Grinstein Edgar, Jundt Franziska, Weinert Inge, Wernet Peter, Royer Hans-Dieter
Institut für Transplantationsdiagnostik und Zelltherapeutika, Heinrich Heine Universität Düsseldorf, Moorenstrasse 5, 40225 Düsseldorf, Germany.
Oncogene. 2002 Feb 28;21(10):1485-92. doi: 10.1038/sj.onc.1205211.
Sp1 binding sites have been identified in enhancer/promoter regions of several growth and cell cycle regulated genes, and it has been shown that Sp1 is increasingly phosphorylated in G1 phase of the cell cycle. Interactions of Sp1 with proteins involved in control of cell cycle and tumor formation have been reported. Here we show that expression of Sp1 protein predominates in the G1 phase of the cell cycle in epithelial cells. This is achieved by proteasome-dependent degradation. Inhibition of endogeneous Sp1 activity by a dominant-negative Sp1 mutant was associated with a cell cycle arrest in G1 phase, a strongly reduced expression of cyclin D1, the EGF-receptor and increased levels of p27Kip1. We have thus identified Sp1 as an important regulator of the cell cycle in G1 phase.
在几个生长和细胞周期调控基因的增强子/启动子区域已鉴定出Sp1结合位点,并且已表明Sp1在细胞周期的G1期磷酸化程度越来越高。已有报道Sp1与参与细胞周期控制和肿瘤形成的蛋白质之间存在相互作用。在此我们表明,Sp1蛋白的表达在上皮细胞周期的G1期占主导地位。这是通过蛋白酶体依赖性降解实现的。显性负性Sp1突变体对内源性Sp1活性的抑制与G1期细胞周期停滞、细胞周期蛋白D1、表皮生长因子受体的表达大幅降低以及p27Kip1水平升高有关。因此,我们已确定Sp1是G1期细胞周期的重要调节因子。