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US5175082A Expired / Lapsed US ⏱️ 0.0 years remaining

Method of characterizing genomic dna

Assignee: Imperial Chemical Industries Ltd
•
Filing: 1987-03-19
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Granted: 1992-12-29
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Expires: 2007-03-19
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Abstract

Abstract Test samples of genomic DNA may be characterized by the use of polynucleotide probes each of which is specific for an informative genetic locus. Such probes may be prepared by the use of probes which are capable of differentiating DNA by reference to more than one polymorphic minisatellite region or hypervariable locus. The polynucleotides and probes of the invention are of use for genetic identification purposes, paternity and maternity testing and particularly in forensic medicine.

Inventors

  • 👤 Alec J. Jeffreys

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-11-05 10:54
CPC Classifications
C; C12; C12N; C12N15/00; C12N15/09; C12N15/10; C12Q; C12Q1/00; C12Q1/68; C12Q1/6813; C12Q1/6827; C12Q1/6876; C12Q2600/00; C12Q2600/156; C12Q2600/172

Claims Analysis

Total Claims: 9
Claim 1
Independent Claim 137 words
A method of characterizing a test sample of genomic DNA from a donor by reference to one or more controls which method comprises: i) fragmenting said sample DNA with at least one restriction enzyme which does not cleave a sequence corresponding to a tandem repeat, ii) probing the DNA fragments with a polynucleotide probe which specifically hybridizes to a single minisatellite region (to the exclusion of other regions), wherein said probe consists essentially of up to 10,000 tandem repeats of a repeat sequence unit being one of ##STR7## wherein Y is C, T or U, X is G or C, R is A or G and T is T or U, or a sequence complementary thereto of identical length, iii) detecting hybridized fragments of DNA, and iv) comparing the hybridized fragments with the said control or controls.
Claim 2
Independent Claim 137 words
A method of characterizing a test sample of genomic DNA from a donor by reference to one or more controls which method comprises: i) fragmenting said sample DNA with at least one restriction enzyme which does not cleave a sequence corresponding to a tandem repeat, ii) probing the DNA fragments with a polynucleotide probe which specifically hybridizes to a single minisatellite region (to the exclusion of other regions), wherein said probe consists essentially of up to 10,000 tandem repeats of a repeat sequence unit being one of ##STR7## wherein Y is C, T or U, X is G or C, R is A or G and T is T or U, or a sequence complementary thereto of identical length, iii) detecting hybridized fragments of DNA, and iv) comparing the hybridized fragments with the said control or controls.
Claim 3
Dependent Claim 49 words
The method according to claim 1 wherein said method establishes the identity of the test sample donor with one or more control sample donors, wherein the control sample(s) are fragmented in an identical manner and a comparison is made of the hybridized fragments from the control and test samples.
Claim 4
Dependent Claim 50 words
The method according to claim 1 wherein said method establishes a family connection between the test sample donor and one or more control sample donors, wherein the control sample(s) are fragmented in an identical manner and a comparison is made of the hybridized fragments from the control and test samples.
Claim 5
Dependent Claim 38 words
The method as claimed in claim 1 wherein said probing is effected using at least two of said polynucleotide probes either in a sequence of tests or in a single test using a mixture of said polynucleotide probes.
Claim 6
Dependent Claim 22 words
The method as claimed in claim 1 wherein the repeat unit sequence of the polynucleotide probe consists of one of sequences 3-9.
Claim 7
Dependent Claim 18 words
The method as claimed in claim 1 wherein the polynucleotide probe is from 9 bp to 45 bp.
Claim 8
Dependent Claim 17 words
The method as claimed in claim 1 wherein the polynucleotide probe is wholly in single stranded form.
Claim 9
Dependent Claim 26 words
A method as claimed in claim 1 wherein the polynucleotide probe is selected from the group consisting of pλg3, λMS1, λMS8(1), λMS8(2), λMS31, λMS32 and λMS43.

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1995-12-29 1996-06-29 1996-12-29 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1999-12-29 2000-06-29 2000-12-29 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 2003-12-29 2004-06-29 2004-12-29 $7700.00 Window Closed / Lapsed

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