An Artifact Derived from a Pseudogene Led to the Discovery of MicroRNA Binding Site Polymorphism in the 3 %26apos;-Untranslated Region of the Human Dihydrofolate Reductase Gene

作者：Hayashi Hideki; Tazoe Yui; Horino Masato; Fujimaki Katoh Chihiro; Tsuboi Seiji; Matsuyama Taiji; Kosuge Kazuhiro; Yamada Hiroshi; Tsuji Daiki; Inoue Kazuyuki; Itoh Kunihiko^*

来源：Drug Metabolism and Pharmacokinetics, 2012, 27(2): 263-267.

DOI：10.2133/dmpk.DMPK-11-NT-092

• dihydrofolate reductase
• genetic polymorphism
• pseudogene
• microRNA
• methotrexate

A novel single-nucleotide polymorphism (SNP) in the 3%26apos;-untranslated region of the human dihydrofolate reductase (DHFR) gene with enhanced expression was identified in 2001. In 2007, it was reported that this SNP, DHFR C829T, was located close to a microRNA binding site and contributed to the stability of mRNA. Many researchers have analyzed this SNP in several races including Asians and Caucasians. However, the mutation allele is not yet confirmed in most populations. In this study, we reinvestigated the frequency of this SNP using three methods. First, this SNP in genomic DNA was analyzed by a PCR-restriction fragment length polymorphism method. Second, this SNP in mRNA was analyzed by a single nucleotide extension method following a reverse transcription reaction. Third, the mRNA expression level was analyzed by a real-time PCR method. The findings in our study, regarding the discovery of this SNP, suggest that the SNP is an artifact caused by contamination by the genomic DNA of the pseudogene DHFRP1. This study is a reinvestigation of a newly discovered genetic polymorphism.

• 出版日期2012-4-25