand of the nucleic acid containing the sequence corresponding to the second primer, the first sequence being between the polymo ⁇ hic restriction site and the sequence corresponding to the second primer, the oligonucleotide being immobilized on a second solid support.
  • the invention features a kit for detecting the presence or absence of a polymo ⁇ hic restriction site in a nucleic acid, the kit containing: (a) a first and a second primer flanking the polymo ⁇ hic restriction site, the first primer being tagged with a detectable label, the second primer being unlabeled; (b) a first oligonucleotide complementary to the single-stranded ends generated in the nucleic acid upon digestion of the nucleic acid with the restriction enzyme corresponding to the polymo ⁇ hic restriction site, the oligonucleotide being tagged with the first member of a first specific binding pair; (c) the second member of the first specific binding pair, immobilized on a first solid support; and (d) a second oligonucleotide complementary to a sequence in the strand of the nucleic acid complementary to the second primer, the sequence being between the polymo ⁇ hic restriction site and either the sequence corresponding to the first primer or the
  • the invention features a kit for detecting the presence or absence of a polymo ⁇ hic restriction site in a nucleic acid, the kit containing: (a) a first and a second primer flanking the polymo ⁇ hic restriction site, the first primer containing a first sequence not complementary to or present in the nucleic acid, the second primer containing a second sequence not complementary to or present in the nucleic acid; (b) a third and a fourth primer, the third primer containing the first sequence or a sequence complementary to the first sequence, the third primer being tagged with the first member of a specific binding pair, the fourth primer containing the second sequence or a sequence complementary to the second sequence, the fourth primer being tagged with a detectable label.
  • the kit further contains the second member of the specific binding pair, immobilized on a solid support.
  • the kit further contains an oligonucleotide complementary to the single-stranded ends generated in the nucleic acid upon digestion of the nucleic acid with the restriction enzyme corresponding to the polymo ⁇ hic restriction site, the oligonucleotide being tagged with a second detectable label.
  • the invention features a kit for detecting the presence or absence of a polymo ⁇ hic restriction site in a nucleic acid, the kit containing: (a) a first and a second primer flanking the polymo ⁇ hic restriction site, the first primer containing a first sequence not complementary to or present in the nucleic acid; (b) a third primer containing the first sequence, the third primer being tagged with a detectable label; (c) an oligonucleotide complementary to a second sequence in the strand of the nucleic acid containing the sequence complementary to the second primer, the second sequence being between the polymo ⁇ hic restriction site and the sequence complementary to the second primer, the oligonucleotide being tagged with a first member of a specific binding pair; and (d) the second member of the specific binding pair, immobilized on a solid support.
  • the invention features a kit for detecting the presence or absence of a polymo ⁇ hic restriction site in a nucleic acid, the kit containing: (a) a first and a second primer flanking the polymo ⁇ hic restriction site, the first primer containing a first sequence not complementary to or present in the nucleic acid, the second primer containing a second sequence not complementary to or present in the nucleic acid; (b) a third and a fourth primer, the third primer containing the first sequence or a sequence complementary to the first sequence, the third primer being tagged with a first detectable label, the fourth primer containing the second sequence or a sequence complementary to the second sequence, the fourth primer being tagged with a second detectable label; (c) a first oligonucleotide, the first oligonucleotide being complementary to a third sequence in the strand of the nucleic acid complementary to the second primer, the third sequence being between the polymo ⁇ hic restriction site and either the sequence complementary to the
  • the invention features a kit for detecting the presence or absence of a polymo ⁇ hic restriction site in a nucleic acid, the kit containing: (a) a first and a second primer flanking the polymo ⁇ hic restriction site, the first primer containing a first sequence not complementary to or present in the nucleic acid, the second primer containing a second sequence not complementary to or present in the nucleic acid; (b) a third and a fourth primer, the third primer containing the first sequence or a sequence complementary to the first sequence, the third primer being tagged with the first member of a first specific binding pair, the fourth primer containing the second sequence or a sequence complementary to the second sequence, the fourth primer being tagged with a detectable label; (c) the second member of the first specific binding pair, immobilized on a first solid support; (d) an oligonucleotide complementary to a third sequence in the strand of the nucleic acid corresponding to the second primer, the sequence being between the polymo
  • the invention features a kit for detecting the presence or absence of a polymo ⁇ hic restriction site in a nucleic acid, the kit containing: (a) a first and a second primer flanking the polymo ⁇ hic restriction site, the first primer containing a first sequence not complementary to or present in the nucleic acid; (b) a third primer containing the first sequence, the third primer being tagged with a detectable label; (c) a first oligonucleotide complementary to the single-stranded ends generated in the nucleic acid upon digestion of the nucleic acid with the restriction enzyme corresponding to the polymo ⁇ hic restriction site, the oligonucleotide being tagged with the first member of a first specific binding pair; (d) the second member of the first specific binding pair, immobilized on a first solid support; (e) a second oligonucleotide complementary to a second sequence in the strand of the nucleic acid corresponding to the first primer, the kit containing: (a)
  • the invention features a kit for detecting the presence or absence of a polymo ⁇ hic restriction site in a nucleic acid, the kit containing: (a) a first and a second primer flanking the polymo ⁇ hic restriction site, the first primer containing a first sequence not complementary to or present in the nucleic acid, the second primer containing a second sequence not complementary to or present in the nucleic acid; (b) a third and a fourth primer, the third primer containing the first sequence or a sequence complementary to the first sequence, the third primer being tagged with the first member of a first specific binding pair, the fourth primer containing the second sequence or a sequence complementary to the second sequence, the fourth primer being tagged with a detectable label; (c) the second member of the first specific binding pair, immobilized on a first solid support; and (d) an oligonucleotide complementary to a third sequence in the strand of the nucleic acid corresponding to the second primer, the third sequence being between
  • the invention features a kit for detecting the presence or absence of a polymo ⁇ hic restriction site in a nucleic acid, the kit containing: (a) a first and a second primer flanking the polymo ⁇ hic restriction site, the first primer containing a first sequence not complementary to or present in the nucleic acid; (b) a third primer containing the first sequence, the third primer being tagged with a detectable label; (c) a first oligonucleotide complementary to the single-stranded ends generated in the nucleic acid upon digestion of the nucleic acid with the restriction enzyme corresponding to the polymo ⁇ hic restriction site, the oligonucleotide being tagged with the first member of a first specific binding pair; (d) the second member of the first specific binding pair, immobilized on a first solid support; and (e) a second oligonucleotide complementary to a second sequence in the strand of the nucleic acid corresponding to the first
  • the invention features a method for detecting the presence or absence of a polymo ⁇ hic restriction site in a nucleic acid, involving the steps of: (a) amplifying the nucleic acid by PCR using a first and a second primer flanking the polymo ⁇ hic restriction site, whereby the resultant PCR product is of a defined size readily resolved by gel electrophoresis; (b) digesting the PCR product of step (a) with the restriction endonuclease corresponding to the polymo ⁇ hic restriction site, the digestion products being differentially sized; (c) separating the reaction products of step (b) by gel electrophoresis; and (d) detecting the separated reaction products, the presence of only uncleaved products being an indication of a homozygote lacking the polymo ⁇ hic restriction site, the presence of only cleaved products being an indication of a homozygote containing the polymo ⁇ hic restriction site, and the presence of both clea
  • the invention features a kit for detecting the presence or absence of a polymo ⁇ hic restriction site in a nucleic acid, the kit containing: a first and a second primer flanking the polymo ⁇ hic restriction site and capable of generating a PCR product of a defined size that is readily resolved by gel electrophoresis.
  • the first and/or the second primers are detectably labeled.
  • the PCR product generated is between 100 and 1000 base pairs in length.
  • the invention features a method for identifying a polymo ⁇ hic restriction site in a nucleic acid, involving the steps of: (a) digesting DNA isolated from a first sample with a first restriction endonuclease; (b) ligating to each of the ends of the reaction products of step (a) a first adaptor; (c) digesting the products of step (b) with a second restriction endonuclease; (d) ligating to each of the ends of the reaction products generated in step (c) a second adaptor; (e) amplifying the reaction products of step (d) by PCR using a first primer complementary to the first adaptor and a second primer complementary to the second adaptor, the second primer being tagged with a first member of a specific binding pair (preferably, biotin); (f) in a separate set of reactions, digesting DNA isolated from a second sample with the first restriction endonuclease; (g) ligating to each of the ends of the ends of the
  • DNA adaptor and a third DNA adaptor, the first and third DNA adaptors having regions complementary to the ends generated by a first restriction endonuclease ends but differing in overall sequence and the second DNA adaptor having a region complementary to the ends generated by a second restriction endonuclease, the second restriction endonuclease site corresponding to the polymo ⁇ hic restriction site; and (b) a first primer, a second primer, and a third primer, the first primer being complementary to the first DNA adaptor, the second primer being complementary to the second DNA adaptor and being tagged with a first member of a specific binding pair, and the third primer being complementary to the third DNA adaptor.
  • This kit may further contain the second member of the specific binding pair immobilized on a solid support.
  • the invention features a method for detecting the presence or absence of a polymo ⁇ hic restriction site in a nucleic acid.
  • the nucleic acid is amplified by PCR using a first and a second primer flanking the polymo ⁇ hic restriction site.
  • the first primer is tagged with a detectable label
  • the amplifying generates a PCR product containing a first strand tagged with the detectable label and an unlabeled second strand.
  • the PCR product is then digested with a restriction endonuclease corresponding to the polymo ⁇ hic restriction site to generate a digestion product, which is denatured to generate a denatured product.
  • the denatured product is contacted with a first probe, which contains a sequence that hybridizes to a first sequence in the first strand that is between the polymo ⁇ hic restriction site and the sequence in the first strand that is complementary to the second primer.
  • the first probe is also immobilized on a first binding element.
  • the first binding element is monitored for the presence of the detectable label, and detection of the detectable label on the first binding element indicates the absence of the polymo ⁇ hic restriction site in the nucleic acid, and a failure to detect the detectable label on the first binding element indicates the presence of the polymo ⁇ hic restriction site in the nucleic acid.
  • the first binding element is a region on a solid support, such as a glass plate or a microchip.
  • This method can also include contacting the denatured product with a second, a third, or a fourth probe.
  • the second probe which is immobilized on a second binding element, contains a sequence that hybridizes to a second sequence in the first strand that is between the polymo ⁇ hic restriction site and the sequence in the first strand that corresponds to the first primer.
  • the third probe which is immobilized on a third binding element, contains a sequence that hybridizes to a third sequence in the second strand that is between the polymo ⁇ hic restriction site and the sequence in the second strand corresponding to the second primer.
  • the fourth probe which is immobilized on a fourth binding element, contains a sequence that hybridizes to a fourth sequence in the second strand that is between the polymo ⁇ hic restriction site and the sequence in the second strand that is complementary to the first primer.
  • the second, third, or fourth binding element can be monitored for the presence of the detectable label.
  • the first, second, third, and fourth binding elements can each be distinct regions on a solid support, such as a glass plate or a microchip.
  • the invention features a method for detecting the presence or absence of a polymo ⁇ hic restriction site in a nucleic acid.
  • the nucleic acid is amplified by PCR using a first and a second primer flanking the polymo ⁇ hic restriction site.
  • the first primer is tagged with a first detectable label and the second primer is tagged with a second detectable label.
  • the amplifying generates a PCR product containing a first strand tagged with the first detectable label and a second strand tagged with the second detectable label.
  • the first and second detectable labels can be identical or distinct.
  • the PCR product is treated with a restriction endonuclease corresponding to the polymo ⁇ hic restriction site to generate a digestion product, which is denatured to generate a denatured product.
  • the denatured product is contacted with a first and a second probe.
  • the first probe which is immobilized on a first binding element, contains a sequence that hybridizes to a first sequence in the first strand that is between the polymo ⁇ hic restriction site and the sequence in the first strand that is complementary to the second primer.
  • the second probe which is immobilized on a second binding element, contains a sequence that hybridizes to a second sequence in the second strand that is between the polymo ⁇ hic restriction site and the sequence in the second strand that is complementary to the first primer.
  • the first and second binding elements can each be distinct regions on a solid support, such as a glass plate or a microchip.
  • the first binding element is monitored for the presence of the first detectable label and the second binding element is monitored for the presence of the second detectable label. Detection of the first detectable label on the first binding element and detection of the second detectable label on the second binding element indicates the absence of the polymo ⁇ hic restriction site in the nucleic acid, and a failure to detect the first detectable label on the first binding element and a failure to detect the second detectable label on the second binding element indicates the presence of the polymo ⁇ hic restriction site in the nucleic acid.
  • This method can also include contacting the denatured product with a third or a fourth probe.
  • the third probe which is immobilized on a third binding element, contains a sequence that hybridizes to a third sequence in the first strand that is between the polymo ⁇ hic restriction site and the sequence in the first strand corresponding to the first primer.
  • the fourth probe which is immobilized on a fourth binding element, contains a sequence that hybridizes to a fourth sequence in the second strand that is between the polymo ⁇ hic restriction site and the sequence in the second strand corresponding to the second primer.
  • the third or fourth binding element can be monitored for the presence of the first or second detectable label.
  • the first, second, third, and fourth binding elements can be each distinct regions on a solid support, such as a glass plate or a microchip.
  • the invention features a method for detecting the presence or absence of a polymo ⁇ hic restriction site in a nucleic acid.
  • the nucleic acid is amplified by PCR using a first and a second primer flanking the polymo ⁇ hic restriction site. The amplifying generates a PCR product containing a first strand containing a sequence corresponding to the first primer and a second strand containing a sequence corresponding to the second primer.
  • the PCR product is treated with a restriction endonuclease corresponding to the polymo ⁇ hic restriction site to generate a digestion product, which is denatured to generate a denatured product.
  • the denatured product is contacted with an oligonucleotide to generate a first reaction product.
  • the oligonucleotide contains a 3' portion that hybridizes to a first region in the first strand that flanks the polymo ⁇ hic restriction site on the side of the polymo ⁇ hic restriction site containing a sequence corresponding to the first primer.
  • the oligonucleotide is blocked so that it cannot serve as a primer for DNA polymerase.
  • the oligonucleotide contains a
  • the first reaction product is treated with a DNA polymerase to extend the unblocked, primed 3' end to generate a second reaction product, which is amplified by
  • the first and the second detectable labels in this method can be identical or distinct.
  • the second PCR product is denatured to generate a second denatured product, which is contacted with a first and a second probe.
  • the first probe which is immobilized on a first binding element, contains a sequence that hybridizes to a first sequence in the second strand that is between the polymo ⁇ hic restriction site and the sequence in the second strand that is complementary to the first primer.
  • the second probe which is immobilized on a second binding element, contains a sequence that hybridizes to a second sequence in the first strand that is between the polymo ⁇ hic restriction site and the sequence in the first strand that is complementary to the second primer.
  • the first and second binding elements can each be distinct regions on a solid support, such as a glass support or a microchip.
  • the first binding element is monitored for the presence of the second detectable label and the second binding element is monitored for the presence of the first detectable label. Detection of the second detectable label on the first binding element and detection of the first detectable label on the second binding element indicates a heterozygote, detection of the second detectable label on the first binding element and a failure to detect the first detectable label on the second binding element indicates a homozygote containing the polymo ⁇ hic restriction site, and detection of the first detectable label on the second binding element and a failure to detect the second detectable label on the first binding element indicates a homozygote lacking the polymo ⁇ hic restriction site.
  • This method can also include contacting the second denatured product with a third or a fourth probe.
  • the third probe which is immobilized on a third binding element, contains a sequence that hybridizes to a third sequence in the first strand that is between the polymo ⁇ hic restriction site and the sequence in the first strand corresponding to the first primer.
  • the fourth probe which is immobilized on a fourth binding element, contains a sequence that hybridizes to a fourth sequence in the second strand that is between the polymo ⁇ hic restriction site and the sequence in the second strand corresponding to the second primer.
  • the third or fourth binding element can be monitored for the presence of the first or second detectable label.
  • the first, second, third, and fourth binding elements can each be distinct regions on a solid support, such as a glass plate or a microchip.
  • the invention features a kit for detecting the presence or absence of a polymo ⁇ hic restriction site in a nucleic acid.
  • the kit can contain one or more sets of a first and a second primer flanking the polymo ⁇ hic restriction site.
  • the first primer is tagged with a detectable label, so that amplifying the nucleic acid by PCR with the first and second primers generates a PCR product containing a first strand tagged with the detectable label and a second strand.
  • the kit also can include one or more first probes, each of which containing a sequence that hybridizes to a first sequence in the first strand that is between the polymo ⁇ hic restriction site and the sequence in the first strand that is complementary to the second primer.
  • Each of the first probes is immobilized on a first binding element.
  • This kit can also contain one or more sets of a second, third, or fourth probe.
  • Each of the second probes, which is immobilized on a second binding element contains a sequence that hybridizes to a second sequence in the first strand that is between the polymo ⁇ hic restriction site and the sequence in the first strand that corresponds to the first primer.
  • Each of the third probes, which is immobilized on a third binding element contains a sequence that hybridizes to a third sequence in the second strand that is between the polymo ⁇ hic restriction site and the sequence in the second strand co ⁇ esponding to the second primer.
  • Each of the fourth probes which is immobilized on a fourth binding element, contains a sequence that hybridizes to a fourth sequence in the second strand that is between the polymo ⁇ hic restriction site and the sequence in the second strand that is complementary to the first primer.
  • the first binding element in this kit can be a region on a solid support, such as a glass plate or a microchip.
  • the first, second, third, and fourth binding elements can each be distinct regions on a solid support, such as a glass plate or a microchip.
  • One or more second primers in this kit can each contain a second detectable label.
  • the kit can further contain a second probe, which is immobilized on a second binding element, and contains a sequence that hybridizes to a second sequence in the second strand that is between the polymo ⁇ hic restriction site and the sequence in the second strand that is complementary to the first primer.
  • the kit can also contain one or more sets of a third or a fourth probe.
  • Each of the third probes, which are immobilized on a third binding element contain a sequence that hybridizes to a third sequence in the first strand that is between the polymo ⁇ hic restriction site and the sequence in the first strand co ⁇ esponding to the first primer.
  • each of the fourth probes which are immobilized on a fourth binding element, contain a sequence that hybridizes to a fourth sequence in the second strand that is between the polymo ⁇ hic restriction site and the sequence in the second strand corresponding to the second primer.
  • the kit can further contain one or more second probes, which are immobilized on a second binding element, that each contain a sequence that hybridizes to a second sequence in the first strand that is between the polymo ⁇ hic restriction site and the sequence in the first strand that co ⁇ esponds to the first primer.
  • the invention features a kit for detecting the presence or absence of a polymo ⁇ hic restriction site in a nucleic acid.
  • This kit can contain one or more sets of a first and a second PCR primer flanking the polymo ⁇ hic restriction site.
  • the first primer can be tagged with a first detectable label, so that amplifying the nucleic acid by PCR using the first and second primers generates a PCR product containing a first strand tagged with the first detectable label and a second strand.
