Literature DB >> 11571714

Simultaneous allele-specific amplification: a strategy using modified primer-template mismatches for SNP detection--application to prothrombin 20210A (factor II) and factor V Leiden (1691A) gene mutations.

S A DelRio-LaFreniere1, R C McGlennen.   

Abstract

BACKGROUND: Inherited thrombophilia is caused by mutations in genes central to the clotting cascade. Analysis of the factor V Leiden (FVL) and prothrombin G20210A mutations are the most prevalent in thrombophilia. METHODS AND
RESULTS: We have optimized an allele-specific PCR assay for the simultaneous detection of both wild-type and mutant alleles. This method is adapted for clinical use with the FVL and prothrombin G20210A assays and is significant in its intentional use of nucleotide mismatches at the 3' end of allele-specific primers. Two internal allele-specific primers are designed to amplify in opposite directions on opposite strands that reduce differential amplification. Our results show concordance with methods involving PCR with restriction endonuclease digestion, yet are simpler to perform.
CONCLUSION: The simultaneous allele-specific amplification method allows simultaneous detection of wild-type and mutant alleles by PCR using four distinct primers. Nucleotide mismatches in the primers reduce competitive amplification.

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Year:  2001        PMID: 11571714     DOI: 10.1007/bf03262054

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


  33 in total

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4.  Simultaneous detection of FV Q506 and prothrombin 20210 A variation by allele-specific PCR.

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5.  Coinheritance of the HR2 haplotype in the factor V gene confers an increased risk of venous thromboembolism to carriers of factor V R506Q (factor V Leiden).

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7.  Preeclampsia and genetic risk factors for thrombosis: a case-control study.

Authors:  C J De Groot; K W Bloemenkamp; E J Duvekot; F M Helmerhorst; R M Bertina; F Van Der Meer; H De Ronde; S G Oei; H H Kanhai; F R Rosendaal
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8.  Allele-specific PCR amplification of factor V Leiden to identify patients at risk for thromboembolism.

Authors:  R Blasczyk; J Wehling; M Ritter; A Neubauer; H Riess
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9.  Thrombotic risk during pregnancy: a population study.

Authors:  P Lindqvist; B Dahlbäck; K Marŝál
Journal:  Obstet Gynecol       Date:  1999-10       Impact factor: 7.661

10.  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
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