Ribieras S, Lefèbvre O, Tomasetto C, Rio M C
Institut de Génétique et de Biologie Moléculaire et Cellulaire, CNRS/INSERM U184/ULP, BP 163, 67404 Illkirch Cedex, C.U. de, Strasbourg, France.
Gene. 2001 Mar 21;266(1-2):67-75. doi: 10.1016/s0378-1119(01)00380-8.
The mammalian Trefoil Factors (TFFs), TFF1/pS2, TFF2/SP and TFF3/ITF, are expressed and secreted throughout the gastrointestinal tract with a specific and complementary pattern. These proteins exhibit common functions in the protection and repair process of the gastrointestinal epithelial barrier. Here, we report the clustered organization of the three mouse TFF genes in a 40 kb DNA segment, in a head to tail orientation in the following order: TFF1, TFF2, and TFF3. Computer comparison of the mouse TFF promoter sequences to their human counterparts revealed conserved boxes in both mouse and human genes. Promoter methylation analyses showed that, in tissues where these genes are normally expressed, the proximal promoters of TFF1 and TFF2 are specifically not methylated and that of TFF3 is partially demethylated. In contrast, in organs that do not express TFFs, the promoters of the three genes are methylated. These findings strongly argue for the involvement of epigenetic mechanisms in the regulation of TFF expression in normal and pathological conditions.
哺乳动物三叶因子(TFFs),即TFF1/pS2、TFF2/SP和TFF3/ITF,在整个胃肠道以特定且互补的模式表达和分泌。这些蛋白质在胃肠道上皮屏障的保护和修复过程中发挥共同作用。在此,我们报道了三个小鼠TFF基因在一个40 kb DNA片段中呈头尾相连的簇状排列,顺序如下:TFF1、TFF2和TFF3。对小鼠TFF启动子序列与其人类对应序列进行计算机比较,发现在小鼠和人类基因中均存在保守框。启动子甲基化分析表明,在这些基因正常表达的组织中,TFF1和TFF2的近端启动子未发生特异性甲基化,但TFF3的近端启动子发生了部分去甲基化。相反,在不表达TFFs的器官中,这三个基因的启动子均发生了甲基化。这些发现有力地证明了表观遗传机制参与了正常和病理条件下TFF表达的调控。