Yu Zhengquan, Mannik Jaana, Soto Amelia, Lin Kevin K, Andersen Bogi
Department of Medicine, University of California, Irvine, CA 92697-4030, USA.
EMBO J. 2009 Jul 8;28(13):1890-903. doi: 10.1038/emboj.2009.142. Epub 2009 Jun 4.
Skin and bladder epithelia form effective permeability barriers through the activation of distinct differentiation gene programs. Using a genome-wide gene-expression study, we identified transcriptional regulators whose expression correlates highly with that of differentiation markers in both the bladder and skin, including the Grainyhead factor Get1/Grhl3, which is already known to be important for epidermal barrier formation. In the bladder, Get1 is most highly expressed in the differentiated umbrella cells and its mutation in mice leads to a defective bladder epithelial barrier formation due to the failure of apical membrane specialization. Genes encoding components of the specialized urothelial membrane, the uroplakins, were downregulated in Get1(-/-) mice. At least one of these genes, uroplakin II, is a direct target of Get1. The urothelial-specific activation of the uroplakin II gene is due to selective binding of Get1 to the uroplakin II promoter in urothelial cells, which is most likely regulated by histone modifications. These results show a crucial role for Get1 in urothelial differentiation and barrier formation.
皮肤和膀胱上皮通过激活不同的分化基因程序形成有效的渗透屏障。通过全基因组基因表达研究,我们鉴定出了转录调节因子,其表达与膀胱和皮肤中的分化标志物高度相关,其中包括颗粒头因子Get1/Grhl3,已知其对表皮屏障形成很重要。在膀胱中,Get1在分化的伞状细胞中表达最高,其在小鼠中的突变会导致膀胱上皮屏障形成缺陷,原因是顶端膜特化失败。编码特殊尿路上皮膜成分uroplakins的基因在Get1(-/-)小鼠中表达下调。这些基因中至少有一个,即uroplakin II,是Get1的直接靶点。uroplakin II基因的尿路上皮特异性激活是由于Get1在尿路上皮细胞中与uroplakin II启动子的选择性结合,这很可能受组蛋白修饰调控。这些结果表明Get1在尿路上皮分化和屏障形成中起关键作用。