  • the first primer can be unlabeled.
  • This kit can also include one or more oligonucleotides containing a 3' portion that hybridizes to a first region in the first strand that flanks the polymo ⁇ hic restriction site on the side of the polymo ⁇ hic restriction site containing a sequence co ⁇ esponding to the first primer.
  • the oligonucleotide is blocked so that it cannot serve as a primer for DNA polymerase.
  • the oligonucleotide contains a 5' portion that does not hybridize to a second region in the first strand that flanks the polymo ⁇ hic restriction site on the side of the polymo ⁇ hic restriction site containing a sequence that is complementary to the second primer.
  • This kit can also include one or more third primers, each of which that hybridizes to a sequence that is complementary to the 5' portion of the oligonucleotide. The third primer can be tagged with a second detectable label.
  • kits are also included in this kit.
  • Each of the first probes which are immobilized on a first solid support, contain a sequence that hybridizes to a first sequence in the second strand that is between the polymo ⁇ hic restriction site and the sequence in the second strand that is complementary to the first primer.
  • Each of the second probes which are immobilized on a second solid support, contain a sequence that hybridizes to a second sequence in the first strand that is between the polymo ⁇ hic restriction site and the sequence in the first strand that is complementary to the second primer.
  • the first and the second detectable labels in this kit can be distinct or identical.
  • the first and second binding elements can each be distinct regions on a solid support, such as a glass support or a microchip.
  • This kit can further contain one or more sets of a third or a fourth probe.
  • Each of the third probes, which are immobilized on a third binding element contain a sequence that hybridizes to a third sequence in the first strand that is between the polymo ⁇ hic restriction site and the sequence in the first strand co ⁇ esponding to the first primer.
  • Each of the fourth probes, which are immobilized on a fourth binding element contain a sequence that hybridizes to a fourth sequence in the second strand that is between the polymo ⁇ hic restriction site and the sequence in the second strand co ⁇ esponding to the second primer.
  • the one or more sets of the first, second, third, and fourth binding elements in this kit can each be distinct regions on a solid support, such as a glass plate or a microchip.
  • the detectable label is selected from the group consisting of digoxigenin, fluorescent labels (e.g., fluorescein and rhodamine), enzymes (e.g., horseradish peroxidase and alkaline phosphatase), biotin (which can be detected by anti-biotin specific antibodies or enzyme-conjugated avidin derivatives), radioactive labels (e.g., 2 P and 125 I), colorimetric reagents, and chemiluminescent reagents.
  • fluorescent labels e.g., fluorescein and rhodamine
  • enzymes e.g., horseradish peroxidase and alkaline phosphatase
  • biotin which can be detected by anti-biotin specific antibodies or enzyme-conjugated avidin derivatives
  • radioactive labels e.g., 2 P and 125 I
  • colorimetric reagents e.g., 2 P and 125 I
  • chemiluminescent reagents
  • the specific binding pairs are selected from the group consisting of avidin-biotin, streptavidin- biotin, hybridizing nucleic acid pairs, interacting protein pairs, antibody-antigen pairs, reagents containing chemically reactive groups (e.g., reactive amino groups), and nucleic acid sequence-nucleic acid binding protein pairs.
  • the solid supports used in the methods of the invention are selected from the group consisting of agarose, acrylamide, and polystyrene beads; polystyrene microtiter plates (for use in, e.g., ELISA); silicon, gold, or glass chips (e.g., microchips), slides, or plates; and nylon and nitrocellulose membranes (for use in, e.g., dot or slot blot assays).
  • heterozygote refers to an individual with different alleles at co ⁇ esponding loci on homologous chromosomes. Accordingly, the term “heterozygous,” as used herein, describes an individual or strain having different allelic genes at one or more paired loci on homologous chromosomes.
  • homozygote refers to an individual with the same allele at co ⁇ esponding loci on homologous chromosomes. Accordingly, the term “homozygous,” as used herein, describes an individual or a strain having identical allelic genes at one or more paired loci on homologous chromosomes.
  • co ⁇ esponding as used herein to describe a nucleic acid strand, e.g., a nucleic acid strand co ⁇ esponding to a particular PCR primer, is meant to indicate that the strand contains the sequence of the particular PCR primer.
  • the term When used to compare a polymo ⁇ hic restriction site to a restriction endonuclease site, the term again indicates that the two sequences are identical.
  • An advantage of certain detection methods of the present invention over many other methods used to detect genetic polymo ⁇ hisms is that gel electrophoresis is not required in the analysis.
  • the methods of the present invention are readily adaptable for automation, allowing large numbers of samples to be processed in relatively short periods of time, at lower costs.
  • detection of an a ⁇ ay of samples is carried out simultaneously on a solid support, such as a glass slide or a microchip, further reducing processing time and cost. Detection of signals on a ⁇ ays can be carried out quantitatively or qualitatively.
  • Those detection methods of the invention utilizing gel electrophoresis are also advantageous because they provide a rapid and inexpensive approach to the identification of large numbers of PCR-based genetic and RFLP markers.
  • the method of the invention useful for cloning genetic polymo ⁇ hisms also represents an improvement over cu ⁇ ent methods. Because the process of selecting out a tagged (e.g., biotinylated) DNA having a polymo ⁇ hism involves a specific hybridization step, candidate DNA from any source may be utilized. For example, DNA from random clones, CDNA libraries, YAC libraries, or any other DNA collection may be screened; pure preparations of genomic DNAs are not required. Moreover, like other methods of the invention, this cloning procedure is rapid and inexpensive.
  • All methods of the invention are useful in clinical diagnostic testing, genomic mapping, positional cloning of genes defined by mutation (such as those that cause inherited disease in humans or resistance to pathogens in crop plants), DNA finge ⁇ rinting (e.g., for forensic analysis and paternity testing), crop and livestock breeding programs, and other related applications.
  • the detection methods of the invention are useful for bacterial typing utilizing known conserved polymo ⁇ hic sequences diagnostic of the bacterium.
  • this approach is useful for distinguishing one bacterium from another (e.g., for the identification of Salmonella in a food sample); polymo ⁇ hism-containing sequences prefe ⁇ ed for this approach include those present in conserved ribosomal RNA genes.
  • this approach is useful for screening bacteria (e.g., clinical isolates) for antibiotic resistance; in this case, known polymo ⁇ hic restriction sites within the antibiotic resistance marker are utilized.
  • the instant methods of bacterial typing decrease false positive results frequently obtained using cu ⁇ ent PCR-based techniques.
  • Fig. 1 is a schematic of a RFLP detection method involving the use of a first PCR primer tagged with a detectable label (X) and a second PCR primer tagged with the first member of a specific binding pair (Y).
  • the products are digested with the restriction endonuclease (R) co ⁇ esponding to the polymo ⁇ hic restriction site, contacted with the second member of the specific binding pair immobilized on a solid support, and the level of the detectable label (X) bound to the solid support is determined.
  • R restriction endonuclease
  • Fig. 2 is a schematic of a RFLP detection method involving the use of a first PCR primer tagged with a first detectable label (X) and a second PCR primer tagged with the first member of a specific binding pair (Y).
  • the products are digested with the restriction endonuclease (R) co ⁇ esponding to the polymo ⁇ hic restriction site, and an oligonucleotide tagged with a second detectable label (Z) is annealed and ligated to the single-stranded ends generated in the digestion.
  • R restriction endonuclease
  • Z second detectable label
  • Fig. 3 is a schematic of a RFLP detection method involving the use of a first
  • PI detectable label
  • P2 second unlabeled PCR primer
  • R restriction endonuclease
  • Both digested and undigested reactions are then denatured and contacted with an oligonucleotide tagged with the first member of a specific binding pair, the oligonucleotide being complementary to the PI strand and located to the right of the restriction site (R) near to, but not overlapping, primer P2.
  • the reactions are then contacted with the second member of the specific binding pair immobilized on a solid support, and the levels of PI in digested versus undigested reactions are compared.
  • Fig. 4 is a schematic of a RFLP detection method involving the use of a first PCR primer tagged with a first detectable label (PI) and a second PCR primer tagged with a second detectable label (P2).
  • the products are digested with the restriction endonuclease (R) co ⁇ esponding to the polymo ⁇ hic restriction site, denatured, and contacted with a first oligonucleotide complementary to the PI strand and located to the right of the restriction site (R) near to, but not overlapping primer P2, and a second oligonucleotide complementary to the P2 strand and located to the right of the restriction site (R) near to, but not overlapping the sequence complementary to primer P2.
  • R restriction endonuclease
  • Both the first and second oligonucleotides are tagged with the first member of a specific binding pair (Y).
  • the reactions are then contacted with the second member of the specific binding pair immobilized on a solid support, and the ratio of PI to P2 bound to the solid support is determined.
  • Fig. 5 is a schematic of a RFLP detection method involving the use of a first
  • PCR primer tagged with a detectable label X
  • Y first specific binding pair
  • the products are digested with the restriction enzyme (R) co ⁇ esponding to the polymo ⁇ hic restriction site, and are contacted with the second member of the first specific binding pair immobilized on a first solid support.
  • Fig. 6 is a schematic of a RFLP detection method involving the use of a first unlabeled PCR primer and a second PCR primer tagged with a detectable label (X).
  • the products are digested with the restriction enzyme (R) co ⁇ esponding to the polymo ⁇ hic restriction site, and contacted with an oligonucleotide complementary to the single-stranded ends generated in the digestion, the oligonucleotide being tagged with the first member of a specific binding pair.
  • R restriction enzyme
  • the products are then contacted with the second member of the first specific binding pair, bound to a first solid support.
  • the filtrate is then bound to a solid support with the anchor sequence (or contacted with an oligonucleotide complementary to the X strand, the oligonucleotide being tagged with the first member of a second specific binding pair, and then contacted with the second member of the second specific binding pair immobilized on a second solid support), and the levels of the detectable label bound to the first solid support and the anchor sequence (or second solid support) are determined.
  • Fig. 7 is a schematic of a RFLP detection method involving the use of PCR primers flanking the polymo ⁇ hic restriction site (the "Alu I" site). Following PCR amplification, the reaction products are digested with the restriction endonuclease co ⁇ esponding to the polymo ⁇ hic restriction site (Alu I), and the fragments are run on an agarose gel. The separated fragments are detected as an indication of the presence or absence of the polymo ⁇ hic marker.
  • Fig. 8 is a schematic of a typical gel analysis according the method described in
  • Figs. 9A-9E are schematics of a method for cloning polymo ⁇ hic restriction fragments.
  • Fig. 10 is a schematic of a non-gel based method for detection of CAPS markers.
  • Fig. 11 is a schematic of parallel processing of 100 CAPS markers on a microchip containing an a ⁇ ay of oligonucleotide probes.
  • Fig. 12 is a schematic of a method for detecting a cleaved end of a CAPS marker.
  • Fig. 13 is a schematic of a method for distinguishing heterozygous CAPS alleles from homozygous CAPS alleles, involving the use of the method for detecting a cleaved end of a CAPS marker shown in Fig. 12.
  • the present invention provides several methods for detecting Cleaved Amplified Polymo ⁇ hic Sequences (CAPS; Konieczny et al., The Plant Journal 4(2):403-410, 1993).
  • CAPS Cleaved Amplified Polymo ⁇ hic Sequences
  • a nucleic acid containing a polymo ⁇ hic restriction site is amplified using primers flanking the restriction site. The resulting
  • PCR product is digested with the restriction endonuclease co ⁇ esponding to the polymo ⁇ hic restriction site, and the digested products are analyzed by gel electrophoresis.
  • the detection methods of the present invention vary greatly from one another in detail, however they share three central features: (1) the nucleic acid containing the polymo ⁇ hic restriction site is amplified by PCR using differently labeled primers flanking the polymo ⁇ hic restriction site, (2) the resulting PCR product is digested with the restriction endonuclease co ⁇ esponding to the polymo ⁇ hic restriction site (which will cleave the DNA of some individuals but not cleave the DNA of others, depending on the presence of the polymo ⁇ hism), and (3) the resulting digestion products are analyzed by detection of the labels they contain, and/or labels attached to oligonucleotides complementary to the digestion products, in order to determine the identity of the polymo ⁇ hic restriction site.
  • the methods of the invention allow rapid and efficient analyses of a large number of samples.
  • the nucleic acid sample containing the polymo ⁇ hic restriction site being analyzed can be obtained from any source, e.g., a tissue homogenate, blood, amniotic fluid, chorionic villus samples, and a bacterial culture; and can be obtained from these sources using standard methods. Only a minute quantity of nucleic acid is required, and can be DNA or RNA (in the case of RNA, a reverse transcription step is required before the PCR step).
  • PCR methods used in the methods of the present invention are ca ⁇ ied out using standard methods (see, e.g., Ausubel et al., Cu ⁇ ent Protocols in Molecular Biology, John Wiley and Sons, New York, 1989; Erlich, PCR Technology, Stockton Press, New York, 1989; Innis et al., PCR Protocols: A Guide to Methods and Applications, Academic Press, Harcourt Brace Javanovich, New York, 1990; Sambrook et al., Molecular Cloning: A Laboratory Manual, Cold Spring Harbor Laboratory Press, Cold Spring Harbor, New York, 1989). Restriction enzyme digestion is also carried out by standard methods using any of a number of available restriction endonucleases (see, e.g., Ausubel et al., supra; New England Biolabs,
  • the primers and oligonucleotides used in the methods of the present invention are preferably DNA, and can be synthesized using standard techniques and, when appropriate, detectably labeled using standard methods (Ausubel et al., supra).
  • Detectable labels that can be used to tag the primers and oligonucleotides used in the methods of the invention include, but are not limited to, digoxigenin, fluorescent labels (e.g., fluorescein and rhodamine), enzymes (e.g., horseradish peroxidase and alkaline phosphatase), biotin (which can be detected by anti-biotin specific antibodies or enzyme-conjugated avidin derivatives), radioactive labels (e.g., 32 P and 125 I), colorimetric reagents, and chemiluminescent reagents.
  • the labels used in the methods of the invention are detected using standard methods.
  • the specific binding pairs useful in the methods of the invention include, but are not limited to, avidin-biotin, streptavidin-biotin, hybridizing nucleic acid pairs, interacting protein pairs, antibody-antigen pairs, reagents containing chemically reactive groups (e.g., reactive amino groups), and nucleic acid sequence-nucleic acid binding protein pairs.
  • the solid supports useful in the methods of the invention include, but are not limited to, agarose, acrylamide, and polystyrene beads; polystyrene microtiter plates (for use in, e.g., ELISA); and nylon and nitrocellulose membranes (for use in, e.g., dot or slot blot assays).
  • Some methods of the invention employ solid supports containing a ⁇ ays of nucleic acid probes.
  • solid supports made of materials such as glass (e.g., glass plates), silicon or silicon-glass (e.g., microchips), or gold (e.g., gold plates) can be used.
  • Methods for attaching nucleic acid probes to precise regions on such solid surfaces e.g., photolithographic methods, are well known in the art, and can be used to make solid supports for use in the invention.
  • kits which contain the reagents required for carrying out the assays.
  • the kits can contain reagents for carrying out the analysis of a single polymo ⁇ hic restriction site (for use in, e.g., diagnostic methods) or multiple polymo ⁇ hic restriction sites (for use in, e.g., genomic mapping).
  • multiple sets of the appropriate primers and oligonucleotides are provided in the kit.
  • the kits may contain the enzymes used in the methods, and the reagents for detecting the labels, e.g., the substrates for enzyme labels, etc.
  • the kits can also contain solid substrates for used in carrying out the method of the invention.
  • the kits can contain solid substrates, such as glass plates or silicon or glass microchips, containing a ⁇ ays of nucleic acid probes.
  • the invention provides methods and kits for generating and detecting the presence or absence of a polymo ⁇ hic restriction site in a nucleic acid.
  • Examples I-IX and XII-XIV describe eight variations of the methods of the invention.
  • Example X describes a prefe ⁇ ed use for the methods of the invention.
  • Example XI describes a prefe ⁇ ed method for cloning polymo ⁇ hic restriction fragments.
  • the following examples are meant to illustrate, but not limit, the methods of the present invention. Other suitable modifications and adaptations of the variety of conditions and parameters of molecular biology which are obvious to those skilled in the art are within the spirit and scope of the present invention.
  • the nucleic acid containing the polymo ⁇ hism is amplified by PCR using a first and a second primer flanking the polymo ⁇ hic restriction site, the first primer being tagged with the first member of a specific binding pair, the second primer being tagged with a detectable label.
  • the resulting PCR product is digested with the restriction endonuclease co ⁇ esponding to the polymo ⁇ hic restriction site and the digested products are contacted with the second member of the specific binding pair, immobilized on a solid support. The level of the detectable label bound to the solid support is then measured.
  • the presence of the detectable label bound to the solid support is an indication of the absence of the polymo ⁇ hic restriction site in the nucleic acid, while the absence of the detectable label bound to the solid support is an indication of the presence of the polymo ⁇ hic restriction site in the nucleic acid.
  • An embodiment of this method is shown in Fig. 1.
  • Example II This method is identical to that described in Example I, with the added step of annealing and ligating to the single-stranded ends generated in the digestion reaction, an oligonucleotide tagged with a second detectable label. After applying the reaction to the second member of the specific binding pair, the levels of both the first and the second detectable labels bound to the solid support are determined.
  • the presence of only the first detectable label bound to the solid support is an indication of a homozygote lacking the polymo ⁇ hic restriction site
  • the presence of only the second detectable label bound to the solid support is an indication of a homozygote containing the polymo ⁇ hic restriction site
  • the presence of both the first and the second detectable labels bound to the solid support is an indication of a heterozygote.
  • An embodiment of this method is shown in Fig. 2.
  • the cleaved ends of the CAPS products can be labeled by using a method described in further detail below in Example XIV. Briefly, in this method, the denatured product is contacted with an oligonucleotide to generate a first reaction product.
  • the oligonucleotide contains a 3' portion that hybridizes to a first region in the first strand that flanks the polymo ⁇ hic restriction site on the side of the polymorphic restriction site containing a sequence co ⁇ esponding to the first primer.
  • the 3' end of the oligonucleotide is blocked by, e.g., a di-deoxynucleotide, so that it cannot serve as a primer for DNA polymerase.
  • the oligonucleotide contains a 5' portion that does not hybridize to a second region in the first strand that flanks the polymorphic restriction site on the side of the polymo ⁇ hic restriction site containing a sequence that is complementary to the second primer.
  • the use of such an oligonucleotide to label a cleaved end of a CAPS marker is illustrated in Fig. 12. This method can also be applied to the CAPS detection techniques of, for example, Examples VI and VIII.
  • the nucleic acid is amplified using a first and a second primer flanking the polymo ⁇ hic restriction site, the first primer being tagged with a detectable label, the second primer being unlabeled.
  • a portion of the PCR reaction is digested with the restriction endonuclease co ⁇ esponding to the polymo ⁇ hic restriction site, while another portion is left undigested. Both the digested and undigested portions are then denatured, and contacted with an oligonucleotide tagged with the first member of a specific binding pair.
  • the oligonucleotide is complementary to a sequence in the strand of the PCR product containing the detectable label, the sequence being between the polymo ⁇ hic restriction site and the sequence complementary to the second primer.
  • the reaction is then contacted with the second member of the specific binding pair, immobilized on a solid support, and the ratio of the levels of the detectable label bound to the solid support between undigested and digested samples is determined.
  • a ratio of 1 :0 between equivalent portions of undigested and digested samples is an indication of a homozygote containing the polymo ⁇ hic restriction site
  • a ratio of 1: 1 between equivalent portions of undigested and digested samples is an indication of a homozygote lacking the polymo ⁇ hic restriction site
  • a ratio of 2: 1 between equivalent portions of undigested and digested samples is an indication of a heterozygote. While the sample volumes used for detection and comparison need not be equivalent, the appropriate calculations must be carried out to account for this adjustment prior to determining the ratio of detectable label in digested and undigested samples. An embodiment of this method is shown in Fig. 3.
  • the nucleic acid is amplified by PCR using a first primer and a second primer flanking the polymo ⁇ hic restriction site, the first primer being tagged with a first detectable label, and the second primer being tagged with a second detectable label.
  • the PCR product is digested with the restriction endonuclease co ⁇ esponding to the polymo ⁇ hic restriction site, denatured, and contacting with a first and a second oligonucleotide.
  • the first oligonucleotide is complementary to a first sequence in the strand of the PCR product containing the first detectable label, the first sequence being between the polymo ⁇ hic restriction site and the sequence co ⁇ esponding to the first primer.
  • the first oligonucleotide is tagged with the first member of a first specific binding pair.
  • the second oligonucleotide is complementary to a second sequence in the strand of the PCR product containing the second detectable label.
  • the second sequence is on the same side of the polymo ⁇ hic restriction site as the first sequence, and is not contained within, or complementary to, either the first or the second primer.
  • the second oligonucleotide is tagged with the first member of a second specific binding pair.
