Alberghina Lilia, Rossi Riccardo L, Wanke Valeria, Querin Lorenzo, Vanoni Marco
Dipartimento di Biotecnologie e Bioscienze, Università di Milano-Bicocca, Milano-Italy.
Ital J Biochem. 2003 Mar;52(1):55-7.
The regulation of cell cycle progression via the attainment of a critical cell size is a conserved feature from simpler unicellular organisms to mammalian cells that is obtaining much attention recently. Genome wide analysis of Saccharomyces cerevisiae deletion strains, genetic epistasis, DNA microarray analysis have recently revealed an increasingly complex network of cell size modulation mechanisms. A systems biology-based approach, that is needed to structure the underlying complexity of cell cycle regulatory mechanisms, is described.
通过达到临界细胞大小来调控细胞周期进程,这是从简单的单细胞生物到哺乳动物细胞都具有的保守特征,最近备受关注。对酿酒酵母缺失菌株的全基因组分析、遗传上位性分析、DNA微阵列分析,最近揭示了一个日益复杂的细胞大小调节机制网络。本文描述了一种基于系统生物学的方法,该方法对于构建细胞周期调控机制的潜在复杂性是必要的。