Rep M, Reiser V, Gartner U, Thevelein J M, Hohmann S, Ammerer G, Ruis H
Laboratorium voor Moleculaire Celbiologie, Katholieke Universiteit Leuven, B-3001 Heverlee, Flanders, Belgium.
Mol Cell Biol. 1999 Aug;19(8):5474-85. doi: 10.1128/MCB.19.8.5474.
After a sudden shift to high osmolarity, Saccharomyces cerevisiae cells respond by transiently inducing the expression of stress-protective genes. Msn2p and Msn4p have been described as two transcription factors that determine the extent of this response. In msn2 msn4 mutants, however, many promoters still show a distinct rise in transcriptional activity upon osmotic stress. Here we describe two structurally related nuclear factors, Msn1p and a newly identified protein, Hot1p (for high-osmolarity-induced transcription), which are also involved in osmotic stress-induced transcription. hot1 single mutants are specifically compromised in the transient induction of GPD1 and GPP2, which encode enzymes involved in glycerol biosynthesis, and exhibit delayed glycerol accumulation after stress exposure. Similar to a gpd1 mutation, a hot1 defect can rescue cells from inappropriately high HOG pathway activity. In contrast, Hot1p has little influence on the osmotic stress induction of CTT1, where Msn1p appears to play a more prominent role. Cells lacking Msn1p, Msn2p, Msn4p, and Hot1p are almost devoid of the short-term transcriptional response of the genes GPD1, GPP2, CTT1, and HSP12 to osmotic stress. Such cells also show a distinct reduction in the nuclear residence of the mitogen-activated protein kinase Hog1p upon osmotic stress. Thus, Hot1p and Msn1p may define an additional tier of transcriptional regulators that control responses to high-osmolarity stress.
在突然转变为高渗透压后,酿酒酵母细胞通过瞬时诱导应激保护基因的表达做出反应。Msn2p和Msn4p已被描述为决定这种反应程度的两种转录因子。然而,在msn2 msn4突变体中,许多启动子在渗透胁迫下仍显示出转录活性的明显升高。在这里,我们描述了两种结构相关的核因子,Msn1p和一种新鉴定的蛋白质Hot1p(高渗透压诱导转录),它们也参与渗透胁迫诱导的转录。hot1单突变体在瞬时诱导GPD1和GPP2(编码参与甘油生物合成的酶)方面存在特异性缺陷,并且在应激暴露后甘油积累延迟。与gpd1突变类似,hot1缺陷可以使细胞免受过高的HOG途径活性的影响。相反,Hot1p对CTT1的渗透胁迫诱导影响很小,而Msn1p在其中似乎发挥更突出的作用。缺乏Msn1p、Msn2p、Msn4p和Hot1p的细胞几乎没有GPD1、GPP2、CTT1和HSP12基因对渗透胁迫的短期转录反应。此类细胞在渗透胁迫下丝裂原活化蛋白激酶Hog1p的核内滞留也明显减少。因此,Hot1p和Msn1p可能定义了另一层转录调节因子,它们控制对高渗透压胁迫的反应。