Kumar Raj, Calhoun William J
Division of Gastroenterology.
Biologics. 2008 Dec;2(4):845-54. doi: 10.2147/btt.s3820.
Post-translational modifications such as phosphorylation are known to play an important role in the gene regulation by the transcription factors including the nuclear hormone receptor superfamily of which the glucocorticoid receptor (GR) is a member. Protein phosphorylation often switches cellular activity from one state to another. Like many other transcription factors, the GR is a phosphoprotein, and phosphorylation plays an important role in the regulation of GR activity. Cell signaling pathways that regulate phosphorylation of the GR and its associated proteins are important determinants of GR function under various physiological conditions. While the role of many phosphorylation sites in the GR is still not fully understood, the role of others is clearer. Several aspects of transcription factor function, including DNA binding affinity, interaction of transactivation domains with the transcription initiation complex, and shuttling between the cytoplasmic compartments, have all been linked to site-specific phosphorylation. All major phosphorylation sites in the human GR are located in the N-terminal domain including the major transactivation domain, AF1. Available literature clearly indicates that many of these potential phosphorylation sites are substrates for multiple kinases, suggesting the potential for a very complex regulatory network. Phosphorylated GR interacts favorably with critical coregulatory proteins and subsequently enhances transcriptional activity. In addition, the activities and specificities of coregulators may be subject to similar regulation by phosphorylation. Regulation of the GR activity due to phosphorylation appears to be site-specific and dependent upon specific cell signaling cascade. Taken together, site-specific phosphorylation and related kinase pathways play an important role in the action of the GR, and more precise mechanistic information will lead to fuller understanding of the complex nature of gene regulation by the GR- and related transcription factors. This review provides currently available information regarding the role of GR phosphorylation in its action, and highlights the possible underlying mechanisms of action.
已知诸如磷酸化等翻译后修饰在包括核激素受体超家族(糖皮质激素受体(GR)是其成员之一)在内的转录因子进行的基因调控中发挥重要作用。蛋白质磷酸化常常将细胞活性从一种状态转变为另一种状态。与许多其他转录因子一样,GR是一种磷蛋白,磷酸化在GR活性的调控中起重要作用。调节GR及其相关蛋白磷酸化的细胞信号通路是各种生理条件下GR功能的重要决定因素。虽然GR中许多磷酸化位点的作用仍未完全了解,但其他一些位点的作用则较为明确。转录因子功能的几个方面,包括DNA结合亲和力、反式激活结构域与转录起始复合物的相互作用以及在细胞质区室之间穿梭,都与位点特异性磷酸化有关。人GR中的所有主要磷酸化位点都位于N端结构域,包括主要的反式激活结构域AF1。现有文献清楚地表明,这些潜在磷酸化位点中的许多都是多种激酶的底物,这表明可能存在一个非常复杂的调控网络。磷酸化的GR与关键的共调节蛋白有良好的相互作用,随后增强转录活性。此外,共调节因子的活性和特异性可能受到类似的磷酸化调节。由于磷酸化导致的GR活性调节似乎是位点特异性的,并且依赖于特定的细胞信号级联反应。综上所述,位点特异性磷酸化和相关激酶途径在GR的作用中起重要作用,更精确的机制信息将有助于更全面地理解GR及相关转录因子进行基因调控的复杂本质。本综述提供了目前关于GR磷酸化在其作用中的作用的可用信息,并强调了可能的潜在作用机制。