Friedrich J Karsten, Panov Kostya I, Cabart Pavel, Russell Jackie, Zomerdijk Joost C B M
Division of Gene Regulation and Expression, School of Life Sciences, Wellcome Trust Biocentre, University of Dundee, Scotland, UK.
J Biol Chem. 2005 Aug 19;280(33):29551-8. doi: 10.1074/jbc.M501595200. Epub 2005 Jun 21.
Knowledge of the role of components of the RNA polymerase I transcription machinery is paramount to understanding regulation of rDNA expression. We describe key findings for the roles of essential transcription factor SL1 and activator upstream binding factor (UBF). We demonstrate that human SL1 can direct accurate Pol I transcription in the absence of UBF and can interact with the rDNA promoter independently and stably, consistent with studies of rodent SL1 but contrary to previous reports of human SL1. UBF itself does not bind stably to rDNA but rapidly associates and dissociates. We show that SL1 significantly reduces the rate of dissociation of UBF from the rDNA promoter. Our findings challenge the idea that UBF activates transcription through recruitment of SL1 at the rDNA promoter and suggest that the rate of pre-initiation complex (PIC) formation is primarily determined by the rate of association of SL1, rather than UBF, with the promoter. Therefore, we propose that SL1 directs PIC formation, functioning in core promoter binding, RNA polymerase I recruitment, and UBF stabilization and that SL1-promoter complex formation is a necessary prerequisite to the assembly of functional and stable PICs that include the UBF activator in mammalian cells.
了解RNA聚合酶I转录机制各组分的作用对于理解rDNA表达的调控至关重要。我们描述了关键转录因子SL1和激活因子上游结合因子(UBF)作用的主要发现。我们证明,在没有UBF的情况下,人类SL1可以指导准确的Pol I转录,并且可以独立且稳定地与rDNA启动子相互作用,这与啮齿动物SL1的研究结果一致,但与之前关于人类SL1的报道相反。UBF本身并不稳定地结合在rDNA上,而是快速结合和解离。我们表明,SL1显著降低了UBF从rDNA启动子上解离的速率。我们的研究结果挑战了UBF通过在rDNA启动子上招募SL1来激活转录的观点,并表明起始前复合物(PIC)的形成速率主要由SL1而非UBF与启动子的结合速率决定。因此,我们提出SL1指导PIC的形成,在核心启动子结合、RNA聚合酶I招募以及UBF稳定化中发挥作用,并且SL1-启动子复合物的形成是在哺乳动物细胞中组装包含UBF激活因子的功能性和稳定PIC的必要前提。