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Response of Schizosaccharomyces pombe to Zinc Deficiency

机译:粟酒裂殖酵母对缺锌的反应

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A component of the cellular response to zinc deficiency operates via control of transcript abundance. Therefore, microarray analysis was employed to identify Schizosaccharomyces pombe genes whose mRNA levels are regulated by intracellular zinc status. A set of 57 genes whose mRNA levels were substantially reduced in response to zinc deficiency was identified, while the mRNA levels of 63 genes were increased by this condition. In order to investigate the mechanisms that control these responses, a genetic screen was employed to identify mutants with defective zinc-responsive gene expression. Two strains (II-1 and V7) that were identified by this screen harbor mutations that are linked to zrt1+, which encodes a putative Zrt/IRT-like protein (ZIP) zinc uptake transporter. Importantly, zrt1+ mRNA levels are increased in response to zinc deprivation, and cells lacking functional Zrt1 are highly impaired in their ability to proliferate at limiting zinc concentrations. Furthermore, zrt1 null cells were found to have severely reduced zinc contents, indicating that Zrt1 functions as a key regulator of intracellular zinc levels in fission yeast. The deletion of fet4+, another zinc-responsive gene encoding a putative metal ion transporter, exacerbated the phenotypes associated with the loss of Zrt1, suggesting that Fet4 also plays a role in zinc uptake under limiting conditions.
机译:细胞对锌缺乏的反应的一部分是通过控制转录本丰度来发挥作用的。因此,通过微阵列分析来鉴定粟酒裂殖酵母基因,这些基因的mRNA水平受细胞内锌状态的调节。鉴定出一组57个基因,其mRNA水平响应于锌缺乏而大大降低,而63种基因的mRNA水平通过这种条件而增加。为了研究控制这些反应的机制,采用了遗传筛选来鉴定具有缺陷的锌反应性基因表达的突变体。通过此筛选鉴定出的两个菌株(II-1和V7)带有与 zrt1 + 相关的突变,该突变编码一种假定的Zrt / IRT样蛋白(ZIP )锌吸收转运蛋白。重要的是, zrt1 + mRNA水平会因缺锌而增加,而缺乏功能性Zrt1的细胞在极限锌浓度下的增殖能力会大大受损。此外,发现 zrt1 空细胞的锌含量大大降低,这表明Zrt1是裂变酵母中细胞内锌水平的关键调节剂。另一个编码假定的金属离子转运蛋白的锌敏感基因 fet4 + 的缺失加剧了与Zrt1丢失相关的表型,表明Fet4在在限制条件下摄取锌。

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