Sasano Yu, Sakata Tetsuro, Okusaki Sakurako, Sugiyama Minetaka, Kaneko Yoshinobu, Harashima Satoshi
Department of Applied Microbial Technology, Faculty of Biotechnology and Life Science, Sojo University.
Department of Biotechnology, Graduate School of Engineering, Osaka University.
Genes Genet Syst. 2018 Dec 22;93(5):199-207. doi: 10.1266/ggs.18-00014. Epub 2018 Nov 16.
To achieve inorganic phosphate (Pi) homeostasis, cells must be able to sense intracellular and extracellular Pi concentrations. In the Pi signaling (PHO) pathway in Saccharomyces cerevisiae, high Pi represses genes involved in Pi uptake (e.g., PHO84) and Pi utilization (PHO5); conversely, the cyclin-dependent kinase inhibitor Pho81 inhibits the activity of the Pho80-Pho85 cyclin-cyclin dependent kinase complex in low-Pi conditions, leading to induction of these genes. However, how yeast senses Pi availability remains unresolved. To identify factors involved in Pi sensing upstream of the Pho81-Pho80-Pho85 complex, we generated and screened suppressor mutants of a Δpho84 strain that shows constitutive PHO5 expression. By a series of genetic tests, including dominance-recessiveness, complementation and tetrad analyses, three sef (suppressor of pho84 [pho eighty-four]) mutants (sef8, sef9 and sef10) were shown to contain a novel single mutation. The sef mutants suppressed the phenotype of constitutive PHO5 expression at the transcriptional level, but did not show restored Pi uptake capacity. An epistasis-hypostasis test revealed that the sef mutations were hypostatic to pho80 mutation, indicating that their gene products function upstream of the Pho81-Pho80-Pho85 complex in the PHO pathway. The sef mutations identified are associated with gene(s) that may be involved in the homeostasis of an intracellular Pi level-sensing mechanism in S. cerevisiae.
为实现无机磷酸盐(Pi)稳态,细胞必须能够感知细胞内和细胞外的Pi浓度。在酿酒酵母的Pi信号传导(PHO)途径中,高Pi水平会抑制参与Pi摄取(如PHO84)和Pi利用(PHO5)的基因;相反,细胞周期蛋白依赖性激酶抑制剂Pho81在低Pi条件下会抑制Pho80 - Pho85细胞周期蛋白 - 细胞周期蛋白依赖性激酶复合物的活性,从而导致这些基因的诱导。然而,酵母如何感知Pi的可用性仍未得到解决。为了鉴定在Pho81 - Pho80 - Pho85复合物上游参与Pi感知的因子,我们构建并筛选了显示组成型PHO5表达的Δpho84菌株的抑制突变体。通过一系列遗传测试,包括显性 - 隐性、互补和四分体分析,三个sef(pho84[pho八十四]的抑制子)突变体(sef8、sef9和sef10)被证明含有一个新的单突变。sef突变体在转录水平上抑制了组成型PHO5表达的表型,但未显示出恢复的Pi摄取能力。上位性 - 下位性测试表明,sef突变对pho80突变是下位性的,这表明它们的基因产物在PHO途径中Pho81 - Pho80 - Pho85复合物的上游发挥作用。所鉴定出的sef突变与可能参与酿酒酵母细胞内Pi水平感知机制稳态的基因有关。