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An epigenetic regulator emerges as microtubule minus-end binding and stabilizing factor in mitosis

Author

Listed:
  • Sylvain Meunier

    (Cell and Developmental Biology Programme, Centre for Genomic Regulation (CRG)
    Universitat Pompeu Fabra (UPF))

  • Maria Shvedunova

    (Max Planck Institute of Immunobiology and Epigenetics
    Faculty of Biology, University of Freiburg)

  • Nhuong Van Nguyen

    (Max Planck Institute of Immunobiology and Epigenetics
    Faculty of Biology, University of Freiburg)

  • Leonor Avila

    (Cell and Developmental Biology Programme, Centre for Genomic Regulation (CRG)
    Universitat Pompeu Fabra (UPF))

  • Isabelle Vernos

    (Cell and Developmental Biology Programme, Centre for Genomic Regulation (CRG)
    Universitat Pompeu Fabra (UPF)
    Institució Catalana de Recerca i Estudis Avançats (ICREA))

  • Asifa Akhtar

    (Max Planck Institute of Immunobiology and Epigenetics)

Abstract

The evolutionary conserved NSL complex is a prominent epigenetic regulator controlling expression of thousands of genes. Here we uncover a novel function of the NSL complex members in mitosis. As the cell enters mitosis, KANSL1 and KANSL3 undergo a marked relocalisation from the chromatin to the mitotic spindle. By stabilizing microtubule minus ends in a RanGTP-dependent manner, they are essential for spindle assembly and chromosome segregation. Moreover, we identify KANSL3 as a microtubule minus-end-binding protein, revealing a new class of mitosis-specific microtubule minus-end regulators. By adopting distinct functions in interphase and mitosis, KANSL proteins provide a link to coordinate the tasks of faithful expression and inheritance of the genome during different phases of the cell cycle.

Suggested Citation

  • Sylvain Meunier & Maria Shvedunova & Nhuong Van Nguyen & Leonor Avila & Isabelle Vernos & Asifa Akhtar, 2015. "An epigenetic regulator emerges as microtubule minus-end binding and stabilizing factor in mitosis," Nature Communications, Nature, vol. 6(1), pages 1-10, November.
  • Handle: RePEc:nat:natcom:v:6:y:2015:i:1:d:10.1038_ncomms8889
    DOI: 10.1038/ncomms8889
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    Cited by:

    1. Ting Li & Dingyi Lu & Chengcheng Yao & Tingting Li & Hua Dong & Zhan Li & Guang Xu & Jiayi Chen & Hao Zhang & Xiaoyu Yi & Haizhen Zhu & Guangqin Liu & Kaiqing Wen & Haixin Zhao & Jun Gao & Yakun Zhang, 2022. "Kansl1 haploinsufficiency impairs autophagosome-lysosome fusion and links autophagic dysfunction with Koolen-de Vries syndrome in mice," Nature Communications, Nature, vol. 13(1), pages 1-16, December.

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