Geusz M E, Fletcher C, Block G D, Straume M, Copeland N G, Jenkins N A, Kay S A, Day R N
NSF Center for Biological Timing, University of Virginia, Charlottesville 22903, USA.
Curr Biol. 1997 Oct 1;7(10):758-66. doi: 10.1016/s0960-9822(06)00334-4.
The AP-1 family of transcription factors has been implicated in the control of the expression of many genes in response to environmental signals. Previous studies have provided temporal profiles for c-fos expression by taking measurements from many animals at several points in time, but these studies provide limited information about dynamic changes in expression. Here, we have devised a method of continuously measuring c-fos expression.
A transgenic mouse line expressing the human c-fos promoter linked to the firefly luciferase reporter gene (fos/luc) was generated to continuously monitor c-fos gene expression. A second transgenic mouse line expressing luciferase under the control of the cytomegalovirus promoter (CMV/luc) served as a control. Luminescence originating from identifiable brain regions was imaged from fos/luc brain slice cultures. Expression of the fos/luc transgene accurately reflected transcriptional responses of the endogenous c-fos gene. Dynamic changes in fos/luc expression in suprachiasmatic nuclei (SCN) explant cultures were monitored continuously, and luminescence showed almost 24 hour rhythms lasting up to five circadian cycles. In contrast, bioluminescence monitored from CMV/luc SCN explant cultures was not rhythmic.
The fos/luc transgenic mouse will be useful for long-term, non-invasive monitoring of c-fos transcriptional responses to the changing cellular environment. Circadian rhythms in c-fos expression can be monitored non-invasively in real time from the SCN, clearly demonstrating that c-fos transcription is regulated by the circadian clock.
转录因子AP-1家族参与了许多基因对环境信号应答的表达调控。以往的研究通过在多个时间点对许多动物进行测量,提供了c-fos表达的时间概况,但这些研究提供的关于表达动态变化的信息有限。在此,我们设计了一种连续测量c-fos表达的方法。
构建了一个表达与萤火虫荧光素酶报告基因相连的人c-fos启动子的转基因小鼠品系(fos/luc),以连续监测c-fos基因表达。另一个在巨细胞病毒启动子(CMV/luc)控制下表达荧光素酶的转基因小鼠品系用作对照。从fos/luc脑片培养物中对来自可识别脑区的发光进行成像。fos/luc转基因的表达准确反映了内源性c-fos基因的转录应答。对视交叉上核(SCN)外植体培养物中fos/luc表达的动态变化进行了连续监测,发光显示出持续长达五个昼夜周期的近24小时节律。相比之下,从CMV/luc SCN外植体培养物中监测到的生物发光没有节律。
fos/luc转基因小鼠将有助于对c-fos对不断变化的细胞环境的转录应答进行长期、非侵入性监测。可以从SCN实时非侵入性地监测c-fos表达的昼夜节律,清楚地表明c-fos转录受昼夜节律时钟调控。