Jóźwiak Paweł, Oracz Joanna, Dziedzic Angela, Szelenberger Rafał, Żyżelewicz Dorota, Bijak Michał, Krześlak Anna
Department of Cytobiochemistry, Faculty of Biology and Environmental Protection, University of Lodz, 90-236 Lodz, Poland.
Institute of Food Technology and Analysis, Faculty of Biotechnology and Food Sciences, Lodz University of Technology, 90-924 Lodz, Poland.
Cancers (Basel). 2024 Mar 5;16(5):1048. doi: 10.3390/cancers16051048.
O-linked β-N-acetylglucosamine (O-GlcNAc) is a reversible post-translational modification involved in the regulation of cytosolic, nuclear, and mitochondrial proteins. The interplay between O-GlcNAcylation and phosphorylation is critical to control signaling pathways and maintain cellular homeostasis. The addition of O-GlcNAc moieties to target proteins is catalyzed by O-linked N-acetylglucosamine transferase (OGT). Of the three splice variants of OGT described, one is destined for the mitochondria (mOGT). Although the effects of O-GlcNAcylation on the biology of normal and cancer cells are well documented, the role of mOGT remains poorly understood. In this manuscript, the effects of mOGT on mitochondrial protein phosphorylation, electron transport chain (ETC) complex activity, and the expression of VDAC porins were investigated. We performed studies using normal and breast cancer cells with upregulated mOGT or its catalytically inactive mutant. Proteomic approaches included the isolation of O-GlcNAc-modified proteins of the electron transport chain, followed by their analysis using mass spectrometry. We found that mitochondrial OGT regulates the activity of complexes I-V of the respiratory chain and identified a group of 19 ETC components as mOGT substrates in mammary cells. Furthermore, we observed that the upregulation of mOGT inhibited the interaction of VDAC1 with hexokinase II. Our results suggest that the deregulation of mOGT reprograms cellular energy metabolism via interaction with and O-GlcNAcylation of proteins involved in ATP production in mitochondria and its exchange between mitochondria and the cytosol.
O-连接的β-N-乙酰葡糖胺(O-GlcNAc)是一种可逆的翻译后修饰,参与胞质、核和线粒体蛋白的调控。O-GlcNAc糖基化和磷酸化之间的相互作用对于控制信号通路和维持细胞稳态至关重要。O-连接的N-乙酰葡糖胺转移酶(OGT)催化将O-GlcNAc部分添加到靶蛋白上。在已描述的OGT的三种剪接变体中,有一种定位于线粒体(mOGT)。尽管O-GlcNAc糖基化对正常细胞和癌细胞生物学特性的影响已有充分记录,但mOGT的作用仍知之甚少。在本手稿中,研究了mOGT对线粒体蛋白磷酸化、电子传递链(ETC)复合物活性以及电压依赖性阴离子通道(VDAC)孔蛋白表达的影响。我们使用mOGT上调或其催化失活突变体的正常细胞和乳腺癌细胞进行了研究。蛋白质组学方法包括分离电子传递链的O-GlcNAc修饰蛋白,然后使用质谱进行分析。我们发现线粒体OGT调节呼吸链复合物I-V的活性,并在乳腺细胞中鉴定出一组19种ETC成分作为mOGT底物。此外,我们观察到mOGT的上调抑制了VDAC1与己糖激酶II的相互作用。我们的结果表明,mOGT的失调通过与线粒体中参与ATP产生及其与细胞质之间交换的蛋白质相互作用和O-GlcNAc糖基化来重新编程细胞能量代谢。