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TRIM52 maintains cellular fitness and is under tight proteolytic control by multiple giant E3 ligases

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  • Alexandra Shulkina

    (Dr.-Bohr-Gasse 9
    Dr.-Bohr-Gasse 9
    a Doctoral School of the University of Vienna and the Medical University of Vienna)

  • Kathrin Hacker

    (Dr.-Bohr-Gasse 9
    Dr.-Bohr-Gasse 9)

  • Julian F. Ehrmann

    (a Doctoral School of the University of Vienna and the Medical University of Vienna
    Vienna BioCenter (VBC)
    Harvard Medical School
    Boston Children’s Hospital)

  • Valentina Budroni

    (Dr.-Bohr-Gasse 9
    Dr.-Bohr-Gasse 9
    a Doctoral School of the University of Vienna and the Medical University of Vienna)

  • Ariane Mandlbauer

    (Johns Hopkins School of Medicine)

  • Johannes Bock

    (Dr.-Bohr-Gasse 9
    Dr.-Bohr-Gasse 9)

  • Daniel B. Grabarczyk

    (Vienna BioCenter (VBC))

  • Genevieve Edobor

    (Dr.-Bohr-Gasse 9
    Dr.-Bohr-Gasse 9)

  • Luisa Cochella

    (Johns Hopkins School of Medicine)

  • Tim Clausen

    (Vienna BioCenter (VBC)
    Vienna BioCenter (VBC))

  • Gijs A. Versteeg

    (Dr.-Bohr-Gasse 9
    Dr.-Bohr-Gasse 9)

Abstract

Tripartite motif 52 (TRIM52) exhibits strong positive selection in humans, yet is lost in many other mammals. In contrast to what one would expect for such a non-conserved factor, TRIM52 loss compromises cell fitness. We set out to determine the cellular function of TRIM52. Genetic and proteomic analyses revealed TRIM52 physically and functionally interacts with the DNA repair machinery. Our data suggest that TRIM52 limits topoisomerase 2 adducts, thereby preventing cell-cycle arrest. Consistent with a fitness-promoting function, TRIM52 is upregulated in various cancers, prompting us to investigate its regulatory pathways. We found TRIM52 to be targeted for ultra-rapid proteasomal degradation by the giant E3 ubiquitin ligases BIRC6, HUWE1, and UBR4/KCMF1. BIRC6 mono-ubiquitinates TRIM52, with subsequent extension by UBR4/KCMF1. These findings suggest a role for TRIM52 in maintaining genome integrity, and regulation of its own abundance through multi-ligase degradation.

Suggested Citation

  • Alexandra Shulkina & Kathrin Hacker & Julian F. Ehrmann & Valentina Budroni & Ariane Mandlbauer & Johannes Bock & Daniel B. Grabarczyk & Genevieve Edobor & Luisa Cochella & Tim Clausen & Gijs A. Verst, 2025. "TRIM52 maintains cellular fitness and is under tight proteolytic control by multiple giant E3 ligases," Nature Communications, Nature, vol. 16(1), pages 1-19, December.
    • Handle: RePEc:nat:natcom:v:16:y:2025:i:1:d:10.1038_s41467-025-59129-y
    DOI: 10.1038/s41467-025-59129-y
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    References listed on IDEAS

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    1. Melanie Almeida & Matthias Hinterndorfer & Hanna Brunner & Irina Grishkovskaya & Kashish Singh & Alexander Schleiffer & Julian Jude & Sumit Deswal & Robert Kalis & Milica Vunjak & Thomas Lendl & Richa, 2021. "AKIRIN2 controls the nuclear import of proteasomes in vertebrates," Nature, Nature, vol. 599(7885), pages 491-496, November.
    2. Petra Ebner & Isabella Poetsch & Luiza Deszcz & Thomas Hoffmann & Johannes Zuber & Fumiyo Ikeda, 2018. "The IAP family member BRUCE regulates autophagosome–lysosome fusion," Nature Communications, Nature, vol. 9(1), pages 1-15, December.
    3. Shuo-Shuo Liu & Tian-Xia Jiang & Fan Bu & Ji-Lan Zhao & Guang-Fei Wang & Guo-Heng Yang & Jie-Yan Kong & Yun-Fan Qie & Pei Wen & Li-Bin Fan & Ning-Ning Li & Ning Gao & Xiao-Bo Qiu, 2024. "Molecular mechanisms underlying the BIRC6-mediated regulation of apoptosis and autophagy," Nature Communications, Nature, vol. 15(1), pages 1-16, December.
    4. Diane L. Haakonsen & Michael Heider & Andrew J. Ingersoll & Kayla Vodehnal & Samuel R. Witus & Takeshi Uenaka & Marius Wernig & Michael Rapé, 2024. "Stress response silencing by an E3 ligase mutated in neurodegeneration," Nature, Nature, vol. 626(8000), pages 874-880, February.
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