  • a first portion of the reaction is then contacted with the second member of the first specific binding pair, immobilized on a first solid support, while a second portion of the reaction is contacted with the second member of the second specific binding pair, immobilized on a second solid support.
  • the ratio of the levels of the first and second detectable labels bound to the first and second solid supports is then determined.
  • a ratio of 1 :0 between equivalent amounts of the first and second portions is an indication of a homozygote containing the polymo ⁇ hic restriction site
  • a ratio of 1 :1 between equivalent amounts of the first and second portions is an indication of a homozygote lacking the polymo ⁇ hic restriction site
  • a ratio of 2: 1 between equivalent amounts of the first and second portions is an indication of a heterozygote.
  • the ratios differ, as follows.
  • the ratio of the levels of the first and second detectable labels bound to the first and second solid supports is 0: 1 between equivalent amounts of the first and second portions in the case of a homozygote containing the polymo ⁇ hic restriction site.
  • the ratio is 1 : 1 between equivalent amounts of the first and second portions in the case of a homozygote lacking the polymo ⁇ hic restriction site, and the ratio is 1 :2 between equivalent amounts of the first and second portions in the case of a heterozygote.
  • the nucleic acid is amplified by PCR using a first and a second primer flanking the polymo ⁇ hic restriction site, the first primer being tagged with the first member of a first specific binding pair, the second primer being tagged with a detectable label.
  • the PCR product is digested with the restriction endonuclease co ⁇ esponding to the polymo ⁇ hic restriction site, and the reaction is then contacted with the second member of the first specific binding pair, immobilized on a first solid support.
  • the material not bound to the first solid support is denatured and contacted with an oligonucleotide complementary to a sequence in the strand of the PCR product containing the detectable label.
  • the sequence is between the polymo ⁇ hic restriction site and the sequence co ⁇ esponding to the second primer, and the oligonucleotide is tagged with the first member of a second specific binding pair.
  • the reaction is then contacted with the second member of the second specific binding pair, immobilized on a second solid support, and the ratio of the level of the detectable label bound to the first solid support compared to the level of the detectable label bound to the second solid support is determined.
  • a ratio of 0: 1 is an indication of a homozygote containing the polymo ⁇ hic restriction site
  • a ratio of 1 :0 is an indication of a homozygote lacking the polymo ⁇ hic restriction site
  • a ratio of 1 : 1 is an indication of a heterozygote.
  • the nucleic acid is amplified by PCR using a first and a second primer flanking the polymo ⁇ hic restriction site, the first primer being tagged with a detectable label, the second primer being unlabeled.
  • the PCR product is digested with the restriction endonuclease co ⁇ esponding to the polymo ⁇ hic restriction site, and a first oligonucleotide tagged with the first member of a first specific binding pair is annealed and ligated to the single-stranded ends generated in the digestion reaction.
  • the reaction is then contacted with the second member of the first specific binding pair, immobilized on a first solid support.
  • the material not bound to the first solid support is denatured, and contacted with a second oligonucleotide complementary to a sequence in the strand of the PCR product containing the detectable label, the sequence being between the polymo ⁇ hic restriction site and either the sequence co ⁇ esponding to the first primer or the sequence complementary to the second primer.
  • the second oligonucleotide is tagged with the first member of a second specific binding pair.
  • the reaction is then contacted with the second member of the second specific binding pair, immobilized on a second solid support, and the ratio of the level of the detectable label bound to the first solid support compared to the level of the detectable label bound to the second solid support is determined.
  • a ratio of 1 :0 is an indication of a homozygote containing the polymo ⁇ hic restriction site
  • a ratio of 0:1 is an indication of a homozygote lacking the polymo ⁇ hic restriction site
  • a ratio of 1 : 1 is an indication of a heterozygote.
  • the nucleic acid is amplified by PCR using a first and a second primer flanking the polymo ⁇ hic restriction site, the first primer being tagged with the first member of a first specific binding pair, the second primer being tagged with a detectable label.
  • the PCR product is digested with the restriction endonuclease co ⁇ esponding to the polymo ⁇ hic restriction site, and contacted with the second member of the first specific binding pair, immobilized on a first solid support.
  • the material not bound to the first solid support is denatured and contacted with an oligonucleotide complementary to a sequence in the strand of the PCR product containing the detectable label.
  • the sequence is between the polymo ⁇ hic restriction site and the sequence co ⁇ esponding to the second primer, and the oligonucleotide is immobilized on a second solid support (e.g., a nylon or nitrocellulose membrane).
  • the ratio of the level of detectable label bound to the first solid support to the level of detectable label bound to the second solid support is then determined.
  • a ratio of 0: 1 is an indication of a homozygote containing the polymo ⁇ hic restriction site
  • a ratio of 1 :0 is an indication of a homozygote lacking the polymo ⁇ hic restriction site
  • a ratio of 1 : 1 is an indication of a heterozygote.
  • the nucleic acid is amplified by PCR using a first and a second primer flanking the polymo ⁇ hic restriction site, the first primer being tagged with a detectable label, the second primer being unlabeled.
  • the PCR product is digested with the restriction endonuclease co ⁇ esponding to the polymo ⁇ hic restriction site, and a first oligonucleotide tagged with the first member of a first specific binding pair is annealed and ligated to the single-stranded ends generated in the digestion reaction.
  • the reaction is contacted with the second member of the first specific binding pair, immobilized on a first solid support.
  • the material not bound to the first solid support is denatured, and contacted with a second oligonucleotide complementary to a sequence in the strand of the PCR product containing the detectable label.
  • the sequence is between the polymo ⁇ hic restriction site and either the sequence co ⁇ esponding to the first primer or the sequence complementary to the second primer, and the second oligonucleotide is immobilized on a second solid support (e.g., a nylon or nitrocellulose membrane).
  • the ratio of the level of the detectable label bound to the first solid support to the level of the detectable label bound to the second solid support is then determined.
  • a ratio of 1 :0 is an indication of a homozygote containing the polymo ⁇ hic restriction site
  • a ratio of 0: 1 is an indication of a homozygote lacking the polymo ⁇ hic restriction site
  • a ratio of 1 : 1 is an indication of a heterozygote.
  • PCR primers containing nucleic acid tags on their 5' ends can also be used in the methods of the invention. These primers can be used in pairs, or in combination with un-tagged primers, in the initial cycles of PCR, followed by the addition of a "universal primer(s)" complementary to the nucleic acid tags in the first primers, and contain detectable labels (e.g., biotin, fluorescent, or ELISA tags).
  • detectable labels e.g., biotin, fluorescent, or ELISA tags.
  • the use of nucleic acid tagged primers in the early rounds of PCR is a cost-effective measure, as only one set of primers, the universal primers, which can be used in the analysis of many different polymorphic sites, need to be detectably labeled.
  • the sets of primers specific for individual polymo ⁇ hic restriction sites do not have to be tagged with detectable labels, but rather need only to be complementary to the universal primers in their 5* ends.
  • the nucleic acid is amplified by PCR using a first and a second primer flanking the polymo ⁇ hic restriction site.
  • the PCR product is digested with the restriction endonuclease co ⁇ esponding to the polymo ⁇ hic restriction site, and, as shown in Fig. 7, the digestion products are run on a gel (preferably an agarose gel).
  • the first and second primers are preferably designed to generate a PCR product that is easily resolvable on an agarose gel (e.g., preferably larger than 100 base pairs and smaller than 1000 base pairs), and the polymo ⁇ hic restriction site is preferably located at an asymmetric position within the amplified fragment.
  • primers are designed to produce PCR amplified products of 300 base pairs, and cleavage at the RFLP site yields products of 200 base pairs and 100 base pairs.
  • sets of primer pairs are provided that detect a number of RFLP markers.
  • Each set of primers may be provided, for example, in one of the wells of a 96-well microtiter plate, and PCR reactions run independently. Following restriction digestion, the reaction products are transfe ⁇ ed to an agarose gel and separated by electrophoresis. A typical result of this method is shown in Fig. 8.
  • Detection of the amplified and cleaved products after electrophoretic separation can be ca ⁇ ied out by standard methods of DNA staining (e.g., ethidium bromide staining) or blotting (e.g., Southern blotting).
  • DNA staining e.g., ethidium bromide staining
  • blotting e.g., Southern blotting
  • one or both of the PCR primers can be detectably labeled, and the labels can be detected as described above.
  • RFLP subtraction provides a large number of polymo ⁇ hic genetic markers, while the methods of the present invention provide efficient methods for their analysis.
  • RFLP subtraction results in the purification of fragments that are present in one population (the tracer) but absent in another (the driver). Purification is achieved by removing all of the fragments in the tracer DNA that have counte ⁇ arts in the driver DNA using subtractive hybridization (Innis et al., PCR Protocols: A Guide to Methods and Applications, Academic Press, Harcourt Brace Javanovich, New York, 1990).
  • the tracer is a size fraction of digested DNA from one strain and the driver is the same size fraction from a polymo ⁇ hic strain.
  • the products obtained after removing the common sequences are RFLPs; they are sized tracer fragments whose driver counte ⁇ arts are not found in the same size fraction.
  • RFLP subtraction preparation of the driver and tracer, subtractive hybridization, and removal of non-hybridizing sequences from the tracer.
  • genomic DNA from two different strains is digested with a restriction endonuclease, and the ends of the restriction fragments from each strain are capped with different oligonucleotide adapters.
  • the low molecular weight fragments are then purified from a slice of an agarose gel and amplified using one of the adapter strands as a PCR primer.
  • a biotinylated primer can be used to amplify the driver so that driver DNA can be removed following the subtractive hybridizations by binding to avidin coated beads.
  • Figure 9 shows a prefe ⁇ ed method for cloning polymo ⁇ hic restriction fragments.
  • the object of this method is to clone restriction fragments from organism B (generated by restriction endonuclease A) that do not contain cleavage sites for restriction endonuclease B, and which correspond to restriction fragments in organism A (generated by restriction endonuclease A) that do contain at least one restriction site for restriction endonuclease B.
  • These polymo ⁇ hic restriction fragments are useful as CAPS markers for the detection methods described above.
  • Fig. 9A genomic DNA isolated from polymo ⁇ hic individuals A and B is separately digested with restriction enzyme A, which preferably leaves so-called sticky ends.
  • restriction enzyme A which preferably leaves so-called sticky ends.
  • a different oligonucleotide adaptor (#3) is ligated to the restriction fragments from individual B.
  • Fig. 9B the restriction fragments from Fig. 9A are cleaved with restriction endonuclease B, which again preferably leaves sticky ends.
  • an oligonucleotide adaptor (#2), with complementary sticky ends for enzyme B, is ligated to the restriction fragments generated by cleavage with enzyme B.
  • the DNA fragments from individual A are amplified using the PCR with an oligonucleotide primer complementary to adaptor #1 and with a biotinylated oligonucleotide primer complementary to adaptor #2.
  • Fig. 9D the amplified products originating from individual A are mixed with the non-amplified fragments of Fig. 9B from individual B.
  • the mixed DNA fragments are then heat denatured, annealed, and adsorbed onto an avidin-coated solid support (e.g., beads).
  • the avidin coated support containing the adsorbed fragments is thoroughly washed.
  • the adsorbed fragments may be eluted, re-amplified with the same primers as above, adsorbed onto a fresh avidin-containing support, and thoroughly washed. This step can be repeated as many times as is necessary or desired.
  • the fragments adsorbed to the avidin-coated beads are eluted and amplified using PCR with primers complementary to adaptor #3.
  • the amplified products should co ⁇ espond to the desired restriction fragments described above.
  • amplified fragments are cloned and then tested individually using the Southern DNA blot hybridization method for their ability to display the desired RFLP.
  • Example XII the nucleic acid is amplified by PCR using a first and a second primer flanking the polymo ⁇ hic restriction site, with the first primer being tagged with a detectable label.
  • the amplification generates a PCR product containing a first strand tagged with the detectable label and a second, unlabeled strand.
  • the PCR product is digested with the restriction endonuclease co ⁇ esponding to the polymo ⁇ hic restriction site and the digestion product is denatured.
  • the denatured product is contacted with a first probe that (1) contains a sequence that hybridizes to a first sequence in the first strand of the PCR product, and (2) is immobilized on a first binding element.
  • the first sequence is between the polymo ⁇ hic restriction site and the sequence in the first strand that is complementary to the second primer.
  • the first binding element is monitored for the presence of the detectable label.
  • this method can employ the use of a second, a third, or a fourth probe.
  • the second probe contains a sequence that hybridizes to a second sequence which is in the first strand and is between the polymo ⁇ hic restriction site and the sequence in the first strand that co ⁇ esponds to the first primer.
  • the third probe contains a sequence that hybridizes to a third sequence which is in the second strand and is between the polymo ⁇ hic restriction site and the sequence in the second strand co ⁇ esponding to the second primer.
  • the fourth probe contains a sequence that hybridizes to a fourth sequence which is in the second strand and is between the polymo ⁇ hic restriction site and the sequence in the second strand that is complementary to the first primer.
  • the second, third, and fourth probes are immobilized on a second, third, and fourth binding element, respectively.
  • the second binding element can be monitored for the presence of the detectable label as a positive control, while the third or fourth binding elements can be monitored for the presence of the detectable label as negative controls.
  • the first, second, third, and fourth binding elements in this and in other methods of the invention, can be present on a solid support having similar sets of binding elements for testing different nucleic acids (see, for example, Fig. 1 1).
  • binding elements for example, the first, second, third, and fourth binding elements, used in this method of the invention can be present as distinct regions on a single solid support.
  • they can be specific sets of nucleic acids bound to distinct regions on a glass plate or on a microchip, such as a glass, silicon, or glass- silicon microchip (see above).
  • a nucleic acid is amplified by PCR using a first and a second primer flanking the polymo ⁇ hic restriction site.
  • the first primer is tagged with a first detectable label and the second primer is tagged with a second detectable label.
  • the amplification thus generates a PCR product containing a first strand tagged with the first detectable label and a second strand tagged with the second detectable label.
  • the first and second labels can be identical or distinct.
  • the PCR product is treated with a restriction endonuclease co ⁇ esponding to the polymo ⁇ hic restriction site to generate a digestion product, which is denatured to generate a denatured product.
  • the denatured product is contacted with a first and a second probe.
  • the first probe which is immobilized on a first binding element, contains a sequence that hybridizes to a first sequence in the first strand that is between the polymo ⁇ hic restriction site and the sequence in the first strand that is complementary to the second primer.
  • the second probe which is immobilized on a second binding element, contains a sequence that hybridizes to a second sequence in the second strand that is between the polymo ⁇ hic restriction site and the sequence in the second strand that is complementary to the first primer.
  • the first binding element is monitored for the presence of the first detectable label and the second binding element is monitored for the presence of the second detectable label. Detection of the first detectable label on the first binding element and detection of the second detectable label on the second binding element indicates the absence of the polymo ⁇ hic restriction site in the nucleic acid, while a failure to detect the first detectable label on the first binding element and a failure to detect the second detectable label on the second binding element indicates the presence of the polymo ⁇ hic restriction site in the nucleic acid.
  • this method can involve the use of a third and fourth probe.
  • the third probe which is immobilized on a third binding element, contains a sequence that hybridizes to a third sequence which is in the first strand and that is between the polymo ⁇ hic restriction site and the sequence in the first strand co ⁇ esponding to the first primer.
  • the fourth probe which is immobilized on a fourth binding element, contains a sequence that hybridizes to a fourth sequence which is in the second strand and that is between the polymo ⁇ hic restriction site and the sequence in the second strand co ⁇ esponding to the second primer.
  • the third or fourth binding elements can be monitored for the presence of the first or second detectable labels as controls.
  • the third binding element can be monitored for the presence of the first detectable label and the fourth binding element can be monitored for the presence of the second detectable label.
  • the first and second, or the first, second, third, and fourth binding elements can be present as distinct regions on a solid support, such as glass (e.g., a glass plate) or a microchip (e.g., a silicon or a silicon-glass microchip).
  • a solid support such as glass (e.g., a glass plate) or a microchip (e.g., a silicon or a silicon-glass microchip). Embodiments of this method are illustrated in Figs. 10 and 11.
  • the nucleic acid is amplified by PCR using a first and a second primer flanking the polymo ⁇ hic restriction site.
  • the amplification generates a PCR product containing a first strand containing a sequence co ⁇ esponding to the first primer and a second strand containing a sequence co ⁇ esponding to the second primer.
  • the PCR product is treated with a restriction endonuclease co ⁇ esponding to the polymo ⁇ hic restriction site to generate a digestion product, which is denatured to generate a denatured product.
  • the denatured product is contacted with an oligonucleotide to generate a first reaction product.
  • the oligonucleotide contains a 3' portion that hybridizes to a first region in the first strand that flanks the polymo ⁇ hic restriction site on the side of the polymo ⁇ hic restriction site containing a sequence co ⁇ esponding to the first primer.
  • the 3' end of the oligonucleotide is blocked by, e.g., a di-deoxynucleotide, so that it cannot serve as a primer for DNA polymerase.
  • the oligonucleotide contains a 5' portion that does not hybridize to a second region in the first strand that flanks the polymo ⁇ hic restriction site on the side of the polymo ⁇ hic restriction site containing a sequence that is complementary to the second primer.
  • the use of such an oligonucleotide to label a cleaved end of a CAPS marker is illustrated in Fig. 12.
  • the first reaction product is treated with a DNA polymerase to extend the unblocked, primed 3' end to generate a second reaction product, which is amplified by PCR using the first primer, tagged with a first detectable label, and a third primer, which hybridizes to a sequence that is complementary to the 5' portion of the oligonucleotide, to generate a second PCR product.
  • the third primer is tagged with a second detectable label.
  • the first and second detectable labels can be identical or distinct.
  • the second PCR product is denatured to generate a second denatured product, which is contacted with a first and a second probe.
  • the first probe which is immobilized on a first binding element, contains a sequence that hybridizes to a first sequence in the second strand that is between the polymo ⁇ hic restriction site and the sequence in the second strand that is complementary to the first primer.
  • the second probe which is immobilized on a second binding element, contains a sequence that hybridizes to a second sequence in the first strand that is between the polymo ⁇ hic restriction site and the sequence in the first strand that is complementary to the second primer.
  • the first binding element is monitored for the presence of the second detectable label and the second binding element is monitored for the presence of the first detectable label. Detection of the second detectable label on the first binding element and detection of the first detectable label on the second binding element indicates a heterozygote, detection of the second detectable label on the first binding element and a failure to detect the first detectable label on the second binding element indicates a homozygote containing the polymo ⁇ hic restriction site, and detection of the first detectable label on the second binding element and a failure to detect the second detectable label on the first binding element indicates a homozygote lacking the polymo ⁇ hic restriction site.
  • this method can employ a third or a fourth probe.
  • the third probe which is immobilized on a third binding element, contains a sequence that hybridizes to a third sequence in the first strand that is between the polymo ⁇ hic restriction site and the sequence in the first strand co ⁇ esponding to the first primer.
  • the fourth probe which is immobilized on a fourth binding element, contains a sequence that hybridizes to a fourth sequence in the second strand that is between the polymo ⁇ hic restriction site and the sequence in the second strand co ⁇ esponding to the second primer.
  • the third or fourth binding elements can be monitored for the presence of the first or second detectable labels as controls.
  • the third binding element can be monitored for the presence of the first detectable label.
  • the first and second, or the first, second, third, and fourth binding elements can be present as distinct regions on a solid support, such as a glass (e.g., a glass plate) or silicon (e.g., a microchip) support.
  • a solid support such as a glass (e.g., a glass plate) or silicon (e.g., a microchip) support. This embodiment is illustrated in Fig. 13.
  • oligonucleotides as described above provides several advantages. For example, because there can be a significant amount of overlap between the oligonucleotide and the cleaved product, highly stringent conditions can be used in the annealing reaction, leading to increased specificity.
  • the 5' end of the oligonucleotide can be the same for many CAPS markers, as it is by design not homologous to any amplified sequences co ⁇ esponding to a CAPS marker for an organism of interest.

