Duke Institute for Genome Sciences and Policy, Duke University Medical Center, Durham, North Carolina, USA.
PLoS One. 2012;7(10):e47967. doi: 10.1371/journal.pone.0047967. Epub 2012 Oct 17.
The E2F6 protein functions as an Rb-independent repressor of gene transcription. We have previously provided evidence suggesting a role for E2F6 in repression of E2F-responsive genes at S phase. Here, we have identified BRG1, the ATPase subunit of the SWI/SNF chromatin-remodeling complex, as an E2F6 interacting protein. Immunoprecipitation experiments demonstrate that BRG1 binds specifically to E2F6 and E2F4 but not the activator E2Fs. E2F6 was also able to interact with BAF155, a BRG1-associated factor, in the SWI/SNF complex. Chromatin immunoprecipitation assays demonstrate the binding of BRG1 coincident with E2F6 on G1/S gene promoters during S phase. Collectively, our studies suggest that E2F6 may recruit BRG1 in transcriptional regulation of genes important for G1/S phase transition of the cell cycle.
E2F6 蛋白作为一种 RB 非依赖性基因转录抑制剂发挥作用。我们之前的研究结果表明,E2F6 在 S 期抑制 E2F 反应基因中起作用。在这里,我们鉴定出 BRG1(SWI/SNF 染色质重塑复合物的 ATP 酶亚基)是 E2F6 的相互作用蛋白。免疫沉淀实验表明,BRG1 特异性结合 E2F6 和 E2F4,但不与激活型 E2Fs 结合。E2F6 还能够与 SWI/SNF 复合物中的 BAF155(BRG1 相关因子)相互作用。染色质免疫沉淀实验表明,BRG1 在 S 期与 E2F6 共同结合于 G1/S 期基因启动子上。总的来说,我们的研究表明,E2F6 可能在细胞周期 G1/S 期转换过程中对重要基因的转录调控中募集 BRG1。