Literature DB >> 15087605

Identification of three genetic risk factors for venous thrombosis using a multiplex allele-specific PCR assay: comparison of conventional and new alternative methods for the preparation of DNA from clinical samples.

Antonio Angelini1, Concetta Di Febbo, Giovanna Baccante, Marcello Di Nisio, Carmine Di Ilio, Franco Cuccurullo, Ettore Porreca.   

Abstract

The demand for thrombophilia testing at the molecular level is increasing and with it the need for a simple and rapid and cost-saving procedure for the preparation of genomic DNA from whole blood samples. The aim of this paper is to compare the efficiency of two conventional commercial procedures (Genomic, Eurobio-Labtek, and Nucleospin, Macherey-Nagel) and two our alternative approaches (microwave irradiation and resin-binding method) for extraction DNA and their suitability and convenience for multiple sample preparation for simultaneous identification of the factor V Leiden, prothrombin 20210 and methylene tetrahydrofolate reductase (MTHFR) 677 variants by multiplex allele specific amplification (ASA-PCR). We have found that chemical-based kit (Genomic) produced higher DNA recovery (mean recovery 40 +/- 4.2 microg/ml; A260/A280 ratio 1,81 +/- 0.05) within 40 min., while the mini spin colum kit (Nucleospin Quickpure) obtained lower yield but the best DNA quality (mean recovery 25.7 +/- 2.3 microg/ml; A (260)/ A (280) ratio = 1,83 +/- 0.06) with fewer processing time (25 min). Costs of each extraction varied from 3.28 Euro for Genomic to 3.6 Euro for Nucleospin. Microwave radiation and resin-based method (GeneFizz) were single step/single tube procedures, that provided template DNA suitable for ASA-PCR assay, without any purification steps. The costs varied from 0.12 Euro for microwave to 1,23 Euro for resin based procedure. In conclusion, our alternative procedures were much faster (<15 min per extraction) and convenient (5.00-7.00 Euro per test) but equally sensitive compared to conventional DNA extraction methods. Moreover, these procedures are easily adaptable to the routine processing of high number of clinical samples and coupled with ASA-PCR assay result particularly suitable for a large scale screening for the diagnosis and prevention of the thrombotic risk.

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Year:  2003        PMID: 15087605     DOI: 10.1023/B:THRO.0000024057.37588.2a

Source DB:  PubMed          Journal:  J Thromb Thrombolysis        ISSN: 0929-5305            Impact factor:   2.300


  13 in total

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Authors:  F R Rosendaal
Journal:  Thromb Haemost       Date:  1999-08       Impact factor: 5.249

Review 2.  PCR amplification of specific alleles: rapid detection of known mutations and polymorphisms.

Authors:  C D Bottema; S S Sommer
Journal:  Mutat Res       Date:  1993-07       Impact factor: 2.433

3.  Multiplex ASA PCR for a simultaneous determination of factor V Leiden gene, G-->A 20210 prothrombin gene and C-->T 677 MTHFR gene mutations.

Authors:  N Hézard; P Cornillet-Lefebvre; L Gillot; G Potron; P Nguyen
Journal:  Thromb Haemost       Date:  1998-05       Impact factor: 5.249

4.  The mutation Ala677-->Val in the methylene tetrahydrofolate reductase gene: a risk factor for arterial disease and venous thrombosis.

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Journal:  Thromb Haemost       Date:  1997-05       Impact factor: 5.249

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Journal:  Biotechniques       Date:  1995-05       Impact factor: 1.993

6.  Polymerase chain reaction amplification of specific alleles: a general method of detection of mutations, polymorphisms, and haplotypes.

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Journal:  Methods Enzymol       Date:  1993       Impact factor: 1.600

7.  Prevalence of prothrombin G20210A, factor V G1691A (Leiden), and methylenetetrahydrofolate reductase (MTHFR) C677T in seven different populations determined by multiplex allele-specific PCR.

Authors:  M J Hessner; R A Luhm; S L Pearson; D J Endean; K D Friedman; R R Montgomery
Journal:  Thromb Haemost       Date:  1999-05       Impact factor: 5.249

8.  Multiple analysis of three common genetic alterations associated with thrombophilia.

Authors:  N M Pecheniuk; N A Marsh; T P Walsh
Journal:  Blood Coagul Fibrinolysis       Date:  2000-03       Impact factor: 1.276

9.  Mutation in blood coagulation factor V associated with resistance to activated protein C.

Authors:  R M Bertina; B P Koeleman; T Koster; F R Rosendaal; R J Dirven; H de Ronde; P A van der Velden; P H Reitsma
Journal:  Nature       Date:  1994-05-05       Impact factor: 49.962

10.  Direct PCR of whole blood and hair shafts by microwave treatment.

Authors:  M Ohhara; Y Kurosu; M Esumi
Journal:  Biotechniques       Date:  1994-10       Impact factor: 1.993

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  2 in total

1.  Improved method of detection and molecular typing of Borrelia burgdorferi sensu lato in clinical samples by polymerase chain reaction without DNA purification.

Authors:  N Rudenko; M Golovchenko; J Nemec; J Volkaert; N Mallátová; L Grubhoffer
Journal:  Folia Microbiol (Praha)       Date:  2005       Impact factor: 2.099

2.  Metabolic detoxification and ace-1 target site mutations associated with acetamiprid resistance in Aedes aegypti L.

Authors:  Roopa Rani Samal; Kungreiliu Panmei; P Lanbiliu; Sarita Kumar
Journal:  Front Physiol       Date:  2022-08-30       Impact factor: 4.755

  2 in total

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