Firtel R A
Department of Biology, Center for Molecular Genetics, University of California at San Diego, La Jolla 92093-0634, USA.
Curr Opin Genet Dev. 1996 Oct;6(5):545-54. doi: 10.1016/s0959-437x(96)80082-7.
cAMP functions as the key extracellular signaling molecule controlling Dictyostelium development acting through classic G-protein-coupled/serpentine receptors. Whereas aggregation is controlled by nanomolar pulses of cAMP, a more continuous micromolar signal controls multicellular differentiation by activating a transcriptional cascade via a receptor-mediated but non G-protein-coupled pathway. Potential mechanisms by which extracellular cAMP functions to differentially control aggregation followed by morphogenesis and cell-type differentiation are discussed. This review also summarizes new findings elucidating pathways controlling cell-type regulation in this organism, including signaling cascades mediated by glycogen synthase kinase 3 and cAMP-dependent protein kinase, key regulators of cell-type differentiation in metazoans, and newly identified transcription factors.
环磷酸腺苷(cAMP)作为关键的细胞外信号分子,通过经典的G蛋白偶联/蛇形受体控制盘基网柄菌的发育。聚集由纳摩尔级的cAMP脉冲控制,而更持续的微摩尔级信号则通过受体介导但非G蛋白偶联的途径激活转录级联反应来控制多细胞分化。本文讨论了细胞外cAMP以不同方式控制聚集、随后的形态发生和细胞类型分化的潜在机制。本综述还总结了阐明该生物体中细胞类型调控途径的新发现,包括由糖原合酶激酶3和cAMP依赖性蛋白激酶介导的信号级联反应,后生动物中细胞类型分化的关键调节因子,以及新发现的转录因子。