Structural basis of three different transcription activation strategies adopted by a single regulator SoxS. Issue 19 (16th October 2022)

• Record Type: Journal Article
• Authors: Shi, Jing; Wang, Lu; Wen, Aijia; Wang, Fulin; Zhang, Yuqiong; Yu, Libing; Li, Fangfang; Jin, Yuanling; Feng, Zhenzhen; Li, Jiacong; Yang, Yujiao; Gao, Fei; Zhang, Yu; Feng, Yu; Wang, Shuang; Zhao, Wei; Lin, Wei
• Is Part Of: Nucleic acids research. Volume 50:Issue 19(2022)
• Page Start: 11359
• Page End: 11373
• Publication Date: 2022-10-16
• Subjects: Nucleic acids -- Periodicals; Molecular biology -- Periodicals; 572.805
• DOI: 10.1093/nar/gkac898
• Languages: English
• ISSNs: 0305-1048

Abstract

Abstract: Transcription activation is established through extensive protein–protein and protein–DNA interactions that allow an activator to engage and remodel RNA polymerase. SoxS, a global transcription activator, diversely regulates subsets of stress response genes with different promoters, but the detailed SoxS-dependent transcription initiation mechanisms remain obscure. Here, we report cryo-EM structures of three SoxS-dependent transcription activation complexes (SoxS-TAC I, SoxS-TAC II and SoxS-TAC III ) comprising of Escherichia coli RNA polymerase (RNAP), SoxS protein and three representative classes of SoxS-regulated promoters. The structures reveal that SoxS monomer orchestrates transcription initiation through specific interactions with the promoter DNA and different conserved domains of RNAP. In particular, SoxS is positioned in the opposite orientation in SoxS-TAC III to that in SoxS-TAC I and SoxS-TAC II, unveiling a novel mode of transcription activation. Strikingly, two universally conserved C-terminal domains of alpha subunit (αCTD) of RNAP associate with each other, bridging SoxS and region 4 of σ 70 . We show that SoxS interacts with RNAP directly and independently from DNA, remodeling the enzyme to activate transcription from cognate SoxS promoters while repressing transcription from UP-element containing promoters. Our data provide a comprehensive summary of SoxS-dependent promoter architectures and offer new insights into the αCTD contribution to transcription control in bacteria.