Stark Michal, Gonen Nitzan, Assaraf Yehuda G
Dept. of Biology, Technion-Israel Institute of Technology, Haifa, Israel.
Biochem Biophys Res Commun. 2009 Oct 9;388(1):79-85. doi: 10.1016/j.bbrc.2009.07.116. Epub 2009 Jul 28.
The proton-coupled folate transporter (PCFT) is the dominant intestinal folate transporter, however, its promoter has yet to be revealed. Hence, we here cloned a 3.1kb fragment upstream to the first ATG of the human PCFT gene and generated sequential deletion constructs evaluated in luciferase reporter assay. This analysis mapped the minimal promoter to 157bp upstream to the first ATG. Crucial GC-box sites were identified within the minimal promoter and in its close vicinity which substantially contribute to promoter activity, as their disruption resulted in 94% loss of luciferase activity. We also identified upstream enhancer elements including YY1 and AP1 which, although distantly located, prominently transactivated the minimal promoter, as their inactivation resulted in 50% decrease in reporter activity. This is the first functional identification of the minimal PCFT promoter harboring crucial GC-box elements that markedly contribute to its transcriptional activation via putative interaction with distal YY1 and AP1 enhancer elements.
质子偶联叶酸转运体(PCFT)是肠道中主要的叶酸转运体,然而,其启动子尚未被揭示。因此,我们在此克隆了人类PCFT基因第一个ATG上游3.1kb的片段,并构建了一系列缺失构建体,通过荧光素酶报告基因检测进行评估。该分析将最小启动子定位到第一个ATG上游157bp处。在最小启动子及其紧邻区域内鉴定出关键的GC盒位点,这些位点对启动子活性有重要贡献,因为它们的破坏导致荧光素酶活性丧失94%。我们还鉴定出上游增强子元件,包括YY1和AP1,尽管它们位置较远,但能显著激活最小启动子,因为它们的失活导致报告基因活性降低50%。这是首次对含有关键GC盒元件的最小PCFT启动子进行功能鉴定,这些元件通过与远端YY1和AP1增强子元件的假定相互作用,对其转录激活有显著贡献。