a First Department of Oral and Maxillofacial Surgery, Graduate School of Dentistry, Osaka University , Osaka , Japan.
b Department of Molecular Genetics, Research Institute for Microbial Diseases, Osaka University , Osaka , Japan.
Cell Cycle. 2019 Aug;18(16):1976-1994. doi: 10.1080/15384101.2019.1637201. Epub 2019 Jul 4.
Clathrin regulates mitotic progression, in addition to membrane trafficking. However, the detailed regulatory mechanisms of clathrin during mitosis remain elusive. Here, we demonstrate novel regulation of clathrin during mitotic phase of the cell cycle. Clathrin heavy chain (CHC) was phosphorylated at T606 by its association partner cyclin G-associated kinase (GAK). This phosphorylation was required for proper cell proliferation and tumor growth of cells implanted into nude mice. Immunofluorescence analysis showed that the localization of CHC-pT606 signals changed during mitosis. CHC-pT606 signals localized in the nucleus and at the centrosome during interphase, whereas CHC signals were mostly cytoplasmic. Co-immunoprecipitation suggested that CHC formed a complex with GAK and polo-like kinase 1 (PLK1). Depletion of GAK using siRNA induced metaphase arrest and aberrant localization of CHC-pT606, which abolished Kiz-pT379 (as a phosphorylation target of PLK1) signals on chromatin at metaphase. Taken together, we propose that the GAK_CHC-pT606_PLK1_Kiz-pT379 axis plays a role in proliferation of cancer cells.
网格蛋白调节有丝分裂进程,除了膜运输。然而,网格蛋白在有丝分裂过程中的详细调节机制仍不清楚。在这里,我们证明了细胞周期有丝分裂阶段网格蛋白的新调节。网格蛋白重链(CHC)通过与其关联伙伴细胞周期蛋白 G 相关激酶(GAK)的结合而在 T606 处被磷酸化。这种磷酸化对于细胞的正常增殖和植入裸鼠的细胞的肿瘤生长是必需的。免疫荧光分析显示,CHC-pT606 信号在有丝分裂过程中的定位发生了变化。CHC-pT606 信号在间期定位于核和中心体,而 CHC 信号主要位于细胞质中。共免疫沉淀表明 CHC 与 GAK 和 polo 样激酶 1(PLK1)形成复合物。使用 siRNA 耗尽 GAK 会诱导中期停滞和 CHC-pT606 的异常定位,这会使中期染色质上的 Kiz-pT379(PLK1 的磷酸化靶标)信号消失。总之,我们提出 GAK_CHC-pT606_PLK1_Kiz-pT379 轴在癌细胞的增殖中发挥作用。