Yu Wenxi, Ye Cunqi, Greenberg Miriam L
From the Department of Biological Sciences, Wayne State University, Detroit, Michigan 48202.
From the Department of Biological Sciences, Wayne State University, Detroit, Michigan 48202
J Biol Chem. 2016 May 13;291(20):10437-44. doi: 10.1074/jbc.M116.714816. Epub 2016 Mar 7.
myo-Inositol, the precursor of all inositol compounds, has pivotal roles in cell metabolism and signaling pathways. Although physiological studies indicate a strong correlation between abnormal intracellular inositol levels and neurological disorders, very little is known about the regulation of inositol synthesis in mammalian cells. In this study, we report that IP6K1, an inositol hexakisphosphate kinase that catalyzes the synthesis of inositol pyrophosphate, regulates inositol synthesis in mammalian cells. Ip6k1 ablation led to profound changes in DNA methylation and expression of Isyna1 (designated mIno1), which encodes the rate-limiting enzyme inositol-3-phosphate synthase. Interestingly, IP6K1 preferentially bound to the phospholipid phosphatidic acid, and this binding was required for IP6K1 nuclear localization and the regulation of mIno1 transcription. This is the first demonstration of IP6K1 as a novel negative regulator of inositol synthesis in mammalian cells.
肌醇是所有肌醇化合物的前体,在细胞代谢和信号通路中起关键作用。尽管生理学研究表明细胞内肌醇水平异常与神经疾病之间存在密切关联,但对于哺乳动物细胞中肌醇合成的调控却知之甚少。在本研究中,我们报告称IP6K1(一种催化肌醇焦磷酸合成的肌醇六磷酸激酶)可调控哺乳动物细胞中的肌醇合成。Ip6k1基因敲除导致DNA甲基化以及编码限速酶肌醇-3-磷酸合酶的Isyna1(命名为mIno1)的表达发生深刻变化。有趣的是,IP6K1优先与磷脂酸结合,而这种结合是IP6K1核定位以及mIno1转录调控所必需的。这是首次证明IP6K1是哺乳动物细胞中肌醇合成的新型负调控因子。