Carvalho Lilian D S, Teixeira Leonardo K, Carrossini Nina, Caldeira Anita T N, Ansel K Mark, Rao Anjana, Viola João P B
Division of Cellular Biology, National Cancer Institute (INCA), Rio de Janeiro, Brazil.
Cell Cycle. 2007 Jul 15;6(14):1789-95. doi: 10.4161/cc.6.14.4473. Epub 2007 May 21.
The NFAT (Nuclear Factor of Activated T cells) family of transcription factors plays a central role in the regulation of several genes related to the immune response. Recently, NFAT proteins have been implicated in the proliferation and differentiation of different cell types. Previous studies have shown that NFAT1-deficient mice display lymphocyte hyperproliferation, shortened cell cycle duration, and cyclin overexpression. Here, we demonstrate that cyclin A2 expression is upregulated in the absence of NFAT1 in lymphocytes. Ectopic expression of NFAT1 in CHO cells decreases cyclin A2 levels. Indeed, NFAT1 binds to a consensus binding site found at the mouse cyclin A2 promoter in vitro and in vivo. Luciferase reporter assays show that NFAT1 downregulates cyclin A2 expression by directly binding to the cyclin A2 promoter. Together, these results indicate that the NFAT1 transcription factor represses cyclin A2 expression in lymphocytes, and may act as a silencer of gene transcription during the cell cycle.
活化T细胞核因子(NFAT)家族转录因子在调控多个与免疫反应相关的基因中发挥核心作用。最近,NFAT蛋白与不同细胞类型的增殖和分化有关。先前的研究表明,NFAT1缺陷型小鼠表现出淋巴细胞过度增殖、细胞周期持续时间缩短以及细胞周期蛋白过表达。在此,我们证明在淋巴细胞中,缺乏NFAT1时细胞周期蛋白A2的表达会上调。在CHO细胞中异位表达NFAT1会降低细胞周期蛋白A2的水平。实际上,NFAT1在体外和体内均与小鼠细胞周期蛋白A2启动子上的共有结合位点结合。荧光素酶报告基因检测表明,NFAT1通过直接结合细胞周期蛋白A2启动子来下调其表达。这些结果共同表明,NFAT1转录因子在淋巴细胞中抑制细胞周期蛋白A2的表达,并且可能在细胞周期中作为基因转录的沉默子。