Liu Liangliang, Xie Ning, Rennie Paul, Challis John R G, Gleave Martin, Lye Stephen J, Dong Xuesen
Vancouver Prostate Center, Department of Urologic Sciences, University of British Columbia, Vancouver, British Columbia, Canada.
Mol Endocrinol. 2011 Jul;25(7):1197-210. doi: 10.1210/me.2010-0517. Epub 2011 May 12.
Originally identified as essential pre-mRNA splicing factors, non-POU-domain-containing, octamer binding protein (p54nrb) and PTB-associated RNA splicing factor (PSF) are also steroid receptor corepressors. The mechanisms by which p54nrb and PSF regulate gene transcription remain unclear. Both p54nrb and PSF contain protein phosphatase 1 (PP1) consensus binding RVxF motifs, suggesting that PP1 may regulate phosphorylation status of p54nrb and PSF and thus their function in gene transcription. In this report, we demonstrated that PP1 forms a protein complex with both p54nrb and PSF. PP1 interacts directly with the RVxF motif only in p54nrb, but not in PSF. Association with PP1 results in dephosphorylation of both p54nrb and PSF in vivo and the loss of their transcriptional corepressor activities. Using the CD44 minigene as a reporter, we showed that PP1 regulates p54nrb and PSF alternative splicing activities that determine exon skipping vs. inclusion in the final mature RNA for translation. In addition, changes in transcriptional corepression and RNA splicing activities of p54nrb and PSF are correlated with alterations in protein interactions of p54nrb and PSF with transcriptional corepressors such as Sin3A and histone deacetylase 1, and RNA splicing factors such as U1A and U2AF. Furthermore, we demonstrated a novel function of the RVxF motif within PSF that enhances its corepression and RNA splicing activities independent of PP1. We conclude that the RVxF motifs play an important role in controlling the multifunctional properties of p54nrb and PSF in the regulation of gene transcription.
非POU结构域含八聚体结合蛋白(p54nrb)和PTB相关RNA剪接因子(PSF)最初被鉴定为必需的前体mRNA剪接因子,它们也是类固醇受体共抑制因子。p54nrb和PSF调节基因转录的机制仍不清楚。p54nrb和PSF都含有蛋白磷酸酶1(PP1)的共有结合RVxF基序,这表明PP1可能调节p54nrb和PSF的磷酸化状态,从而影响它们在基因转录中的功能。在本报告中,我们证明PP1与p54nrb和PSF都形成了蛋白复合物。PP1仅直接与p54nrb中的RVxF基序相互作用,而不与PSF中的该基序相互作用。与PP1结合导致p54nrb和PSF在体内去磷酸化,并丧失其转录共抑制活性。以CD44小基因为报告基因,我们表明PP1调节p54nrb和PSF的可变剪接活性,这些活性决定了外显子在最终成熟RNA中是被跳过还是被包含用于翻译。此外,p54nrb和PSF的转录共抑制和RNA剪接活性的变化与p54nrb和PSF与转录共抑制因子(如Sin3A和组蛋白去乙酰化酶1)以及RNA剪接因子(如U1A和U2AF)的蛋白相互作用的改变相关。此外,我们证明了PSF内RVxF基序的一种新功能,即独立于PP1增强其共抑制和RNA剪接活性。我们得出结论,RVxF基序在控制p54nrb和PSF在基因转录调控中的多功能特性方面发挥着重要作用。