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Structure of the transcription open complex of distinct σI factors

Author

Listed:
  • Jie Li

    (Chinese Academy of Sciences
    Chinese Academy of Sciences
    Chinese Academy of Sciences
    Shandong Energy Institute)

  • Haonan Zhang

    (University of Chinese Academy of Sciences
    Chinese Academy of Sciences)

  • Dongyu Li

    (University of Chinese Academy of Sciences
    Chinese Academy of Sciences)

  • Ya-Jun Liu

    (Chinese Academy of Sciences
    Chinese Academy of Sciences
    Chinese Academy of Sciences
    Shandong Energy Institute)

  • Edward A. Bayer

    (The Weizmann Institute of Science
    Ben-Gurion University of the Negev)

  • Qiu Cui

    (Chinese Academy of Sciences
    Chinese Academy of Sciences
    Chinese Academy of Sciences
    Shandong Energy Institute)

  • Yingang Feng

    (Chinese Academy of Sciences
    Chinese Academy of Sciences
    Chinese Academy of Sciences
    Shandong Energy Institute)

  • Ping Zhu

    (University of Chinese Academy of Sciences
    Chinese Academy of Sciences)

Abstract

Bacterial σI factors of the σ70-family are widespread in Bacilli and Clostridia and are involved in the heat shock response, iron metabolism, virulence, and carbohydrate sensing. A multiplicity of σI paralogues in some cellulolytic bacteria have been shown to be responsible for the regulation of the cellulosome, a multienzyme complex that mediates efficient cellulose degradation. Here, we report two structures at 3.0 Å and 3.3 Å of two transcription open complexes formed by two σI factors, SigI1 and SigI6, respectively, from the thermophilic, cellulolytic bacterium, Clostridium thermocellum. These structures reveal a unique, hitherto-unknown recognition mode of bacterial transcriptional promoters, both with respect to domain organization and binding to promoter DNA. The key characteristics that determine the specificities of the σI paralogues were further revealed by comparison of the two structures. Consequently, the σI factors represent a distinct set of the σ70-family σ factors, thus highlighting the diversity of bacterial transcription.

Suggested Citation

  • Jie Li & Haonan Zhang & Dongyu Li & Ya-Jun Liu & Edward A. Bayer & Qiu Cui & Yingang Feng & Ping Zhu, 2023. "Structure of the transcription open complex of distinct σI factors," Nature Communications, Nature, vol. 14(1), pages 1-12, December.
  • Handle: RePEc:nat:natcom:v:14:y:2023:i:1:d:10.1038_s41467-023-41796-4
    DOI: 10.1038/s41467-023-41796-4
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    References listed on IDEAS

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    1. Dingwei He & Linlin You & Xiaoxian Wu & Jing Shi & Aijia Wen & Zhi Yan & Wenhui Mu & Chengli Fang & Yu Feng & Yu Zhang, 2022. "Pseudomonas aeruginosa SutA wedges RNAP lobe domain open to facilitate promoter DNA unwinding," Nature Communications, Nature, vol. 13(1), pages 1-10, December.
    2. Yeqing Zong & Haoqian M. Zhang & Cheng Lyu & Xiangyu Ji & Junran Hou & Xian Guo & Qi Ouyang & Chunbo Lou, 2017. "Insulated transcriptional elements enable precise design of genetic circuits," Nature Communications, Nature, vol. 8(1), pages 1-13, December.
    3. Kathryn Tunyasuvunakool & Jonas Adler & Zachary Wu & Tim Green & Michal Zielinski & Augustin Žídek & Alex Bridgland & Andrew Cowie & Clemens Meyer & Agata Laydon & Sameer Velankar & Gerard J. Kleywegt, 2021. "Highly accurate protein structure prediction for the human proteome," Nature, Nature, vol. 596(7873), pages 590-596, August.
    4. Wei Lin & Sukhendu Mandal & David Degen & Min Sung Cho & Yu Feng & Kalyan Das & Richard H. Ebright, 2019. "Structural basis of ECF-σ-factor-dependent transcription initiation," Nature Communications, Nature, vol. 10(1), pages 1-14, December.
    5. Jing Shi & Aijia Wen & Sha Jin & Bo Gao & Yang Huang & Yu Feng, 2021. "Transcription activation by a sliding clamp," Nature Communications, Nature, vol. 12(1), pages 1-10, December.
    6. Linlin You & Jing Shi & Liqiang Shen & Lingting Li & Chengli Fang & Chengzhi Yu & Wenbo Cheng & Yu Feng & Yu Zhang, 2019. "Structural basis for transcription antitermination at bacterial intrinsic terminator," Nature Communications, Nature, vol. 10(1), pages 1-11, December.
    7. Remo Rohs & Sean M. West & Alona Sosinsky & Peng Liu & Richard S. Mann & Barry Honig, 2009. "The role of DNA shape in protein–DNA recognition," Nature, Nature, vol. 461(7268), pages 1248-1253, October.
    8. Hande Boyaci & James Chen & Rolf Jansen & Seth A. Darst & Elizabeth A. Campbell, 2019. "Structures of an RNA polymerase promoter melting intermediate elucidate DNA unwinding," Nature, Nature, vol. 565(7739), pages 382-385, January.
    9. Lingting Li & Chengli Fang & Ningning Zhuang & Tiantian Wang & Yu Zhang, 2019. "Structural basis for transcription initiation by bacterial ECF σ factors," Nature Communications, Nature, vol. 10(1), pages 1-14, December.
    10. John Jumper & Richard Evans & Alexander Pritzel & Tim Green & Michael Figurnov & Olaf Ronneberger & Kathryn Tunyasuvunakool & Russ Bates & Augustin Žídek & Anna Potapenko & Alex Bridgland & Clemens Me, 2021. "Highly accurate protein structure prediction with AlphaFold," Nature, Nature, vol. 596(7873), pages 583-589, August.
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