Interlinked bistable mechanisms generate robust mitotic transitions. Issue 20 (18th October 2017)

• Record Type: Journal Article
• Authors: Hutter, Lukas H.; Rata, Scott; Hochegger, Helfrid; Novák, Béla
• Is Part Of: Cell cycle. Volume 16:Issue 20(2017)
• Page Start: 1885
• Page End: 1892
• Publication Date: 2017-10-18
• Subjects: CDK1 -- PP2A:B55 -- spindle assembly checkpoint -- error correction -- biochemical switches -- mitosis -- Greatwall -- Aurora B -- cyclins -- cancer cells -- checkpoint control; Cell cycle -- Periodicals; 571.84377
• DOI: 10.1080/15384101.2017.1371885
• Languages: English
• ISSNs: 1538-4101

Abstract

ABSTRACT: The transitions between phases of the cell cycle have evolved to be robust and switch-like, which ensures temporal separation of DNA replication, sister chromatid separation, and cell division. Mathematical models describing the biochemical interaction networks of cell cycle regulators attribute these properties to underlying bistable switches, which inherently generate robust, switch-like, and irreversible transitions between states. We have recently presented new mathematical models for two control systems that regulate crucial transitions in the cell cycle: mitotic entry and exit, 1 and the mitotic checkpoint. 2 Each of the two control systems is characterized by two interlinked bistable switches. In the case of mitotic checkpoint control, these switches are mutually activating, whereas in the case of the mitotic entry/exit network, the switches are mutually inhibiting. In this Perspective we describe the qualitative features of these regulatory motifs and show that having two interlinked bistable mechanisms further enhances robustness and irreversibility. We speculate that these network motifs also underlie other cell cycle transitions and cellular transitions between distinct biochemical states.