Chang Chiung-Wen, Chou Han-Yi, Lin Yu-Sheng, Huang Kuo-Hsiang, Chang Ching-Jin, Hsu Tsui-Chun, Lee Sheng-Chung
Institute of Molecular Medicine, College of Medicine, National Taiwan University, Taipei, Taiwan.
BMC Mol Biol. 2008 Jul 1;9:61. doi: 10.1186/1471-2199-9-61.
As an epigenetic regulator, the transcriptional intermediary factor 1beta (TIF1beta)/KAP1/TRIM28) has been linked to gene expression and chromatin remodeling at specific loci by association with members of the heterochromatin protein 1 (HP1) family and various other chromatin factors. The interaction between TIF1beta and HP1 is crucial for heterochromatin formation and maintenance. The HP1-box, PXVXL, of TIF1beta is responsible for its interaction with HP1. However, the underlying mechanism of how the interaction is regulated remains poorly understood.
This work demonstrates that TIF1beta is phosphorylated on Ser473, the alteration of which is dynamically associated with cell cycle progression and functionally linked to transcriptional regulation. Phosphorylation of TIF1beta/Ser473 coincides with the induction of cell cycle gene cyclin A2 at the S-phase. Interestingly, chromatin immunoprecipitation demonstrated that the promoter of cyclin A2 gene is occupied by TIF1beta and that such occupancy is inversely correlated with Ser473 phosphorylation. Additionally, when HP1beta was co-expressed with TIF1beta/S473A, but not TIF1beta/S473E, the colocalization of TIF1beta/S473A and HP1beta to the promoters of Cdc2 and Cdc25A was enhanced. Non-phosphorylated TIF1beta/Ser473 allowed greater TIF1beta association with the regulatory regions and the consequent repression of these genes. Consistent with possible inhibition of TIF1beta's corepressor function, the phosphorylation of the Ser473 residue, which is located near the HP1-interacting PXVXL motif, compromised the formation of TIF1beta-HP1 complex. Finally, we found that the phosphorylation of TIF1beta/Ser473 is mediated by the PKCdelta pathway and is closely linked to cell proliferation.
The modulation of HP1beta-TIF1beta interaction through the phosphorylation/de-phosphorylation of TIF1beta/Ser473 may constitute a molecular switch that regulates the expression of particular genes. Higher levels of phosphorylated TIF1beta/Ser473 may be associated with the expression of key regulatory genes for cell cycle progression and the proliferation of cells.
作为一种表观遗传调节因子,转录中介因子1β(TIF1β/KAP1/TRIM28)通过与异染色质蛋白1(HP1)家族成员及其他各种染色质因子的结合,与特定基因座处的基因表达和染色质重塑相关联。TIF1β与HP1之间的相互作用对于异染色质的形成和维持至关重要。TIF1β的HP1结合框PXVXL负责其与HP1的相互作用。然而,这种相互作用如何被调控的潜在机制仍知之甚少。
本研究表明,TIF1β在Ser473位点发生磷酸化,其变化与细胞周期进程动态相关,并在功能上与转录调控相联系。TIF1β/Ser473的磷酸化与S期细胞周期基因细胞周期蛋白A2的诱导同时发生。有趣的是,染色质免疫沉淀显示细胞周期蛋白A2基因的启动子被TIF1β占据,且这种占据与Ser473磷酸化呈负相关。此外,当HP1β与TIF1β/S473A共表达时,而非与TIF1β/S473E共表达时,TIF1β/S473A与HP1β在Cdc2和Cdc25A启动子处的共定位增强。未磷酸化的TIF1β/Ser473使TIF1β与调控区域的结合更强,从而导致这些基因的抑制。与可能抑制TIF1β的共抑制因子功能一致,位于与HP1相互作用的PXVXL基序附近的Ser473残基的磷酸化损害了TIF1β-HP1复合物的形成。最后,我们发现TIF1β/Ser473的磷酸化由PKCδ途径介导,且与细胞增殖密切相关。
通过TIF1β/Ser473的磷酸化/去磷酸化对HP1β-TIF1β相互作用的调节可能构成一个调节特定基因表达的分子开关。较高水平的磷酸化TIF1β/Ser473可能与细胞周期进程和细胞增殖的关键调控基因的表达相关。