Following a brief description of the operational procedures of systems biology (SB), the cell cycle of budding yeast is discussed as a Successful example of a top-down SB analysis After the reconstruction of the steps that have led to the identification of a sizer plus timer network in the G1 to S transition, it is shown that basic functions of the cell cycle (the setting of the critical cell size and the accuracy of DNA replication) are system-level properties. detected only by integrating molecular analysis with modelling and simulation of their underlying networks. A detailed network structure of a second relevant regulatory step of the cell cycle, the exit from mitosis, derived from extensive data mining, is constructed and discussed. To reach a quantitative understanding of how nutrients control. through signalling. metabolism and transcription, cell growth and cycle is a very relevant aim of SB. Since we know that about 900 gene products are required for cell cycle execution and control in budding yeast, it is quite clear that a purely systematic approach would require too much time Therefore lines for a modular SB approach, which prioritises molecular and computational investigations for faster cell Cycle understanding, are proposed The relevance of the insight coming from the cell cycle SB studies in developing a new framework for tackling very complex biological processes. such as cancer and aging, is discussed (C) 2009 Elsevier Inc. All rights reserved.