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A fast-acting lipid checkpoint in G1 prevents mitotic defects

Author

Listed:
  • Marielle S. Köberlin

    (Stanford University School of Medicine
    Stanford University School of Medicine)

  • Yilin Fan

    (Stanford University School of Medicine
    Massachusetts General Hospital and Harvard Medical School)

  • Chad Liu

    (Stanford University School of Medicine
    Chan Zuckerberg Biohub)

  • Mingyu Chung

    (Stanford University School of Medicine
    Stanford University School of Medicine)

  • Antonio F. M. Pinto

    (Salk Institute for Biological Studies)

  • Peter K. Jackson

    (Stanford University School of Medicine
    Stanford University School of Medicine)

  • Alan Saghatelian

    (Salk Institute for Biological Studies)

  • Tobias Meyer

    (Stanford University School of Medicine
    Weill Cornell Medicine)

Abstract

Lipid synthesis increases during the cell cycle to ensure sufficient membrane mass, but how insufficient synthesis restricts cell-cycle entry is not understood. Here, we identify a lipid checkpoint in G1 phase of the mammalian cell cycle by using live single-cell imaging, lipidome, and transcriptome analysis of a non-transformed cell. We show that synthesis of fatty acids in G1 not only increases lipid mass but extensively shifts the lipid composition to unsaturated phospholipids and neutral lipids. Strikingly, acute lowering of lipid synthesis rapidly activates the PERK/ATF4 endoplasmic reticulum (ER) stress pathway that blocks cell-cycle entry by increasing p21 levels, decreasing Cyclin D levels, and suppressing Retinoblastoma protein phosphorylation. Together, our study identifies a rapid anticipatory ER lipid checkpoint in G1 that prevents cells from starting the cell cycle as long as lipid synthesis is low, thereby preventing mitotic defects, which are triggered by low lipid synthesis much later in mitosis.

Suggested Citation

  • Marielle S. Köberlin & Yilin Fan & Chad Liu & Mingyu Chung & Antonio F. M. Pinto & Peter K. Jackson & Alan Saghatelian & Tobias Meyer, 2024. "A fast-acting lipid checkpoint in G1 prevents mitotic defects," Nature Communications, Nature, vol. 15(1), pages 1-17, December.
  • Handle: RePEc:nat:natcom:v:15:y:2024:i:1:d:10.1038_s41467-024-46696-9
    DOI: 10.1038/s41467-024-46696-9
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    References listed on IDEAS

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    1. Lindsey R. Pack & Leighton H. Daigh & Mingyu Chung & Tobias Meyer, 2021. "Clinical CDK4/6 inhibitors induce selective and immediate dissociation of p21 from cyclin D-CDK4 to inhibit CDK2," Nature Communications, Nature, vol. 12(1), pages 1-12, December.
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