Yadav Kamlesh Kumar, Rajasekharan Ram
Lipidomic Centre, Department of Lipid Science, CSIR-Central Food Technological Research Institute, Mysore, Karnataka, 570020, India.
Academy of Scientific and Innovative Research, CSIR-CFTRI, Mysore, India.
Curr Genet. 2016 Nov;62(4):841-851. doi: 10.1007/s00294-016-0590-6. Epub 2016 Mar 15.
PHM8 is a very important enzyme in nonpolar lipid metabolism because of its role in triacylglycerol (TAG) biosynthesis under phosphate stress conditions. It is positively regulated by the PHO4 transcription factor under low phosphate conditions; however, its regulation has not been explored under normal physiological conditions. General control nonderepressible (GCN4), a basic leucine-zipper transcription factor activates the transcription of amino acids, purine biosynthesis genes and many stress response genes under various stress conditions. In this study, we demonstrate that the level of TAG is regulated by the transcription factor GCN4. GCN4 directly binds to its consensus recognition sequence (TGACTC) in the PHM8 promoter and controls its expression. The analysis of cells expressing the P -lacZ reporter gene showed that mutations (TGACTC-GGGCCC) in the GCN4-binding sequence caused a significant increase in β-galactosidase activity. Mutation in the GCN4 binding sequence causes an increase in PHM8 expression, lysophosphatidic acid phosphatase activity and TAG level. PHM8, in conjunction with DGA1, a mono- and diacylglycerol transferase, controls the level of TAG. These results revealed that GCN4 negatively regulates PHM8 and that deletion of GCN4 causes de-repression of PHM8, which is responsible for the increased TAG content in gcn4∆ cells.
PHM8是一种在非极性脂质代谢中非常重要的酶,因为它在磷酸盐胁迫条件下的三酰甘油(TAG)生物合成中发挥作用。在低磷酸盐条件下,它受PHO4转录因子的正向调控;然而,在正常生理条件下其调控机制尚未被探究。一般控制非抑制性(GCN4),一种碱性亮氨酸拉链转录因子,在各种胁迫条件下激活氨基酸、嘌呤生物合成基因以及许多应激反应基因的转录。在本研究中,我们证明TAG水平受转录因子GCN4的调控。GCN4直接结合到PHM8启动子中的共有识别序列(TGACTC)并控制其表达。对表达P -lacZ报告基因的细胞分析表明,GCN4结合序列中的突变(TGACTC-GGGCCC)导致β-半乳糖苷酶活性显著增加。GCN4结合序列中的突变导致PHM8表达增加、溶血磷脂酸磷酸酶活性增加以及TAG水平升高。PHM8与单酰甘油和二酰甘油转移酶DGA1共同控制TAG水平。这些结果表明GCN4对PHM8起负调控作用,并且GCN4的缺失导致PHM8去抑制,这是gcn4∆细胞中TAG含量增加的原因。