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Title: Method for producing labeled single-stranded nucleic acid probes

Abstract

Disclosed is a method for the introduction of unidirectional deletions in a cloned DNA segment. More specifically, the method comprises providing a recombinant DNA construct comprising a DNA segment of interest inserted in a cloning vector, the cloning vector having an f1 endonuclease recognition sequence adjacent to the insertion site of the DNA segment of interest. The recombinant DNA construct is then contacted with the protein pII encoded by gene II of phage f1 thereby generating a single-stranded nick. The nicked DNA is then contacted with E. coli Exonuclease III thereby expanding the single-stranded nick into a single-stranded gap. The single-stranded gapped DNA is then contacted with a single-strand-specific endonuclease thereby producing a linearized DNA molecule containing a double-stranded deletion corresponding in size to the single-stranded gap. The DNA treated in this manner is then incubated with DNA ligase under conditions appropriate for ligation. Also disclosed is a method for producing single-stranded DNA probes. In this embodiment, single-stranded gapped DNA, produced as described above, is contacted with a DNA polymerase in the presence of labeled nucleotides to fill in the gap. This DNA is then linearized by digestion with a restriction enzyme which cuts outside the DNA segment of interest.more » The product of this digestion is then denatured to produce a labeled single-stranded nucleic acid probe.« less

Inventors:
 [1];  [2];  [3]
  1. (Bellport, NY)
  2. (Middle Island, NY)
  3. (Upton, NY)
Issue Date:
Research Org.:
ASSOC UNIVERSITIES INC
OSTI Identifier:
872595
Patent Number(s):
5968786
Application Number:
09/215,817
Assignee:
Brookhaven Science Associates (Upton, NY) BNL
DOE Contract Number:  
AC02-76CH00016
Resource Type:
Patent
Country of Publication:
United States
Language:
English
Subject:
method; producing; labeled; single-stranded; nucleic; acid; probes; disclosed; introduction; unidirectional; deletions; cloned; dna; segment; specifically; comprises; providing; recombinant; construct; comprising; inserted; cloning; vector; f1; endonuclease; recognition; sequence; adjacent; insertion; site; contacted; protein; pii; encoded; ii; phage; generating; nick; nicked; coli; exonuclease; iii; expanding; gap; gapped; single-strand-specific; linearized; molecule; containing; double-stranded; deletion; corresponding; size; treated; manner; incubated; ligase; conditions; appropriate; ligation; embodiment; produced; described; polymerase; presence; nucleotides; fill; digestion; restriction; enzyme; cuts; outside; product; denatured; produce; probe; stranded dna; dna probes; molecule containing; comprises providing; acid probes; dna polymerase; method comprises; nucleic acid; recombinant dna; dna segment; single-stranded nucleic; cloning vector; acid probe; cloned dna; dna molecule; single-stranded dna; restriction enzyme; recognition sequence; sequence adjacent; producing single-stranded; method comprise; unidirectional deletions; dna construct; f1 endonuclease; dna probe; dna ligase; endonuclease recognition; construct comprising; labeled single-stranded; labeled nucleotides; insertion site; nuclease recognition; stranded nucleic; producing single; /435/

Citation Formats

Dunn, John J., Quesada, Mark A., and Randesi, Matthew. Method for producing labeled single-stranded nucleic acid probes. United States: N. p., 1999. Web.
Dunn, John J., Quesada, Mark A., & Randesi, Matthew. Method for producing labeled single-stranded nucleic acid probes. United States.
Dunn, John J., Quesada, Mark A., and Randesi, Matthew. Tue . "Method for producing labeled single-stranded nucleic acid probes". United States. https://www.osti.gov/servlets/purl/872595.
@article{osti_872595,
title = {Method for producing labeled single-stranded nucleic acid probes},
author = {Dunn, John J. and Quesada, Mark A. and Randesi, Matthew},
abstractNote = {Disclosed is a method for the introduction of unidirectional deletions in a cloned DNA segment. More specifically, the method comprises providing a recombinant DNA construct comprising a DNA segment of interest inserted in a cloning vector, the cloning vector having an f1 endonuclease recognition sequence adjacent to the insertion site of the DNA segment of interest. The recombinant DNA construct is then contacted with the protein pII encoded by gene II of phage f1 thereby generating a single-stranded nick. The nicked DNA is then contacted with E. coli Exonuclease III thereby expanding the single-stranded nick into a single-stranded gap. The single-stranded gapped DNA is then contacted with a single-strand-specific endonuclease thereby producing a linearized DNA molecule containing a double-stranded deletion corresponding in size to the single-stranded gap. The DNA treated in this manner is then incubated with DNA ligase under conditions appropriate for ligation. Also disclosed is a method for producing single-stranded DNA probes. In this embodiment, single-stranded gapped DNA, produced as described above, is contacted with a DNA polymerase in the presence of labeled nucleotides to fill in the gap. This DNA is then linearized by digestion with a restriction enzyme which cuts outside the DNA segment of interest. The product of this digestion is then denatured to produce a labeled single-stranded nucleic acid probe.},
doi = {},
journal = {},
number = ,
volume = ,
place = {United States},
year = {1999},
month = {10}
}

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