TFIIB-related factor 1 is a nucleolar protein that promotes RNA polymerase I-directed transcription and tumour cell growth

Author:

Wang Juan12,Chen Qiyue1,Wang Xin3,Zhao Shasha1,Deng Huan1,Guo Baoqiang4,Zhang Cheng1,Song Xiaoye1,Deng Wensheng1ORCID,Zhang Tongcun1,Ni Hongwei2

Affiliation:

1. School of Life Science and Health, Wuhan University of Science and Technology , Wuhan 430065 , China

2. School of Materials and Metallurgy, Wuhan University of Science and Technology , Wuhan 430081 , China

3. Faculty of Biology, Medicine, and Health, University of Manchester , Manchester M13 9PL , UK

4. School of Healthcare Science, Manchester Metropolitan University , Manchester M1 5GD , UK

Abstract

Abstract 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.

Funder

Natural Science Foundation of China

China Postdoctoral Science Foundation

Publisher

Oxford University Press (OUP)

Subject

Genetics (clinical),Genetics,Molecular Biology,General Medicine

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