| Literature DB >> 26291670 |
Alex Pinder1, Dorothy Loo1, Brittney Harrington1, Vanessa Oakes1, Michelle M Hill1, Brian Gabrielli2.
Abstract
Cell cycle progression from G2 phase into mitosis is regulated by a complex network of mechanisms, all of which finally control the timing of Cyclin B/CDK1 activation. PLK1 regulates a network of events that contribute to regulating G2/M phase progression. Here we have used a proteomics approach to identify proteins that specifically bind to the Polobox domain of PLK1. This identified a panel of proteins that were either associated with PLK1 in G2 phase and/or mitosis, the strongest interaction being with the MAPK scaffold protein JIP4. PLK1 binding to JIP4 was found in G2 phase and mitosis, and PLK1 binding was self-primed by PLK1 phosphorylation of JIP4. PLK1 binding is required for JIP4-dependent p38MAPK activation in G2 phase during normal cell cycle progression, but not in either G2 phase or mitotic stress response. Finally, JIP4 is a target for caspase-dependent cleavage in mitotically arrested cells. The role for the PLK1-JIP4 regulated p38MAPK activation in G2 phase is unclear, but it does not affect either progression into or through mitosis.Entities:
Keywords: G2 phase; JIP4; Mitosis; PLK1; p38MAPK
Mesh:
Substances:
Year: 2015 PMID: 26291670 DOI: 10.1016/j.cellsig.2015.08.009
Source DB: PubMed Journal: Cell Signal ISSN: 0898-6568 Impact factor: 4.315