Molecular Systems Biology of Sic1 in Yeast Cell Cycle Regulation Through Multiscale Modeling

Conference paper

DOI: 10.1007/978-1-4419-7210-1_7

Volume 736 of the book series Advances in Experimental Medicine and Biology (AEMB)
Cite this paper as:
Barberis M. (2012) Molecular Systems Biology of Sic1 in Yeast Cell Cycle Regulation Through Multiscale Modeling. In: Goryanin I., Goryachev A. (eds) Advances in Systems Biology. Advances in Experimental Medicine and Biology, vol 736. Springer, New York, NY

Abstract

Cell cycle control is highly regulated to guarantee the precise timing of events essential for cell growth, i.e., DNA replication onset and cell division. Failure of this control plays a role in cancer and molecules called cyclin-dependent kinase (Cdk) inhibitors (Ckis) exploit a critical function in cell cycle timing. Here we present a multiscale modeling where experimental and computational studies have been employed to investigate structure, function and temporal dynamics of the Cki Sic1 that regulates cell cycle progression in Saccharomyces cerevisiae. Structural analyses reveal molecular details of the interaction between Sic1 and Cdk/cyclin complexes, and biochemical investigation reveals Sic1 function in analogy to its human counterpart p27Kip1, whose deregulation leads to failure in timing of kinase activation and, therefore, to cancer. Following these findings, a bottom-up systems biology approach has been developed to characterize modular networks addressing Sic1 regulatory function. Through complementary experimentation and modeling, we suggest a mechanism that underlies Sic1 function in controlling temporal waves of cyclins to ensure correct timing of the phase-specific Cdk activities.

Copyright information

© Springer Science+Business Media, LLC 2012

Authors and Affiliations

  1. 1.Institute for BiologyHumboldt University BerlinBerlinGermany
  2. 2.Max Planck Institute for Molecular GeneticsBerlinGermany