Maeda Takuya, Sugiura Reiko, Kita Ayako, Saito Mariko, Deng Lu, He Yi, Yabin Lu, Fujita Yasuko, Takegawa Kaoru, Shuntoh Hisato, Kuno Takayoshi
Division of Molecular Pharmacology and Pharmacogenomics, Department of Genome Sciences, Kobe University Graduate School of Medicine, Kobe 650-0017, Japan.
Genes Cells. 2004 Jan;9(1):71-82. doi: 10.1111/j.1356-9597.2004.00699.x.
Schizosaccharomyces pombe pmr1+ gene is homologous to Saccharomyces cerevisiae PMR1 gene, which encodes the P-type Ca2+/Mn2+-ATPase. Addition of Mn2+, as well as Ca2+, to the medium induced pmr1+ gene expression in a calcineurin-dependent manner. The pmr1 knockout (Deltapmr1) cells exhibited hypersensitivity to EGTA. A screen for high gene dosage-suppressors of the EGTA-hypersensitive phenotype of Deltapmr1 led to the identification of pdt1+ gene, which encodes an Nramp-related metal transporter. The Deltapmr1 cells showed round cell morphology. Although Deltapdt1 cells appeared normal in the regular medium, it showed round cell morphology similar to that of the Deltapmr1 cells when Mn2+ was removed from the medium. The removal of Mn2+ also exacerbated the round morphology of the Deltapmr1 cells. The Deltapmr1Deltapdt1 double mutants grew very slowly and showed extremely aberrant cell morphology with round, enlarged and depolarized shape. The addition of Mn2+, but not Ca2+, to the medium completely suppressed the morphological defects, while both Mn2+ and Ca2+ markedly improved the slow growth of the double mutants. These results suggest that Pmr1 and Pdt1 cooperatively regulate cell morphogenesis through the control of Mn2+ homeostasis, and that calcineurin functions as a Mn2+ sensor as well as a Mn2+ homeostasis regulator.
粟酒裂殖酵母pmr1⁺基因与酿酒酵母PMR1基因同源,后者编码P型Ca²⁺/Mn²⁺ - ATP酶。向培养基中添加Mn²⁺以及Ca²⁺会以钙调神经磷酸酶依赖性方式诱导pmr1⁺基因表达。pmr1基因敲除(Δpmr1)细胞对乙二醇双四乙酸(EGTA)表现出超敏性。对Δpmr1细胞EGTA超敏表型的高基因剂量抑制子进行筛选,从而鉴定出pdt1⁺基因,该基因编码一种与天然抗性相关巨噬蛋白(Nramp)相关的金属转运蛋白。Δpmr1细胞呈现圆形细胞形态。尽管Δpdt1细胞在常规培养基中看起来正常,但当从培养基中去除Mn²⁺时,它会表现出与Δpmr1细胞相似的圆形细胞形态。去除Mn²⁺也加剧了Δpmr1细胞的圆形形态。Δpmr1Δpdt1双突变体生长非常缓慢,并表现出极其异常的细胞形态,呈圆形、增大且去极化。向培养基中添加Mn²⁺而非Ca²⁺可完全抑制形态缺陷,而Mn²⁺和Ca²⁺均能显著改善双突变体的缓慢生长。这些结果表明,Pmr1和Pdt1通过控制Mn²⁺稳态协同调节细胞形态发生,并且钙调神经磷酸酶既作为Mn²⁺传感器又作为Mn²⁺稳态调节剂发挥作用。