Literature DB >> 14530454

Sequential DEXAS: a method for obtaining DNA sequences from genomic DNA and blood in one reaction.

Michael Motz1, Gregor Sagner, Svante Pääbo, Christian Kilger.   

Abstract

Sequential DEXAS (direct exponential amplification and sequencing), a one step amplification and sequencing procedure that allows accurate, inexpensive and rapid DNA sequence determination directly from genomic DNA, is described. This method relies on the simultaneous use of two DNA polymerases that differ both in their ability to incorporate dideoxynucleotides and in the time at which they are activated during the reaction. One enzyme, which incorporates deoxynucleotides and performs amplification of the target DNA sequence, is supplied in an active state whereas the other enzyme, which incorporates dideoxynucleotides and performs the sequencing reaction, is supplied in an inactive state but becomes activated by a temperature step during the thermocycling. Thus, in the initial stage of the reaction, target amplification occurs, while in the second stage the sequencing reaction takes place. We show that Sequential DEXAS yields high quality sequencing results directly from genomic DNA as well as directly from human blood without any prior isolation or purification of DNA.

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Year:  2003        PMID: 14530454      PMCID: PMC219489          DOI: 10.1093/nar/gng112

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


  17 in total

1.  Purification and characterization of PCR-inhibitory components in blood cells.

Authors:  W A Al-Soud; P Rådström
Journal:  J Clin Microbiol       Date:  2001-02       Impact factor: 5.948

2.  Y-chromosomal SNPs in Finno-Ugric-speaking populations analyzed by minisequencing on microarrays.

Authors:  M Raitio; K Lindroos; M Laukkanen; T Pastinen; P Sistonen; A Sajantila; A C Syvänen
Journal:  Genome Res       Date:  2001-03       Impact factor: 9.043

3.  Coupled amplification and sequencing of genomic DNA.

Authors:  G Ruano; K K Kidd
Journal:  Proc Natl Acad Sci U S A       Date:  1991-04-01       Impact factor: 11.205

4.  A fluorogenic allele-specific amplification method for DNA-based screening for inherited metabolic disorders.

Authors:  Y Matsubara; K Fujii; P Rinaldo; K Narisawa
Journal:  Acta Paediatr Suppl       Date:  1999-12

5.  Analysis of any point mutation in DNA. The amplification refractory mutation system (ARMS).

Authors:  C R Newton; A Graham; L E Heptinstall; S J Powell; C Summers; N Kalsheker; J C Smith; A F Markham
Journal:  Nucleic Acids Res       Date:  1989-04-11       Impact factor: 16.971

6.  Specific synthesis of DNA in vitro via a polymerase-catalyzed chain reaction.

Authors:  K B Mullis; F A Faloona
Journal:  Methods Enzymol       Date:  1987       Impact factor: 1.600

7.  Mutation detection by pyrosequencing: sequencing of exons 5-8 of the p53 tumor suppressor gene.

Authors:  C A Garcia; A Ahmadian; B Gharizadeh; J Lundeberg; M Ronaghi; P Nyrén
Journal:  Gene       Date:  2000-08-08       Impact factor: 3.688

8.  Chip-based genotyping by mass spectrometry.

Authors:  K Tang; D J Fu; D Julien; A Braun; C R Cantor; H Köster
Journal:  Proc Natl Acad Sci U S A       Date:  1999-08-31       Impact factor: 11.205

9.  Amplification of DNA from whole blood.

Authors:  J Burckhardt
Journal:  PCR Methods Appl       Date:  1994-02

Review 10.  Dicarboxylic acid anhydrides as dissociating agents of protein-containing structures.

Authors:  E Palacián; P J González; M Piñeiro; F Hernández
Journal:  Mol Cell Biochem       Date:  1990-09-21       Impact factor: 3.396

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