4.8 Article

Acetylation of Aurora B by TIP60 ensures accurate chromosomal segregation

期刊

NATURE CHEMICAL BIOLOGY
卷 12, 期 4, 页码 226-+

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NATURE PUBLISHING GROUP
DOI: 10.1038/NCHEMBIO.2017

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资金

  1. Natural Science Foundation of China [31430054, 31320103904, 91313303, 2002CB713700, 31501095, 81270466, 31371363, 31271439, 91213303]
  2. 973 projects [2014CB964803, 2012CB917200, 2012CB945002, 2013CB911203, 2002CB713701]
  3. MOE Innovative team [IRT13038]
  4. Fundamental Research Funds for the Central Universities [WK2070000066]
  5. Chinese Academy of Sciences Center of Excellence [2015HSC-UE010]
  6. US National Institutes of Health [DK56292, CA164133]

向作者/读者索取更多资源

Faithful segregation of chromosomes in mammalian cells requires bi-orientation of sister chromatids, which relies on the sensing of correct attachments between spindle microtubules and kinetochores. Although the mechanisms underlying cyclin-dependent kinase 1 (CDK1) activation, which triggers mitotic entry, have been extensively studied, the regulatory mechanisms that couple CDK1-cyclin B activity to chromosome stability are not well understood. Here, we identified a signaling axis in which Aurora B activity is modulated by CDK1-cyclin B via the acetyltransferase TIP60 in human cell division. CDK1-cyclin B phosphorylates Ser90 of TIP60, which elicits TIP60-dependent acetylation of Aurora B and promotes accurate chromosome segregation in mitosis. Mechanistically, TIP60 acetylation of Aurora B at Lys215 protects Aurora B's activation loop from dephosphorylation by the phosphatase PP2A to ensure a robust, error-free metaphase-anaphase transition. These findings delineate a conserved signaling cascade that integrates protein phosphorylation and acetylation with cell cycle progression for maintenance of genomic stability.

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