Abstract − Analytical Sciences, 26(4), 503 (2010).
Genotyping of Polymorphisms in Alcohol and Aldehyde Dehydrogenase Genes by Direct Application of PCR-RFLP on Dried Blood without DNA Extraction
  Mariko HAYASHIDA,* Kyoko IWAO-KOIZUMI,* Shigenori MURATA,* Akira YOKOYAMA,** and Kenji KINOSHITA*
  *School of Pharmaceutical Sciences, Mukogawa Women’s University, Koshien, Nishinomiya 663-8179, Japan
**National Institute on Alcoholism, Kurihama National Hospital, Yokosuka, Kanagawa 239-0841, Japan
  **National Institute on Alcoholism, Kurihama National Hospital, Yokosuka, Kanagawa 239-0841, Japan
We have developed a simple, labor-saving, inexpensive, and rapid single nucleotide polymorphism (SNP) genotyping method that works directly on whole human blood.  This single-tube genotyping method was used to successfully and reliably genotype ADH1B and ALDH2 polymorphisms without DNA isolation using a 1.2-mm disc of dried blood and the KOD FX PCR enzyme kit.  SNP genotyping was performed by a polymerase chain reaction–restriction fragment length polymorphism (PCR-RFLP) method.  In addition to the labor and expense advantages, the possibility of sample contamination was considerably decreased, since the DNA extraction step was eliminated.  In the post-genome era, a simple and inexpensive method for diagnostic analysis is in high demand, and this method will be very useful for genetic diagnoses in biological and medical laboratories.
  
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