| Literature DB >> 31272276 |
Yusuke Yabuno1, Toshihiro Uchihashi1, Towa Sasakura2, Hiroyuki Shimizu2, Yoko Naito2,3, Kohshiro Fukushima2, Kaori Ota2, Mikihiko Kogo1, Hiroshi Nojima2, Norikazu Yabuta2,4.
Abstract
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.Entities:
Keywords: CHC; GAK; Kizuna; PLK1; centrosome; mitosis
Year: 2019 PMID: 31272276 PMCID: PMC6681784 DOI: 10.1080/15384101.2019.1637201
Source DB: PubMed Journal: Cell Cycle ISSN: 1551-4005 Impact factor: 4.534