Literature DB >> 10837092

Correct heteroduplex formation for mutation detection analysis.

M J Smith1, K E Humphrey, R Cappai, K Beyreuther, C L Masters, R G Cotton.   

Abstract

BACKGROUND: The majority of mutation detection methods for unknown mutations are polymerase chain reaction (PCR)-based methods dependent on the formation of heteroduplexes between wild-type and mutant strands of DNA. METHODS AND
RESULTS: This report discusses the difficulties associated with forming heteroduplexes with a large DNA fragment and the implications for subsequent mutation detection by the chemical cleavage of mismatch technique and other methods reliant on heteroduplex formation. It was found that the size and sequence context of the fragment being investigated inhibited correct heteroduplex formation. The problem was overcome by dividing the sequence into two overlapping fragments.
CONCLUSIONS: Early identification of this problem in other fragments will help with the rapid optimization of PCR-based mutation detection methods.

Mesh:

Substances:

Year:  2000        PMID: 10837092     DOI: 10.1007/bf03262025

Source DB:  PubMed          Journal:  Mol Diagn        ISSN: 1084-8592


  21 in total

1.  Detection of point mutations in human DNA by analysis of RNA conformation polymorphism(s).

Authors:  P V Danenberg; T Horikoshi; M Volkenandt; K Danenberg; H J Lenz; L C Shea; A P Dicker; A Simoneau; P A Jones; J R Bertino
Journal:  Nucleic Acids Res       Date:  1992-02-11       Impact factor: 16.971

2.  Comprehensive detection of single base changes in human genomic DNA using denaturing gradient gel electrophoresis and a GC clamp.

Authors:  E S Abrams; S E Murdaugh; L S Lerman
Journal:  Genomics       Date:  1990-08       Impact factor: 5.736

3.  Sensitive and fast mutation detection by solid phase chemical cleavage.

Authors:  L L Hansen; J Justesen; T A Kruse
Journal:  Hum Mutat       Date:  1996       Impact factor: 4.878

4.  Exhaustive mutation scanning by fluorescence-assisted mismatch analysis discloses new genotype-phenotype correlations in angiodema.

Authors:  E Verpy; M Biasotto; M Brai; G Misiano; T Meo; M Tosi
Journal:  Am J Hum Genet       Date:  1996-08       Impact factor: 11.025

5.  Modification of the melting properties of duplex DNA by attachment of a GC-rich DNA sequence as determined by denaturing gradient gel electrophoresis.

Authors:  R M Myers; S G Fischer; T Maniatis; L S Lerman
Journal:  Nucleic Acids Res       Date:  1985-05-10       Impact factor: 16.971

6.  Molecular analysis of the presenilin 1 (S182) gene in "sporadic" cases of Alzheimer's disease: identification and characterisation of unusual splice variants.

Authors:  R Anwar; T P Moynihan; H Ardley; N Brindle; P L Coletta; N Cairns; A F Markham; P A Robinson
Journal:  J Neurochem       Date:  1996-04       Impact factor: 5.372

7.  A variant of Alzheimer's disease with spastic paraparesis and unusual plaques due to deletion of exon 9 of presenilin 1.

Authors:  R Crook; A Verkkoniemi; J Perez-Tur; N Mehta; M Baker; H Houlden; M Farrer; M Hutton; S Lincoln; J Hardy; K Gwinn; M Somer; A Paetau; H Kalimo; R Ylikoski; M Pöyhönen; S Kucera; M Haltia
Journal:  Nat Med       Date:  1998-04       Impact factor: 53.440

8.  Ultrarapid mutation detection by multiplex, solid-phase chemical cleavage.

Authors:  G Rowley; S Saad; F Giannelli; P M Green
Journal:  Genomics       Date:  1995-12-10       Impact factor: 5.736

9.  The structure of the presenilin 1 (S182) gene and identification of six novel mutations in early onset AD families.

Authors: 
Journal:  Nat Genet       Date:  1995-10       Impact factor: 38.330

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