Dittmer Jürgen
Universität Halle-Wittenberg Universitätsklinik und Poliklinik für Gynäkologie Magdeburger Str, 24 06097 Halle, Saale, Germany.
Mol Cancer. 2003 Aug 20;2:29. doi: 10.1186/1476-4598-2-29.
The Ets1 proto-oncoprotein is a member of the Ets family of transcription factors that share a unique DNA binding domain, the Ets domain. The DNA binding activity of Ets1 is controlled by kinases and transcription factors. Some transcription factors, such as AML-1, regulate Ets1 by targeting its autoinhibitory module. Others, such as Pax-5, alter Ets1 DNA binding properties. Ets1 harbors two phosphorylation sites, threonine-38 and an array of serines within the exon VII domain. Phosphorylation of threonine-38 by ERK1/2 activates Ets1, whereas phosphorylation of the exon VII domain by CaMKII or MLCK inhibits Ets1 DNA binding activity. Ets1 is expressed by numerous cell types. In haemotopoietic cells, it contributes to the regulation of cellular differentiation. In a variety of other cells, including endothelial cells, vascular smooth muscle cells and epithelial cancer cells, Ets1 promotes invasive behavior. Regulation of MMP1, MMP3, MMP9 and uPA as well as of VEGF and VEGF receptor gene expression has been ascribed to Ets1. In tumors, Ets1 expression is indicative of poorer prognosis.
Ets1原癌蛋白是Ets转录因子家族的成员之一,该家族共享一个独特的DNA结合结构域,即Ets结构域。Ets1的DNA结合活性受激酶和转录因子的调控。一些转录因子,如AML-1,通过靶向其自身抑制模块来调节Ets1。其他转录因子,如Pax-5,则改变Ets1的DNA结合特性。Ets1有两个磷酸化位点,即苏氨酸-38和外显子VII结构域内的一系列丝氨酸。ERK1/2对苏氨酸-38的磷酸化激活Ets1,而CaMKII或MLCK对外显子VII结构域的磷酸化则抑制Ets1的DNA结合活性。Ets1在多种细胞类型中表达。在造血细胞中,它有助于调节细胞分化。在包括内皮细胞、血管平滑肌细胞和上皮癌细胞在内的多种其他细胞中,Ets1促进侵袭行为。MMP1、MMP3、MMP9和uPA以及VEGF和VEGF受体基因表达的调控都归因于Ets1。在肿瘤中,Ets1的表达表明预后较差。