Fred Wyszkowski Cancer Research Laboratory, Faculty of Biology, Technion-Israel Institute of Technology, Haifa 32000, Israel.
J Biol Chem. 2010 Oct 29;285(44):33602-13. doi: 10.1074/jbc.M110.135640. Epub 2010 Aug 19.
Folates are essential vitamins that play a key role as one-carbon donors in a spectrum of biosynthetic pathways including RNA and DNA synthesis. The proton-coupled folate transporter (PCFT/SLC46A1) mediates obligatory intestinal folate absorption. Loss-of-function mutations in PCFT result in hereditary folate malabsorption, an autosomal recessive disorder characterized by very low folate levels in the blood and cerebrospinal fluid. Hereditary folate malabsorption manifests within the first months after birth with anemia, immune deficiency, and neurological deficits. Here we studied the role of inducible trans-activators of PCFT gene expression. Bioinformatics identified three putative nuclear respiratory factor 1 (NRF-1) binding sites in the minimal promoter. The following evidence establish that PCFT is an NRF-1-responsive gene; electrophoretic mobility shift assay showed NRF-1 binding to native but not mutant NRF-1 sites, whereas antibody-mediated supershift analysis and chromatin immunoprecipitation revealed NRF-1 binding to its consensus sites within the PCFT promoter. Moreover, mutational inactivation of individual or all NRF-1 binding sites resulted in 40-60% decrease in luciferase reporter activity. Consistently, overexpression of NRF-1 or a constitutively active NRF-1 VP-16 construct resulted in increased reporter activity and PCFT mRNA levels. Conversely, introduction of a dominant-negative NRF-1 construct markedly repressed reporter activity and PCFT mRNA levels; likewise, introduction of NRF-1 siRNA duplexes to cells resulted in decreased PCFT transcript levels. Moreover, NRF-1 silencing down-regulated genes encoding for key folate transporters and enzymes in folate metabolism. These novel findings identify NRF-1 as a major inducible transcriptional regulator of PCFT gene expression. The implications of this linkage between folate transport and metabolism with mitochondria biogenesis and respiration are discussed.
叶酸是必需的维生素,作为一碳供体在一系列生物合成途径中发挥关键作用,包括 RNA 和 DNA 的合成。质子偶联叶酸转运体(PCFT/SLC46A1)介导必需的肠道叶酸吸收。PCFT 的功能丧失突变导致遗传性叶酸吸收不良,这是一种常染色体隐性遗传病,其特征是血液和脑脊液中的叶酸水平非常低。遗传性叶酸吸收不良在出生后的头几个月内表现为贫血、免疫缺陷和神经功能缺损。在这里,我们研究了诱导 PCFT 基因表达的反式激活因子的作用。生物信息学在最小启动子中鉴定了三个假定的核呼吸因子 1(NRF-1)结合位点。以下证据证实 PCFT 是一种 NRF-1 反应性基因;电泳迁移率变动分析显示 NRF-1 与天然而非突变的 NRF-1 结合位点结合,而抗体介导的超迁移分析和染色质免疫沉淀显示 NRF-1 与 PCFT 启动子内的其共有位点结合。此外,单个或所有 NRF-1 结合位点的突变失活导致荧光素酶报告基因活性降低 40-60%。一致地,NRF-1 的过表达或组成型激活的 NRF-1 VP-16 构建体导致报告基因活性和 PCFT mRNA 水平增加。相反,引入显性负 NRF-1 构建体显著抑制报告基因活性和 PCFT mRNA 水平;同样,向细胞中引入 NRF-1 siRNA 双链体导致 PCFT 转录物水平降低。此外,NRF-1 沉默下调了叶酸代谢中关键叶酸转运体和酶的基因表达。这些新发现确定 NRF-1 是 PCFT 基因表达的主要诱导转录调节因子。讨论了这种叶酸转运和代谢与线粒体生物发生和呼吸之间的联系的意义。