Clinical Chemistry
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


Clinical Chemistry 47: 852-857, 2001;
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Web of Science (14)
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Teupser, D.
Right arrow Articles by Thiery, J.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Teupser, D.
Right arrow Articles by Thiery, J.
Related Collections
Right arrow Molecular Diagnostics and Genetics
Right arrow Lipids, Lipoproteins, and Cardiovascular Risk Factors
(Clinical Chemistry. 2001;47:852-857.)
© 2001 American Association for Clinical Chemistry, Inc.


Articles

Fluorescence-based Detection of the CETP TaqIB Polymorphism: False Positives with the TaqMan-based Exonuclease Assay Attributable to a Previously Unknown Gene Variant

Daniel Teupser1a, Wolfgang Rupprecht2, Peter Lohse2 and Joachim Thiery1

1 Institute of Laboratory Medicine, Clinical Chemistry, and Molecular Diagnostics, University Hospital Leipzig, Liebigstrasse 27, 04103 Leipzig, Germany.

2 Institute of Clinical Chemistry, Grosshadern, University Hospital Munich, Marchioninistrasse 15, 81377 Munich, Germany.

aAuthor for correspondence. Fax 49-341-9722209; e-mail daniel{at}teupser.de.

Background: Previous studies have shown an association between the TaqIB polymorphism of the cholesteryl ester transfer protein (CETP) gene with plasma CETP and HDL concentrations and the progression of coronary artery disease (CAD). The aim of the present study was to determine the performance of two new fluorescence-based detection systems in the analysis of the TaqIB genotype.

Methods: CAD patients (n = 150) with known TaqIB genotype, as determined by restriction fragment length polymorphism (RFLP) analysis, were selected, including three groups of 50 patients, carrying the B1/1, B1/2, and B2/2 genotypes, respectively. The genotypes were also analyzed by fluorescence-based allele-specific TaqMan PCR and melting curve analysis (LightCycler). In addition, DNA sequencing was applied.

Results: The TaqIB genotypes obtained by fluorescence analysis corresponded to those determined by RFLP analysis with the exception of three heterozygous patients (B1/2), who were misclassified as homozygous B2 carriers with the TaqMan system. Melting curve analysis of these samples demonstrated an additional melting point at 59.1 °C, which was also found in four patients homozygous for the B1 allele. DNA sequencing revealed a previously unknown C270T nucleotide exchange in intron 1 of the CETP gene, only nine base pairs from the TaqIB site.

Conclusions: Determination of the TaqIB polymorphism with the TaqMan system led to misclassifications because of a previously unknown C270T polymorphism of the CETP gene. The base substitution was detected with the LightCycler because of the occurrence of an additional melting point. Our data indicate the importance of thorough evaluation of new gene analysis systems before using them on a routine basis.




The following articles in journals at HighWire Press have cited this article:


Home page
Clin. Chem.Home page
J. Marki-Zay, C. L. Klein, D. Gancberg, H. G. Schimmel, and L. Dux
European External Quality Control Study on the Competence of Laboratories to Recognize Rare Sequence Variants Resulting in Unusual Genotyping Results
Clin. Chem., April 1, 2009; 55(4): 739 - 747.
[Abstract] [Full Text] [PDF]


Home page
Clin. Chem.Home page
M. T. Seipp, D. Pattison, J. D. Durtschi, M. Jama, K. V. Voelkerding, and C. T. Wittwer
Quadruplex Genotyping of F5, F2, and MTHFR Variants in a Single Closed Tube by High-Resolution Amplicon Melting
Clin. Chem., January 1, 2008; 54(1): 108 - 115.
[Abstract] [Full Text] [PDF]


Home page
Clin. Chem.Home page
H. El Housni, P. Heimann, J. Parma, and G. Vassart
Single-Nucleotide Polymorphism Genotyping by Melting Analysis of Dual-Labeled Probes: Examples Using Factor V Leiden and Prothrombin 20210A Mutations
Clin. Chem., October 1, 2003; 49(10): 1669 - 1672.
[Full Text] [PDF]


Home page
J. Lipid Res.Home page
S. M. Boekholdt and J. F. Thompson
Natural genetic variation as a tool in understanding the role of CETP in lipid levels and disease
J. Lipid Res., July 1, 2003; 44(6): 1080 - 1093.
[Abstract] [Full Text] [PDF]


Home page
Clin. Chem.Home page
M. Erali, B. Schmidt, E. Lyon, and C. Wittwer
Evaluation of Electronic Microarrays for Genotyping Factor V, Factor II, and MTHFR
Clin. Chem., May 1, 2003; 49(5): 732 - 739.
[Abstract] [Full Text] [PDF]


Home page
Clin. Chem.Home page
K. Xu, R. H. Lipsky, W. Mangal, E. Ferro, and D. Goldman
Single-Nucleotide Polymorphism Allele Frequencies Determined by Quantitative Kinetic Assay of Pooled DNA
Clin. Chem., September 1, 2002; 48(9): 1605 - 1608.
[Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 2001 by the American Association for Clinical Chemistry.