Literature DB >> 7937161

A program for selecting DNA fragments to detect mutations by denaturing gel electrophoresis methods.

S Brossette1, R M Wartell.   

Abstract

A computer program was developed to automate the selection of DNA fragments for detecting mutations within a long DNA sequence by denaturing gel electrophoresis methods. The program, MELTSCAN, scans through a user specified DNA sequence calculating the melting behavior of overlapping DNA fragments covering the sequence. Melting characteristics of the fragments are analyzed to determine the best fragment for detecting mutations at each base pair position in the sequence. The calculation also determines the optimal fragment for detecting mutations within a user specified mutational hot spot region. The program is built around the statistical mechanical model of the DNA melting transition. The optimal fragment for a given position is selected using the criteria that its melting curve has at least two steps, the base pair position is in the fragment's lowest melting domain, and the melting domain has the smallest number of base pairs among fragments that meet the first two criteria. The program predicted fragments for detecting mutations in the cDNA and genomic DNA of the human p53 gene.

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Year:  1994        PMID: 7937161      PMCID: PMC331956          DOI: 10.1093/nar/22.20.4321

Source DB:  PubMed          Journal:  Nucleic Acids Res        ISSN: 0305-1048            Impact factor:   16.971


  17 in total

1.  Attachment of a 40-base-pair G + C-rich sequence (GC-clamp) to genomic DNA fragments by the polymerase chain reaction results in improved detection of single-base changes.

Authors:  V C Sheffield; D R Cox; L S Lerman; R M Myers
Journal:  Proc Natl Acad Sci U S A       Date:  1989-01       Impact factor: 11.205

2.  Inverted repeat sequences can influence the melting transitions of linear DNAs.

Authors:  C R McCampbell; R M Wartell; R R Plaskon
Journal:  Biopolymers       Date:  1989-10       Impact factor: 2.505

3.  Computational simulation of DNA melting and its application to denaturing gradient gel electrophoresis.

Authors:  L S Lerman; K Silverstein
Journal:  Methods Enzymol       Date:  1987       Impact factor: 1.600

4.  A general method for saturation mutagenesis of cloned DNA fragments.

Authors:  R M Myers; L S Lerman; T Maniatis
Journal:  Science       Date:  1985-07-19       Impact factor: 47.728

5.  Detecting base pair substitutions in DNA fragments by temperature-gradient gel electrophoresis.

Authors:  R M Wartell; S H Hosseini; C P Moran
Journal:  Nucleic Acids Res       Date:  1990-05-11       Impact factor: 16.971

6.  Temperature-gradient gel electrophoresis. Thermodynamic analysis of nucleic acids and proteins in purified form and in cellular extracts.

Authors:  V Rosenbaum; D Riesner
Journal:  Biophys Chem       Date:  1987-05-09       Impact factor: 2.352

7.  Selecting DNA fragments for mutation detection by temperature gradient gel electrophoresis: application to the p53 gene cDNA.

Authors:  S H Ke; P J Kelly; R M Wartell; S Hunter; V A Varma
Journal:  Electrophoresis       Date:  1993-07       Impact factor: 3.535

8.  Theory of DNA melting curves.

Authors:  M Fixman; J J Freire
Journal:  Biopolymers       Date:  1977-12       Impact factor: 2.505

9.  Mutations in the p53 gene occur in diverse human tumour types.

Authors:  J M Nigro; S J Baker; A C Preisinger; J M Jessup; R Hostetter; K Cleary; S H Bigner; N Davidson; S Baylin; P Devilee
Journal:  Nature       Date:  1989-12-07       Impact factor: 49.962

10.  Human p53 cellular tumor antigen: cDNA sequence and expression in COS cells.

Authors:  R Zakut-Houri; B Bienz-Tadmor; D Givol; M Oren
Journal:  EMBO J       Date:  1985-05       Impact factor: 11.598

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