Abstract

The invention features methods for detecting polymorphic restriction sites in nucleic acids and kits for carrying out these methods.

Description

CLEAVED AMPLIFIED RFLP DETECTION METHODS This invention was made with Government support under Contract No. GM 48707 awarded by the National Institutes of Health and Contract No. MCB-9406240 awarded by the National Science Foundation. The Government has certain rights in the invention.
Background of the Invention This invention relates to the generation and detection of genetic polymorphisms .
Genetic maps consisting primarily of restriction fragment length polymorphic (RFLP) markers are being constructed for many organisms, including man. Traditional approaches for detecting RFLPs involve Southern blot hybridization. Recently, techniques based on the polymerase chain reaction (PCR; Mullis et al., Methods Enzymol. 155:350-355, 1987) have been used in addition to, or in place of, traditional RFLP markers in genetic analysis (Cox et al., BioEssays 13:193-198, 1991). In contrast to traditional RFLP markers, PCR-generated markers can be scored using a small sample of DNA, without the use of radioactivity, and without the need for time-consuming DNA blotting procedures. One widely used PCR-based approach involves the use of single short PCR primers of arbitrary sequence called RAPD primers (for random amplified polymorphic DNA; Reiter et al., Proc. Natl. Acad. Sci. USA 89: 1477-1481 , 1992; Williams et al., Theoret. Appl. Genet. 82:489-498, 1991). A second category of PCR- based markers are called SSLPs (for simple sequence length polymorphism). The method employing SSLPs is based on amplification across tandem repeats of one or a few nucleotides known as "microsatellites." Microsatellites occur frequently and randomly in most eukaryotic genomes and display a high degree of polymorphism due to variation in the numbers of repeated units.
A third category of PCR-based markers are called AFLPs (for amplified fragment length polymoφhisms). In the method employing these markers, DNA from two polymoφhic strains are cleaved with one or two restriction endonucleases, and adapters are ligated to the ends of the cleaved fragments. The fragments are then amplified using primers complementary to the adapter(s). The primers contain short stretches of random nucleotides at their 3' ends, which result in limiting the number of amplified fragments generated.
Summary of the Invention We have developed novel PCR-based methods for detecting the presence or absence of a polymoφhic restriction site in a nucleic acid involving the use of differentially labeled PCR primers and oligonucleotides.
Accordingly, in one aspect, the invention features a method for detecting the presence or absence of a polymoφhic restriction site in a nucleic acid, involving the steps of (a) amplifying the nucleic acid by PCR using a first and a second primer flanking the polymoφhic restriction site, the first primer being tagged with the first member of a specific binding pair, the second primer being tagged with a detectable label; (b) digesting the PCR product of step (a) with the restriction endonuclease corresponding to the polymoφhic restriction site; (c) contacting the reaction product of step (b) with the second member of the specific binding pair, immobilized on a solid support; and (d) measuring the level of the detectable label bound to the solid support, the presence of the detectable label bound to the solid support being an indication of the absence of the polymoφhic restriction site in the nucleic acid.
In a second aspect, the invention features a method for detecting the presence or absence of a polymoφhic restriction site in a nucleic acid, involving the steps of: (a) amplifying the nucleic acid by PCR using a first and a second primer flanking the polymoφhic restriction site, the first primer being tagged with the first member of a specific binding pair, the second primer being tagged with a first detectable label; (b) digesting the PCR product of step (a) with the restriction endonuclease corresponding to the polymoφhic restriction site; (c) annealing and ligating to the single-stranded ends generated in the reaction of step (b) an oligonucleotide tagged with a second detectable label; (d) contacting the reaction product of step (c) with the second member of the specific binding pair, immobilized on a solid support; and (e) determining the levels of the first and second detectable labels bound to the solid support, the presence of only the first detectable label bound to the solid support being an indication of a homozygote lacking the polymoφhic restriction site, the presence of only the second detectable label bound to the solid support being an indication of a homozygote containing the polymoφhic restriction site, and the presence of both the first and second detectable labels bound to the solid support being an indication of a heterozygote.
In a third aspect, the invention features a method for detecting the presence or absence of a polymoφhic restriction site in a nucleic acid, the method involving the steps of: (a) amplifying the nucleic acid by PCR using a first and a second primer flanking the polymoφhic restriction site, the first primer being tagged with a detectable label, the second primer being unlabeled; (b) digesting a portion of the reaction of step (a) with the restriction endonuclease corresponding to the polymoφhic restriction site, while leaving another portion of the reaction of step (a) undigested; (c) denaturing the digested and undigested portions from step (b); (d) contacting the product of step (c) with an oligonucleotide complementary to a sequence in the strand of the product of step (c) containing the detectable label, the sequence being between the polymoφhic restriction and the sequence complementary to the second primer, the oligonucleotide being tagged with a first member of a specific binding pair; (e) contacting the reaction product of step (d) with the second member of the specific binding pair, immobilized on a solid support; and (f) determining the ratio of the levels of the detectable label bound to the solid support between undigested and digested samples, a ratio of 1 :0 between equivalent portions of the undigested and digested samples being an indication of a homozygote containing the polymoφhic restriction site, a ratio of 1 : 1 between equivalent portions of the undigested and digested samples being an indication of a homozygote lacking the polymoφhic restriction site, and a ratio of 2:1 between equivalent portions of the undigested and digested samples being an indication of a heterozygote. In a fourth aspect, the invention features a method for detecting the presence or absence of a polymoφhic restriction site in a nucleic acid, involving the steps of: (a) amplifying the nucleic acid by PCR using a first and a second primer flanking the polymoφhic restriction site, the first primer being tagged with a first detectable label, the second primer being tagged with a second detectable label; (b) digesting the reaction product of step (a) with the restriction endonuclease corresponding to the polymoφhic restriction site; (c) denaturing the reaction product of step (b); (d) contacting the product of step (c) with a first and a second oligonucleotide, the first oligonucleotide being complementary to a first sequence in the strand of the product of step (c) containing the first detectable label, the first sequence being between the polymoφhic restriction site and the sequence corresponding to the first primer, the first oligonucleotide being tagged with the first member of a first specific binding pair, the second oligonucleotide being complementary to a second sequence in the strand of the product of step (c) containing the second detectable label, the second sequence being on the same side of the polymoφhic restriction site as the first sequence, the second sequence not being contained within or being complementary to either of the first or second primers, the second oligonucleotide being tagged with the first member of a second specific binding pair; (e) contacting a first portion of the reaction product of step (d) with the second member of the first specific binding pair, immobilized on a first solid support; (f) contacting a second portion of the reaction product of step (d) with the second member of the second specific binding pair, immobilized on a second solid support; and (g) determining the ratio of the levels of the first and second detectable labels bound to the first and second solid supports, a ratio of 1 :0 between equivalent amounts of the first and second portions being an indication of a homozygote containing the polymoφhic restriction site, a ratio of 1 : 1 between equivalent amounts of the first and second portions being an indication of a homozygote lacking the polymoφhic restriction site, and a ratio of 2: 1 between equivalent amounts of the first and second portions being an indication of a heterozygote.
In a fifth aspect, the invention features a method for detecting the presence or absence of a polymoφhic restriction site in a nucleic acid, involving the steps of: (a) amplifying the nucleic acid by PCR using a first and a second primer flanking the polymoφhic restriction site, the first primer being tagged with a first detectable label, the second primer being tagged with a second detectable label; (b) digesting the reaction product of step (a) with the restriction endonuclease corresponding to the polymoφhic restriction site; (c) denaturing the reaction product of step (b); (d) contacting the product of step (c) with a first and a second oligonucleotide, the first oligonucleotide being complementary to a first sequence in the strand of the product of step (c) containing the first detectable label, the first sequence being between the polymoφhic restriction site and the sequence complementary to the second primer, the first oligonucleotide being tagged with the first member of a first specific binding pair, the second oligonucleotide being complementary to a second sequence in the strand of the product of step (c) containing the second detectable label, the second sequence being on the same side of the polymoφhic restriction site as the first sequence, the second sequence not being contained within or being complementary to either of the first or second primers, the second oligonucleotide being tagged with the first member of a second specific binding pair; (e) contacting a first portion of the reaction product of step (d) with the second member of the first specific binding pair, immobilized on a first solid support; (f) contacting a second portion of the reaction product of step (d) with the second member of the second specific binding pair, immobilized on a second solid support; and (g) determining the ratio of the levels of the first and second detectable labels bound to the first and second solid supports, a ratio of 0: 1 between equivalent amounts of the first and second portions being an indication of a homozygote containing the polymoφhic restriction site, a ratio of 1 : 1 between equivalent amounts of the first and second portions being an indication of a homozygote lacking the polymoφhic restriction site, and a ratio of 1 :2 between equivalent amounts of the first and second portions being an indication of a heterozygote.
In a sixth aspect, the invention method for detecting the presence or absence of a polymoφhic restriction site in a nucleic acid, involving the steps of: (a) amplifying the nucleic acid by PCR using a first and a second primer flanking the polymoφhic restriction site, the first primer being tagged with a first detectable label, the second primer being tagged with a second detectable label; (b) digesting the reaction product of step (a) with the restriction endonuclease corresponding to the polymoφhic restriction site; (c) denaturing the reaction product of step (b); (d) contacting the product of step (c) with a first and a second oligonucleotide, the first oligonucleotide being complementary to a first sequence in the strand of the product of step (c) containing the first detectable label, the first sequence being between the polymoφhic restriction site and the sequence corresponding to the first primer, the first oligonucleotide being tagged with the first member of a specific binding pair, the second oligonucleotide being complementary to a second sequence in the strand of the product of step (c) containing the second detectable label, the second sequence being on the same side of the polymoφhic restriction site as the first sequence, the second sequence not being contained within or being complementary to either of the first or second primers, the second oligonucleotide being tagged with the first member of the specific binding pair; (e) contacting the reaction product of step (d) with the second member of the specific binding pair, immobilized on a solid support; and
(f) determining the ratio of the levels of the first and second detectable labels bound to the solid support, a ratio of 1 :0 being an indication of a homozygote containing the polymoφhic restriction site, a ratio of 1 : 1 being an indication of a homozygote lacking the polymoφhic restriction site, and a ratio of 2:1 being an indication of a heterozygote.
In a seventh aspect, the invention features a method for detecting the presence or absence of a polymoφhic restriction site in a nucleic acid, involving the steps of: (a) amplifying the nucleic acid by PCR using a first and a second primer flanking the polymoφhic restriction site, the first primer being tagged with a first detectable label, the second primer being tagged with a second detectable label; (b) digesting the reaction product of step (a) with the restriction endonuclease corresponding to the polymoφhic restriction site; (c) denaturing the reaction product of step (b); (d) contacting the product of step (c) with a first and a second oligonucleotide, the first oligonucleotide being complementary to a first sequence in the strand of the product of step (c) containing the first detectable label, the first sequence being between the polymoφhic restriction site and the sequence complementary to the second primer, the first oligonucleotide being tagged with the first member of a specific binding pair, the second oligonucleotide being complementary to a second sequence in the strand of the product of step (c) containing the second detectable label, the second sequence being on the same side of the polymoφhic restriction site as the first sequence, the second sequence not being contained within or being complementary to either of the first or second primers, the second oligonucleotide being tagged with the first member of the specific binding pair; (e) contacting the reaction product of step (d) with the second member of the specific binding pair, immobilized on a solid support; and (f) determining the ratio of the levels of the first and second detectable labels bound to the solid support, a ratio of 0:1 being an indication of a homozygote containing the polymoφhic restriction site, a ratio of 1 : 1 being an indication of a homozygote lacking the polymoφhic restriction site, and a ratio of 1 :2 being an indication of a heterozygote.
In an eighth aspect, the invention features a method for detecting the presence or absence of a polymoφhic restriction site in a nucleic acid, involving the steps of: (a) amplifying the nucleic acid by PCR using a first and a second primer flanking the polymoφhic restriction site, the first primer being tagged with the first member of a first specific binding pair, the second primer being tagged with a detectable label; (b) digesting the reaction product of step (a) with the restriction endonuclease corresponding to the polymoφhic restriction site; (c) contacting the reaction product of step (b) with the second member of the first specific binding pair, immobilized on a first solid support; (d) denaturing the reaction product of step (c) not bound to the first solid support; (e) contacting the product of step (d) with an oligonucleotide complementary to a sequence in the strand of the product of step (d) containing the detectable label, the sequence being between the polymoφhic restriction site and the sequence corresponding to the second primer, the oligonucleotide being tagged with the first member of a second specific binding pair; (f) contacting the reaction product of step (e) with the second member of the second specific binding pair, immobilized on a second solid support; and (g) determining the ratio of the level of the detectable label bound to the first solid support to the level of the detectable label bound to the second solid support, a ratio of 0: 1 being an indication of a homozygote containing the polymoφhic restriction site, in a case where the total amount of the reaction product from step (c) not bound to the first solid support was used in steps (d), (e), and (f); a ratio of 1 :0 being an indication of a homozygote lacking the polymoφhic restriction site, in a case where the total amount of the reaction product from step (c) not bound to the first solid support was used in steps (d), (e), and (f); and a ratio of 1 : 1 being an indication of a heterozygote, in a case where the total amount of the reaction product from step (c) not bound to the first solid support was used in steps (d), (e), and (f).
In a ninth aspect, the invention features a method for detecting the presence or absence of a polymoφhic restriction site in a nucleic acid, involving the steps of: (a) amplifying the nucleic acid by PCR using a first and a second primer flanking the polymoφhic restriction site, the first primer being tagged with a detectable label, the second primer being unlabeled; (b) digesting the reaction product of step (a) with the restriction endonuclease corresponding to the polymoφhic restriction site; (c) annealing and ligating to the single-stranded ends generated in the reaction of step (b) a first oligonucleotide tagged with the first member of a first specific binding pair; (d) contacting the reaction product of step (c) with the second member of the first specific binding pair, immobilized on a first solid support; (e) denaturing the reaction product of step (d) not bound to the first solid support; (f) contacting the product of step (e) with a second oligonucleotide complementary to a sequence in the strand of the product of step (e) containing the detectable label, the sequence being between the polymoφhic restriction site and either the sequence corresponding to the first primer or the sequence complementary to the second primer, the second oligonucleotide being tagged with the first member of a second specific binding pair; (g) contacting the reaction product of step (f) with the second member of the second specific binding pair, immobilized on a second solid support; and (h) determining the ratio of the level of the detectable label bound to the first solid support to the level of the detectable label bound to the second solid support, a ratio of 1 :0 being an indication of a homozygote containing the polymoφhic restriction site, in a case where the total amount of the reaction product from step (d) not bound to the first solid support was used in steps (e), (f), and (g); a ratio of 0: 1 being an indication of a homozygote lacking the polymoφhic restriction site, in a case where the total amount of the reaction product from step (d) not bound to the first solid support was used in steps
(e), (f), and (g); and a ratio of 1 : 1 being an indication of a heterozygote; in a case where the total amount of the reaction product from step (d) not bound to the first solid support was used in steps (e), (f), and (g).
In a tenth aspect, the invention features a method for detecting the presence or absence of a polymoφhic restriction site in a nucleic acid, involving the steps of: (a) amplifying the nucleic acid by PCR using a first and a second primer flanking the polymoφhic restriction site, the first primer being tagged with the first member of a first specific binding pair, the second primer being tagged with a detectable label; (b) digesting the reaction product of step (a) with the restriction endonuclease corresponding to the polymoφhic restriction site; (c) contacting the reaction product of step (b) with the second member of the first specific binding pair, immobilized on a first solid support; (d) denaturing the reaction product from step (c) not bound to the first solid support; (e) contacting the product of step (d) with an oligonucleotide complementary to a sequence in the strand of the product of step (d) containing the detectable label, the sequence being between the polymoφhic restriction site and the sequence corresponding to the second primer, the oligonucleotide being immobilized on a second solid support; and (f) determining the ratio of the level of the detectable label bound to the first solid support to the level of the detectable label bound to the second solid support, a ratio of 0:1 being an indication of a homozygote containing the polymoφhic restriction site, in a case where the total amount of the reaction product from step (c) not bound to the first solid support was used in steps (d) and (e); a ratio of 1 :0 being an indication of a homozygote lacking the polymoφhic restriction site, in a case where the total amount of the reaction product from step (c) not bound to the first solid support was used in steps (d) and (e); and a ratio of 1 : 1 being an indication of a heterozygote, in a case where the total amount of the reaction product from step (c) not bound to the first solid support was used in steps (d) and (e).
In an eleventh aspect, the invention features a method for detecting the presence or absence of a polymoφhic restriction site in a nucleic acid, involving the steps of: (a) amplifying the nucleic acid by PCR using a first and a second primer flanking the polymoφhic restriction site, the first primer being tagged with a detectable label, the second primer being unlabeled; (b) digesting the reaction product of step (a) with the restriction endonuclease corresponding to the polymoφhic restriction site; (c) annealing and ligating to the single-stranded ends generated in the reaction of step (b) a first oligonucleotide tagged with the first member of a first specific binding pair; (d) contacting the reaction product of step (c) with the second member of the first specific binding pair, immobilized on a first solid support; (e) denaturing the reaction product of step (d) not bound to the first solid support; (f) contacting the product of step (e) with a second oligonucleotide complementary to a sequence in the strand of the product of step (e) containing the detectable label, the sequence being between the polymoφhic restriction site and either the sequence corresponding to the first primer or the sequence complementary to the second primer, the second oligonucleotide being immobilized on a second solid support; and (g) determining the ratio of the level of the detectable label bound to the first solid support to the level of the detectable label bound to the second solid support, a ratio of 1 :0 being an indication of a homozygote containing the polymoφhic restriction site, in a case where the total amount of the reaction product from step (d) not bound to the first solid support was used in steps (e) and (f); a ratio of 0: 1 being an indication of a homozygote lacking the polymoφhic restriction site, in a case where the total amount of the reaction product from step (d) not bound to the first solid support was used in steps (e) and (f); and a ratio of 1 : 1 being an indication of a heterozygote, in a case where the total amount of the reaction product from step (d) not bound to the first solid support was used in steps (e) and (f).
In a twelfth aspect, the invention features a method for detecting the presence or absence of a polymoφhic restriction site in a nucleic acid, involving the steps of: (a) amplifying the nucleic acid by PCR using a first and a second primer flanking the polymoφhic restriction site, the first primer containing a first sequence not complementary to or present in the nucleic acid, the second primer containing a second sequence not complementary to or present in the nucleic acid; (b) amplifying the product of step (a) by PCR using a third and a fourth primer, the third primer containing the first sequence or a sequence complementary to the first sequence, the third primer being tagged with the first member of a specific binding pair, the fourth primer containing the second sequence or a sequence complementary to the second sequence, the fourth primer being tagged with a detectable label; (c) digesting the product of step (b) with the restriction endonuclease corresponding to the polymoφhic restriction site; (d) contacting the reaction product of step (c) with the second member of the specific binding pair, immobilized on a solid support; and (e) measuring the level of the detectable label bound to the solid support, the presence of the detectable label bound to the solid support being an indication of the absence of the polymoφhic restriction site in the nucleic acid.
In a thirteenth aspect, the invention features a method for detecting the presence or absence of a polymoφhic restriction site in a nucleic acid, involving the steps of: (a) amplifying the nucleic acid by PCR using a first and a second primer flanking the polymoφhic restriction site, the first primer containing a first sequence not complementary to or present in the nucleic acid, the second primer containing a second sequence not complementary to or present in the nucleic acid; (b) amplifying the product of step (a) by PCR using a third and a fourth primer, the third primer containing the first sequence or a sequence complementary to the first sequence, the third primer being tagged with the first member of a specific binding pair, the fourth primer containing the second sequence or a sequence complementary to the second sequence, the fourth primer being tagged with a detectable label; (c) digesting the PCR product of step (b) with the restriction endonuclease corresponding to the polymoφhic restriction site; (d) annealing and ligating to the single-stranded ends generated in the reaction of step (c) an oligonucleotide tagged with a second detectable label; (e) contacting the reaction product of step (d) with the second member of the specific binding pair, immobilized on a solid support; and (f) determining the levels of the first and second detectable labels bound to the solid support, the presence of only the first detectable label bound to the solid support being an indication of a homozygote lacking the polymoφhic restriction site, the presence of only the second detectable label bound to the solid support being an indication of a homozygote containing the polymoφhic restriction site, and the presence of both the first and second detectable labels bound to the solid support being an indication of a heterozygote. In a fourteenth aspect, the invention features a method for detecting the presence or absence of a polymoφhic restriction site in a nucleic acid, involving the steps of: (a) amplifying the nucleic acid by PCR using a first and a second primer flanking the polymoφhic restriction site, the first primer containing a first sequence not complementary to or present in the nucleic acid; (b) amplifying the product of step
(a) by PCR using a third primer and the second primer, the third primer containing the first sequence, the third primer being tagged with a detectable label; (c) digesting a portion of the reaction of step (b) with the restriction endonuclease corresponding to the polymoφhic restriction site, while leaving another portion of the reaction of step (b) undigested; (d) denaturing the digested and undigested portions from step (c); (e) contacting the product of step (d) with an oligonucleotide complementary to a second sequence in the strand of the product of step (d) containing the detectable label, the second sequence being between the polymoφhic restriction site and the sequence complementary to the second primer, the oligonucleotide being tagged with a first member of a specific binding pair; (f) contacting the reaction product of step (e) with the second member of the specific binding pair, immobilized on a solid support; and (g) determining the ratio of the levels of the detectable label bound to the solid support between undigested and digested samples, a ratio of 1 :0 between equivalent portions of the undigested and digested samples being an indication of a homozygote containing the polymoφhic restriction site, a ratio of 1 : 1 between equivalent portions of the undigested and digested samples being an indication of a homozygote lacking the polymoφhic restriction site, and a ratio of 2: 1 between equivalent portions of the undigested and digested samples being an indication of a heterozygote.
In a fifteenth aspect, the invention features a method for detecting the presence or absence of a polymoφhic restriction site in a nucleic acid, involving the steps of:
(a) amplifying the nucleic acid by PCR using a first and a second primer flanking the polymoφhic restriction site, the first primer containing a first sequence not complementary to or present in the nucleic acid, the second primer containing a second sequence not complementary to or present in the nucleic acid; (b) amplifying the product of step (a) by PCR using a third and a fourth primer, the third primer containing the first sequence or a sequence complementary to the first sequence, the third primer being tagged with a first detectable label, the fourth primer containing the second sequence or a sequence complementary to the second sequence, the fourth primer being tagged with a second detectable label; (c) digesting the reaction product of step (b) with the restriction endonuclease corresponding to the polymoφhic restriction site; (d) denaturing the reaction product of step (c); (e) contacting the product of step (d) with a first and a second oligonucleotide, the first oligonucleotide being complementary to a third sequence in the strand of the product of step (d) containing the first detectable label, the third sequence being between the polymoφhic restriction site and the sequence corresponding to or complementary to the first primer, the first oligonucleotide being tagged with the first member of a first specific binding pair, the second oligonucleotide being complementary to a fourth sequence in the strand of the product of step (d) containing the second detectable label, the fourth sequence being on the same side of the polymoφhic restriction site as the third sequence, the fourth sequence not being contained within or being complementary to any of the primers, the second oligonucleotide being tagged with the first member of a second specific binding pair; (f) contacting a first portion of the reaction product of step (e) with the second member of the first specific binding pair, immobilized on a first solid support; (g) contacting a second portion of the reaction product of step (e) with the second member of the second specific binding pair, immobilized on a second solid support; and (h) determining the ratio of the levels of the first and second detectable labels bound to the first and second solid supports, a ratio of 1:0 between equivalent amounts of the first and second portions being an indication of a homozygote containing the polymoφhic restriction site, a ratio of 1 : 1 between equivalent amounts of the first and second portions being an indication of a homozygote lacking the polymoφhic restriction site, and a ratio of 2: 1 between equivalent amounts of the first and second portions being an indication of a heterozygote.
In a sixteenth aspect, the invention features a method for detecting the presence or absence of a polymoφhic restriction site in a nucleic acid, involving the steps of: (a) amplifying the nucleic acid by PCR using a first and a second primer flanking the polymoφhic restriction site, the first primer containing a first sequence not complementary to or present in the nucleic acid, the second primer containing a second sequence not complementary to or present in the nucleic acid; (b) amplifying the product of step (a) by PCR using a third and a fourth primer, the third primer containing the first sequence or a sequence complementary to the first sequence, the third primer being tagged with a first detectable label, the fourth primer containing the second sequence or a sequence complementary to the second sequence, the fourth primer being tagged with a second detectable label; (c) digesting the reaction product of step (b) with the restriction endonuclease corresponding to the polymoφhic restriction site; (d) denaturing the reaction product of step (c); (e) contacting the product of step (d) with a first and a second oligonucleotide, the first oligonucleotide being complementary to a third sequence in the strand of the product of step (d) containing the first detectable label, the third sequence being between the polymoφhic restriction site and the sequence corresponding to or complementary to the second primer, the first oligonucleotide being tagged with the first member of a first specific binding pair, the second oligonucleotide being complementary to a fourth sequence in the strand of the product of step (d) containing the second detectable label, the fourth sequence being on the same side of the polymoφhic restriction site as the third sequence, the fourth sequence not being contained within or being complementary to any of the primers, the second oligonucleotide being tagged with the first member of a second specific binding pair; (f) contacting a first portion of the reaction product of step (e) with the second member of the first specific binding pair, immobilized on a first solid support; (g) contacting a second portion of the reaction product of step (e) with the second member of the second specific binding pair, immobilized on a second solid support; and (h) determining the ratio of the levels of the first and second detectable labels bound to the first and second solid supports, a ratio of 0: 1 between equivalent amounts of the first and second portions being an indication of a homozygote containing the polymoφhic restriction site, a ratio of 1 : 1 between equivalent amounts of the first and second portions being an indication of a homozygote lacking the polymoφhic restriction site, and a ratio of 1 :2 between equivalent amounts of the first and second portions being an indication of a heterozygote. In a seventeenth aspect, the invention features a method for detecting the presence or absence of a polymoφhic restriction site in a nucleic acid, involving the steps of: (a) amplifying the nucleic acid by PCR using a first and a second primer flanking the polymoφhic restriction site, the first primer containing a first sequence not complementary to or present in the nucleic acid, the second primer containing a second sequence not complementary to or present in the nucleic acid; (b) amplifying the product of step (a) by PCR using a third and a fourth primer, the third primer containing the first sequence or a sequence complementary to the first sequence, the third primer being tagged with a first detectable label, the fourth primer containing the second sequence or a sequence complementary to the second sequence, the fourth primer being tagged with a second detectable label; (c) digesting the reaction product of step (b) with the restriction endonuclease corresponding to the polymoφhic restriction site; (d) denaturing the reaction product of step (c); (e) contacting the product of step (d) with a first and a second oligonucleotide, the first oligonucleotide being complementary to a third sequence in the strand of the product of step (d) containing the first detectable label, the third sequence being between the polymoφhic restriction site and the sequence corresponding to or complementary to the first primer, the first oligonucleotide being tagged with the first member of a specific binding pair, the second oligonucleotide being complementary to a fourth sequence in the strand of the product of step (d) containing the second detectable label, the fourth sequence being on the same side of the polymoφhic restriction site as the third sequence, the fourth sequence not being contained within or being complementary to any of the primers, the second oligonucleotide being tagged with the first member of the specific binding pair; (f) contacting the reaction product of step (e) with the second member of the specific binding pair, immobilized on a solid support; and (g) determining the ratio of the levels of the first and second detectable labels bound to the solid support, a ratio of 1 :0 being an indication of a homozygote containing the polymoφhic restriction site, a ratio of 1 : 1 being an indication of a homozygote lacking the polymoφhic restriction site, and a ratio of 2: 1 being an indication of a heterozygote.
