Ogawa N, DeRisi J, Brown P O
Department of Biochemistry, Howard Hughes Medical Institute, Stanford University School of Medicine, Stanford, California 94305-5307, USA.
Mol Biol Cell. 2000 Dec;11(12):4309-21. doi: 10.1091/mbc.11.12.4309.
The PHO regulatory pathway is involved in the acquisition of phosphate (P(i)) in the yeast Saccharomyces cerevisiae. When extracellular P(i) concentrations are low, several genes are transcriptionally induced by this pathway, which includes the Pho4 transcriptional activator, the Pho80-Pho85 cyclin-CDK pair, and the Pho81 CDK inhibitor. In an attempt to identify all the components regulated by this system, a whole-genome DNA microarray analysis was employed, and 22 PHO-regulated genes were identified. The promoter regions of 21 of these genes contained at least one copy of a sequence that matched the Pho4 recognition site. Eight of these genes, PHM1-PHM8, had no previously defined function in phosphate metabolism. The amino acid sequences of PHM1 (YFL004w), PHM2 (YPL019c), PHM3 (YJL012c), and PHM4 (YER072w) are 32-56% identical. The phm3 and phm4 single mutants and the phm1 phm2 double mutant were each severely deficient in accumulation of inorganic polyphosphate (polyP) and P(i). The phenotype of the phm5 mutant suggests that PHM5 (YDR452w) is essential for normal catabolism of polyP in the yeast vacuole. Taken together, the results reveal important new features of a genetic system that plays a critical role in P(i) acquisition and polyP metabolism in yeast.
PHO调控途径参与酿酒酵母中磷酸盐(P(i))的摄取。当细胞外P(i)浓度较低时,该途径会转录诱导多个基因,其中包括Pho4转录激活因子、Pho80 - Pho85细胞周期蛋白 - CDK对以及Pho81 CDK抑制剂。为了鉴定受该系统调控的所有组分,我们采用了全基因组DNA微阵列分析,并鉴定出22个受PHO调控的基因。其中21个基因的启动子区域包含至少一个与Pho4识别位点匹配的序列拷贝。这些基因中的8个,即PHM1 - PHM8,在磷酸盐代谢中以前没有明确的功能。PHM1(YFL004w)、PHM2(YPL019c)、PHM3(YJL012c)和PHM4(YER072w)的氨基酸序列有32 - 56%的同一性。phm3和phm4单突变体以及phm1 phm2双突变体在无机多聚磷酸盐(polyP)和P(i)的积累方面均严重缺陷。phm5突变体的表型表明PHM5(YDR452w)对于酵母液泡中polyP的正常分解代谢至关重要。综上所述,这些结果揭示了一个在酵母P(i)摄取和polyP代谢中起关键作用的遗传系统的重要新特征。