Hosokawa Masakiyo, Furihata Tomomi, Yaginuma Yumiko, Yamamoto Naoko, Koyano Nao, Fujii Ayako, Nagahara Yuko, Satoh Testuo, Chiba Kan
Faculty of Pharmaceutical Sciences, Chiba Institute of Sciences, Choshi, 288-0025, Japan.
Drug Metab Rev. 2007;39(1):1-15. doi: 10.1080/03602530600952164.
The mammalian carboxylesterases (CESs) comprise a multigene family which gene products play important roles in biotransformation of ester- or amide-type prodrugs. Since expression level of CESs may affect the pharmacokinetic behavior of prodrugs in vivo, it is important to understand the transcriptional regulation mechanism of the CES genes. However, little is known about the gene structure and transcriptional regulation of the mammalian CES genes. In the present study, to investigate the transcriptional regulation of the promoter region of the CES1 and CES2 genes were isolated from mouse, rat and human genomic DNA by PCR amplification. A TATA box was not found the transcriptional start site of all CES promoter. These CES promoters share several common binding sites for transcription factors among the same CES families, suggesting that the orthologous CES genes have evolutionally conserved transcriptional regulatory mechanisms. The result of present study suggested that the mammalian CES promoters were at least partly conserved among the same CES families, and some of the transcription factors may play similar roles in transcriptional regulation of the human and murine CES genes.
哺乳动物羧酸酯酶(CESs)构成一个多基因家族,其基因产物在酯型或酰胺型前药的生物转化中发挥重要作用。由于CESs的表达水平可能影响前药在体内的药代动力学行为,因此了解CES基因的转录调控机制很重要。然而,关于哺乳动物CES基因的基因结构和转录调控知之甚少。在本研究中,为了研究CES1和CES2基因启动子区域的转录调控,通过PCR扩增从小鼠、大鼠和人类基因组DNA中分离出这些基因。在所有CES启动子的转录起始位点均未发现TATA框。这些CES启动子在同一CES家族中共享几个转录因子的常见结合位点,表明直系同源CES基因具有进化上保守的转录调控机制。本研究结果表明,哺乳动物CES启动子在同一CES家族中至少部分保守,并且一些转录因子可能在人类和小鼠CES基因的转录调控中发挥相似作用。