Iwamoto K, Kato T
Laboratory for Molecular Dynamics of Mental Disorders, Brain Science Institute, Wako-city, Saitama, Japan.
Pharmacogenomics J. 2002;2(5):335-40. doi: 10.1038/sj.tpj.6500130.
Serotonin 2C receptor (5-HT(2C)R) transcripts undergo RNA editing, generating pharmacologically different isoforms. To test whether the RNA editing of 5-HT(2C)R is regulated by serotonergic activity, effects of cocaine or reserpine administration in the rat cerebral cortex were examined. Although these drugs have been known to alter serotonin metabolism, no alterations in the RNA editing were found by the sequencing analysis. Towards high throughput analysis, we developed a non-RI method that allows accurate and rapid estimation of RNA editing by combining the primer extension with denaturing high-performance liquid chromatography (DHPLC). By using this, RNA editing efficiencies of 5-HT(2C)R in the midbrain and hippocampus as well as the cerebral cortex were examined, and no alterations were found among these regions. Our method using DHPLC is applicable to examine association of RNA editing with various diseases.
血清素2C受体(5-HT(2C)R)转录本会经历RNA编辑,产生药理学特性不同的异构体。为了测试5-HT(2C)R的RNA编辑是否受血清素能活性调节,研究了给大鼠大脑皮层注射可卡因或利血平的效果。尽管已知这些药物会改变血清素代谢,但测序分析未发现RNA编辑有变化。为了进行高通量分析,我们开发了一种非放射性同位素方法,通过将引物延伸与变性高效液相色谱(DHPLC)相结合,能够准确快速地估计RNA编辑情况。利用该方法,检测了中脑、海马体以及大脑皮层中5-HT(2C)R的RNA编辑效率,这些区域之间未发现变化。我们使用DHPLC的方法适用于研究RNA编辑与各种疾病的关联。