Hirose Shigenori, Mayanagi Taira, Pears Catherine, Amagai Aiko, Loomis William F, Maeda Yasuo
Cell and Developmental Biology, Biological Sciences, University of California, San Diego, La Jolla, CA 92093-0368, USA.
Eukaryot Cell. 2005 Aug;4(8):1477-82. doi: 10.1128/EC.4.8.1477-1482.2005.
When growth stops due to the depletion of nutrients, Dictyostelium cells rapidly turn off vegetative genes and start to express developmental genes. One of the early developmental genes, dia1, is adjacent to a vegetative gene, impA, on chromosome 4. An intergenic region of 654 bp separates the coding regions of these divergently transcribed genes. Constructs carrying the intergenic region expressed a reporter gene (green fluorescent protein gene) that replaced impA in growing cells and a reporter gene that replaced dia1 (DsRed) during development. Deletion of a 112-bp region proximal to the transcriptional start site of impA resulted in complete lack of expression of both reporter genes during growth or development. At the other end of the intergenic region there are two copies of a motif that is also found in the carA regulatory region. Removing one copy of this repeat reduced impA expression twofold. Removing the second copy had no further consequences. Removing the central portion of the intergenic region resulted in high levels of expression of dia1 in growing cells, indicating that this region contains a sequence involved in repression during the vegetative stage. Gel shift experiments showed that a nuclear protein present in growing cells recognizes the sequence GAAGTTCTAATTGATTGAAG found in this region. This DNA binding activity is lost within the first 4 h of development. Different nuclear proteins were found to recognize the repeated sequence proximal to dia1. One of these became prevalent after 4 h of development. Together these regulatory components at least partially account for this aspect of the growth-to-differentiation transition.
当由于营养物质耗尽而停止生长时,盘基网柄菌细胞会迅速关闭营养基因并开始表达发育基因。早期发育基因之一dia1与4号染色体上的一个营养基因impA相邻。一个654 bp的基因间区域将这些反向转录基因的编码区域分隔开。携带该基因间区域的构建体在生长细胞中表达了取代impA的报告基因(绿色荧光蛋白基因)以及在发育过程中取代dia1的报告基因(DsRed)。删除impA转录起始位点近端的一个112 bp区域导致在生长或发育过程中两个报告基因均完全不表达。在基因间区域的另一端有一个基序的两个拷贝,该基序也存在于carA调控区域中。去除这个重复序列的一个拷贝使impA表达降低了两倍。去除第二个拷贝没有进一步的影响。去除基因间区域的中心部分导致dia1在生长细胞中高水平表达,这表明该区域包含一个在营养阶段参与抑制作用的序列。凝胶迁移实验表明,生长细胞中存在的一种核蛋白能够识别该区域中发现的序列GAAGTTCTAATTGATTGAAG。这种DNA结合活性在发育的前4小时内丧失。发现不同的核蛋白能够识别dia1近端的重复序列。其中一种在发育4小时后变得普遍。这些调控元件共同至少部分地解释了从生长到分化转变的这一方面。