Jani Niketa M, Lopes John M
Department of Biological Sciences, Wayne State University, Detroit, MI 48202, USA.
Mol Microbiol. 2008 Dec;70(6):1529-39. doi: 10.1111/j.1365-2958.2008.06506.x. Epub 2008 Oct 23.
In Saccharomyces cerevisiae, transcription of most of the phospholipid biosynthetic genes (e.g. INO1, CHO1, CHO2 and OPI3) is repressed by growth in the presence of inositol and choline and derepressed in their absence. This regulation requires the Ino2p and Ino4p activators and the Opi1p repressor. The PIS1 structural gene is required for the synthesis of the essential lipid phosphatidylinositol. Previous reports show that PIS1 expression is uncoupled from inositol/choline regulation, but is regulated by carbon source, hypoxia and zinc. However, in this study we found that the expression of PIS1 is induced twofold by inositol. This regulation did not require Ino2p and Ino4p, although Ino4p was required for full expression. Ino4p is a basic helix-loop-helix protein that requires a binding partner. Curiously, none of the other basic helix-loop-helix proteins affected PIS1 expression. Inositol induction did require another general regulator of phospholipid biosynthesis, Ume6p. Ume6p was found to be a positive regulator of PIS1 gene expression. Ume6p, and several associated factors, were required for inositol-mediated induction and chromatin immunoprecipitation analysis showed that Ume6p directly regulates PIS1 expression. Thus, we demonstrate novel regulation of the PIS1 gene by Ume6p.
在酿酒酵母中,大多数磷脂生物合成基因(如INO1、CHO1、CHO2和OPI3)的转录在肌醇和胆碱存在的情况下生长时受到抑制,而在其不存在时则去抑制。这种调节需要Ino2p和Ino4p激活剂以及Opi1p阻遏物。PIS1结构基因是合成必需脂质磷脂酰肌醇所必需的。先前的报道表明,PIS1的表达与肌醇/胆碱调节无关,但受碳源、缺氧和锌的调节。然而,在本研究中我们发现,肌醇可使PIS1的表达诱导两倍。这种调节不需要Ino2p和Ino4p,尽管Ino4p是完全表达所必需的。Ino4p是一种基本的螺旋-环-螺旋蛋白,需要一个结合伴侣。奇怪的是,其他基本的螺旋-环-螺旋蛋白均不影响PIS1的表达。肌醇诱导确实需要磷脂生物合成的另一种通用调节因子Ume6p。发现Ume6p是PIS1基因表达的正调节因子。Ume6p以及几个相关因子是肌醇介导的诱导所必需的,染色质免疫沉淀分析表明Ume6p直接调节PIS1的表达。因此,我们证明了Ume6p对PIS1基因的新型调节。