Weinberg M S, Girotti M, Spencer R L
Department of Psychology, University of Colorado at Boulder, 345 UCB, Muenzinger D244, Boulder, CO 80303, USA.
Neuroscience. 2007 Dec 5;150(2):478-86. doi: 10.1016/j.neuroscience.2007.09.013. Epub 2007 Sep 14.
The protein product of the fra-2 gene (Fra-2), a fos-family member, can compete with Fos protein for participation in activating protein-1 (AP-1) transcription factor complexes and each protein can contribute different transactivational consequences to an AP-1 complex. To date, there is limited characterization of fra-2 mRNA expression in the rat forebrain. We examined basal and restraint-induced mRNA expression (in situ hybridization) of fra-2 in the rat forebrain and compared its temporal-spatial pattern to c-fos. In contrast to the very low basal expression of c-fos, fra-2 basal expression was moderately high throughout cortex and some subcortical structures, including prominent basal expression in the hypothalamic paraventricular nucleus (PVN). Restraint-induced fra-2 expression was quantified in the prefrontal cortex (PFC), lateral septum (LS) and PVN. Maximal fra-2 gene induction in the PFC and LS was delayed (60 min) after restraint onset with respect to c-fos (15 min), whereas in the PVN, fra-2 mRNA increased within 15 min of restraint. Additionally we compared c-fos and fra-2 gene expression in rats given shorter or longer restraint durations, but equal total time from stress onset to sample collection, to determine the extent to which the kinetics of gene induction matched that of a hypothalamic-pituitary-adrenal axis hormone response. Rats given 45 min recovery after 15 min restraint showed less c-fos expression in the PVN, less fra-2 expression in the prelimbic and infralimbic PFC, and no difference in the LS compared with rats restrained for 60 min. Thus, the expression of both genes was sensitive to stressor duration, but this sensitivity varied with brain region. Differential basal and stress-induced expression patterns of the fra-2 and c-fos genes are likely to have important functional consequences for AP-1 transcription factor dependent regulation of neural plasticity.
fos家族成员fra - 2基因的蛋白质产物(Fra - 2)可与Fos蛋白竞争参与激活蛋白-1(AP - 1)转录因子复合物,且每种蛋白对AP - 1复合物可产生不同的反式激活作用。迄今为止,大鼠前脑内fra - 2 mRNA表达的特征描述有限。我们检测了大鼠前脑内fra - 2的基础表达及束缚诱导的mRNA表达(原位杂交),并将其时空模式与c - fos进行比较。与c - fos极低的基础表达相反,fra - 2在整个皮质和一些皮质下结构中的基础表达中等偏高,包括下丘脑室旁核(PVN)中有显著的基础表达。在额叶前皮质(PFC)、外侧隔区(LS)和PVN中对束缚诱导的fra - 2表达进行了定量分析。与c - fos(15分钟)相比,束缚开始后PFC和LS中fra - 2基因的最大诱导延迟(60分钟),而在PVN中,束缚后15分钟内fra - 2 mRNA就增加。此外,我们比较了给予较短或较长束缚时间但从应激开始到样本采集总时间相等的大鼠中c - fos和fra - 2基因的表达,以确定基因诱导动力学与下丘脑-垂体-肾上腺轴激素反应的匹配程度。与束缚60分钟的大鼠相比,束缚15分钟后恢复45分钟的大鼠在PVN中c - fos表达较少,在前边缘和下边缘PFC中fra - 2表达较少,而在LS中无差异。因此,这两个基因的表达均对应激源持续时间敏感,但这种敏感性因脑区而异。fra - 2和c - fos基因不同的基础表达和应激诱导表达模式可能对AP - 1转录因子依赖的神经可塑性调节具有重要的功能影响。