Department of Molecular Biophysics and Biochemistry, Yale University, New Haven, CT 06511, USA; Yale Cancer Biology Institute, Yale University, West Haven, CT 06516, USA.
Department of Molecular Biophysics and Biochemistry, Yale University, New Haven, CT 06511, USA; Yale Cancer Biology Institute, Yale University, West Haven, CT 06516, USA.
Cell Rep. 2023 May 30;42(5):112495. doi: 10.1016/j.celrep.2023.112495. Epub 2023 May 9.
Centromere protein A (CENP-A) defines centromere identity and nucleates kinetochore formation for mitotic chromosome segregation. Here, we show that ataxia telangiectasia and Rad3-related (ATR) kinase, a master regulator of the DNA damage response, protects CENP-A occupancy at interphase centromeres in a DNA damage-independent manner. In unperturbed cells, ATR localizes to promyelocytic leukemia nuclear bodies (PML NBs), which house the histone H3.3 chaperone DAXX (death domain-associated protein 6). We find that ATR inhibition reduces DAXX association with PML NBs, resulting in the DAXX-dependent loss of CENP-A and an aberrant increase in H3.3 at interphase centromeres. Additionally, we show that ATR-dependent phosphorylation within the C terminus of DAXX regulates CENP-A occupancy at centromeres and DAXX localization. Lastly, we demonstrate that acute ATR inhibition during interphase leads to kinetochore formation defects and an increased rate of lagging chromosomes. These findings highlight a mechanism by which ATR protects centromere identity and genome stability.
着丝粒蛋白 A(CENP-A)定义着丝粒的身份,并为有丝分裂染色体分离的动粒形成提供核。在这里,我们表明,共济失调毛细血管扩张症和 Rad3 相关激酶(ATR),一种 DNA 损伤反应的主调控因子,以一种不依赖于 DNA 损伤的方式保护间期着丝粒处的 CENP-A 占据。在未受干扰的细胞中,ATR 定位于早幼粒细胞白血病核体(PML NBs),其中包含组蛋白 H3.3 伴侣 DAXX(死亡结构域相关蛋白 6)。我们发现,ATR 抑制减少了 DAXX 与 PML NBs 的结合,导致 DAXX 依赖性 CENP-A 丢失和间期着丝粒处 H3.3 的异常增加。此外,我们表明,DAXX 内 C 末端的 ATR 依赖性磷酸化调节着丝粒处的 CENP-A 占据和 DAXX 定位。最后,我们证明在间期急性抑制 ATR 会导致动粒形成缺陷和滞后染色体的比例增加。这些发现强调了 ATR 保护着丝粒身份和基因组稳定性的机制。