In an eighteenth aspect, the invention features a method for detecting the presence or absence of a polymoφhic restriction site in a nucleic acid, involving (a) amplifying the nucleic acid by PCR using a first and second primer flanking the polymoφhic restriction site, the first primer containing a first sequence not complementary to or present in the nucleic acid, the second primer containing a second sequence not complementary to or present in the nucleic acid; (b) amplifying the product of step (a) by PCR using a third and a fourth primer, the third primer containing the first sequence or a sequence complementary to the first sequence, the third primer being tagged with a first detectable label, the fourth primer containing the second sequence or a sequence complementary to the second sequence, the fourth primer being tagged with a second detectable label; (c) digesting the reaction product of step (b) with the restriction endonuclease corresponding to the polymoφhic restriction site; (d) denaturing the reaction product of step (c); (e) contacting the product of step (d) with a first and a second oligonucleotide, the first oligonucleotide being complementary to a third sequence in the strand of the product of step (d) containing the first detectable label, the third sequence being between the polymoφhic restriction site and the sequence corresponding to or complementary to the second primer, the first oligonucleotide being tagged with the first member of a specific binding pair, the second oligonucleotide being complementary to a fourth sequence in the strand of the product of step (d) containing the second detectable label, the fourth sequence being on the same side of the polymoφhic restriction site as the third sequence, the fourth sequence not being contained within or being complementary to any of the primers, the second oligonucleotide being tagged with the first member of the specific binding pair; (f) contacting the reaction product of step (e) with the second member of the specific binding pair, immobilized on a solid support; and (g) determining the ratio of the levels of the first and second detectable labels bound to the solid support, a ratio of 0:1 being an indication of a homozygote containing the polymoφhic restriction site, a ratio of 1 : 1 being an indication of a homozygote lacking the polymoφhic restriction site, and a ratio of 1 :2 being an indication of a heterozygote.
In a nineteenth aspect, the invention features a method for detecting the presence or absence of a polymoφhic restriction site in a nucleic acid, involving the steps of (a) amplifying the nucleic acid by PCR using a first and a second primer flanking the polymoφhic restriction site, the first primer containing a first sequence not complementary to or present in the nucleic acid, the second primer containing a second sequence not complementary to or present in the nucleic acid; (b) amplifying the product of step (a) by PCR using a third and a fourth primer, the third primer containing the first sequence or a sequence complementary to the first sequence, the third primer being tagged with the first member of a first specific binding pair, the fourth primer containing the second sequence or a sequence complementary to the second sequence, the fourth primer being tagged with a detectable label; (c) digesting the reaction product of step (b) with the restriction endonuclease corresponding to the polymoφhic restriction site; (d) contacting the reaction product of step (c) with the second member of the first specific binding pair, immobilized on a first solid support; (e) denaturing the reaction product of step (d) not bound to the first solid support; (f) contacting the product of step (e) with an oligonucleotide complementary to a third sequence in the strand of the product of step (e) containing the detectable label, the third sequence being between the polymoφhic restriction site and the sequence corresponding to or complementary to the second primer, the oligonucleotide being tagged with the first member of a second specific binding pair; (g) contacting the reaction product of step (f) with the second member of the second specific binding pair, immobilized on a second solid support; and (h) determining the ratio of the level of the detectable label bound to the first solid support to the level of the detectable label bound to the second solid support, a ratio of 0: 1 being an indication of a homozygote containing the polymoφhic restriction site, in a case where the total amount of the reaction product from step (d) not bound to the first solid support was used in steps (e), (f), and (g); a ratio of 1 :0 being an indication of a homozygote lacking the polymoφhic restriction site, in a case where the total amount of the reaction product from step (d) not bound to the first solid support was used in steps (e), (f), and (g); and a ratio of 1 : 1 being an indication of a heterozygote, in a case where the total amount of the reaction product from step (d) not bound to the first solid support was used in steps (e), (f), and (g).
In a twentieth aspect the invention features a method for detecting the presence or absence of a polymoφhic restriction site in a nucleic acid, involving the steps of: (a) amplifying the nucleic acid by PCR using a first and a second primer flanking the polymoφhic restriction site, the first primer containing a first sequence not complementary to or present in the nucleic acid; (b) amplifying the product of step (a) by PCR using a third primer and the second primer, the third primer containing the first sequence, the third primer being tagged with a detectable label; (c) digesting the reaction product of step (b) with the restriction endonuclease corresponding to the polymoφhic restriction site; (d) annealing and ligating to the single-stranded ends generated in the reaction of step (c) a first oligonucleotide tagged with the first member of a first specific binding pair; (e) contacting the reaction product of step (d) with the second member of the first specific binding pair, immobilized on a first solid support; (f) denaturing the reaction product of step (e) not bound to the first solid support; (g) contacting the product of step (f) with a second oligonucleotide complementary to a second sequence in the strand of the product of step (f) containing the detectable label, the second sequence being between the polymoφhic restriction site and either the sequence corresponding to or complementary to the second primer or the sequence corresponding to or complementary to the first primer, the second oligonucleotide being tagged with the first member of a second specific binding pair; (h) contacting the reaction product of step (g) with the second member of the second specific binding pair, immobilized on a second solid support; and (i) determining the ratio of the level of the detectable label bound to the first solid support to the level of the detectable label bound to the second solid support, a ratio of 1 :0 being an indication of a homozygote containing the polymoφhic restriction site, in a case where the total amount of the reaction product from step (c) not bound to the first solid support was used in steps (f), (g), and (h); a ratio of 0:1 being an indication of a homozygote lacking the polymoφhic restriction site, in a case where the total amount of the reaction product from step (e) not bound to the first solid support was used in steps (f), (g), and (h); and a ratio of 1 : 1 being an indication of a heterozygote; in a case where the total amount of the reaction product from step (e) not bound to the first solid support was used in steps (f), (g), and (h).
In a twenty-first aspect, the invention features a method for detecting the presence or absence of a polymoφhic restriction site in a nucleic acid, involving the steps of: (a) amplifying the nucleic acid by PCR using a first and a second primer flanking the polymoφhic restriction site, the first primer containing a first sequence not complementary to or present in the nucleic acid, the second primer containing a second sequence not complementary to or present in the nucleic acid; (b) amplifying the product of step (a) by PCR using a third and a fourth primer, the third primer containing the first sequence or a sequence complementary to the first sequence, the third primer being tagged with the first member of a first specific binding pair, the fourth primer containing the second sequence or a sequence complementary to the second sequence, the fourth primer being tagged with a detectable label; (c) digesting the reaction product of step (b) with the restriction endonuclease corresponding to the polymoφhic restriction site; (d) contacting the reaction product of step (c) with the second member of the first specific binding pair, immobilized on a first solid support;
(e) denaturing the reaction product from step (d) not bound to the first solid support;
(f) contacting the product of step (e) with an oligonucleotide complementary to a third sequence in the strand of the product of step (e) containing the detectable label, the third sequence being between the polymoφhic restriction site and the sequence corresponding to or complementary to the second primer, the oligonucleotide being immobilized on a second solid support; and (g) determining the ratio of the level of the detectable label bound to the first solid support to the level of the detectable label bound to the second solid support, a ratio of 0:1 being an indication of a homozygote containing the polymoφhic restriction site, in a case where the total amount of the reaction product from step (d) not bound to the first solid support was used in steps (e) and (f); a ratio of 1 :0 being an indication of a homozygote lacking the polymoφhic restriction site, in a case where the total amount of the reaction product from step (d) not bound to the first solid support was used in steps (e) and (f); and a ratio of 1 : 1 being an indication of a heterozygote, in a case where the total amount of the reaction product from step (d) not bound to the first solid support was used in steps (e) and (f).
In a twenty-second aspect, the invention features a method for detecting the presence or absence of a polymoφhic restriction site in a nucleic acid, the method involving the steps of: (a) amplifying the nucleic acid by PCR using a first and a second primer flanking the polymoφhic restriction site, the first primer containing a first sequence not complementary to or present in the nucleic acid; (b) amplifying the product of step (a) by PCR using a third primer and the second primer, the third primer containing the first sequence, the third primer being tagged with a detectable label; (c) digesting the reaction product of step (b) with the restriction endonuclease corresponding to the polymoφhic restriction site; (d) annealing and ligating to the single- stranded ends generated in the reaction of step (c) a first oligonucleotide tagged with the first member of a first specific binding pair; (e) contacting the reaction product of step (d) with the second member of the first specific binding pair, immobilized on a first solid support; (f) denaturing the reaction product of step (e) not bound to the first solid support; (g) contacting the product of step (f) with a second oligonucleotide complementary to a second sequence in the strand of the product of step (f) containing the detectable label, the second sequence being between the polymoφhic restriction site and either the sequence corresponding to or complementary to the second primer or the sequence corresponding to or complementary to the first primer, the second oligonucleotide being immobilized on a second solid support; and (h) determining the ratio of the level of the detectable label bound to the first solid support to the level of the detectable label bound to the second solid support, a ratio of 1 :0 being an indication of a homozygote containing the polymoφhic restriction site, in a case where the total amount of the reaction product from step (e) not bound to the first solid support was used in steps (f) and (g); a ratio of 0: 1 being an indication of a homozygote lacking the polymoφhic restriction site, in a case where the total amount of the reaction product from step (e) not bound to the first solid support was used in steps (f) and (g); and a ratio of 1 : 1 being an indication of a heterozygote, in a case where the total amount of the reaction product from step (e) not bound to the first solid support was used in steps (f) and (g).
In a twenty-third aspect, the invention features a kit for detecting the presence or absence of a polymoφhic restriction site in a nucleic acid, the kit containing one or more sets of a first and a second primer flanking the polymoφhic restriction site, the first primer being tagged with the first member of a specific binding pair, the second primer being tagged with a detectable label. In a preferred embodiment, the kit further contains the second member of the specific binding pair, immobilized on a solid support. In another preferred embodiment, the kit further contains an oligonucleotide complementary to the single-stranded ends generated in the nucleic acid upon digestion of the nucleic acid with the restriction enzyme corresponding to the polymoφhic restriction site, the oligonucleotide being tagged with a second detectable label.
In a twenty-fourth aspect, the invention features a kit for detecting the presence or absence of a polymoφhic restriction site in a nucleic acid, the kit containing: (a) a first and a second primer flanking the polymoφhic restriction site, the first primer being tagged with a detectable label, the second primer being unlabeled; (b) an oligonucleotide complementary to a sequence in the strand of the nucleic acid complementary to the second primer, the sequence being between the polymoφhic restriction site and the sequence complementary to the second primer, the oligonucleotide being tagged with a first member of a specific binding pair; and (c) the second member of the specific binding pair, immobilized on a solid support. In a twenty-fifth aspect, the invention features a kit for detecting the presence or absence of a polymoφhic restriction site in a nucleic acid, the kit containing: (a) a first and a second primer flanking the polymoφhic restriction site, the first primer being tagged with a first detectable label, the second primer being tagged with a second detectable label; (b) a first oligonucleotide, the first oligonucleotide being complementary to a first sequence in the strand of the nucleic acid complementary to the second primer, the first sequence being between the polymoφhic restriction site and either the sequence corresponding to the first primer or the sequence complementary to the second primer, the first oligonucleotide being tagged with the first member of a first specific binding pair; (c) a second oligonucleotide, the second oligonucleotide being complementary to a second sequence in the strand of the nucleic acid complementary to the first primer, the second sequence being on the same side of the polymoφhic restriction site as the first sequence, the second sequence not being contained within or being complementary to either of the first or second primers, the second oligonucleotide being tagged with the first member of a second specific binding pair; (d) the second member of the first specific binding pair, immobilized on a first solid support; and (e) the second member of the second specific binding pair, immobilized on a second solid support. In a preferred embodiment, the first and the second specific binding pairs are identical, and the first and the second solid supports are identical.
In a twenty-sixth aspect, the invention features a kit for detecting the presence or absence of a polymoφhic restriction site in a nucleic acid, the kit containing: (a) a first and a second primer flanking the polymoφhic restriction site, the first primer being tagged with the first member of a first specific binding pair, the second primer being tagged with a detectable label; (b) the second member of the first specific binding pair, immobilized on a first solid support; (c) an oligonucleotide complementary to a first sequence in the strand of the nucleic acid containing the sequence corresponding to the second primer, the first sequence being between the polymoφhic restriction site and the sequence corresponding to the second primer, the oligonucleotide being tagged with the first member of a second specific binding pair; and (d) the second member of the second specific binding pair, immobilized on a second solid support.
In a twenty-seventh aspect, the invention features a kit for detecting the presence or absence of a polymoφhic restriction site in a nucleic acid, the kit containing: (a) a first and a second primer flanking the polymoφhic restriction site, the first primer being tagged with a detectable label, the second primer being unlabeled; (b) a first oligonucleotide complementary to the single-stranded ends generated in the nucleic acid upon digestion of the nucleic acid with the restriction enzyme corresponding to the polymoφhic restriction site, the oligonucleotide being tagged with the first member of a first specific binding pair; (c) the second member of the first specific binding pair, immobilized on a first solid support; (d) a second oligonucleotide complementary to a sequence in the strand of the nucleic acid complementary to the second primer, the sequence being between the polymoφhic restriction site and either the sequence corresponding to the first primer or the sequence complementary to the second primer, the second oligonucleotide being tagged with the first member of a second specific binding pair; and (e) the second member of the second specific binding pair, immobilized on a second solid support.
In a twenty-eighth aspect, the invention features a kit for detecting the presence or absence of a polymoφhic restriction site in a nucleic acid, the kit containing: (a) a first and a second primer flanking the polymoφhic restriction site, the first primer being tagged with the first member of a first specific binding pair, the second primer being tagged with a detectable label; (b) the second member of the first specific binding pair, immobilized on a first solid support; and (c) an oligonucleotide complementary to a first sequence in the strand of the nucleic acid containing the sequence corresponding to the second primer, the first sequence being between the polymoφhic restriction site and the sequence corresponding to the second primer, the oligonucleotide being immobilized on a second solid support.
In a twenty-ninth aspect, the invention features a kit for detecting the presence or absence of a polymoφhic restriction site in a nucleic acid, the kit containing: (a) a first and a second primer flanking the polymoφhic restriction site, the first primer being tagged with a detectable label, the second primer being unlabeled; (b) a first oligonucleotide complementary to the single-stranded ends generated in the nucleic acid upon digestion of the nucleic acid with the restriction enzyme corresponding to the polymoφhic restriction site, the oligonucleotide being tagged with the first member of a first specific binding pair; (c) the second member of the first specific binding pair, immobilized on a first solid support; and (d) a second oligonucleotide complementary to a sequence in the strand of the nucleic acid complementary to the second primer, the sequence being between the polymoφhic restriction site and either the sequence corresponding to the first primer or the sequence complementary to the second primer, the second oligonucleotide being immobilized on a second solid support.
In a thirtieth aspect, the invention features a kit for detecting the presence or absence of a polymoφhic restriction site in a nucleic acid, the kit containing: (a) a first and a second primer flanking the polymoφhic restriction site, the first primer containing a first sequence not complementary to or present in the nucleic acid, the second primer containing a second sequence not complementary to or present in the nucleic acid; (b) a third and a fourth primer, the third primer containing the first sequence or a sequence complementary to the first sequence, the third primer being tagged with the first member of a specific binding pair, the fourth primer containing the second sequence or a sequence complementary to the second sequence, the fourth primer being tagged with a detectable label. In a preferred embodiment, the kit further contains the second member of the specific binding pair, immobilized on a solid support. In another preferred embodiment, the kit further contains an oligonucleotide complementary to the single-stranded ends generated in the nucleic acid upon digestion of the nucleic acid with the restriction enzyme corresponding to the polymoφhic restriction site, the oligonucleotide being tagged with a second detectable label. In a thirty-first aspect, the invention features a kit for detecting the presence or absence of a polymoφhic restriction site in a nucleic acid, the kit containing: (a) a first and a second primer flanking the polymoφhic restriction site, the first primer containing a first sequence not complementary to or present in the nucleic acid; (b) a third primer containing the first sequence, the third primer being tagged with a detectable label; (c) an oligonucleotide complementary to a second sequence in the strand of the nucleic acid containing the sequence complementary to the second primer, the second sequence being between the polymoφhic restriction site and the sequence complementary to the second primer, the oligonucleotide being tagged with a first member of a specific binding pair; and (d) the second member of the specific binding pair, immobilized on a solid support. In a thirty-second aspect, the invention features a kit for detecting the presence or absence of a polymoφhic restriction site in a nucleic acid, the kit containing: (a) a first and a second primer flanking the polymoφhic restriction site, the first primer containing a first sequence not complementary to or present in the nucleic acid, the second primer containing a second sequence not complementary to or present in the nucleic acid; (b) a third and a fourth primer, the third primer containing the first sequence or a sequence complementary to the first sequence, the third primer being tagged with a first detectable label, the fourth primer containing the second sequence or a sequence complementary to the second sequence, the fourth primer being tagged with a second detectable label; (c) a first oligonucleotide, the first oligonucleotide being complementary to a third sequence in the strand of the nucleic acid complementary to the second primer, the third sequence being between the polymoφhic restriction site and either the sequence complementary to the second primer or the sequence corresponding to the first primer, the first oligonucleotide being tagged with the first member of a first specific binding pair, (d) a second oligonucleotide, the second oligonucleotide being complementary to a fourth sequence in the strand of the nucleic acid complementary to the first primer, the fourth sequence being on the same side of the polymoφhic restriction site as the third sequence, the fourth sequence not being contained within or being complementary to any of the primers, the second oligonucleotide being tagged with the first member of a second specific binding pair; (e) the second member of the first specific binding pair, immobilized on a first solid support; and (f) the second member of the second specific binding pair, immobilized on a second solid support. In a preferred embodiment, the first and the second specific binding pairs are identical, and the first and the second solid supports are identical.
In a thirty-third aspect, the invention features a kit for detecting the presence or absence of a polymoφhic restriction site in a nucleic acid, the kit containing: (a) a first and a second primer flanking the polymoφhic restriction site, the first primer containing a first sequence not complementary to or present in the nucleic acid, the second primer containing a second sequence not complementary to or present in the nucleic acid; (b) a third and a fourth primer, the third primer containing the first sequence or a sequence complementary to the first sequence, the third primer being tagged with the first member of a first specific binding pair, the fourth primer containing the second sequence or a sequence complementary to the second sequence, the fourth primer being tagged with a detectable label; (c) the second member of the first specific binding pair, immobilized on a first solid support; (d) an oligonucleotide complementary to a third sequence in the strand of the nucleic acid corresponding to the second primer, the sequence being between the polymoφhic restriction site and the sequence corresponding to the second primer, the oligonucleotide being tagged with the first member of a second specific binding pair; and (e) the second member of the second specific binding pair, immobilized on a second solid support.
In a thirty- fourth aspect, the invention features a kit for detecting the presence or absence of a polymoφhic restriction site in a nucleic acid, the kit containing: (a) a first and a second primer flanking the polymoφhic restriction site, the first primer containing a first sequence not complementary to or present in the nucleic acid; (b) a third primer containing the first sequence, the third primer being tagged with a detectable label; (c) a first oligonucleotide complementary to the single-stranded ends generated in the nucleic acid upon digestion of the nucleic acid with the restriction enzyme corresponding to the polymoφhic restriction site, the oligonucleotide being tagged with the first member of a first specific binding pair; (d) the second member of the first specific binding pair, immobilized on a first solid support; (e) a second oligonucleotide complementary to a second sequence in the strand of the nucleic acid corresponding to the first primer, the second sequence being between the polymoφhic restriction site and either the sequence complementary to the second primer or the sequence corresponding to the first primer, the second oligonucleotide being tagged with the first member of a second specific binding pair; and (f) the second member of the second specific binding pair, immobilized on a second solid support.
In a thirty-fifth aspect, the invention features a kit for detecting the presence or absence of a polymoφhic restriction site in a nucleic acid, the kit containing: (a) a first and a second primer flanking the polymoφhic restriction site, the first primer containing a first sequence not complementary to or present in the nucleic acid, the second primer containing a second sequence not complementary to or present in the nucleic acid; (b) a third and a fourth primer, the third primer containing the first sequence or a sequence complementary to the first sequence, the third primer being tagged with the first member of a first specific binding pair, the fourth primer containing the second sequence or a sequence complementary to the second sequence, the fourth primer being tagged with a detectable label; (c) the second member of the first specific binding pair, immobilized on a first solid support; and (d) an oligonucleotide complementary to a third sequence in the strand of the nucleic acid corresponding to the second primer, the third sequence being between the polymoφhic restriction site and the sequence corresponding to the second primer, the oligonucleotide being immobilized on a second solid support.
In a thirty-sixth aspect, the invention features a kit for detecting the presence or absence of a polymoφhic restriction site in a nucleic acid, the kit containing: (a) a first and a second primer flanking the polymoφhic restriction site, the first primer containing a first sequence not complementary to or present in the nucleic acid; (b) a third primer containing the first sequence, the third primer being tagged with a detectable label; (c) a first oligonucleotide complementary to the single-stranded ends generated in the nucleic acid upon digestion of the nucleic acid with the restriction enzyme corresponding to the polymoφhic restriction site, the oligonucleotide being tagged with the first member of a first specific binding pair; (d) the second member of the first specific binding pair, immobilized on a first solid support; and (e) a second oligonucleotide complementary to a second sequence in the strand of the nucleic acid corresponding to the first primer, the sequence being between the polymoφhic restriction site and either the sequence corresponding to or complementary to the second primer or the sequence corresponding to or complementary to the first primer, the second oligonucleotide being immobilized on a second solid support. In a thirty-seventh aspect, the invention features a method for detecting the presence or absence of a polymoφhic restriction site in a nucleic acid, involving the steps of: (a) amplifying the nucleic acid by PCR using a first and a second primer flanking the polymoφhic restriction site, whereby the resultant PCR product is of a defined size readily resolved by gel electrophoresis; (b) digesting the PCR product of step (a) with the restriction endonuclease corresponding to the polymoφhic restriction site, the digestion products being differentially sized; (c) separating the reaction products of step (b) by gel electrophoresis; and (d) detecting the separated reaction products, the presence of only uncleaved products being an indication of a homozygote lacking the polymoφhic restriction site, the presence of only cleaved products being an indication of a homozygote containing the polymoφhic restriction site, and the presence of both cleaved and uncleaved products being an indication of a heterozygote. In a preferred embodiment, one or both of the first and second primers are tagged with a detectable label. In another preferred embodiment, the PCR product is 100-1000 base pairs in length. In a thirty-eighth aspect, the invention features a kit for detecting the presence or absence of a polymoφhic restriction site in a nucleic acid, the kit containing: a first and a second primer flanking the polymoφhic restriction site and capable of generating a PCR product of a defined size that is readily resolved by gel electrophoresis. In a preferred embodiment, the first and/or the second primers are detectably labeled. In another preferred embodiment, the PCR product generated is between 100 and 1000 base pairs in length.
In a thirty-ninth aspect, the invention features a method for identifying a polymoφhic restriction site in a nucleic acid, involving the steps of: (a) digesting DNA isolated from a first sample with a first restriction endonuclease; (b) ligating to each of the ends of the reaction products of step (a) a first adaptor; (c) digesting the products of step (b) with a second restriction endonuclease; (d) ligating to each of the ends of the reaction products generated in step (c) a second adaptor; (e) amplifying the reaction products of step (d) by PCR using a first primer complementary to the first adaptor and a second primer complementary to the second adaptor, the second primer being tagged with a first member of a specific binding pair (preferably, biotin); (f) in a separate set of reactions, digesting DNA isolated from a second sample with the first restriction endonuclease; (g) ligating to each of the ends of the reaction products of step (f) a third adaptor; (h) digesting the products of step (g) with the second restriction endonuclease; (i) denaturing the products of step (e) and the products of step (h); (j) combining the denatured products of step (i) under conditions allowing hybridization; (k) contacting the hybridization products of step (j) with the second member of the specific binding pair (preferably, avidin), the second member being immobilized on a solid support; (1) recovering the hybridization products captured on the solid support; and (m) amplifying the products obtained in step (1) by PCR using a primer complementary to the third adaptor, an amplified product being an indication of a polymoφhic restriction site corresponding to the second restriction endonuclease. In a fortieth aspect, the invention features a kit for identifying a polymoφhic restriction site in a nucleic acid, the kit containing: (a) a first DNA adaptor, a second
