Schnitzler G R, Briscoe C, Brown J M, Firtel R A
Department of Biology, University of California, San Diego, La Jolla 92093-0634, USA.
Cell. 1995 Jun 2;81(5):737-45. doi: 10.1016/0092-8674(95)90535-9.
The transcription factor G box-binding factor (GBF) is required for the developmental switch between aggregative and postaggregative gene expression, cell-type differentiation, and morphogenesis. We show that constitutive expression of GBF allows ectopic expression of postaggregative genes, but only in response to exogenous cAMP. GBF activation requires the serpentine cAMP receptors required for aggregation, but not the coupled G alpha 2 or the G beta subunit, suggesting a novel signaling pathway. In response to high cAMP, g alpha 2-null cells can bypass the aggregation stage, expressing cell type-specific genes and forming fruiting bodies. Our results demonstrate that the same receptors regulate aggregation and cell-type differentiation, but via distinct pathways depending upon whether the receptor perceives a pulsatile or sustained signal.
转录因子G盒结合因子(GBF)是聚集性和聚集后基因表达、细胞类型分化及形态发生之间发育转换所必需的。我们发现,GBF的组成型表达允许聚集后基因的异位表达,但仅对外源cAMP有反应。GBF激活需要聚集所需的蛇形cAMP受体,但不需要偶联的Gα2或Gβ亚基,这提示了一种新的信号通路。在高cAMP作用下,Gα2缺失的细胞可以绕过聚集阶段,表达细胞类型特异性基因并形成子实体。我们的结果表明,相同的受体调节聚集和细胞类型分化,但根据受体感知的是脉动信号还是持续信号,通过不同的途径进行调节。