Weeks Andrew T, Bird Amanda J
Department of Human Nutrition, Ohio State University, Columbus, Ohio, USA.
Department of Human Nutrition, Ohio State University, Columbus, Ohio, USA; Department of Molecular Genetics, Ohio State University, Columbus, Ohio, USA; Center for RNA Biology, Ohio State University, Columbus, Ohio, USA.
J Biol Chem. 2025 Feb;301(2):108156. doi: 10.1016/j.jbc.2025.108156. Epub 2025 Jan 4.
Zinc is an essential micronutrient that serves as a cofactor in a wide variety of enzymes, including Cu-Zn Superoxide Dismutase 1 (Sod1). We have discovered in Schizosaccharomyces pombe that Sod1 mRNA and protein levels are regulated in response to cellular zinc availability. We demonstrate that lower levels of sod1 mRNA and protein accumulate under low zinc conditions and that this regulation does not require the sod1 promoter or known factors that regulate the transcription of sod1 in response to zinc and other environmental stresses. Further analyses using yeast deletion strains and an inactive allele of Caf1 revealed that the reduced accumulation of sod1 mRNA and protein under low zinc conditions depends on the Caf1 and Ccr4 deadenylases of the CCR4-NOT complex. We also found that Caf1 and Ccr4 are both required for growth under zinc-limiting conditions. To gain additional mechanistic insight we used immunoblot analysis to map the regions required for the regulation of the Sod1 protein by zinc. We found that the sod1 ORF and 3'UTR are both necessary and sufficient for the zinc-dependent changes in Sod1 protein abundance. Our studies reveal a novel mechanism of altering mRNA and protein abundance in response to zinc status, which depends on the CCR4-NOT complex.
锌是一种必需的微量营养素,它在多种酶中作为辅助因子发挥作用,包括铜锌超氧化物歧化酶1(Sod1)。我们在粟酒裂殖酵母中发现,Sod1 mRNA和蛋白质水平会根据细胞内锌的可利用性进行调节。我们证明,在低锌条件下,sod1 mRNA和蛋白质的水平会降低,并且这种调节不需要sod1启动子或已知的在锌和其他环境应激反应中调节sod1转录的因子。使用酵母缺失菌株和Caf1的无活性等位基因进行的进一步分析表明,低锌条件下sod1 mRNA和蛋白质积累的减少取决于CCR4-NOT复合物的Caf1和Ccr4去腺苷酸化酶。我们还发现,在锌限制条件下生长,Caf1和Ccr4都是必需的。为了获得更多的机制性见解,我们使用免疫印迹分析来确定锌调节Sod1蛋白所需的区域。我们发现,sod1开放阅读框(ORF)和3'非翻译区(UTR)对于Sod1蛋白丰度的锌依赖性变化都是必要且充分的。我们的研究揭示了一种响应锌状态改变mRNA和蛋白质丰度的新机制,该机制依赖于CCR4-NOT复合物。