Department of Biology, Johns Hopkins University, Baltimore, MD 21218, USA.
Janelia Research Campus, Howard Hughes Medical Institute, Ashburn, VA 20147, USA; Experimental Immunology Branch, National Cancer Institute, Bethesda, MD 20892, USA.
Mol Cell. 2021 Sep 2;81(17):3560-3575.e6. doi: 10.1016/j.molcel.2021.07.022. Epub 2021 Aug 9.
Transcription initiation by RNA polymerase II (RNA Pol II) requires preinitiation complex (PIC) assembly at gene promoters. In the dynamic nucleus, where thousands of promoters are broadly distributed in chromatin, it is unclear how multiple individual components converge on any target to establish the PIC. Here we use live-cell, single-molecule tracking in S. cerevisiae to visualize constrained exploration of the nucleoplasm by PIC components and Mediator's key role in guiding this process. On chromatin, TFIID/TATA-binding protein (TBP), Mediator, and RNA Pol II instruct assembly of a short-lived PIC, which occurs infrequently but efficiently within a few seconds on average. Moreover, PIC exclusion by nucleosome encroachment underscores regulated promoter accessibility by chromatin remodeling. Thus, coordinated nuclear exploration and recruitment to accessible targets underlies dynamic PIC establishment in yeast. Our study provides a global spatiotemporal model for transcription initiation in live cells.
RNA 聚合酶 II(RNA Pol II)的转录起始需要在基因启动子处组装起始前复合物(PIC)。在动态核中,成千上万的启动子广泛分布在染色质中,目前尚不清楚如何将多个单个组件集中在任何目标上以建立 PIC。在这里,我们使用酿酒酵母中的活细胞、单分子跟踪来可视化 PIC 组件在核质中的受限探索以及 Mediator 在指导该过程中的关键作用。在染色质上,TFIID/TATA 结合蛋白(TBP)、Mediator 和 RNA Pol II 指导短寿命 PIC 的组装,该 PIC 偶尔发生,但平均在几秒钟内高效发生。此外,核小体侵入导致 PIC 排除突出了染色质重塑对启动子可及性的调控。因此,核的协调探索和对可及目标的募集是酵母中动态 PIC 建立的基础。我们的研究为活细胞中转录起始提供了一个全局的时空模型。