Department of Biochemistry and Molecular Biology, The University of Iowa, Iowa City, IA 52242, USA.
Department of Cardiovascular and Metabolic Sciences, Lerner Research Institute, Cleveland Clinic, Cleveland, OH 44195, USA.
Nucleic Acids Res. 2022 Sep 9;50(16):9127-9148. doi: 10.1093/nar/gkac678.
The effects of rapid acute depletion of components of RNA polymerase II (Pol II) general transcription factors (GTFs) that are thought to be critical for formation of preinitiation complexes (PICs) and initiation in vitro were quantified in HAP1 cells using precision nuclear run-on sequencing (PRO-Seq). The average dependencies for each factor across >70 000 promoters varied widely even though levels of depletions were similar. Some of the effects could be attributed to the presence or absence of core promoter elements such as the upstream TBP-specificity motif or downstream G-rich sequences, but some dependencies anti-correlated with such sequences. While depletion of TBP had a large effect on most Pol III promoters only a small fraction of Pol II promoters were similarly affected. TFIIB depletion had the largest general effect on Pol II and also correlated with apparent termination defects downstream of genes. Our results demonstrate that promoter activity is combinatorially influenced by recruitment of TFIID and sequence-specific transcription factors. They also suggest that interaction of the preinitiation complex (PIC) with nucleosomes can affect activity and that recruitment of TFIID containing TBP only plays a positive role at a subset of promoters.
使用精确核运转测序(PRO-Seq)技术,在 HAP1 细胞中定量分析了 RNA 聚合酶 II(Pol II)通用转录因子(GTFs)的快速急性耗竭对体外起始复合物(PIC)形成和起始的影响。尽管耗竭水平相似,但每个因子在超过 70,000 个启动子上的平均依赖性差异很大。一些影响可以归因于核心启动子元件的存在或缺失,例如上游 TBP 特异性基序或下游富含 G 的序列,但有些依赖性与这些序列呈负相关。虽然 TBP 的耗竭对大多数 Pol III 启动子有很大影响,但只有一小部分 Pol II 启动子受到类似影响。TFIIB 的耗竭对 Pol II 有最大的普遍影响,并且与基因下游的明显终止缺陷相关。我们的结果表明,启动子活性受到 TFIID 和序列特异性转录因子募集的组合影响。它们还表明,起始前复合物(PIC)与核小体的相互作用可以影响活性,并且仅包含 TBP 的 TFIID 的募集仅在一部分启动子上发挥积极作用。