Sanvisens Nerea, Romero Antonia M, Zhang Caiguo, Wu Xiaorong, An Xiuxiang, Huang Mingxia, Puig Sergi
From the Departamento de Biotecnología, Instituto de Agroquímica y Tecnología de Alimentos (IATA), Consejo Superior de Investigaciones Científicas (CSIC), Paterna, Valencia 46980, Spain and.
the Department of Biochemistry and Molecular Genetics, University of Colorado School of Medicine, Aurora, Colorado 80045.
J Biol Chem. 2016 Apr 29;291(18):9807-17. doi: 10.1074/jbc.M116.720862. Epub 2016 Mar 12.
Ribonucleotide reductase (RNR) is an essential iron-dependent enzyme that catalyzes deoxyribonucleotide synthesis in eukaryotes. Living organisms have developed multiple strategies to tightly modulate RNR function to avoid inadequate or unbalanced deoxyribonucleotide pools that cause DNA damage and genome instability. Yeast cells activate RNR in response to genotoxic stress and iron deficiency by facilitating redistribution of its small heterodimeric subunit Rnr2-Rnr4 from the nucleus to the cytoplasm, where it forms an active holoenzyme with large Rnr1 subunit. Dif1 protein inhibits RNR by promoting nuclear import of Rnr2-Rnr4. Upon DNA damage, Dif1 phosphorylation by the Dun1 checkpoint kinase and its subsequent degradation enhances RNR function. In this report, we demonstrate that Dun1 kinase triggers Rnr2-Rnr4 redistribution to the cytoplasm in response to iron deficiency. We show that Rnr2-Rnr4 relocalization by low iron requires Dun1 kinase activity and phosphorylation site Thr-380 in the Dun1 activation loop, but not the Dun1 forkhead-associated domain. By using different Dif1 mutant proteins, we uncover that Dun1 phosphorylates Dif1 Ser-104 and Thr-105 residues upon iron scarcity. We observe that the Dif1 phosphorylation pattern differs depending on the stimuli, which suggests different Dun1 activating pathways. Importantly, the Dif1-S104A/T105A mutant exhibits defects in nucleus-to-cytoplasm redistribution of Rnr2-Rnr4 by iron limitation. Taken together, these results reveal that, in response to iron starvation, Dun1 kinase phosphorylates Dif1 to stimulate Rnr2-Rnr4 relocalization to the cytoplasm and promote RNR function.
核糖核苷酸还原酶(RNR)是一种必需的铁依赖性酶,可催化真核生物中的脱氧核糖核苷酸合成。生物体已经开发出多种策略来严格调节RNR功能,以避免脱氧核糖核苷酸库不足或失衡,从而导致DNA损伤和基因组不稳定。酵母细胞通过促进其小异二聚体亚基Rnr2-Rnr4从细胞核重新分布到细胞质来响应基因毒性应激和铁缺乏,在细胞质中它与大的Rnr1亚基形成活性全酶。Dif1蛋白通过促进Rnr2-Rnr4的核输入来抑制RNR。在DNA损伤时,Dun1检查点激酶对Dif1的磷酸化及其随后的降解增强了RNR功能。在本报告中,我们证明Dun1激酶在响应铁缺乏时触发Rnr2-Rnr4重新分布到细胞质。我们表明,低铁条件下Rnr2-Rnr4的重新定位需要Dun1激酶活性和Dun1激活环中的磷酸化位点Thr-380,但不需要Dun1叉头相关结构域。通过使用不同的Dif1突变蛋白,我们发现铁缺乏时Dunl磷酸化Dif1的Ser-104和Thr-105残基。我们观察到Dif1的磷酸化模式因刺激而异,这表明存在不同的Dun1激活途径。重要的是,Dif1-S104A/T105A突变体在铁限制下Rnr2-Rnr4从细胞核到细胞质的重新分布中表现出缺陷。综上所述,这些结果表明,在铁饥饿时,Dun1激酶磷酸化Dif1以刺激Rnr2-Rnr4重新定位到细胞质并促进RNR功能。