Startseite Detection of Usual and Atypical Aldehyde Dehydrogenase Alleles by Mismatch Amplification Mutation Assay
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Detection of Usual and Atypical Aldehyde Dehydrogenase Alleles by Mismatch Amplification Mutation Assay

  • Huai-rong Luo , Guang-chou Tu und Ya-ping Zhang
Veröffentlicht/Copyright: 1. Juni 2005
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Clinical Chemistry and Laboratory Medicine (CCLM)
Aus der Zeitschrift Band 39 Heft 12

Abstract

The genotypes of liver mitochondrial high-affinity aldehyde dehydrogenase-2 (ALDH2) are strongly associated with the drinking behavior and the alcohol liver diseases, since the individuals with atypical AlDH22 allele have higher levels of acetaldehyde in their plasma. The atypical AlDH22 allele has a nucleotide base transition (G→A) in its exon 12. Based on this point mutation, we developed a rapid, reliable and inexpensive method, mismatch amplification mutation assay (MAMA), for the determination of human ALDH2 usual and atypical alleles. Two pairs of primers were designed for the amplification of the usual AlDH21 allele and the atypical AlDH22 allele, respectively. If the sample for the detection was heterozygous, it could be amplified by both of the primers. The product of polymerase chain reaction (PCR) of ALDH2 exon 12 could be easily screened by electrophoresis on a 2% agarose gel. The results of the MAMA method were further confirmed by sequencing. In the total of fifty samples from unrelated healthy Chinese Han people from Wuhan, China, the frequency of atypical AlDH22 allele was found to be 12%.

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Published Online: 2005-06-01
Published in Print: 2001-12-07

Copyright © 2001 by Walter de Gruyter GmbH & Co. KG

Artikel in diesem Heft

  1. Contents
  2. Subject Index
  3. Author Index
  4. Summary of the 2nd Sino-European Congress of Laboratory Medicine
  5. Laboratory Diagnosis of Viral Hepatitis in China: The Present and the Future
  6. Molecular Diagnostics in China
  7. Detection of Usual and Atypical Aldehyde Dehydrogenase Alleles by Mismatch Amplification Mutation Assay
  8. Expression of Prostaglandin D Synthase in Ovarian Cancer
  9. Carrier Detection and Prenatal Diagnosis of Hemophilia A
  10. Detection of Oligoclonal Immunoglobulins in the Cerebrospinal Fluid by Immunofixation Electrophoresis
  11. 2nd Sino-European Congress of Laboratory Medicine – Strategies for Laboratory Diagnostics in Medicine
  12. The Problems and Strategy relevant to the Quality Management of Clinical Laboratories
  13. Computer Application to the Laboratory Management in Hospital
  14. The Basis of the Synovial Fluid Analysis
  15. Determination of Tumor Markers in Serum. Pitfalls and Good Practice
  16. Gas Chromatography-Mass Spectrometry Measurement of 6β-OH-Cortisol/Cortisol Ratio in Human Urine: A Specific Marker of Enzymatic Induction
  17. No Variation in Hsp70 mRNA Level during Cardiac Surgery in Pediatric Patients Evaluated by Semiquantitative RT-PCR
  18. Rapid Detection of Macroprolactin in tHe Form of Prolactin-Immunoglobulin G Complexes by Immunoprecipitation with Anti-human IgG-Agarose
  19. Molecular Characterization of Chromosome 22 Deletions by Short Tandem Repeat Polymorphism (STRP) in Patients with Conotruncal Heart Defects
  20. A Simple and Rapid Analysis of Triplet Repeat Diseases by Expand Long PCR
  21. The Effects of Peroxynitrite on Erythrocytes
  22. The Use of Hirudin as Universal Anticoagulant in Haematology, Clinical Chemistry and Blood Grouping
  23. Comparison of Different Immunoassays for CA 19-9
  24. The Evaluation of Analytical Performance of the Precision G Point-of-Care Glucometer
  25. On Painting and Philosophy: Sir Henry Raeburn
  26. Acknowledgement
  27. Meetings and Awards
Heruntergeladen am 26.10.2025 von https://www.degruyterbrill.com/document/doi/10.1515/CCLM.2001.189/pdf
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