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暴露于Cd(2+)的粟酒裂殖酵母Deltapap1转录因子突变体中的基因表达和酶分析。

Gene expressions and enzyme analyses in the Schizosaccharomyces pombe Deltapap1 transcription factor mutant exposed to Cd(2+).

作者信息

Takács Krisztina, Gazdag Zoltán, Raspor Peter, Pesti Miklós

机构信息

Department of General and Environmental Microbiology, University of Pécs, Hungary.

出版信息

J Basic Microbiol. 2007 Feb;47(1):74-83. doi: 10.1002/jobm.200610239.

Abstract

The objective of this study was to investigate the role of the Pap1 transcription factor in response to long-term Cd(2+) stress. The Schizosaccharomyces pombe wild-type strain and the Deltapap1 mutant, treated with 0.5 mM CdSO(4), were used in antioxidant enzyme and gene expression experiments. The Deltapap1 mutant proved to be sensitive to Cd(2+) in the spot test assay, suggesting that the Pap1 transcription factor plays an important role in the response to Cd(2+) stress. The Cd(2+) uptake was the same in both strains. Determination of the superoxide level in the wild-type strain proved that superoxide was generated, suggesting that long-term Cd(2+) treatment could trigger oxidative stress. Furthermore, the Deltapap1 mutant displayed higher amounts of superoxide. These results were supported by the significantly lower amount of peroxide generated in the reaction catalyzed by superoxide dismutase (SOD). The Deltapap1 mutant had a significantly lower glutathione S-transferase specific activity than that of the wild-type strain during long-term Cd(2+) stress, caused by the lower GSH and sulfide assimilation. We have demonstrated that GST III activity was not induced by Cd(2+) stress in the Deltapap1 mutant. The overall low GST activity was not sufficient for the cell to eliminate Cd(2+) caused damage and could result in a Cd(2+)-sensitive phenotype of the Deltapap1 mutant. The RT-PCR and Northern blot experiments proved that gst2 was not induced either by short-term or by long-term Cd(2+) treatment. The SPCC965.06 (a putative K(+) ion channel subunit) gene expression increased, while the hmt1 (an ABC-type vacuolar transporter protein) expression decreased in both strains. No detectable alteration in the mRNA levels of, gpx1, hmt2, sod1, sod, and trx1 was observed. SOD enzyme analyses revealed that the absence of Pap1 protein could result in a lower SODs activity and affect the sulfate assimilation. This is the first report on the fact that the Pap1 transcription factor could play an important role in the cellular post-transcriptional/post-translational enzyme activity induction processes of SODs that occur in response to Cd(2+).

摘要

本研究的目的是调查Pap1转录因子在响应长期镉离子(Cd²⁺)胁迫中的作用。用0.5 mM硫酸镉(CdSO₄)处理的粟酒裂殖酵母野生型菌株和Δpap1突变体用于抗氧化酶和基因表达实验。在点试验分析中,Δpap1突变体被证明对Cd²⁺敏感,这表明Pap1转录因子在响应Cd²⁺胁迫中起重要作用。两种菌株对Cd²⁺的摄取量相同。对野生型菌株中超氧化物水平的测定证明产生了超氧化物,这表明长期Cd²⁺处理可引发氧化应激。此外,Δpap1突变体显示出更高量的超氧化物。超氧化物歧化酶(SOD)催化反应中产生的过氧化物量显著降低,支持了这些结果。在长期Cd²⁺胁迫期间,由于较低的谷胱甘肽(GSH)和硫化物同化作用,Δpap1突变体的谷胱甘肽S -转移酶比活性显著低于野生型菌株。我们已经证明,在Δpap1突变体中,Cd²⁺胁迫不会诱导GST III活性。总体较低的GST活性不足以使细胞消除Cd²⁺造成的损伤,并可能导致Δpap1突变体出现对Cd²⁺敏感的表型。逆转录 - 聚合酶链反应(RT - PCR)和Northern印迹实验证明,短期或长期Cd²⁺处理均不会诱导gst2表达。在两种菌株中,SPCC965.06(一种假定的钾离子通道亚基)基因表达增加,而hmt1(一种ABC型液泡转运蛋白)表达降低。未观察到gpx1、hmt2、sod1、sod和trx1的mRNA水平有可检测到的变化。SOD酶分析表明,Pap1蛋白的缺失可能导致SODs活性降低并影响硫酸盐同化作用。这是关于Pap1转录因子可能在响应Cd²⁺时发生的SODs细胞转录后/翻译后酶活性诱导过程中起重要作用这一事实的首次报道。

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