Literature DB >> 9465076

Conformation sensitive gel electrophoresis for simple and accurate detection of mutations: comparison with denaturing gradient gel electrophoresis and nucleotide sequencing.

J Körkkö1, S Annunen, T Pihlajamaa, D J Prockop, L Ala-Kokko.   

Abstract

Previously, an assay called conformation sensitive gel electrophoresis (CSGE) was developed for scanning PCR products for the presence of single-base and larger base mismatches in DNA. The assay was based on the assumption that mildly denaturing solvents in an appropriate buffer can accentuate the conformational changes produced by single-base mismatches in double-stranded DNA and thereby increase the differential migration in electrophoretic gels of heteroduplexes and homoduplexes. Here the sensitivity of assays by CSGE was improved by limiting the maximal size of the PCR products to 450 bp and making several changes in the conditions for PAGE. With the improved conditions, CSGE detected all 76 previously identified single-base changes in a large series of PCR products from collagen genes that contain multiple exons with highly repetitive and GC-rich sequences. In a survey of 736 alleles of collagen genes, CSGE detected 223 unique single-base mismatches that were confirmed by nucleotide sequencing. CSGE has the advantage over other methods for scanning PCR products in that it is simple, requires no special preparation of PCR products, has a large capacity, and does not use radioactivity.

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Year:  1998        PMID: 9465076      PMCID: PMC19147          DOI: 10.1073/pnas.95.4.1681

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN: 0027-8424            Impact factor:   11.205


  33 in total

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2.  Two new recurrent nucleotide mutations in the COL1A1 gene in four patients with osteogenesis imperfecta: about one-fifth are recurrent.

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Journal:  Hum Mutat       Date:  1997       Impact factor: 4.878

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Journal:  Nat Biotechnol       Date:  1997-05       Impact factor: 54.908

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Journal:  Hum Mutat       Date:  1997       Impact factor: 4.878

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Journal:  Methods Enzymol       Date:  1987       Impact factor: 1.600

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Journal:  Hum Mutat       Date:  1997       Impact factor: 4.878

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Journal:  Methods Enzymol       Date:  1987       Impact factor: 1.600

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Journal:  Proc Natl Acad Sci U S A       Date:  1988-06       Impact factor: 11.205

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Journal:  Science       Date:  1985-12-13       Impact factor: 47.728

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Journal:  Proc Natl Acad Sci U S A       Date:  1986-02       Impact factor: 11.205

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  52 in total

1.  Splicing mutations of 54-bp exons in the COL11A1 gene cause Marshall syndrome, but other mutations cause overlapping Marshall/Stickler phenotypes.

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Journal:  Am J Hum Genet       Date:  1999-10       Impact factor: 11.025

2.  Phylogenetic network of the mtDNA haplogroup U in Northern Finland based on sequence analysis of the complete coding region by conformation-sensitive gel electrophoresis.

Authors:  S Finnilä; I E Hassinen; L Ala-Kokko; K Majamaa
Journal:  Am J Hum Genet       Date:  2000-03       Impact factor: 11.025

3.  The mitochondrial gene tree comes of age.

Authors:  M Richards; V Macaulay
Journal:  Am J Hum Genet       Date:  2001-05-10       Impact factor: 11.025

4.  A novel procedure for simple and efficient genotyping of single nucleotide polymorphisms by using the Zn2+-cyclen complex.

Authors:  Emiko Kinoshita-Kikuta; Eiji Kinoshita; Tohru Koike
Journal:  Nucleic Acids Res       Date:  2002-11-15       Impact factor: 16.971

5.  Two-dimensional conformation-dependent electrophoresis (2D-CDE) to separate DNA fragments containing unmatched bulge from complex DNA samples.

Authors:  Gudmundur H Gunnarsson; Hans G Thormar; Bjarki Gudmundsson; Lina Akesson; Jon J Jonsson
Journal:  Nucleic Acids Res       Date:  2004-02-03       Impact factor: 16.971

6.  Epidermolysis bullosa. II. Type VII collagen mutations and phenotype-genotype correlations in the dystrophic subtypes.

Authors:  Roslyn Varki; Sara Sadowski; Jouni Uitto; Ellen Pfendner
Journal:  J Med Genet       Date:  2006-09-13       Impact factor: 6.318

7.  Sequence variation in the tRNA genes of human mitochondrial DNA.

Authors:  Tiina Vilmi; Jukka S Moilanen; Saara Finnilä; Kari Majamaa
Journal:  J Mol Evol       Date:  2005-05       Impact factor: 2.395

8.  Mismatch-induced DNA unbending upon duplex opening.

Authors:  Chongli Yuan; Elizabeth Rhoades; Daniel M Heuer; Lynden A Archer
Journal:  Biophys J       Date:  2005-08-05       Impact factor: 4.033

9.  Epidermolysis bullosa. I. Molecular genetics of the junctional and hemidesmosomal variants.

Authors:  R Varki; S Sadowski; E Pfendner; J Uitto
Journal:  J Med Genet       Date:  2006-02-10       Impact factor: 6.318

10.  Prevalence of germline TP53 mutations in HER2+ breast cancer patients.

Authors:  Michelle G Rath; Serena Masciari; Rebecca Gelman; Alexander Miron; Penelope Miron; Kathleen Foley; Andrea L Richardson; Ian E Krop; Sigitas J Verselis; Deborah A Dillon; Judy E Garber
Journal:  Breast Cancer Res Treat       Date:  2013-04-12       Impact factor: 4.872

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