Wang Juan, Chen Qiyue, Wang Xin, Zhao Shasha, Deng Huan, Guo Baoqiang, Zhang Cheng, Song Xiaoye, Deng Wensheng, Zhang Tongcun, Ni Hongwei
School of Life Science and Health, Wuhan University of Science and Technology, Wuhan 430065, China.
School of Materials and Metallurgy, Wuhan University of Science and Technology, Wuhan 430081, China.
Hum Mol Genet. 2023 Jan 1;32(1):104-121. doi: 10.1093/hmg/ddac152.
Eukaryotic RNA polymerase I (Pol I) products play fundamental roles in ribosomal assembly, protein synthesis, metabolism and cell growth. Abnormal expression of both Pol I transcription-related factors and Pol I products causes a range of diseases, including ribosomopathies and cancers. However, the factors and mechanisms governing Pol I-dependent transcription remain to be elucidated. Here, we report that transcription factor IIB-related factor 1 (BRF1), a subunit of transcription factor IIIB required for RNA polymerase III (Pol III)-mediated transcription, is a nucleolar protein and modulates Pol I-mediated transcription. We showed that BRF1 can be localized to the nucleolus in several human cell types. BRF1 expression correlates positively with Pol I product levels and tumour cell growth in vitro and in vivo. Pol III transcription inhibition assays confirmed that BRF1 modulates Pol I-directed transcription in an independent manner rather than through a Pol III product-to-45S pre-rRNA feedback mode. Mechanistically, BRF1 binds to the Pol I transcription machinery components and can be recruited to the rDNA promoter along with them. Additionally, alteration of BRF1 expression affects the recruitment of Pol I transcription machinery components to the rDNA promoter and the expression of TBP and TAF1A. These findings indicate that BRF1 modulates Pol I-directed transcription by controlling the expression of selective factor 1 subunits. In summary, we identified a novel role of BRF1 in Pol I-directed transcription, suggesting that BRF1 can independently regulate both Pol I- and Pol III-mediated transcription and act as a key coordinator of Pol I and Pol III.
真核生物RNA聚合酶I(Pol I)产物在核糖体组装、蛋白质合成、代谢和细胞生长中发挥着重要作用。Pol I转录相关因子和Pol I产物的异常表达会引发一系列疾病,包括核糖体病和癌症。然而,调控Pol I依赖性转录的因子和机制仍有待阐明。在此,我们报告转录因子IIB相关因子1(BRF1),它是RNA聚合酶III(Pol III)介导转录所需的转录因子IIIB的一个亚基,是一种核仁蛋白,并调节Pol I介导的转录。我们发现BRF1可在多种人类细胞类型中定位于核仁。BRF1的表达与Pol I产物水平以及体外和体内肿瘤细胞的生长呈正相关。Pol III转录抑制试验证实,BRF1以独立方式调节Pol I指导的转录,而非通过Pol III产物到45S前体rRNA的反馈模式。从机制上讲,BRF1与Pol I转录机制组分结合,并可与它们一起被招募到rDNA启动子。此外,BRF1表达的改变会影响Pol I转录机制组分向rDNA启动子的募集以及TBP和TAF1A的表达。这些发现表明,BRF1通过控制选择性因子1亚基的表达来调节Pol I指导的转录。总之,我们确定了BRF1在Pol I指导转录中的新作用,表明BRF1可独立调节Pol I和Pol III介导的转录,并作为Pol I和Pol III的关键协调因子。