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RNA聚合酶III TFIIB相关因子Brf2介导的氧化还原信号传导

Redox Signaling by the RNA Polymerase III TFIIB-Related Factor Brf2.

作者信息

Gouge Jerome, Satia Karishma, Guthertz Nicolas, Widya Marcella, Thompson Andrew James, Cousin Pascal, Dergai Oleksandr, Hernandez Nouria, Vannini Alessandro

机构信息

Division of Structural Biology, The Institute of Cancer Research, London SW7 3RP, UK.

Center for Integrative Genomics, Faculty of Biology and Medicine, University of Lausanne, 1015 Lausanne, Switzerland.

出版信息

Cell. 2015 Dec 3;163(6):1375-87. doi: 10.1016/j.cell.2015.11.005.

Abstract

TFIIB-related factor 2 (Brf2) is a member of the family of TFIIB-like core transcription factors. Brf2 recruits RNA polymerase (Pol) III to type III gene-external promoters, including the U6 spliceosomal RNA and selenocysteine tRNA genes. Found only in vertebrates, Brf2 has been linked to tumorigenesis but the underlying mechanisms remain elusive. We have solved crystal structures of a human Brf2-TBP complex bound to natural promoters, obtaining a detailed view of the molecular interactions occurring at Brf2-dependent Pol III promoters and highlighting the general structural and functional conservation of human Pol II and Pol III pre-initiation complexes. Surprisingly, our structural and functional studies unravel a Brf2 redox-sensing module capable of specifically regulating Pol III transcriptional output in living cells. Furthermore, we establish Brf2 as a central redox-sensing transcription factor involved in the oxidative stress pathway and provide a mechanistic model for Brf2 genetic activation in lung and breast cancer.

摘要

TFIIB相关因子2(Brf2)是TFIIB样核心转录因子家族的成员。Brf2将RNA聚合酶(Pol)III招募到III型基因外部启动子,包括U6剪接体RNA和硒代半胱氨酸tRNA基因。Brf2仅在脊椎动物中发现,它与肿瘤发生有关,但其潜在机制仍不清楚。我们解析了与天然启动子结合的人Brf2-TBP复合物的晶体结构,详细了解了在依赖Brf2的Pol III启动子处发生的分子相互作用,并突出了人Pol II和Pol III预起始复合物的一般结构和功能保守性。令人惊讶的是,我们的结构和功能研究揭示了一个能够在活细胞中特异性调节Pol III转录输出的Brf2氧化还原感应模块。此外,我们确定Brf2是参与氧化应激途径的核心氧化还原感应转录因子,并为肺癌和乳腺癌中Brf2的基因激活提供了一个机制模型。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9662/4671959/4bdf2787a7d1/fx1.jpg

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