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A unified Watson-Crick geometry drives transcription of six-letter expanded DNA alphabets by E. coli RNA polymerase

Author

Listed:
  • Juntaek Oh

    (University of California, San Diego
    Kyung Hee University)

  • Zelin Shan

    (The Salk Institute for Biological Studies)

  • Shuichi Hoshika

    (Foundation for Applied Molecular Evolution)

  • Jun Xu

    (University of California, San Diego)

  • Jenny Chong

    (University of California, San Diego)

  • Steven A. Benner

    (Foundation for Applied Molecular Evolution)

  • Dmitry Lyumkis

    (The Salk Institute for Biological Studies
    Department of Integrative Structural and Computational Biology
    University of California San Diego)

  • Dong Wang

    (University of California, San Diego
    University of California, San Diego
    University of California, San Diego)

Abstract

Artificially Expanded Genetic Information Systems (AEGIS) add independently replicable unnatural nucleotide pairs to the natural G:C and A:T/U pairs found in native DNA, joining the unnatural pairs through alternative modes of hydrogen bonding. Whether and how AEGIS pairs are recognized and processed by multi-subunit cellular RNA polymerases (RNAPs) remains unknown. Here, we show that E. coli RNAP selectively recognizes unnatural nucleobases in a six-letter expanded genetic system. High-resolution cryo-EM structures of three RNAP elongation complexes containing template-substrate UBPs reveal the shared principles behind the recognition of AEGIS and natural base pairs. In these structures, RNAPs are captured in an active state, poised to perform the chemistry step. At this point, the unnatural base pair adopts a Watson-Crick geometry, and the trigger loop is folded into an active conformation, indicating that the mechanistic principles underlying recognition and incorporation of natural base pairs also apply to AEGIS unnatural base pairs. These data validate the design philosophy of AEGIS unnatural basepairs. Further, we provide structural evidence supporting a long-standing hypothesis that pair mismatch during transcription occurs via tautomerization. Together, our work highlights the importance of Watson-Crick complementarity underlying the design principles of AEGIS base pair recognition.

Suggested Citation

  • Juntaek Oh & Zelin Shan & Shuichi Hoshika & Jun Xu & Jenny Chong & Steven A. Benner & Dmitry Lyumkis & Dong Wang, 2023. "A unified Watson-Crick geometry drives transcription of six-letter expanded DNA alphabets by E. coli RNA polymerase," Nature Communications, Nature, vol. 14(1), pages 1-10, December.
  • Handle: RePEc:nat:natcom:v:14:y:2023:i:1:d:10.1038_s41467-023-43735-9
    DOI: 10.1038/s41467-023-43735-9
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    References listed on IDEAS

    as
    1. Juntaek Oh & Michiko Kimoto & Haoqing Xu & Jenny Chong & Ichiro Hirao & Dong Wang, 2023. "Structural basis of transcription recognition of a hydrophobic unnatural base pair by T7 RNA polymerase," Nature Communications, Nature, vol. 14(1), pages 1-8, December.
    2. Isaac J. Kimsey & Eric S. Szymanski & Walter J. Zahurancik & Anisha Shakya & Yi Xue & Chia-Chieh Chu & Bharathwaj Sathyamoorthy & Zucai Suo & Hashim M. Al-Hashimi, 2018. "Dynamic basis for dG•dT misincorporation via tautomerization and ionization," Nature, Nature, vol. 554(7691), pages 195-201, February.
    3. Alexey Rozov & Natalia Demeshkina & Eric Westhof & Marat Yusupov & Gulnara Yusupova, 2015. "Structural insights into the translational infidelity mechanism," Nature Communications, Nature, vol. 6(1), pages 1-9, November.
    4. Natalia Demeshkina & Lasse Jenner & Eric Westhof & Marat Yusupov & Gulnara Yusupova, 2012. "A new understanding of the decoding principle on the ribosome," Nature, Nature, vol. 484(7393), pages 256-259, April.
    5. Dmitry G. Vassylyev & Marina N. Vassylyeva & Jinwei Zhang & Murali Palangat & Irina Artsimovitch & Robert Landick, 2007. "Structural basis for substrate loading in bacterial RNA polymerase," Nature, Nature, vol. 448(7150), pages 163-168, July.
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