Rapid cycling and precocious termination of G1 phase in cells expressing CDK1AF

• Published in: Molecular biology of the cell 2008-08, Vol.19 (8), p.3426-3441
• Main Authors: Pomerening, Joseph R, Ubersax, Jeffrey A, Ferrell, Jr, James E
• Format: Article
• Language: English
• Subjects: Animals; CDC2 Protein Kinase - genetics; CDC2 Protein Kinase - metabolism; Cell Cycle; Cell Cycle Proteins - metabolism; Cyclin B - metabolism; Cyclin B1; G1 Phase; Gene Expression Regulation; Gene Expression Regulation, Developmental; HeLa Cells; Humans; Mitosis; Models, Biological; Mutation; Nuclear Proteins - metabolism; Protein-Tyrosine Kinases - metabolism; Time Factors; Xenopus
• ISSN: 1059-1524; 1939-4586
• DOI: 10.1091/mbc.E08-02-0172

In Xenopus embryos, the cell cycle is driven by an autonomous biochemical oscillator that controls the periodic activation and inactivation of cyclin B1-CDK1. The oscillator circuit includes a system of three interlinked positive and double-negative feedback loops (CDK1 -> Cdc25 -> CDK1; CDK1 -/ Wee1 -/ CDK1; and CDK1 -/ Myt1 -/ CDK1) that collectively function as a bistable trigger. Previous work established that this bistable trigger is essential for CDK1 oscillations in the early embryonic cell cycle. Here, we assess the importance of the trigger in the somatic cell cycle, where checkpoints and additional regulatory mechanisms could render it dispensable. Our approach was to express the phosphorylation site mutant CDK1AF, which short-circuits the feedback loops, in HeLa cells, and to monitor cell cycle progression by live cell fluorescence microscopy. We found that CDK1AF-expressing cells carry out a relatively normal first mitosis, but then undergo rapid cycles of cyclin B1 accumulation and destruction at intervals of 3-6 h. During these cycles, the cells enter and exit M phase-like states without carrying out cytokinesis or karyokinesis. Phenotypically similar rapid cycles were seen in Wee1 knockdown cells. These findings show that the interplay between CDK1, Wee1/Myt1, and Cdc25 is required for the establishment of G1 phase, for the normal approximately 20-h cell cycle period, and for the switch-like oscillations in cyclin B1 abundance characteristic of the somatic cell cycle. We propose that the HeLa cell cycle is built upon an unreliable negative feedback oscillator and that the normal high reliability, slow pace and switch-like character of the cycle is imposed by a bistable CDK1/Wee1/Myt1/Cdc25 system.