DNA adaptor, and a third DNA adaptor, the first and third DNA adaptors having regions complementary to the ends generated by a first restriction endonuclease ends but differing in overall sequence and the second DNA adaptor having a region complementary to the ends generated by a second restriction endonuclease, the second restriction endonuclease site corresponding to the polymoφhic restriction site; and (b) a first primer, a second primer, and a third primer, the first primer being complementary to the first DNA adaptor, the second primer being complementary to the second DNA adaptor and being tagged with a first member of a specific binding pair, and the third primer being complementary to the third DNA adaptor. This kit may further contain the second member of the specific binding pair immobilized on a solid support.
In a forty-first aspect, the invention features a method for detecting the presence or absence of a polymoφhic restriction site in a nucleic acid. In this method the nucleic acid is amplified by PCR using a first and a second primer flanking the polymoφhic restriction site. The first primer is tagged with a detectable label, and the amplifying generates a PCR product containing a first strand tagged with the detectable label and an unlabeled second strand. The PCR product is then digested with a restriction endonuclease corresponding to the polymoφhic restriction site to generate a digestion product, which is denatured to generate a denatured product. The denatured product is contacted with a first probe, which contains a sequence that hybridizes to a first sequence in the first strand that is between the polymoφhic restriction site and the sequence in the first strand that is complementary to the second primer. The first probe is also immobilized on a first binding element.
The first binding element is monitored for the presence of the detectable label, and detection of the detectable label on the first binding element indicates the absence of the polymoφhic restriction site in the nucleic acid, and a failure to detect the detectable label on the first binding element indicates the presence of the polymoφhic restriction site in the nucleic acid. The first binding element is a region on a solid support, such as a glass plate or a microchip.
This method can also include contacting the denatured product with a second, a third, or a fourth probe. The second probe, which is immobilized on a second binding element, contains a sequence that hybridizes to a second sequence in the first strand that is between the polymoφhic restriction site and the sequence in the first strand that corresponds to the first primer. The third probe, which is immobilized on a third binding element, contains a sequence that hybridizes to a third sequence in the second strand that is between the polymoφhic restriction site and the sequence in the second strand corresponding to the second primer. The fourth probe, which is immobilized on a fourth binding element, contains a sequence that hybridizes to a fourth sequence in the second strand that is between the polymoφhic restriction site and the sequence in the second strand that is complementary to the first primer. In this method, the second, third, or fourth binding element can be monitored for the presence of the detectable label. The first, second, third, and fourth binding elements can each be distinct regions on a solid support, such as a glass plate or a microchip.
In a forty-second aspect, the invention features a method for detecting the presence or absence of a polymoφhic restriction site in a nucleic acid. In this method the nucleic acid is amplified by PCR using a first and a second primer flanking the polymoφhic restriction site. The first primer is tagged with a first detectable label and the second primer is tagged with a second detectable label. The amplifying generates a PCR product containing a first strand tagged with the first detectable label and a second strand tagged with the second detectable label. The first and second detectable labels can be identical or distinct.
The PCR product is treated with a restriction endonuclease corresponding to the polymoφhic restriction site to generate a digestion product, which is denatured to generate a denatured product. The denatured product is contacted with a first and a second probe. The first probe, which is immobilized on a first binding element, contains a sequence that hybridizes to a first sequence in the first strand that is between the polymoφhic restriction site and the sequence in the first strand that is complementary to the second primer. The second probe, which is immobilized on a second binding element, contains a sequence that hybridizes to a second sequence in the second strand that is between the polymoφhic restriction site and the sequence in the second strand that is complementary to the first primer. The first and second binding elements can each be distinct regions on a solid support, such as a glass plate or a microchip. The first binding element is monitored for the presence of the first detectable label and the second binding element is monitored for the presence of the second detectable label. Detection of the first detectable label on the first binding element and detection of the second detectable label on the second binding element indicates the absence of the polymoφhic restriction site in the nucleic acid, and a failure to detect the first detectable label on the first binding element and a failure to detect the second detectable label on the second binding element indicates the presence of the polymoφhic restriction site in the nucleic acid.
This method can also include contacting the denatured product with a third or a fourth probe. The third probe, which is immobilized on a third binding element, contains a sequence that hybridizes to a third sequence in the first strand that is between the polymoφhic restriction site and the sequence in the first strand corresponding to the first primer. The fourth probe, which is immobilized on a fourth binding element, contains a sequence that hybridizes to a fourth sequence in the second strand that is between the polymoφhic restriction site and the sequence in the second strand corresponding to the second primer. The third or fourth binding element can be monitored for the presence of the first or second detectable label. The first, second, third, and fourth binding elements can be each distinct regions on a solid support, such as a glass plate or a microchip. In a forty-third aspect, the invention features a method for detecting the presence or absence of a polymoφhic restriction site in a nucleic acid. In this method, the nucleic acid is amplified by PCR using a first and a second primer flanking the polymoφhic restriction site. The amplifying generates a PCR product containing a first strand containing a sequence corresponding to the first primer and a second strand containing a sequence corresponding to the second primer.
The PCR product is treated with a restriction endonuclease corresponding to the polymoφhic restriction site to generate a digestion product, which is denatured to generate a denatured product. The denatured product is contacted with an oligonucleotide to generate a first reaction product. The oligonucleotide contains a 3' portion that hybridizes to a first region in the first strand that flanks the polymoφhic restriction site on the side of the polymoφhic restriction site containing a sequence corresponding to the first primer. The oligonucleotide is blocked so that it cannot serve as a primer for DNA polymerase. In addition, the oligonucleotide contains a
5' portion that does not hybridize to a second region in the first strand that flanks the polymoφhic restriction site on the side of the polymoφhic restriction site containing a sequence that is complementary to the second primer.
The first reaction product is treated with a DNA polymerase to extend the unblocked, primed 3' end to generate a second reaction product, which is amplified by
PCR using the first primer, tagged with a first detectable label, and a third primer that hybridizes to a sequence that is complementary to the 5' portion of the oligonucleotide, to generate a second PCR product. The third primer is tagged with a second detectable label. The first and the second detectable labels in this method can be identical or distinct.
The second PCR product is denatured to generate a second denatured product, which is contacted with a first and a second probe. The first probe, which is immobilized on a first binding element, contains a sequence that hybridizes to a first sequence in the second strand that is between the polymoφhic restriction site and the sequence in the second strand that is complementary to the first primer. The second probe, which is immobilized on a second binding element, contains a sequence that hybridizes to a second sequence in the first strand that is between the polymoφhic restriction site and the sequence in the first strand that is complementary to the second primer. The first and second binding elements can each be distinct regions on a solid support, such as a glass support or a microchip.
The first binding element is monitored for the presence of the second detectable label and the second binding element is monitored for the presence of the first detectable label. Detection of the second detectable label on the first binding element and detection of the first detectable label on the second binding element indicates a heterozygote, detection of the second detectable label on the first binding element and a failure to detect the first detectable label on the second binding element indicates a homozygote containing the polymoφhic restriction site, and detection of the first detectable label on the second binding element and a failure to detect the second detectable label on the first binding element indicates a homozygote lacking the polymoφhic restriction site.
This method can also include contacting the second denatured product with a third or a fourth probe. The third probe, which is immobilized on a third binding element, contains a sequence that hybridizes to a third sequence in the first strand that is between the polymoφhic restriction site and the sequence in the first strand corresponding to the first primer. The fourth probe, which is immobilized on a fourth binding element, contains a sequence that hybridizes to a fourth sequence in the second strand that is between the polymoφhic restriction site and the sequence in the second strand corresponding to the second primer. The third or fourth binding element can be monitored for the presence of the first or second detectable label. The first, second, third, and fourth binding elements can each be distinct regions on a solid support, such as a glass plate or a microchip.
In a forty- fourth aspect, the invention features a kit for detecting the presence or absence of a polymoφhic restriction site in a nucleic acid. The kit can contain one or more sets of a first and a second primer flanking the polymoφhic restriction site. The first primer is tagged with a detectable label, so that amplifying the nucleic acid by PCR with the first and second primers generates a PCR product containing a first strand tagged with the detectable label and a second strand. The kit also can include one or more first probes, each of which containing a sequence that hybridizes to a first sequence in the first strand that is between the polymoφhic restriction site and the sequence in the first strand that is complementary to the second primer. Each of the first probes is immobilized on a first binding element. This kit can also contain one or more sets of a second, third, or fourth probe. Each of the second probes, which is immobilized on a second binding element, contains a sequence that hybridizes to a second sequence in the first strand that is between the polymoφhic restriction site and the sequence in the first strand that corresponds to the first primer. Each of the third probes, which is immobilized on a third binding element, contains a sequence that hybridizes to a third sequence in the second strand that is between the polymoφhic restriction site and the sequence in the second strand coπesponding to the second primer. Each of the fourth probes, which is immobilized on a fourth binding element, contains a sequence that hybridizes to a fourth sequence in the second strand that is between the polymoφhic restriction site and the sequence in the second strand that is complementary to the first primer.
The first binding element in this kit can be a region on a solid support, such as a glass plate or a microchip. In addition, in this kit, the first, second, third, and fourth binding elements can each be distinct regions on a solid support, such as a glass plate or a microchip.
One or more second primers in this kit can each contain a second detectable label. In addition, the kit can further contain a second probe, which is immobilized on a second binding element, and contains a sequence that hybridizes to a second sequence in the second strand that is between the polymoφhic restriction site and the sequence in the second strand that is complementary to the first primer. The kit can also contain one or more sets of a third or a fourth probe. Each of the third probes, which are immobilized on a third binding element, contain a sequence that hybridizes to a third sequence in the first strand that is between the polymoφhic restriction site and the sequence in the first strand coπesponding to the first primer. Each of the fourth probes, which are immobilized on a fourth binding element, contain a sequence that hybridizes to a fourth sequence in the second strand that is between the polymoφhic restriction site and the sequence in the second strand corresponding to the second primer. The kit can further contain one or more second probes, which are immobilized on a second binding element, that each contain a sequence that hybridizes to a second sequence in the first strand that is between the polymoφhic restriction site and the sequence in the first strand that coπesponds to the first primer. In a forty-fifth aspect, the invention features a kit for detecting the presence or absence of a polymoφhic restriction site in a nucleic acid. This kit can contain one or more sets of a first and a second PCR primer flanking the polymoφhic restriction site. The first primer can be tagged with a first detectable label, so that amplifying the nucleic acid by PCR using the first and second primers generates a PCR product containing a first strand tagged with the first detectable label and a second strand.
Alternatively, the first primer can be unlabeled.
This kit can also include one or more oligonucleotides containing a 3' portion that hybridizes to a first region in the first strand that flanks the polymoφhic restriction site on the side of the polymoφhic restriction site containing a sequence coπesponding to the first primer. The oligonucleotide is blocked so that it cannot serve as a primer for DNA polymerase. In addition, the oligonucleotide contains a 5' portion that does not hybridize to a second region in the first strand that flanks the polymoφhic restriction site on the side of the polymoφhic restriction site containing a sequence that is complementary to the second primer. This kit can also include one or more third primers, each of which that hybridizes to a sequence that is complementary to the 5' portion of the oligonucleotide. The third primer can be tagged with a second detectable label.
Also included in this kit are one or more sets of a first and a second probe. Each of the first probes, which are immobilized on a first solid support, contain a sequence that hybridizes to a first sequence in the second strand that is between the polymoφhic restriction site and the sequence in the second strand that is complementary to the first primer. Each of the second probes, which are immobilized on a second solid support, contain a sequence that hybridizes to a second sequence in the first strand that is between the polymoφhic restriction site and the sequence in the first strand that is complementary to the second primer.
The first and the second detectable labels in this kit can be distinct or identical. In addition, the first and second binding elements can each be distinct regions on a solid support, such as a glass support or a microchip.
This kit can further contain one or more sets of a third or a fourth probe. Each of the third probes, which are immobilized on a third binding element, contain a sequence that hybridizes to a third sequence in the first strand that is between the polymoφhic restriction site and the sequence in the first strand coπesponding to the first primer. Each of the fourth probes, which are immobilized on a fourth binding element, contain a sequence that hybridizes to a fourth sequence in the second strand that is between the polymoφhic restriction site and the sequence in the second strand coπesponding to the second primer.
The one or more sets of the first, second, third, and fourth binding elements in this kit can each be distinct regions on a solid support, such as a glass plate or a microchip.
In a prefeπed embodiment of various of the above aspects, multiple polymoφhic restriction sites are detected by the method or kit. In prefeπed embodiments of various of the above aspects, the detectable label is selected from the group consisting of digoxigenin, fluorescent labels (e.g., fluorescein and rhodamine), enzymes (e.g., horseradish peroxidase and alkaline phosphatase), biotin (which can be detected by anti-biotin specific antibodies or enzyme-conjugated avidin derivatives), radioactive labels (e.g., 2P and 125I), colorimetric reagents, and chemiluminescent reagents. In other prefeπed embodiments of various of the above aspects, the specific binding pairs are selected from the group consisting of avidin-biotin, streptavidin- biotin, hybridizing nucleic acid pairs, interacting protein pairs, antibody-antigen pairs, reagents containing chemically reactive groups (e.g., reactive amino groups), and nucleic acid sequence-nucleic acid binding protein pairs. In related preferred embodiments of various of the above aspects, the solid supports used in the methods of the invention are selected from the group consisting of agarose, acrylamide, and polystyrene beads; polystyrene microtiter plates (for use in, e.g., ELISA); silicon, gold, or glass chips (e.g., microchips), slides, or plates; and nylon and nitrocellulose membranes (for use in, e.g., dot or slot blot assays).
The term "heterozygote," as used herein, refers to an individual with different alleles at coπesponding loci on homologous chromosomes. Accordingly, the term "heterozygous," as used herein, describes an individual or strain having different allelic genes at one or more paired loci on homologous chromosomes.
The term "homozygote," as used herein, refers to an individual with the same allele at coπesponding loci on homologous chromosomes. Accordingly, the term "homozygous," as used herein, describes an individual or a strain having identical allelic genes at one or more paired loci on homologous chromosomes. The term "coπesponding" as used herein to describe a nucleic acid strand, e.g., a nucleic acid strand coπesponding to a particular PCR primer, is meant to indicate that the strand contains the sequence of the particular PCR primer. When used to compare a polymoφhic restriction site to a restriction endonuclease site, the term again indicates that the two sequences are identical. An advantage of certain detection methods of the present invention over many other methods used to detect genetic polymoφhisms is that gel electrophoresis is not required in the analysis. Thus, the methods of the present invention are readily adaptable for automation, allowing large numbers of samples to be processed in relatively short periods of time, at lower costs. In certain of the embodiments, detection of an aπay of samples is carried out simultaneously on a solid support, such as a glass slide or a microchip, further reducing processing time and cost. Detection of signals on aπays can be carried out quantitatively or qualitatively. In addition, in several variations of the methods of the invention (see, e.g., Examples III and IV below), internal controls are provided, thus controlling for variability detected by different practitioners. Furthermore, in several of the variations of the methods of the invention (see Examples III-VIII and XII-XIV below), an oligonucleotide probe hybridizing to a sequence in the PCR product internal to the primers is used to purify the products, thus allowing a reduction in background problems associated with PCR amplification.
Those detection methods of the invention utilizing gel electrophoresis are also advantageous because they provide a rapid and inexpensive approach to the identification of large numbers of PCR-based genetic and RFLP markers. The method of the invention useful for cloning genetic polymoφhisms also represents an improvement over cuπent methods. Because the process of selecting out a tagged (e.g., biotinylated) DNA having a polymoφhism involves a specific hybridization step, candidate DNA from any source may be utilized. For example, DNA from random clones, CDNA libraries, YAC libraries, or any other DNA collection may be screened; pure preparations of genomic DNAs are not required. Moreover, like other methods of the invention, this cloning procedure is rapid and inexpensive.
All methods of the invention are useful in clinical diagnostic testing, genomic mapping, positional cloning of genes defined by mutation (such as those that cause inherited disease in humans or resistance to pathogens in crop plants), DNA fingeφrinting (e.g., for forensic analysis and paternity testing), crop and livestock breeding programs, and other related applications.
In one particular example, the detection methods of the invention are useful for bacterial typing utilizing known conserved polymoφhic sequences diagnostic of the bacterium. In one application, this approach is useful for distinguishing one bacterium from another (e.g., for the identification of Salmonella in a food sample); polymoφhism-containing sequences prefeπed for this approach include those present in conserved ribosomal RNA genes. In another application, this approach is useful for screening bacteria (e.g., clinical isolates) for antibiotic resistance; in this case, known polymoφhic restriction sites within the antibiotic resistance marker are utilized. The instant methods of bacterial typing decrease false positive results frequently obtained using cuπent PCR-based techniques.
Detailed Description The drawings are first described. Drawings
Fig. 1 is a schematic of a RFLP detection method involving the use of a first PCR primer tagged with a detectable label (X) and a second PCR primer tagged with the first member of a specific binding pair (Y). After amplification by PCR, the products are digested with the restriction endonuclease (R) coπesponding to the polymoφhic restriction site, contacted with the second member of the specific binding pair immobilized on a solid support, and the level of the detectable label (X) bound to the solid support is determined.
Fig. 2 is a schematic of a RFLP detection method involving the use of a first PCR primer tagged with a first detectable label (X) and a second PCR primer tagged with the first member of a specific binding pair (Y). After amplification by PCR, the products are digested with the restriction endonuclease (R) coπesponding to the polymoφhic restriction site, and an oligonucleotide tagged with a second detectable label (Z) is annealed and ligated to the single-stranded ends generated in the digestion. The reaction is then contacted with the second member of the specific binding pair bound to a solid support, and the levels of the first and second detectable labels (X and Z) bound to the solid support are determined. Fig. 3 is a schematic of a RFLP detection method involving the use of a first
PCR primer tagged with a detectable label (PI) and a second unlabeled PCR primer (P2). After amplification by PCR, half of the reaction (or one of the identical reactions if carried out in duplicate) is digested with the restriction endonuclease (R) coπesponding to the polymoφhic restriction site. Both digested and undigested reactions are then denatured and contacted with an oligonucleotide tagged with the first member of a specific binding pair, the oligonucleotide being complementary to the PI strand and located to the right of the restriction site (R) near to, but not overlapping, primer P2. The reactions are then contacted with the second member of the specific binding pair immobilized on a solid support, and the levels of PI in digested versus undigested reactions are compared.
Fig. 4 is a schematic of a RFLP detection method involving the use of a first PCR primer tagged with a first detectable label (PI) and a second PCR primer tagged with a second detectable label (P2). After amplification by PCR, the products are digested with the restriction endonuclease (R) coπesponding to the polymoφhic restriction site, denatured, and contacted with a first oligonucleotide complementary to the PI strand and located to the right of the restriction site (R) near to, but not overlapping primer P2, and a second oligonucleotide complementary to the P2 strand and located to the right of the restriction site (R) near to, but not overlapping the sequence complementary to primer P2. Both the first and second oligonucleotides are tagged with the first member of a specific binding pair (Y). The reactions are then contacted with the second member of the specific binding pair immobilized on a solid support, and the ratio of PI to P2 bound to the solid support is determined. Fig. 5 is a schematic of a RFLP detection method involving the use of a first
PCR primer tagged with a detectable label (X) and a second PCR primer tagged with the first member of a first specific binding pair (Y). After amplification by PCR, the products are digested with the restriction enzyme (R) coπesponding to the polymoφhic restriction site, and are contacted with the second member of the first specific binding pair immobilized on a first solid support. The filtrate is then bound to a solid support with the anchor sequence (or contacted with an oligonucleotide complementary to the X strand between the restriction site (R) and the label (X), the oligonucleotide being tagged with the first member of a second specific binding pair, and then contacted with the second member of the second specific binding pair immobilized on a second solid support), and the levels of the detectable label bound to the first solid support and the anchor sequence (or second solid support) are determined. Fig. 6 is a schematic of a RFLP detection method involving the use of a first unlabeled PCR primer and a second PCR primer tagged with a detectable label (X). After amplification by PCR, the products are digested with the restriction enzyme (R) coπesponding to the polymoφhic restriction site, and contacted with an oligonucleotide complementary to the single-stranded ends generated in the digestion, the oligonucleotide being tagged with the first member of a specific binding pair. The products are then contacted with the second member of the first specific binding pair, bound to a first solid support. The filtrate is then bound to a solid support with the anchor sequence (or contacted with an oligonucleotide complementary to the X strand, the oligonucleotide being tagged with the first member of a second specific binding pair, and then contacted with the second member of the second specific binding pair immobilized on a second solid support), and the levels of the detectable label bound to the first solid support and the anchor sequence (or second solid support) are determined.
Fig. 7 is a schematic of a RFLP detection method involving the use of PCR primers flanking the polymoφhic restriction site (the "Alu I" site). Following PCR amplification, the reaction products are digested with the restriction endonuclease coπesponding to the polymoφhic restriction site (Alu I), and the fragments are run on an agarose gel. The separated fragments are detected as an indication of the presence or absence of the polymoφhic marker. Fig. 8 is a schematic of a typical gel analysis according the method described in
Fig. 7.
Figs. 9A-9E are schematics of a method for cloning polymoφhic restriction fragments. Fig. 10 is a schematic of a non-gel based method for detection of CAPS markers.
Fig. 11 is a schematic of parallel processing of 100 CAPS markers on a microchip containing an aπay of oligonucleotide probes.
Fig. 12 is a schematic of a method for detecting a cleaved end of a CAPS marker.
Fig. 13 is a schematic of a method for distinguishing heterozygous CAPS alleles from homozygous CAPS alleles, involving the use of the method for detecting a cleaved end of a CAPS marker shown in Fig. 12.
Methods for Generating and Detecting Genetic Polvmoφhisms
The present invention provides several methods for detecting Cleaved Amplified Polymoφhic Sequences (CAPS; Konieczny et al., The Plant Journal 4(2):403-410, 1993). In the CAPS method, a nucleic acid containing a polymoφhic restriction site is amplified using primers flanking the restriction site. The resulting
PCR product is digested with the restriction endonuclease coπesponding to the polymoφhic restriction site, and the digested products are analyzed by gel electrophoresis.
The detection methods of the present invention vary greatly from one another in detail, however they share three central features: (1) the nucleic acid containing the polymoφhic restriction site is amplified by PCR using differently labeled primers flanking the polymoφhic restriction site, (2) the resulting PCR product is digested with the restriction endonuclease coπesponding to the polymoφhic restriction site (which will cleave the DNA of some individuals but not cleave the DNA of others, depending on the presence of the polymoφhism), and (3) the resulting digestion products are analyzed by detection of the labels they contain, and/or labels attached to oligonucleotides complementary to the digestion products, in order to determine the identity of the polymoφhic restriction site. The methods of the invention allow rapid and efficient analyses of a large number of samples. The nucleic acid sample containing the polymoφhic restriction site being analyzed can be obtained from any source, e.g., a tissue homogenate, blood, amniotic fluid, chorionic villus samples, and a bacterial culture; and can be obtained from these sources using standard methods. Only a minute quantity of nucleic acid is required, and can be DNA or RNA (in the case of RNA, a reverse transcription step is required before the PCR step). The PCR methods used in the methods of the present invention are caπied out using standard methods (see, e.g., Ausubel et al., Cuπent Protocols in Molecular Biology, John Wiley and Sons, New York, 1989; Erlich, PCR Technology, Stockton Press, New York, 1989; Innis et al., PCR Protocols: A Guide to Methods and Applications, Academic Press, Harcourt Brace Javanovich, New York, 1990; Sambrook et al., Molecular Cloning: A Laboratory Manual, Cold Spring Harbor Laboratory Press, Cold Spring Harbor, New York, 1989). Restriction enzyme digestion is also carried out by standard methods using any of a number of available restriction endonucleases (see, e.g., Ausubel et al., supra; New England Biolabs,
Beverly, MA).
The primers and oligonucleotides used in the methods of the present invention are preferably DNA, and can be synthesized using standard techniques and, when appropriate, detectably labeled using standard methods (Ausubel et al., supra). Detectable labels that can be used to tag the primers and oligonucleotides used in the methods of the invention include, but are not limited to, digoxigenin, fluorescent labels (e.g., fluorescein and rhodamine), enzymes (e.g., horseradish peroxidase and alkaline phosphatase), biotin (which can be detected by anti-biotin specific antibodies or enzyme-conjugated avidin derivatives), radioactive labels (e.g., 32P and 125I), colorimetric reagents, and chemiluminescent reagents. The labels used in the methods of the invention are detected using standard methods.
The specific binding pairs useful in the methods of the invention include, but are not limited to, avidin-biotin, streptavidin-biotin, hybridizing nucleic acid pairs, interacting protein pairs, antibody-antigen pairs, reagents containing chemically reactive groups (e.g., reactive amino groups), and nucleic acid sequence-nucleic acid binding protein pairs.
The solid supports useful in the methods of the invention include, but are not limited to, agarose, acrylamide, and polystyrene beads; polystyrene microtiter plates (for use in, e.g., ELISA); and nylon and nitrocellulose membranes (for use in, e.g., dot or slot blot assays).
Some methods of the invention employ solid supports containing aπays of nucleic acid probes. In these cases, solid supports made of materials such as glass (e.g., glass plates), silicon or silicon-glass (e.g., microchips), or gold (e.g., gold plates) can be used. Methods for attaching nucleic acid probes to precise regions on such solid surfaces, e.g., photolithographic methods, are well known in the art, and can be used to make solid supports for use in the invention. (For example, see, Schena et al., Science 270:467-470, 1995; Kozal et al., Nature Medicine 2(7):753-759, 1996; Cheng et al., Nucleic Acids Research 24(2):380-385, 1996; Lipshutz et al., BioTechniques
19(3):442-447, 1995; Pease et al., Proc. Natl. Acad. Sci. USA 91 :5022-5026, 1994; Fodor et al., Nature 364:555-556, 1993; Pirrung et al., U.S. Patent No. 5,143,854; and Fodor et al, WO 92/10092.)
The methods of the invention can be facilitated by the use of kits which contain the reagents required for carrying out the assays. The kits can contain reagents for carrying out the analysis of a single polymoφhic restriction site (for use in, e.g., diagnostic methods) or multiple polymoφhic restriction sites (for use in, e.g., genomic mapping). When multiple samples are analyzed, multiple sets of the appropriate primers and oligonucleotides are provided in the kit. In addition to the primers and oligonucleotides required for carrying out the various methods, the kits may contain the enzymes used in the methods, and the reagents for detecting the labels, e.g., the substrates for enzyme labels, etc. The kits can also contain solid substrates for used in carrying out the method of the invention. For example, the kits can contain solid substrates, such as glass plates or silicon or glass microchips, containing aπays of nucleic acid probes.
