Zimmermann Tim, Kashyap Anubha, Hartmann Urs, Otto Gerd, Galle Peter R, Strand Susanne, Strand Dennis
1st Department of Internal Medicine, Johannes Gutenberg University, Langenbeck Str. 1, 55101 Mainz, Germany.
Biochem Biophys Res Commun. 2008 Feb 22;366(4):1067-73. doi: 10.1016/j.bbrc.2007.12.084. Epub 2007 Dec 26.
The human lgl gene, Hugl-2 (llgl2, Lgl2), codes for a cytoskeletal protein involved in regulating cell polarity. Here, we report the identification and functional characterization of the promoter region ( approximately 1.2kb) of the Hugl-2 gene. Luciferase expression assays show a high basal Hugl-2 promoter activity in different cell lines and primary human hepatocytes. Truncations of the promoter identified a GC-rich region important for this activity. Alignment of human and mouse genomic sequences demonstrate that this is an evolutionary conserved region fcontaining putative binding sites for several transcription factors including Elk-1 and Sp-1. Mithramycin A reduces Hugl-2 expression indicating Sp-1 transcription factors activate Hugl-2. Treatment of primary hepatocytes with epidermal growth factor (EGF) suppresses Hugl-2, suggesting regulation by the EGF-signaling pathway. Downregulation of Hugl-2 by EGF may contribute to loss of cell polarity and tumour progression, therefore supporting a tumour suppressor role for Hugl-2.
人类lgl基因Hugl - 2(llgl2,Lgl2)编码一种参与调节细胞极性的细胞骨架蛋白。在此,我们报告了Hugl - 2基因启动子区域(约1.2kb)的鉴定及功能特征。荧光素酶表达分析显示,Hugl - 2启动子在不同细胞系和原代人肝细胞中具有较高的基础活性。启动子截短实验确定了一个对该活性重要的富含GC的区域。人和小鼠基因组序列比对表明,这是一个进化保守区域,包含几个转录因子(包括Elk - 1和Sp - 1)的假定结合位点。光神霉素A降低了Hugl - 2的表达,表明Sp - 1转录因子激活了Hugl - 2。用表皮生长因子(EGF)处理原代肝细胞会抑制Hugl - 2,提示其受EGF信号通路调控。EGF对Hugl - 2的下调可能导致细胞极性丧失和肿瘤进展,因此支持Hugl - 2具有肿瘤抑制作用。