Adames, Neil R.Schuck, P. LoganChen, Katherine C.Murali, T. M.Tyson, John J.Peccoud, Jean2016-12-092016-12-092015-11-051059-1524http://hdl.handle.net/10919/73622The cell cycle is composed of bistable molecular switches that govern the transitions between gap phases (G1 and G2) and the phases in which DNA is replicated (S) and partitioned between daughter cells (M). Many molecular details of the budding yeast G1–S transition (Start) have been elucidated in recent years, especially with regard to its switch-like behavior due to positive feedback mechanisms. These results led us to reevaluate and expand a previous mathematical model of the yeast cell cycle. The new model incorporates Whi3 inhibition of Cln3 activity, Whi5 inhibition of SBF and MBF transcription factors, and feedback inhibition of Whi5 by G1–S cyclins. We tested the accuracy of the model by simulating various mutants not described in the literature. We then constructed these novel mutant strains and compared their observed phenotypes to the model’s simulations. The experimental results reported here led to further changes of the model, which will be fully described in a later article. Our study demonstrates the advantages of combining model design, simulation, and testing in a coordinated effort to better understand a complex biological network.3966 - 3984 (19) page(s)Creative Commons Attribution-NonCommercial-ShareAlike 3.0 UnportedCell BiologyCELL-CYCLE STARTSYSTEMS-LEVEL FEEDBACKCDC28 PROTEIN-KINASESACCHAROMYCES-CEREVISIAETRANSCRIPTION FACTORSIZE-CONTROLG1 CYCLINSDNA-REPLICATIONS-PHASECLN3-CDC28 KINASEArticle - Refereedhttps://doi.org/10.1091/mbc.E15-06-03582622