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首页> 外文期刊>Eukaryotic cell >Snf1-Like Protein Kinase Ssp2 Regulates Glucose Derepression in Schizosaccharomyces pombe
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Snf1-Like Protein Kinase Ssp2 Regulates Glucose Derepression in Schizosaccharomyces pombe

机译:Snf1样蛋白激酶Ssp2调节粟酒裂殖酵母中的葡萄糖抑制。

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The function of two fission yeast genes, SPCC74.03c/ssp2+ and SPAC23H4.02/ppk9+, encoding an Snf1-like protein kinase were investigated. Deletion of ssp2+ caused a partial defect in glucose derepression of inv1+, fbp1+, and gld1+ and in assimilation of sucrose and glycerol, while a mutation in ppk9+ had no apparent effect. Scr1, a transcription factor involved in glucose repression, localized to the nucleus under glucose-rich conditions and to the cytoplasm during glucose starvation in wild-type cells. In contrast, in the ssp2Δ mutant, Scr1 localized to the nucleus in cells grown in glucose-rich medium as well as in glucose-starved cells. Immunoblot analysis showed that Ssp2 is required for the phosphorylation of Scr1 upon glucose deprivation. Mutation of five putative Ssp2 recognition sites in Scr1 prevented glucose derepression of invertase in glucose-starved cells. These results indicate that Ssp2 regulates phosphorylation and subcellular localization of Scr1 in response to glucose.
机译:两个裂变酵母基因SPCC74.03c / ssp2 + 和SPAC23H4.02 / ppk9 + 的功能,研究了编码Snf1样蛋白激酶的蛋白。删除 ssp2 + 会导致 inv1 + fbp1 + gld1 + 并吸收蔗糖和甘油,而 ppk9 中存在突变+ 没有明显作用。 Scr1是一种参与葡萄糖阻遏的转录因子,在富含葡萄糖的条件下定位于细胞核,而在野生型细胞的葡萄糖饥饿期间定位于细胞质。相反,在 ssp2 Δ突变体中,Scr1在富含葡萄糖的培养基以及缺乏葡萄糖的细胞中定位于细胞核。免疫印迹分析表明,葡萄糖剥夺后Scr1的磷酸化需要Ssp2。 Scr1中五个假定的Ssp2识别位点的突变可防止葡萄糖缺乏细胞中转化酶的葡萄糖抑制。这些结果表明,Ssp2响应葡萄糖调节Scr1的磷酸化和亚细胞定位。

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