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Competitive antagonism of KAT7 crotonylation against acetylation affects procentriole formation and colorectal tumorigenesis

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  • Meng Wang

    (Peking University Health Science Center
    Beijing Key Laboratory of Protein Posttranslational Modifications and Cell Function)

  • Guanqun Mu

    (Peking University Health Science Center)

  • Bingquan Qiu

    (Peking University Health Science Center)

  • Shuo Wang

    (Peking University Health Science Center)

  • Changyu Tao

    (Peking University Health Science Center)

  • Yutong Mao

    (Peking University Health Science Center)

  • Xinhui Zhao

    (Peking University Health Science Center)

  • Jiansong Liu

    (Peking University Health Science Center)

  • Keyu Chen

    (Peking University Health Science Center)

  • Ziyu Li

    (Peking University Cancer Hospital & Institute)

  • Weibin Wang

    (Peking University Health Science Center)

  • Ence Yang

    (Peking University Health Science Center)

  • Yang Yang

    (Peking University Health Science Center
    Beijing Key Laboratory of Protein Posttranslational Modifications and Cell Function)

Abstract

Accurate procentriole formation is critical for centriole duplication. However, the holistic transcriptional regulatory mechanisms underlying this process remain elusive. Here, we show that KAT7 crotonylation, facilitated by the crotonyltransferase hMOF, competes against its acetylation regulated by the deacetylase HDAC2 at the K432 residue upon DNA damage stimulation. This competition diminishes its histone acetyltransferase activity, leading to the inhibition of procentriole formation in colorectal cancer cells. Mechanistically, the reduction of KAT7 histone acetyltransferase activity by the antagonistic effect of KAT7 crotonylation against its acetylation decreases the gene expression associated with procentriole formation by modulating the enrichment of H3K14ac at their promoters and plays an important role in colorectal tumorigenesis. Furthermore, KAT7 crotonylation and acetylation are associated with the prognosis in colorectal cancer patients. Collectively, our findings uncover a previously unidentified role of KAT7 in the regulation of procentriole formation and colorectal tumorigenesis via competitive antagonism of its crotonylation against acetylation.

Suggested Citation

  • Meng Wang & Guanqun Mu & Bingquan Qiu & Shuo Wang & Changyu Tao & Yutong Mao & Xinhui Zhao & Jiansong Liu & Keyu Chen & Ziyu Li & Weibin Wang & Ence Yang & Yang Yang, 2025. "Competitive antagonism of KAT7 crotonylation against acetylation affects procentriole formation and colorectal tumorigenesis," Nature Communications, Nature, vol. 16(1), pages 1-18, December.
  • Handle: RePEc:nat:natcom:v:16:y:2025:i:1:d:10.1038_s41467-025-57546-7
    DOI: 10.1038/s41467-025-57546-7
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    References listed on IDEAS

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    1. Laura MacPherson & Juliana Anokye & Miriam M. Yeung & Enid Y. N. Lam & Yih-Chih Chan & Chen-Fang Weng & Paul Yeh & Kathy Knezevic & Miriam S. Butler & Annabelle Hoegl & Kah-Lok Chan & Marian L. Burr &, 2020. "HBO1 is required for the maintenance of leukaemia stem cells," Nature, Nature, vol. 577(7789), pages 266-270, January.
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