As discussed above, the invention provides methods and kits for generating and detecting the presence or absence of a polymoφhic restriction site in a nucleic acid. Examples I-IX and XII-XIV describe eight variations of the methods of the invention. Example X describes a prefeπed use for the methods of the invention. Example XI describes a prefeπed method for cloning polymoφhic restriction fragments. The following examples are meant to illustrate, but not limit, the methods of the present invention. Other suitable modifications and adaptations of the variety of conditions and parameters of molecular biology which are obvious to those skilled in the art are within the spirit and scope of the present invention.
EXAMPLES Example I.
In this method, the nucleic acid containing the polymoφhism is amplified by PCR using a first and a second primer flanking the polymoφhic restriction site, the first primer being tagged with the first member of a specific binding pair, the second primer being tagged with a detectable label. The resulting PCR product is digested with the restriction endonuclease coπesponding to the polymoφhic restriction site and the digested products are contacted with the second member of the specific binding pair, immobilized on a solid support. The level of the detectable label bound to the solid support is then measured. The presence of the detectable label bound to the solid support is an indication of the absence of the polymoφhic restriction site in the nucleic acid, while the absence of the detectable label bound to the solid support is an indication of the presence of the polymoφhic restriction site in the nucleic acid. An embodiment of this method is shown in Fig. 1.
Example II. This method is identical to that described in Example I, with the added step of annealing and ligating to the single-stranded ends generated in the digestion reaction, an oligonucleotide tagged with a second detectable label. After applying the reaction to the second member of the specific binding pair, the levels of both the first and the second detectable labels bound to the solid support are determined. The presence of only the first detectable label bound to the solid support is an indication of a homozygote lacking the polymoφhic restriction site, the presence of only the second detectable label bound to the solid support is an indication of a homozygote containing the polymoφhic restriction site, and the presence of both the first and the second detectable labels bound to the solid support is an indication of a heterozygote. An embodiment of this method is shown in Fig. 2.
In addition to labeling the cleaved ends of the CAPS products by annealing and ligating an oligonucleotide to the sticky ends generated by the cleavage, as is described above, and, e.g., in Examples VI and VIII, the cleaved ends can be labeled by using a method described in further detail below in Example XIV. Briefly, in this method, the denatured product is contacted with an oligonucleotide to generate a first reaction product. The oligonucleotide contains a 3' portion that hybridizes to a first region in the first strand that flanks the polymoφhic restriction site on the side of the polymorphic restriction site containing a sequence coπesponding to the first primer.
The 3' end of the oligonucleotide is blocked by, e.g., a di-deoxynucleotide, so that it cannot serve as a primer for DNA polymerase. The oligonucleotide contains a 5' portion that does not hybridize to a second region in the first strand that flanks the polymorphic restriction site on the side of the polymoφhic restriction site containing a sequence that is complementary to the second primer. The use of such an oligonucleotide to label a cleaved end of a CAPS marker is illustrated in Fig. 12. This method can also be applied to the CAPS detection techniques of, for example, Examples VI and VIII.
Example III.
In this method, the nucleic acid is amplified using a first and a second primer flanking the polymoφhic restriction site, the first primer being tagged with a detectable label, the second primer being unlabeled. A portion of the PCR reaction is digested with the restriction endonuclease coπesponding to the polymoφhic restriction site, while another portion is left undigested. Both the digested and undigested portions are then denatured, and contacted with an oligonucleotide tagged with the first member of a specific binding pair. The oligonucleotide is complementary to a sequence in the strand of the PCR product containing the detectable label, the sequence being between the polymoφhic restriction site and the sequence complementary to the second primer.
The reaction is then contacted with the second member of the specific binding pair, immobilized on a solid support, and the ratio of the levels of the detectable label bound to the solid support between undigested and digested samples is determined. A ratio of 1 :0 between equivalent portions of undigested and digested samples is an indication of a homozygote containing the polymoφhic restriction site, a ratio of 1: 1 between equivalent portions of undigested and digested samples is an indication of a homozygote lacking the polymoφhic restriction site, and a ratio of 2: 1 between equivalent portions of undigested and digested samples is an indication of a heterozygote. While the sample volumes used for detection and comparison need not be equivalent, the appropriate calculations must be carried out to account for this adjustment prior to determining the ratio of detectable label in digested and undigested samples. An embodiment of this method is shown in Fig. 3.
Example IV.
In this method, the nucleic acid is amplified by PCR using a first primer and a second primer flanking the polymoφhic restriction site, the first primer being tagged with a first detectable label, and the second primer being tagged with a second detectable label.
The PCR product is digested with the restriction endonuclease coπesponding to the polymoφhic restriction site, denatured, and contacting with a first and a second oligonucleotide. The first oligonucleotide is complementary to a first sequence in the strand of the PCR product containing the first detectable label, the first sequence being between the polymoφhic restriction site and the sequence coπesponding to the first primer. The first oligonucleotide is tagged with the first member of a first specific binding pair. The second oligonucleotide is complementary to a second sequence in the strand of the PCR product containing the second detectable label. The second sequence is on the same side of the polymoφhic restriction site as the first sequence, and is not contained within, or complementary to, either the first or the second primer. The second oligonucleotide is tagged with the first member of a second specific binding pair. A first portion of the reaction is then contacted with the second member of the first specific binding pair, immobilized on a first solid support, while a second portion of the reaction is contacted with the second member of the second specific binding pair, immobilized on a second solid support. The ratio of the levels of the first and second detectable labels bound to the first and second solid supports is then determined. A ratio of 1 :0 between equivalent amounts of the first and second portions is an indication of a homozygote containing the polymoφhic restriction site, a ratio of 1 :1 between equivalent amounts of the first and second portions is an indication of a homozygote lacking the polymoφhic restriction site, and a ratio of 2: 1 between equivalent amounts of the first and second portions is an indication of a heterozygote.
In the case where the first sequence (to which the first oligonucleotide is complementary) in the strand containing the first detectable label is between the polymoφhic restriction site and the sequence complementary to the second primer, the ratios differ, as follows. The ratio of the levels of the first and second detectable labels bound to the first and second solid supports is 0: 1 between equivalent amounts of the first and second portions in the case of a homozygote containing the polymoφhic restriction site. The ratio is 1 : 1 between equivalent amounts of the first and second portions in the case of a homozygote lacking the polymoφhic restriction site, and the ratio is 1 :2 between equivalent amounts of the first and second portions in the case of a heterozygote. An embodiment of this method is shown in Fig. 4. Example V.
In this method, the nucleic acid is amplified by PCR using a first and a second primer flanking the polymoφhic restriction site, the first primer being tagged with the first member of a first specific binding pair, the second primer being tagged with a detectable label. The PCR product is digested with the restriction endonuclease coπesponding to the polymoφhic restriction site, and the reaction is then contacted with the second member of the first specific binding pair, immobilized on a first solid support.
The material not bound to the first solid support is denatured and contacted with an oligonucleotide complementary to a sequence in the strand of the PCR product containing the detectable label. The sequence is between the polymoφhic restriction site and the sequence coπesponding to the second primer, and the oligonucleotide is tagged with the first member of a second specific binding pair. The reaction is then contacted with the second member of the second specific binding pair, immobilized on a second solid support, and the ratio of the level of the detectable label bound to the first solid support compared to the level of the detectable label bound to the second solid support is determined. A ratio of 0: 1 is an indication of a homozygote containing the polymoφhic restriction site, a ratio of 1 :0 is an indication of a homozygote lacking the polymoφhic restriction site, and a ratio of 1 : 1 is an indication of a heterozygote. These ratios are coπect in cases where the total amount of the material not bound to the first solid support is used in the following steps, and should be adjusted accordingly, if a different amount of the material is used. An embodiment of this method is shown in Fig. 5.
Example VI.
In this method, the nucleic acid is amplified by PCR using a first and a second primer flanking the polymoφhic restriction site, the first primer being tagged with a detectable label, the second primer being unlabeled. The PCR product is digested with the restriction endonuclease coπesponding to the polymoφhic restriction site, and a first oligonucleotide tagged with the first member of a first specific binding pair is annealed and ligated to the single-stranded ends generated in the digestion reaction. The reaction is then contacted with the second member of the first specific binding pair, immobilized on a first solid support.
The material not bound to the first solid support is denatured, and contacted with a second oligonucleotide complementary to a sequence in the strand of the PCR product containing the detectable label, the sequence being between the polymoφhic restriction site and either the sequence coπesponding to the first primer or the sequence complementary to the second primer. The second oligonucleotide is tagged with the first member of a second specific binding pair. The reaction is then contacted with the second member of the second specific binding pair, immobilized on a second solid support, and the ratio of the level of the detectable label bound to the first solid support compared to the level of the detectable label bound to the second solid support is determined. A ratio of 1 :0 is an indication of a homozygote containing the polymoφhic restriction site, a ratio of 0:1 is an indication of a homozygote lacking the polymoφhic restriction site, and a ratio of 1 : 1 is an indication of a heterozygote. These ratios are coπect in cases where the total amount of the material not bound to the first solid support is used in the following steps, and should be adjusted accordingly, if a different amount of the material is used. An embodiment of this method is shown in Fig. 6.
Example VII.
In this method, the nucleic acid is amplified by PCR using a first and a second primer flanking the polymoφhic restriction site, the first primer being tagged with the first member of a first specific binding pair, the second primer being tagged with a detectable label. The PCR product is digested with the restriction endonuclease coπesponding to the polymoφhic restriction site, and contacted with the second member of the first specific binding pair, immobilized on a first solid support.
The material not bound to the first solid support is denatured and contacted with an oligonucleotide complementary to a sequence in the strand of the PCR product containing the detectable label. The sequence is between the polymoφhic restriction site and the sequence coπesponding to the second primer, and the oligonucleotide is immobilized on a second solid support (e.g., a nylon or nitrocellulose membrane).
The ratio of the level of detectable label bound to the first solid support to the level of detectable label bound to the second solid support is then determined. A ratio of 0: 1 is an indication of a homozygote containing the polymoφhic restriction site, a ratio of 1 :0 is an indication of a homozygote lacking the polymoφhic restriction site, and a ratio of 1 : 1 is an indication of a heterozygote. These ratios are coπect in cases where the total amount of the material not bound to the first solid support is used in the following steps, and should be adjusted accordingly, if a different amount of the material is used. An embodiment of this method is shown in Fig. 5.
Example VIII.
In this method, the nucleic acid is amplified by PCR using a first and a second primer flanking the polymoφhic restriction site, the first primer being tagged with a detectable label, the second primer being unlabeled. The PCR product is digested with the restriction endonuclease coπesponding to the polymoφhic restriction site, and a first oligonucleotide tagged with the first member of a first specific binding pair is annealed and ligated to the single-stranded ends generated in the digestion reaction. The reaction is contacted with the second member of the first specific binding pair, immobilized on a first solid support. The material not bound to the first solid support is denatured, and contacted with a second oligonucleotide complementary to a sequence in the strand of the PCR product containing the detectable label. The sequence is between the polymoφhic restriction site and either the sequence coπesponding to the first primer or the sequence complementary to the second primer, and the second oligonucleotide is immobilized on a second solid support (e.g., a nylon or nitrocellulose membrane).
The ratio of the level of the detectable label bound to the first solid support to the level of the detectable label bound to the second solid support is then determined.
A ratio of 1 :0 is an indication of a homozygote containing the polymoφhic restriction site, a ratio of 0: 1 is an indication of a homozygote lacking the polymoφhic restriction site, and a ratio of 1 : 1 is an indication of a heterozygote. These ratios are coπect in cases where the total amount of the material not bound to the first solid support is used in the following steps, and should be adjusted accordingly, if a different amount of the material is used. An embodiment of this method is shown in Fig. 6.
PCR primers containing nucleic acid tags on their 5' ends can also be used in the methods of the invention. These primers can be used in pairs, or in combination with un-tagged primers, in the initial cycles of PCR, followed by the addition of a "universal primer(s)" complementary to the nucleic acid tags in the first primers, and contain detectable labels (e.g., biotin, fluorescent, or ELISA tags). The use of nucleic acid tagged primers in the early rounds of PCR is a cost-effective measure, as only one set of primers, the universal primers, which can be used in the analysis of many different polymorphic sites, need to be detectably labeled. The sets of primers specific for individual polymoφhic restriction sites do not have to be tagged with detectable labels, but rather need only to be complementary to the universal primers in their 5* ends.
Example IX. In another method of the invention, the nucleic acid is amplified by PCR using a first and a second primer flanking the polymoφhic restriction site. The PCR product is digested with the restriction endonuclease coπesponding to the polymoφhic restriction site, and, as shown in Fig. 7, the digestion products are run on a gel (preferably an agarose gel). To simplify the gel reading, the first and second primers are preferably designed to generate a PCR product that is easily resolvable on an agarose gel (e.g., preferably larger than 100 base pairs and smaller than 1000 base pairs), and the polymoφhic restriction site is preferably located at an asymmetric position within the amplified fragment. Using this technique, short gel runs can be used for analysis, and the cleaved products are easily detected. In the particular example shown in Fig. 8, primers are designed to produce PCR amplified products of 300 base pairs, and cleavage at the RFLP site yields products of 200 base pairs and 100 base pairs. In a preferred method of carrying out this method, sets of primer pairs are provided that detect a number of RFLP markers. Each set of primers may be provided, for example, in one of the wells of a 96-well microtiter plate, and PCR reactions run independently. Following restriction digestion, the reaction products are transfeπed to an agarose gel and separated by electrophoresis. A typical result of this method is shown in Fig. 8.
Detection of the amplified and cleaved products after electrophoretic separation can be caπied out by standard methods of DNA staining (e.g., ethidium bromide staining) or blotting (e.g., Southern blotting). Alternatively, one or both of the PCR primers can be detectably labeled, and the labels can be detected as described above.
Example X.
A prefeπed use of the methods of the invention is in conjunction with a method called RFLP subtraction. RFLP subtraction provides a large number of polymoφhic genetic markers, while the methods of the present invention provide efficient methods for their analysis.
Carrying out RFLP subtraction results in the purification of fragments that are present in one population (the tracer) but absent in another (the driver). Purification is achieved by removing all of the fragments in the tracer DNA that have counteφarts in the driver DNA using subtractive hybridization (Innis et al., PCR Protocols: A Guide to Methods and Applications, Academic Press, Harcourt Brace Javanovich, New York, 1990). In RFLP subtraction, the tracer is a size fraction of digested DNA from one strain and the driver is the same size fraction from a polymoφhic strain. The products obtained after removing the common sequences are RFLPs; they are sized tracer fragments whose driver counteφarts are not found in the same size fraction.
There are three steps in RFLP subtraction: preparation of the driver and tracer, subtractive hybridization, and removal of non-hybridizing sequences from the tracer. To prepare the driver and tracer DNA, genomic DNA from two different strains is digested with a restriction endonuclease, and the ends of the restriction fragments from each strain are capped with different oligonucleotide adapters. The low molecular weight fragments are then purified from a slice of an agarose gel and amplified using one of the adapter strands as a PCR primer. A biotinylated primer can be used to amplify the driver so that driver DNA can be removed following the subtractive hybridizations by binding to avidin coated beads.
Three rounds of subtractive hybridization are performed to remove tracer sequences that also occur in the driver. A small amount of tracer is mixed with an excess of biotinylated driver, the mixture is denatured and allowed to re-anneal. Most tracer sequences will hybridize to complementary biotinylated driver strands. Some tracer sequences, however, are not represented in the driver because they reside on large restriction fragments (i.e., they are RFLPs) or are missing from the driver genome. These fragments will have no complementary biotinylated strands with which to anneal. The biotinylated driver DNA, and any tracer that has annealed to it, is then removed using avi din-coated beads. The unbound fraction is then subjected to two more rounds of subtractive hybridization, tracer DNA remaining after the third round is amplified, and poorly hybridizing sequences are removed. Example XI.
Figure 9 shows a prefeπed method for cloning polymoφhic restriction fragments. The object of this method is to clone restriction fragments from organism B (generated by restriction endonuclease A) that do not contain cleavage sites for restriction endonuclease B, and which correspond to restriction fragments in organism A (generated by restriction endonuclease A) that do contain at least one restriction site for restriction endonuclease B. These polymoφhic restriction fragments are useful as CAPS markers for the detection methods described above.
Refeπing to the method outlined in Figs. 9A-9E, in Fig. 9A, genomic DNA isolated from polymoφhic individuals A and B is separately digested with restriction enzyme A, which preferably leaves so-called sticky ends. An oligonucleotide adaptor (#1), with complementary sticky ends, is ligated to the restriction fragments from individual A. A different oligonucleotide adaptor (#3) is ligated to the restriction fragments from individual B. In Fig. 9B, the restriction fragments from Fig. 9A are cleaved with restriction endonuclease B, which again preferably leaves sticky ends. In the case of the DNA fragments from individual A, an oligonucleotide adaptor (#2), with complementary sticky ends for enzyme B, is ligated to the restriction fragments generated by cleavage with enzyme B. In Fig. 9C, the DNA fragments from individual A are amplified using the PCR with an oligonucleotide primer complementary to adaptor #1 and with a biotinylated oligonucleotide primer complementary to adaptor #2.
In Fig. 9D, the amplified products originating from individual A are mixed with the non-amplified fragments of Fig. 9B from individual B. The mixed DNA fragments are then heat denatured, annealed, and adsorbed onto an avidin-coated solid support (e.g., beads). The avidin coated support containing the adsorbed fragments is thoroughly washed. If desired, the adsorbed fragments may be eluted, re-amplified with the same primers as above, adsorbed onto a fresh avidin-containing support, and thoroughly washed. This step can be repeated as many times as is necessary or desired.
In Fig. 9E, the fragments adsorbed to the avidin-coated beads are eluted and amplified using PCR with primers complementary to adaptor #3. The amplified products should coπespond to the desired restriction fragments described above.
These amplified fragments are cloned and then tested individually using the Southern DNA blot hybridization method for their ability to display the desired RFLP.
Example XII. In this method, the nucleic acid is amplified by PCR using a first and a second primer flanking the polymoφhic restriction site, with the first primer being tagged with a detectable label. The amplification generates a PCR product containing a first strand tagged with the detectable label and a second, unlabeled strand. The PCR product is digested with the restriction endonuclease coπesponding to the polymoφhic restriction site and the digestion product is denatured. The denatured product is contacted with a first probe that (1) contains a sequence that hybridizes to a first sequence in the first strand of the PCR product, and (2) is immobilized on a first binding element. The first sequence is between the polymoφhic restriction site and the sequence in the first strand that is complementary to the second primer. The first binding element is monitored for the presence of the detectable label.
Detection of the detectable label on the first binding element indicates the absence of the polymoφhic restriction site in the nucleic acid, and a failure to detect the detectable label on the first binding element indicates the presence of the polymoφhic restriction site in the nucleic acid. In addition to the first probe described above, this method can employ the use of a second, a third, or a fourth probe. The second probe contains a sequence that hybridizes to a second sequence which is in the first strand and is between the polymoφhic restriction site and the sequence in the first strand that coπesponds to the first primer. The third probe contains a sequence that hybridizes to a third sequence which is in the second strand and is between the polymoφhic restriction site and the sequence in the second strand coπesponding to the second primer. The fourth probe contains a sequence that hybridizes to a fourth sequence which is in the second strand and is between the polymoφhic restriction site and the sequence in the second strand that is complementary to the first primer. The second, third, and fourth probes are immobilized on a second, third, and fourth binding element, respectively. The second binding element can be monitored for the presence of the detectable label as a positive control, while the third or fourth binding elements can be monitored for the presence of the detectable label as negative controls. The first, second, third, and fourth binding elements, in this and in other methods of the invention, can be present on a solid support having similar sets of binding elements for testing different nucleic acids (see, for example, Fig. 1 1).
The binding elements, for example, the first, second, third, and fourth binding elements, used in this method of the invention can be present as distinct regions on a single solid support. For example, they can be specific sets of nucleic acids bound to distinct regions on a glass plate or on a microchip, such as a glass, silicon, or glass- silicon microchip (see above).
Example XIII.
In this method a nucleic acid is amplified by PCR using a first and a second primer flanking the polymoφhic restriction site. The first primer is tagged with a first detectable label and the second primer is tagged with a second detectable label. The amplification thus generates a PCR product containing a first strand tagged with the first detectable label and a second strand tagged with the second detectable label. In this method, the first and second labels can be identical or distinct.
The PCR product is treated with a restriction endonuclease coπesponding to the polymoφhic restriction site to generate a digestion product, which is denatured to generate a denatured product. The denatured product is contacted with a first and a second probe. The first probe, which is immobilized on a first binding element, contains a sequence that hybridizes to a first sequence in the first strand that is between the polymoφhic restriction site and the sequence in the first strand that is complementary to the second primer. The second probe, which is immobilized on a second binding element, contains a sequence that hybridizes to a second sequence in the second strand that is between the polymoφhic restriction site and the sequence in the second strand that is complementary to the first primer.
The first binding element is monitored for the presence of the first detectable label and the second binding element is monitored for the presence of the second detectable label. Detection of the first detectable label on the first binding element and detection of the second detectable label on the second binding element indicates the absence of the polymoφhic restriction site in the nucleic acid, while a failure to detect the first detectable label on the first binding element and a failure to detect the second detectable label on the second binding element indicates the presence of the polymoφhic restriction site in the nucleic acid.
In addition to the first and second probes described above, this method can involve the use of a third and fourth probe. The third probe, which is immobilized on a third binding element, contains a sequence that hybridizes to a third sequence which is in the first strand and that is between the polymoφhic restriction site and the sequence in the first strand coπesponding to the first primer. The fourth probe, which is immobilized on a fourth binding element, contains a sequence that hybridizes to a fourth sequence which is in the second strand and that is between the polymoφhic restriction site and the sequence in the second strand coπesponding to the second primer.
The third or fourth binding elements can be monitored for the presence of the first or second detectable labels as controls. For example, the third binding element can be monitored for the presence of the first detectable label and the fourth binding element can be monitored for the presence of the second detectable label.
The first and second, or the first, second, third, and fourth binding elements can be present as distinct regions on a solid support, such as glass (e.g., a glass plate) or a microchip (e.g., a silicon or a silicon-glass microchip). Embodiments of this method are illustrated in Figs. 10 and 11.
Example XIV
In this method, the nucleic acid is amplified by PCR using a first and a second primer flanking the polymoφhic restriction site. The amplification generates a PCR product containing a first strand containing a sequence coπesponding to the first primer and a second strand containing a sequence coπesponding to the second primer.
The PCR product is treated with a restriction endonuclease coπesponding to the polymoφhic restriction site to generate a digestion product, which is denatured to generate a denatured product. The denatured product is contacted with an oligonucleotide to generate a first reaction product. The oligonucleotide contains a 3' portion that hybridizes to a first region in the first strand that flanks the polymoφhic restriction site on the side of the polymoφhic restriction site containing a sequence coπesponding to the first primer. The 3' end of the oligonucleotide is blocked by, e.g., a di-deoxynucleotide, so that it cannot serve as a primer for DNA polymerase. The oligonucleotide contains a 5' portion that does not hybridize to a second region in the first strand that flanks the polymoφhic restriction site on the side of the polymoφhic restriction site containing a sequence that is complementary to the second primer. The use of such an oligonucleotide to label a cleaved end of a CAPS marker is illustrated in Fig. 12.
As illustrated in Fig. 12., the first reaction product is treated with a DNA polymerase to extend the unblocked, primed 3' end to generate a second reaction product, which is amplified by PCR using the first primer, tagged with a first detectable label, and a third primer, which hybridizes to a sequence that is complementary to the 5' portion of the oligonucleotide, to generate a second PCR product. The third primer is tagged with a second detectable label. In this method, the first and second detectable labels can be identical or distinct. The second PCR product is denatured to generate a second denatured product, which is contacted with a first and a second probe. The first probe, which is immobilized on a first binding element, contains a sequence that hybridizes to a first sequence in the second strand that is between the polymoφhic restriction site and the sequence in the second strand that is complementary to the first primer. The second probe, which is immobilized on a second binding element, contains a sequence that hybridizes to a second sequence in the first strand that is between the polymoφhic restriction site and the sequence in the first strand that is complementary to the second primer.
The first binding element is monitored for the presence of the second detectable label and the second binding element is monitored for the presence of the first detectable label. Detection of the second detectable label on the first binding element and detection of the first detectable label on the second binding element indicates a heterozygote, detection of the second detectable label on the first binding element and a failure to detect the first detectable label on the second binding element indicates a homozygote containing the polymoφhic restriction site, and detection of the first detectable label on the second binding element and a failure to detect the second detectable label on the first binding element indicates a homozygote lacking the polymoφhic restriction site.
In addition to the first and second probes described above, this method can employ a third or a fourth probe. The third probe, which is immobilized on a third binding element, contains a sequence that hybridizes to a third sequence in the first strand that is between the polymoφhic restriction site and the sequence in the first strand coπesponding to the first primer. The fourth probe, which is immobilized on a fourth binding element, contains a sequence that hybridizes to a fourth sequence in the second strand that is between the polymoφhic restriction site and the sequence in the second strand coπesponding to the second primer.
The third or fourth binding elements can be monitored for the presence of the first or second detectable labels as controls. For example, the third binding element can be monitored for the presence of the first detectable label.
The first and second, or the first, second, third, and fourth binding elements can be present as distinct regions on a solid support, such as a glass (e.g., a glass plate) or silicon (e.g., a microchip) support. This embodiment is illustrated in Fig. 13.
Use of oligonucleotides as described above provides several advantages. For example, because there can be a significant amount of overlap between the oligonucleotide and the cleaved product, highly stringent conditions can be used in the annealing reaction, leading to increased specificity. In addition, the 5' end of the oligonucleotide can be the same for many CAPS markers, as it is by design not homologous to any amplified sequences coπesponding to a CAPS marker for an organism of interest. These advantages also apply to other methods employing such an oligonucleotide, as are described below.
Other Embodiments The above examples are, therefore, to be construed as merely illustrative, and not limitative of the remainder of the disclosure in any way whatsoever.
From the above description, one skilled in the art can easily ascertain the essential characteristics of the present invention, and without departing form the spirit and scope thereof, can make various changes and modifications of the invention to adapt it to various usages and conditions. All publications cited herein are fully incoφorated by reference herein in their entirety. Other embodiments are in the claims set forth below.

