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首页> 外文期刊>Journal of Basic Microbiology: An International Journal on Morphology, Physiology, Genetics, and Ecology of Microorganisms >Gene expressions and enzyme analyses in the Schizosaccharomyces pombe Deltapap1 transcription factor mutant exposed to Cd(2+).
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Gene expressions and enzyme analyses in the Schizosaccharomyces pombe Deltapap1 transcription factor mutant exposed to Cd(2+).

机译: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。

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摘要

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 thatof 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+).
机译:这项研究的目的是调查Pap1转录因子在长期Cd(2+)应激反应中的作用。用0.5 mM CdSO(4)处理的粟酒裂殖酵母野生型菌株和Deltapap1突变体用于抗氧化酶和基因表达实验。 Deltapap1突变体被证明对Cd(2+)敏感,即点测试,表明Pap1转录因子在对Cd(2+)胁迫的应答中起重要作用。两种菌株中Cd(2+)的吸收均相同。野生型菌株中超氧化物水平的测定证明产生了超氧化物,表明长期的Cd(2+)处理可触发氧化应激。此外,Deltapap1突变体显示更高数量的超氧化物。这些结果得到了超氧化物歧化酶(SOD)催化的反应中生成的过氧化物的明显降低的支持。在较低的GSH和硫化物同化作用下,长期Cd(2+)胁迫期间,Deltapap1突变体的谷胱甘肽S-转移酶比活性明显低于野生型菌株。我们已经证明,GST III活性不是由Deltapap1突变体中的Cd(2+)胁迫诱导的。总体上较低的GST活性不足以使细胞消除Cd(2+)引起的损害,并可能导致Deltapap1突变体的Cd(2+)敏感表型。 RT-PCR和Northern blot实验证明,短期或长期Cd(2+)处理均不会诱导gst2。在两个菌株中,SPCC965.06(推定的K(+)离子通道亚基)基因表达增加,而hmt1(ABC型液泡转运蛋白)表达减少。在gpx1,hmt2,sod1,sod和trx1的mRNA水平上未发现可检测的变化。 SOD酶分析表明,Pap1蛋白的缺乏可能导致SOD活性降低并影响硫酸盐的同化作用。这是关于Pap1转录因子在响应Cd(2+)发生的SOD的细胞转录后/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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