Ogawa N, Noguchi K, Sawai H, Yamashita Y, Yompakdee C, Oshima Y
Department of Biotechnology, Faculty of Engineering, Osaka University, Japan.
Mol Cell Biol. 1995 Feb;15(2):997-1004. doi: 10.1128/MCB.15.2.997.
The PHO81 gene is thought to encode an inhibitor of the negative regulators (Pho80p and Pho85p) in the phosphatase (PHO) regulon. Transcription of PHO81 is regulated by Pi signals through the same PHO regulatory system. Elimination of the PHO81 promoter or its substitution by the GAL1 promoter revealed that stimulation of the PHO regulatory system requires both increased transcription of PHO81 and a Pi starvation signal. The predicted Pho81p protein contains 1,179 amino acids (aa) and has six repeats of an ankyrin-like sequence in its central region. The minimum amino acid sequence required for Pho81p function was narrowed down to a 141-aa segment (aa 584 to 724), which contains the fifth and sixth repeats of the ankyrin-like motif. The third to sixth repeats of the ankyrin-like motif of Pho81p have significant similarities to that of p16INK4, which inhibits activity of the human cyclin D-CDK4 kinase complex. Deletion analyses revealed that the N- and C-terminal regions of Pho81p behave as negative and positive regulatory domains, respectively, for the minimal 141-aa region. The negative regulatory activity of the N-terminal domain was antagonized by a C-terminal segment of Pho81p supplied in trans. All four known classes of PHO81c mutations that show repressible acid phosphatase activity in high-Pi medium affect the N-terminal half of Pho81p. An in vitro assay showed that a glutathione S-transferase-Pho81p fusion protein inhibits the Pho85p protein kinase. Association of Pho81p with Pho85p or with the Pho80p-Pho85p complex was demonstrated by the two-hybrid system.
PHO81基因被认为编码磷酸酶(PHO)调节子中负调节因子(Pho80p和Pho85p)的一种抑制剂。PHO81的转录受磷酸根信号通过相同的PHO调节系统调控。去除PHO81启动子或用GAL1启动子替换它,结果表明,PHO调节系统的激活既需要PHO81转录增加,也需要磷酸根饥饿信号。预测的Pho81p蛋白含有1179个氨基酸(aa),其中心区域有六个锚蛋白样序列重复。Pho81p功能所需的最小氨基酸序列被缩小到一个141个氨基酸的片段(第584至724位氨基酸),该片段包含锚蛋白样基序的第五和第六个重复。Pho81p锚蛋白样基序的第三至第六个重复与p16INK4的该基序有显著相似性,p16INK4抑制人细胞周期蛋白D - CDK4激酶复合物的活性。缺失分析表明,对于最小的141个氨基酸区域,Pho81p的N端和C端区域分别表现为负调节域和正调节域。N端结构域的负调节活性被反式提供的Pho81p的C端片段拮抗。在高磷酸根培养基中表现出可抑制酸性磷酸酶活性的所有四种已知类型的PHO81c突变都影响Pho81p的N端一半。体外试验表明,谷胱甘肽S - 转移酶 - Pho81p融合蛋白抑制Pho85p蛋白激酶。通过双杂交系统证明了Pho81p与Pho85p或与Pho80p - Pho85p复合物的结合。