Department of Nutritional Sciences, University of Wisconsin-Madison, Madison, Wisconsin 53706, USA.
J Biol Chem. 2011 Feb 25;286(8):6844-54. doi: 10.1074/jbc.M110.203927. Epub 2010 Dec 22.
Previous studies suggested that the zinc-responsive Zap1 transcriptional activator directly regulates the expression of over 80 genes in Saccharomyces cerevisiae. Many of these genes play key roles to enhance the ability of yeast cells to grow under zinc-limiting conditions. Zap1 is unusual among transcriptional activators in that it contains two activation domains, designated AD1 and AD2, which are regulated independently by zinc. These two domains are evolutionarily conserved among Zap1 orthologs suggesting that they are both important for Zap1 function. In this study, we have examined the roles of AD1 and AD2 in low zinc growth and the regulation of Zap1 target gene expression. Using alleles that are specifically disrupted for either AD1 or AD2 function, we found that these domains are not redundant, and both are important for normal growth in low zinc. AD1 plays the primary role in zinc-responsive gene regulation, whereas AD2 is required for maximal expression of only a few target promoters. AD1 alone is capable of driving full expression of most Zap1 target genes and dictates the kinetics of Zap1 gene induction in response to zinc withdrawal. Surprisingly, we found that AD1 is less active in zinc-limited cells under heat stress and AD2 plays a more important role under those conditions. These results suggest that AD2 may contribute more to Zap1 function when zinc deficiency is combined with other environmental stresses. In the course of these studies, we also found that the heat shock response is induced under conditions of severe zinc deficiency.
先前的研究表明,锌响应型 Zap1 转录激活因子直接调控酿酒酵母中超过 80 个基因的表达。这些基因中的许多在增强酵母细胞在缺锌条件下生长的能力方面发挥着关键作用。Zap1 在转录激活因子中是不寻常的,因为它包含两个激活结构域,分别称为 AD1 和 AD2,它们分别由锌调节。这两个结构域在 Zap1 同源物中是进化保守的,这表明它们对 Zap1 功能都很重要。在这项研究中,我们研究了 AD1 和 AD2 在低锌生长和 Zap1 靶基因表达调控中的作用。使用专门破坏 AD1 或 AD2 功能的等位基因,我们发现这些结构域不是冗余的,并且对于在低锌下的正常生长都是重要的。AD1 在锌响应基因调控中起着主要作用,而 AD2 仅对于少数靶启动子的最大表达是必需的。AD1 本身能够驱动大多数 Zap1 靶基因的充分表达,并决定了 Zap1 基因对锌去除的诱导动力学。令人惊讶的是,我们发现 AD1 在热应激下的缺锌细胞中活性较低,而 AD2 在这些条件下发挥更重要的作用。这些结果表明,当锌缺乏与其他环境压力结合时,AD2 可能对 Zap1 功能的贡献更大。在这些研究过程中,我们还发现,在严重缺锌的条件下会诱导热休克反应。