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细胞周期S期期间,CTP:磷酸胆碱胞苷转移酶α表达的激活由转录因子Sp1介导。

Activation of CTP:phosphocholine cytidylyltransferase alpha expression during the S phase of the cell cycle is mediated by the transcription factor Sp1.

作者信息

Banchio Claudia, Schang Luis M, Vance Dennis E

机构信息

Department of Biochemistry and Canadian Institutes of Health Research Group on Molecular and Cell Biology of Lipids, University of Alberta, Edmonton, Alberta, T6G 2S2, Canada.

出版信息

J Biol Chem. 2003 Aug 22;278(34):32457-64. doi: 10.1074/jbc.M304810200. Epub 2003 Jun 6.

Abstract

An essential step during cell division is induction of phosphatidylcholine biosynthesis. In this pathway, CTP:phosphocholine cytidylyltransferase alpha (CT alpha) plays an important regulatory role. Previous studies (Golfman, L. S., Bakovic, M., and Vance, D. E. (2001) J. Biol. Chem. 276, 43688-43692) demonstrated that CT alpha mRNA accumulates during S phase in preparation for cellular mitosis. We now demonstrate that increased binding of the transcription factor Sp1 to the proximal promoter of CT alpha is responsible for increased transcription during the S phase. The Sp1 binding element present in position -67/-62 is essential for activation, and the Sp1 site in position -31/-9 is required to enhance transcription. Inhibition of Sp1 expression by RNA interference abolished the enhanced expression of CT alpha. Immunoprecipitation studies demonstrated that Sp1 interacts with cyclin E, cyclin A, and cyclin-dependent kinase 2 during the S phase. We conclude that Sp1 binding to the CT alpha proximal promoter is necessary to enhance transcription during the S phase. This is the first elucidation of a mechanism by which expression of a key enzyme in phospholipid biosynthesis is regulated during the cell cycle.

摘要

细胞分裂过程中的一个关键步骤是诱导磷脂酰胆碱的生物合成。在这条途径中,CTP:磷酸胆碱胞苷转移酶α(CTα)发挥着重要的调节作用。先前的研究(Golfman, L. S., Bakovic, M., and Vance, D. E. (2001) J. Biol. Chem. 276, 43688 - 43692)表明,CTα mRNA在S期积累,为细胞有丝分裂做准备。我们现在证明,转录因子Sp1与CTα近端启动子结合增加是S期转录增加的原因。位于-67/-62位置的Sp1结合元件对激活至关重要,而位于-31/-9位置的Sp1位点对增强转录是必需的。通过RNA干扰抑制Sp1表达消除了CTα增强的表达。免疫沉淀研究表明,在S期Sp1与细胞周期蛋白E、细胞周期蛋白A和细胞周期蛋白依赖性激酶2相互作用。我们得出结论,Sp1与CTα近端启动子结合是S期增强转录所必需的。这是首次阐明在细胞周期中调节磷脂生物合成关键酶表达的机制。

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