Tanabe Hiroyuki, Haraguchi Isao, Yoshioka Sachiko
Laboratory of Biochemistry, Faculty of Agriculture, Kinki University, Nara 631-8505, Japan.
Biosci Biotechnol Biochem. 2002 Dec;66(12):2567-72. doi: 10.1271/bbb.66.2567.
The alpha-51D gene encodes surface protein 51D, which specifies serotype 51D of Paramecium tetraurelia stock 51. Previously, we isolated the gene as one expressed at much higher levels in a short-lived mutant than in its parental wild-type stock and characterized its expression to be up-regulated with increased clonal age of the wild-type stock. Here we investigated the transcriptional mechanism for the serotype expression in light of its possible causal relationship to the Paramecium clonal life span. DNA-protein binding analyses of the upstream of the alpha-51D gene identified a stretch of DNA sequence that interacted specifically with macronuclear proteins prepared from the 51D-expressing mutant. The DNA sequence was mapped to the 23 bp between -310 and -288, counting from the initiation position of 51D transcription. A protein with a binding ability for this DNA element was purified to homogeneity from the macronuclear proteins by chromatography using the specific DNA-protein interaction. In vitro transcriptional analyses showed that both the purified protein and its target domain are essential for increased synthesis of the 51D transcript. These results showed that the DNA-protein interaction is required for induction of the 51D expression in the mutant. However, aged wild-type paramecia, in which the serotype is also highly expressed, lacked the same specific transcriptional activity as detected in the mutant, suggesting another DNA-protein interaction involved in the 51D up-regulation.
α-51D基因编码表面蛋白51D,它决定了四膜虫51号品系的51D血清型。此前,我们将该基因分离出来,发现它在一个短命突变体中的表达水平远高于其亲本野生型品系,并发现其表达随着野生型品系克隆年龄的增加而上调。在此,我们根据其与四膜虫克隆寿命可能的因果关系,研究了血清型表达的转录机制。对α-51D基因上游进行DNA-蛋白质结合分析,确定了一段DNA序列,它与从表达51D的突变体中制备的大核蛋白发生特异性相互作用。该DNA序列定位于从51D转录起始位置开始计数的-310至-288之间的23个碱基对处。通过利用特异性DNA-蛋白质相互作用的色谱法,从大核蛋白中纯化出一种对该DNA元件具有结合能力的蛋白质,使其达到同质。体外转录分析表明,纯化的蛋白质及其靶结构域对于增加51D转录本的合成都是必不可少的。这些结果表明,DNA-蛋白质相互作用是突变体中51D表达诱导所必需的。然而,血清型也高度表达的老龄野生型草履虫缺乏在突变体中检测到的相同特异性转录活性,这表明在51D上调中涉及另一种DNA-蛋白质相互作用。