Siol Oliver, Dingermann Theodor, Winckler Thomas
Universität Jena, Lehrstuhl für Pharmazeutische Biologie, Semmelweisstrasse 10, D-07743 Jena, Germany.
Eukaryot Cell. 2006 Apr;5(4):658-64. doi: 10.1128/EC.5.4.658-664.2006.
Aggregation of Dictyostelium discoideum amoebae into multicellular structures is organized by cyclic AMP (cAMP), which acts as a chemoattractant, as a second messenger, and as a morphogen. Aggregation of D. discoideum cells depends on the expression of adenylyl cyclase ACA, which provides extracellular cAMP for signal relay and intracellular cAMP for the induction of genes required at multicellular stages. We have identified a DNA-binding activity specific for a highly A+T-enriched motif in the upstream region of the ACA-encoding gene, acaA. The factor shows DNA-binding characteristics very similar to those of C-module-binding factor (CbfA). Although CbfA was originally identified as a putative regulator of the activity of D. discoideum retrotransposon TRE5-A, it also was found to be essential for aggregation of D. discoideum cells. The identified DNA-binding activity was absent in mutant cells depleted of CbfA, and CbfA could be precipitated using an acaA promoter fragment. We propose that CbfA binds to the acaA promoter to provide a basal transcription activity that is required for induction of ACA expression after the onset of D. discoideum development.
盘基网柄菌变形虫聚集形成多细胞结构是由环磷酸腺苷(cAMP)介导的,cAMP作为一种趋化因子、第二信使和形态发生素发挥作用。盘基网柄菌细胞的聚集依赖于腺苷酸环化酶ACA的表达,ACA为信号传递提供细胞外cAMP,并为多细胞阶段所需基因的诱导提供细胞内cAMP。我们在编码ACA的基因acaA的上游区域鉴定出一种对高度富含A+T的基序具有特异性的DNA结合活性。该因子显示出与C模块结合因子(CbfA)非常相似的DNA结合特性。尽管CbfA最初被鉴定为盘基网柄菌反转录转座子TRE5-A活性的假定调节因子,但它也被发现是盘基网柄菌细胞聚集所必需的。在缺乏CbfA的突变细胞中不存在所鉴定的DNA结合活性,并且可以使用acaA启动子片段沉淀CbfA。我们提出,CbfA与acaA启动子结合以提供基础转录活性,这是盘基网柄菌发育开始后诱导ACA表达所必需的。