Nguyen Tuan, Lindner Ricco, Tedeschi Andrea, Forsberg Kirsi, Green Andrew, Wuttke Anja, Gaub Perrine, Di Giovanni Simone
Laboratory for NeuroRegeneration and Repair, Department of Neurology, Hertie Institute for Clinical Brain Research, Germany.
J Biol Chem. 2009 Jul 10;284(28):18816-23. doi: 10.1074/jbc.M109.015719. Epub 2009 May 14.
Transcription is essential for neurite and axon outgrowth during development. Recent work points to the involvement of nuclear factor of activated T cells (NFAT) in the regulation of genes important for axon growth and guidance. However, NFAT has not been reported to directly control the transcription of axon outgrowth-related genes. To identify transcriptional targets, we performed an in silico promoter analysis and found a putative NFAT site within the GAP-43 promoter. Using in vitro and in vivo experiments, we demonstrated that NFAT-3 regulates GAP-43, but unexpectedly, does not promote but represses the expression of GAP-43 in neurons and in the developing brain. Specifically, in neuron-like PC-12 cells and in cultured cortical neurons, the overexpression of NFAT-3 represses GAP-43 activation mediated by neurotrophin signaling. Using chromatin immunoprecipitation assays, we also show that prior to neurotrophin activation, endogenous NFAT-3 occupies the GAP-43 promoter in PC-12 cells, in cultured neurons, and in the mouse brain. Finally, we observe that NFAT-3 is required to repress the physiological expression of GAP-43 and other pro-axon outgrowth genes in specific developmental windows in the mouse brain. Taken together, our data reveal an unexpected role for NFAT-3 as a direct transcriptional repressor of GAP-43 expression and suggest a more general role for NFAT-3 in the control of the neuronal outgrowth program.
转录对于发育过程中的神经突和轴突生长至关重要。最近的研究表明,活化T细胞核因子(NFAT)参与了对轴突生长和导向重要的基因的调控。然而,尚未有报道称NFAT可直接控制轴突生长相关基因的转录。为了确定转录靶点,我们进行了计算机启动子分析,并在GAP - 43启动子内发现了一个假定的NFAT位点。通过体外和体内实验,我们证明NFAT - 3调节GAP - 43,但出乎意料的是,它在神经元和发育中的大脑中并不促进反而抑制GAP - 43的表达。具体而言,在神经元样PC - 12细胞和培养的皮质神经元中,NFAT - 3的过表达抑制了神经营养因子信号介导的GAP - 43激活。使用染色质免疫沉淀试验,我们还表明,在神经营养因子激活之前,内源性NFAT - 3在PC - 12细胞、培养的神经元和小鼠大脑中占据GAP - 43启动子。最后,我们观察到在小鼠大脑的特定发育阶段,NFAT - 3是抑制GAP - 43和其他促轴突生长基因的生理表达所必需的。综上所述,我们的数据揭示了NFAT - 3作为GAP - 43表达的直接转录抑制因子的意外作用,并表明NFAT - 3在控制神经元生长程序中具有更广泛的作用。