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酿酒酵母中钠离子应激反应所需的钙调神经磷酸酶非依赖途径的鉴定。

Identification of a calcineurin-independent pathway required for sodium ion stress response in Saccharomyces cerevisiae.

作者信息

Ganster R W, McCartney R R, Schmidt M C

机构信息

Department of Molecular Genetics and Biochemistry, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania 15261, USA.

出版信息

Genetics. 1998 Sep;150(1):31-42. doi: 10.1093/genetics/150.1.31.

Abstract

The calcium-dependent protein phosphatase calcineurin plays an essential role in ion homeostasis in yeast. In this study, we identify a parallel ion stress response pathway that is independent of the calcineurin signaling pathway. Cells with null alleles in both STD1 and its homologue, MTH1, manifest numerous phenotypes observed in calcineurin mutants, including sodium, lithium, manganese, and hydroxyl ion sensitivity, as well as alpha factor toxicity. Furthermore, increased gene dosage of STD1 suppresses the ion stress phenotypes in calcineurin mutants and confers halotolerance in wild-type cells. However, Std1p functions in a calcineurin-independent ion stress response pathway, since a std1 mth1 mutant is FK506 sensitive under conditions of ion stress. Mutations in other genes known to regulate gene expression in response to changes in glucose concentration, including SNF3, RGT2, and SNF5, also affect cell growth under ion stress conditions. Gene expression studies indicate that the regulation of HAL1 and PMR2 expression is affected by STD1 gene dosage. Taken together, our data demonstrate that response to ion stress requires the participation of both calcineurin-dependent and -independent pathways.

摘要

钙依赖性蛋白磷酸酶钙调神经磷酸酶在酵母的离子稳态中起着至关重要的作用。在本研究中,我们鉴定出一条与钙调神经磷酸酶信号通路无关的平行离子应激反应途径。STD1及其同源物MTH1中具有无效等位基因的细胞表现出在钙调神经磷酸酶突变体中观察到的众多表型,包括对钠、锂、锰和氢氧根离子的敏感性,以及α因子毒性。此外,增加STD1的基因剂量可抑制钙调神经磷酸酶突变体中的离子应激表型,并赋予野生型细胞耐盐性。然而,Std1p在一条独立于钙调神经磷酸酶的离子应激反应途径中发挥作用,因为在离子应激条件下,std1 mth1突变体对FK506敏感。其他已知在响应葡萄糖浓度变化时调节基因表达的基因(包括SNF3、RGT2和SNF5)中的突变,也会影响离子应激条件下的细胞生长。基因表达研究表明,HAL1和PMR2的表达调控受STD1基因剂量的影响。综上所述,我们的数据表明,对离子应激的反应需要钙调神经磷酸酶依赖性和非依赖性途径的参与。

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