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Metabolic labeling based methylome profiling enables functional dissection of histidine methylation in C3H1 zinc fingers

Author

Listed:
  • Keyun Wang

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

  • Li Zhang

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

  • Sirui Zhang

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

  • Ye Liu

    (Chinese Academy of Sciences)

  • Jiawei Mao

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

  • Zhen Liu

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

  • Lin Xu

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

  • Kejia Li

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

  • Jianshu Wang

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

  • Yanni Ma

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

  • Jiayi Wang

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

  • Haitao Li

    (Tsinghua University)

  • Zefeng Wang

    (University of Chinese Academy of Sciences, Chinese Academy of Sciences
    Southern University of Science and Technology)

  • Guohui Li

    (Chinese Academy of Sciences)

  • Hong Cheng

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

  • Mingliang Ye

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

Abstract

Protein methylation is a functionally important post-translational modification that occurs on diverse amino acid residues. The current proteomics approaches are inefficient to discover the methylation on residues other than Arg and Lys, which hinders the deep understanding of the functional role of rare protein methylation. Herein, we present a methyl-specific metabolic labeling approach for global methylome mapping, which enable the acquisition of methylome dataset covering diverse methylation types. Interestingly, of the identified methylation events, His methylation is found to be preferably occurred in C3H1 zinc fingers (ZFs). These His methylation events are determined to be Nπ specific and catalyzed by CARNMT1. The His methylation is found to stabilize the structure of ZFs. U2AF1 is used as a proof-of-concept to highlight the functional importance of His methylation in ZFs in RNA binding and RNA metabolism. The results of this study enable novel understanding of how protein methylation regulates cellular processes.

Suggested Citation

  • Keyun Wang & Li Zhang & Sirui Zhang & Ye Liu & Jiawei Mao & Zhen Liu & Lin Xu & Kejia Li & Jianshu Wang & Yanni Ma & Jiayi Wang & Haitao Li & Zefeng Wang & Guohui Li & Hong Cheng & Mingliang Ye, 2024. "Metabolic labeling based methylome profiling enables functional dissection of histidine methylation in C3H1 zinc fingers," Nature Communications, Nature, vol. 15(1), pages 1-14, December.
  • Handle: RePEc:nat:natcom:v:15:y:2024:i:1:d:10.1038_s41467-024-51979-2
    DOI: 10.1038/s41467-024-51979-2
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    References listed on IDEAS

    as
    1. Alex W. Wilkinson & Jonathan Diep & Shaobo Dai & Shuo Liu & Yaw Shin Ooi & Dan Song & Tie-Mei Li & John R. Horton & Xing Zhang & Chao Liu & Darshan V. Trivedi & Katherine M. Ruppel & José G. Vilches-M, 2019. "SETD3 is an actin histidine methyltransferase that prevents primary dystocia," Nature, Nature, vol. 565(7739), pages 372-376, January.
    2. 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.
    3. Cara Lunn Shirai & Brian S. White & Manorama Tripathi & Roberto Tapia & James N. Ley & Matthew Ndonwi & Sanghyun Kim & Jin Shao & Alexa Carver & Borja Saez & Robert S. Fulton & Catrina Fronick & Miche, 2017. "Mutant U2AF1-expressing cells are sensitive to pharmacological modulation of the spliceosome," Nature Communications, Nature, vol. 8(1), pages 1-10, April.
    4. Hisashi Yoshida & Sam-Yong Park & Gyosuke Sakashita & Yuko Nariai & Kanako Kuwasako & Yutaka Muto & Takeshi Urano & Eiji Obayashi, 2020. "Elucidation of the aberrant 3′ splice site selection by cancer-associated mutations on the U2AF1," Nature Communications, Nature, vol. 11(1), pages 1-9, December.
    5. 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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