Claims

1. A method for detecting the presence or absence of a polymoφhic restriction site in a nucleic acid, said method comprising the steps of:
(a) amplifying said nucleic acid by PCR using a first and a second primer flanking said polymoφhic restriction site, said first primer being tagged with a detectable label, wherein said amplifying generates a PCR product comprising a first strand tagged with said detectable label and an unlabeled second strand;
(b) treating said PCR product with a restriction endonuclease coπesponding to said polymorphic restriction site to generate a digestion product;
(c) denaturing said digestion product to generate a denatured product; (d) contacting said denatured product with a first probe, said first probe comprising a sequence that hybridizes to a first sequence in said first strand, said first sequence being between said polymoφhic restriction site and the sequence in said first strand that is complementary to said second primer, said first probe being immobilized on a first binding element; (e) monitoring said first binding element for the presence of said detectable label, wherein detection of said detectable label on said first binding element indicates the absence of said polymoφhic restriction site in said nucleic acid, and a failure to detect said detectable label on said first binding element indicates the presence of said polymoφhic restriction site in said nucleic acid.
2. The method of claim 1, further comprising the steps of:
(a) contacting said denatured product with a second, a third, or a fourth probe, said second probe comprising a sequence that hybridizes to a second sequence in said first strand, said second sequence being between said polymoφhic restriction site and the sequence in said first strand that coπesponds to said first primer, said second probe being immobilized on a second binding element; said third probe comprising a sequence that hybridizes to a third sequence in said second strand, said third sequence being between said polymoφhic restriction site and the sequence in said second strand coπesponding to said second primer, said third probe being immobilized on a third binding element; said fourth probe comprising a sequence that hybridizes to a fourth sequence in said second strand, said fourth sequence being between said polymoφhic restriction site and the sequence in said second strand that is complementary to said first primer, said fourth probe being immobilized on a fourth binding element; and
(b) monitoring said second, third, or fourth binding element for the presence of said detectable label.
3. The method of claim 1 , wherein said first binding element is a region on a solid support.
4. A method for detecting the presence or absence of a polymoφhic restriction site in a nucleic acid, said method comprising the steps of:
(a) amplifying said nucleic acid by PCR using a first and a second primer flanking said polymoφhic restriction site, said first primer being tagged with a first detectable label, said second primer being tagged with a second detectable label, wherein said amplifying generates a PCR product comprising a first strand tagged with said first detectable label and a second strand tagged with said second detectable label; (b) treating said PCR product with a restriction endonuclease coπesponding to said polymoφhic restriction site to generate a digestion product;
(c) denaturing said digestion product to generate a denatured product;
(d) contacting said denatured product with a first and a second probe, said first probe comprising a sequence that hybridizes to a first sequence in said first strand, said first sequence being between said polymoφhic restriction site and the sequence in said first strand that is complementary to said second primer, said first probe being immobilized on a first binding element; said second probe comprising a sequence that hybridizes to a second sequence in said second strand, said second sequence being between said polymoφhic restriction site and the sequence in said second strand that is complementary to said first primer, said second probe being immobilized on a second binding element;
(e) monitoring said first binding element for the presence of said first detectable label and monitoring said second binding element for the presence of said second detectable label, wherein detection of said first detectable label on said first binding element and detection of said second detectable label on said second binding element indicates the absence of said polymoφhic restriction site in said nucleic acid, and a failure to detect said first detectable label on said first binding element and a failure to detect said second detectable label on said second binding element indicates the presence of said polymoφhic restriction site in said nucleic acid.
5. The method of claim 4, further comprising the steps of:
(a) contacting said denatured product with a third or a fourth probe, said third probe comprising a sequence that hybridizes to a third sequence in said first strand, said third sequence being between said polymoφhic restriction site and the sequence in said first strand coπesponding to said first primer, said third probe being immobilized on a third binding element; said fourth probe comprising a sequence that hybridizes to a fourth sequence in said second strand, said fourth sequence being between said polymoφhic restriction site and the sequence in said second strand coπesponding to said second primer, said fourth probe being immobilized on a fourth binding element; and
(b) monitoring said third or fourth binding element for the presence of said first or second detectable label.
6. A method for detecting the presence or absence of a polymoφhic restriction site in a nucleic acid, said method comprising the steps of: (a) amplifying said nucleic acid by PCR using a first and a second primer flanking said polymoφhic restriction site, wherein said amplifying generates a PCR product comprising a first strand comprising a sequence coπesponding to said first primer and a second strand comprising a sequence coπesponding to said second primer;
(b) treating said PCR product with a restriction endonuclease coπesponding to said polymoφhic restriction site to generate a digestion product;
(c) denaturing said digestion product to generate a denatured product;
(d) contacting said denatured product with an oligonucleotide to generate a first reaction product, said oligonucleotide comprising a 3' portion that hybridizes to a first region in said first strand, said first region flanking said polymoφhic restriction site on the side of said polymoφhic restriction site comprising a sequence coπesponding to said first primer, said oligonucleotide being blocked so that it cannot serve as a primer for DNA polymerase, said oligonucleotide comprising a 5' portion that does not hybridize to a second region in said first strand, said second region flanking said polymoφhic restriction site on the side of said polymoφhic restriction site comprising a sequence that is complementary to said second primer;
(e) treating said first reaction product with a DNA polymerase to extend the unblocked, primed 3' end to generate a second reaction product; (0 amplifying said second reaction product by PCR using said first primer, tagged with a first detectable label, and a third primer that hybridizes to a sequence that is complementary to said 5' portion of said oligonucleotide to generate a second PCR product, said third primer being tagged with a second detectable label;
(g) denaturing said second PCR product to generate a second denatured product;
(h) contacting said second denatured product with a first and a second probe, said first probe comprising a sequence that hybridizes to a first sequence in said second strand, said first sequence being between said polymoφhic restriction site and the sequence in said second strand that is complementary to said first primer, said first probe being immobilized on a first binding element; said second probe comprising a sequence that hybridizes to a second sequence in said first strand, said second sequence being between said polymoφhic restriction site and the sequence in said first 5 strand that is complementary to said second primer, said second probe being immobilized on a second binding element;
(i) monitoring said first binding element for the presence of said second detectable label and monitoring said second binding element for the presence of said first detectable label, wherein detection of said second detectable label on said first o binding element and detection of said first detectable label on said second binding element indicates a heterozygote, detection of said second detectable label on said first binding element and a failure to detect said first detectable label on said second binding element indicates a homozygote comprising said polymoφhic restriction site, and detection of said first detectable label on said second binding element and a failure 5 to detect said second detectable label on said first binding element indicates a homozygote lacking said polymoφhic restriction site.
7. The method of claim 6, further comprising the steps of: (a) contacting said second denatured product with a third or a fourth probe, said 0 third probe comprising a sequence that hybridizes to a third sequence in said first strand, said third sequence being between said polymoφhic restriction site and the sequence in said first strand coπesponding to said first primer, said third probe being immobilized on a third binding element; said fourth probe comprising a sequence that hybridizes to a fourth sequence in said second strand, said fourth sequence being 5 between said polymoφhic restriction site and the sequence in said second strand coπesponding to said second primer, said fourth probe being immobilized on a fourth binding element; and (b) monitoring said third or fourth binding element for the presence of said first or second detectable label.
8. The method of claim 2, 5, or 7, wherein said first, second, third, and fourth binding elements are each distinct regions on a solid support.
9. The method of claim 4 or 6, wherein said first and second binding elements are each distinct regions on a solid support.
10. The method of claim 4 or 6, wherein said first and said second detectable labels are identical.
11. The method of claim 3, 8, or 9, wherein said solid support is a microchip.
12. The method of claim 3, 8, or 9, wherein said solid support is glass.
13. A kit for detecting the presence or absence of a polymoφhic restriction site in a nucleic acid, said kit comprising: one or more sets of a first and a second primer flanking said polymoφhic restriction site, said first primer being tagged with a detectable label, wherein amplifying said nucleic acid by PCR with said first and second primers generates a PCR product comprising a first strand tagged with said detectable label and a second strand; and one or more first probes, wherein each of said first probes comprises a sequence that hybridizes to a first sequence in said first strand, said first sequence being between said polymoφhic restriction site and the sequence in said first strand that is complementary to said second primer, and each of said first probes is immobilized on a first binding element.
14. The kit of claim 13, further comprising one or more sets of a second, third, or fourth probe, each of said second probes comprising a sequence that hybridizes to a second sequence in said first strand, said second sequence being between said polymoφhic restriction site and the sequence in said first strand that coπesponds to said first primer, said second probe being immobilized on a second binding element; each of said third probes comprising a sequence that hybridizes to a third sequence in said second strand, said third sequence being between said polymoφhic restriction site and the sequence in said second strand coπesponding to said second primer, said third probe being immobilized on a third binding element; and each of said fourth probes comprising a sequence that hybridizes to a fourth sequence in said second strand, said fourth sequence being between said polymoφhic restriction site and the sequence in said second strand that is complementary to said first primer, said fourth probe being immobilized on a fourth binding element.
15. The kit of claim 13, wherein said first binding element is a region on a solid support.
16. The kit of claim 13, wherein said one or more second primers each comprises a second detectable label and said kit further comprises a second probe comprising a sequence that hybridizes to a second sequence in said second strand, said second sequence being between said polymoφhic restriction site and the sequence in said second strand that is complementary to said first primer, and said second probe being immobilized on a second binding element.
17. The kit of claim 16, further comprising one or more sets of a third or a fourth probe, each of said third probes comprising a sequence that hybridizes to a third sequence in said first strand, said third sequence being between said polymoφhic restriction site and the sequence in said first strand coπesponding to said first primer, said third probe being immobilized on a third binding element; each of said fourth probes comprising a sequence that hybridizes to a fourth sequence in said second strand, said fourth sequence being between said polymoφhic restriction site and the sequence in said second strand coπesponding to said second primer, and said fourth probe being immobilized on a fourth binding element.
18. The kit of claim 13, further comprising one or more second probes, each comprising a sequence that hybridizes to a second sequence in said first strand, said second sequence being between said polymoφhic restriction site and the sequence in said first strand that coπesponds to said first primer, and said second probe being immobilized on a second binding element.
19. A kit for detecting the presence or absence of a polymoφhic restriction site in a nucleic acid, said kit comprising: one or more sets of a first and a second PCR primer flanking said polymoφhic restriction site, said first primer being tagged with a first detectable label, wherein amplifying said nucleic acid by PCR using said first and second primers generates a PCR product comprising a first strand tagged with said first detectable label and a second strand; one or more oligonucleotides comprising a 3' portion that hybridizes to a first region in said first strand, said first region flanking said polymoφhic restriction site on the side of said polymoφhic restriction site comprising a sequence coπesponding to said first primer, said oligonucleotide being blocked so that it cannot serve as a primer for DNA polymerase, said oligonucleotide comprising a 5' portion that does not hybridize to a second region in said first strand, said second region flanking said polymoφhic restriction site on the side of said polymoφhic restriction site comprising a sequence that is complementary to said second primer; one or more third primers, each of which that hybridizes to a sequence that is complementary to said 5' portion of said oligonucleotide, said third primer being tagged with a second detectable label; one or more sets of a first and a second probe, each of said first probes comprising a sequence that hybridizes to a first sequence in said second strand, said first sequence being between said polymoφhic restriction site and the sequence in said second strand that is complementary to said first primer, said first probe being immobilized on a first binding element; each of said second probes comprising a sequence that hybridizes to a second sequence in said first strand, said second sequence being between said polymoφhic restriction site and the sequence in said first strand that is complementary to said second primer, and said second probe being immobilized on a second binding element.
20. The kit of claim 19, further comprising one or more sets of a third or a fourth probe, each of said third probes comprising a sequence that hybridizes to a third sequence in said first strand, said third sequence being between said polymoφhic restriction site and the sequence in said first strand coπesponding to said first primer, said third probe being immobilized on a third binding element; each of said fourth probes comprising a sequence that hybridizes to a fourth sequence in said second strand, said fourth sequence being between said polymoφhic restriction site and the sequence in said second strand coπesponding to said second primer, and said fourth probe being immobilized on a fourth binding element.
21. The kit of claim 19, wherein said first and said second detectable labels are identical.
22. The kit of claim 19, wherein said first and second binding elements are each distinct regions on a solid support.
23. The kit of claim 14 or 20, wherein said first, second, third, and fourth binding elements are each distinct regions on a solid support.
24. The kit of claim 15, 22, or 23, wherein said solid support is glass.
25. The kit of claim 15, 22, or 23, wherein said solid support is a microchip.
EP19970942525 1996-09-18 1997-09-17 Cleaved amplified rflp detection methods Withdrawn EP0948645A4 (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US715484 1996-09-18
US08/715,484 US6004783A (en) 1994-03-18 1996-09-18 Cleaved amplified RFLP detection methods
PCT/US1997/016467 WO1998012352A1 (en) 1996-09-18 1997-09-17 Cleaved amplified rflp detection methods

Publications (2)

Publication Number Publication Date
EP0948645A1 true EP0948645A1 (en) 1999-10-13
EP0948645A4 EP0948645A4 (en) 2002-11-05

Family

ID=24874229

Family Applications (1)

Application Number Title Priority Date Filing Date
EP19970942525 Withdrawn EP0948645A4 (en) 1996-09-18 1997-09-17 Cleaved amplified rflp detection methods

Country Status (3)

Country Link
EP (1) EP0948645A4 (en)
CA (1) CA2266750A1 (en)
WO (1) WO1998012352A1 (en)

Families Citing this family (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AU763135B2 (en) * 1998-03-27 2003-07-17 Johnson & Johnson Research Pty. Limited Catalytic nucleic acid-based diagnostic methods
ATE274069T1 (en) * 1998-11-09 2004-09-15 Methexis Genomics N V ANALYSIS OF BAMPLICONS OBTAINED BY RESTRICTION ENDONUCLEASE
EP1157131A2 (en) * 1999-02-22 2001-11-28 Lynx Therapeutics, Inc. Polymorphic dna fragments and uses thereof
AU2001285155A1 (en) * 2000-08-21 2002-03-04 Lynx Therapeutics, Inc. Polymorphic dna fragments and uses thereof
AU2002227055A1 (en) * 2000-11-01 2002-05-15 The General Hospital Corporation Bacterial strain typing
AUPR221400A0 (en) 2000-12-20 2001-01-25 Murdoch Childrens Research Institute, The Diagnostic assay
AU2002215696B2 (en) * 2000-12-20 2007-07-19 Murdoch Childrens Research Institute Method for detecting whether an organism is homozygous or heterozygous using labelled primers and RFLP
ES2301342B1 (en) * 2006-03-14 2009-05-01 Oryzon Genomics, S.A. "METHOD OF ANALYSIS OF NUCLEIC ACIDS".

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1989010414A1 (en) * 1988-04-28 1989-11-02 Robert Bruce Wallace AMPLIFIED SEQUENCE POLYMORPHISMS (ASPs)
WO1995025538A1 (en) * 1994-03-18 1995-09-28 The General Hospital Corporation Cleaved amplified rflp detection methods

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4775619A (en) * 1984-10-16 1988-10-04 Chiron Corporation Polynucleotide determination with selectable cleavage sites
US4925785A (en) * 1986-03-07 1990-05-15 Biotechnica Diagnostics, Inc. Nucleic acid hybridization assays
US5629158A (en) * 1989-03-22 1997-05-13 Cemu Bitecknik Ab Solid phase diagnosis of medical conditions
US5523225A (en) * 1993-09-13 1996-06-04 Regents Of The University Of Colorado DNA sequence encoding human cystathionine β-synthase

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1989010414A1 (en) * 1988-04-28 1989-11-02 Robert Bruce Wallace AMPLIFIED SEQUENCE POLYMORPHISMS (ASPs)
WO1995025538A1 (en) * 1994-03-18 1995-09-28 The General Hospital Corporation Cleaved amplified rflp detection methods

Non-Patent Citations (3)

* Cited by examiner, † Cited by third party
Title
NAIF H M ET AL: "EARLY DETECTION OF BOVINE LEUKEMIA VIRUS BY USING AN ENZYME-LINKED ASSAY FOR POLYMERASE CHAIN REACTION-AMPLIFIED PROVIRAL DNA IN EXPERIMENTALLY INFECTED CATTLE" JOURNAL OF CLINICAL MICROBIOLOGY, WASHINGTON, DC, US, vol. 30, no. 3, March 1992 (1992-03), pages 675-679, XP002917080 ISSN: 0095-1137 *
See also references of WO9812352A1 *
UGOZZOLI L: "DETECTION OF SPECIFIC ALLELES BY USING ALLELE-SPECIFIC PRIMER EXTENSION FOLLOWED BY CAPTURE ON SOLID SUPPORT" GENETIC ANALYSIS TECHNIQUES AND APPLICATIONS, ELSEVIER SCIENCE PUBLISHING, NEW YORK, US, vol. 9, no. 4, 1 August 1992 (1992-08-01), pages 107-112, XP000330552 ISSN: 1050-3862 *

Also Published As

Publication number Publication date
WO1998012352A1 (en) 1998-03-26
EP0948645A4 (en) 2002-11-05
CA2266750A1 (en) 1998-03-26

Similar Documents

Publication Publication Date Title
US6004783A (en) Cleaved amplified RFLP detection methods
US6110709A (en) Cleaved amplified modified polymorphic sequence detection methods
US6156502A (en) Arbitrary sequence oligonucleotide fingerprinting
US5834181A (en) High throughput screening method for sequences or genetic alterations in nucleic acids
US6027877A (en) Use of immobilized mismatch binding protein for detection of mutations and polymorphisms, purification of amplified DNA samples and allele identification
US6294336B1 (en) Method for analyzing the nucleotide sequence of a polynucleotide by oligonucleotide extension on an array
US6972174B2 (en) Method for detecting single nucleotide polymorphisms (SNP's) and point mutations
US20050191636A1 (en) Detection of STRP, such as fragile X syndrome
US20020094525A1 (en) Methods for the detection of multiple single nucleotide polymorphisms in a single reaction
Delahunty et al. Testing the feasibility of DNA typing for human identification by PCR and an oligonucleotide ligation assay.
CA2294053A1 (en) Methods for the detection of multiple single nucleotide polymorphisms in a single reaction
CA2497740A1 (en) Multiplexed analysis of polymorphic loci by probe elongation-mediated detection
US6794133B1 (en) Broad range PCR amplification techniques
WO1999029901A1 (en) Broad range pcr amplification techniques
EP1173612A2 (en) METHOD FOR THE DETECTION AND/OR ANALYSIS, BY MEANS OF PRIMER EXTENSION TECHNIQUES, OF SINGLE NUCLEOTIDE POLYMORPHISMS IN RESTRICTION FRAGMENTS, IN PARTICULAR IN AMPLIFIED RESTRICTION FRAGMENTS GENERATED USING AFLP$m(3)
EP0948645A1 (en) Cleaved amplified rflp detection methods
WO2005026389A2 (en) Ligation-based method of analysis of single nucleotide polymorphisms on genomic dna
JP4731081B2 (en) Method for selectively isolating nucleic acids
AU2002357968A1 (en) Method and integrated device for the detection of cytosine methylations
CA2110059C (en) Three highly informative microsatellite repeat polymorphic dna markers
Li et al. Tag/anti-tag liquid-phase primer extension array: a flexible and versatile genotyping platform
US20040014056A1 (en) Identification of genetic markers
Bates et al. Instrumentation for Automated Molecular Marker Acquisition and Data Analysis
ZIEGLE STEPHEN RE BATES, DAVID A. KNORR, JENNIFER W. WELLER, JANET S. ZIEGLE
WO2004044242A1 (en) Polymorphism assay

Legal Events

Date Code Title Description
PUAI Public reference made under article 153(3) epc to a published international application that has entered the european phase

Free format text: ORIGINAL CODE: 0009012

17P Request for examination filed

Effective date: 19990416

AK Designated contracting states

Kind code of ref document: A1

Designated state(s): DE FR GB

R17P Request for examination filed (corrected)

Effective date: 19990416

A4 Supplementary search report drawn up and despatched
AK Designated contracting states

Kind code of ref document: A4

Designated state(s): DE FR GB

A4 Supplementary search report drawn up and despatched

Effective date: 20021105

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: THE APPLICATION IS DEEMED TO BE WITHDRAWN

18D Application deemed to be withdrawn

Effective date: 20030116