Department of Biochemistry, University of Oxford, Oxford, UK.
Open Biol. 2013 Mar 13;3(3):120179. doi: 10.1098/rsob.120179.
Progression through the eukaryotic cell cycle is characterized by specific transitions, where cells move irreversibly from stage i-1 of the cycle into stage i. These irreversible cell cycle transitions are regulated by underlying bistable switches, which share some common features. An inhibitory protein stalls progression, and an activatory protein promotes progression. The inhibitor and activator are locked in a double-negative feedback loop, creating a one-way toggle switch that guarantees an irreversible commitment to move forward through the cell cycle, and it opposes regression from stage i to stage i-1. In many cases, the activator is an enzyme that modifies the inhibitor in multiple steps, whereas the hypo-modified inhibitor binds strongly to the activator and resists its enzymatic activity. These interactions are the basis of a reaction motif that provides a simple and generic account of many characteristic properties of cell cycle transitions. To demonstrate this assertion, we apply the motif in detail to the G1/S transition in budding yeast and to the mitotic checkpoint in mammalian cells. Variations of the motif might support irreversible cellular decision-making in other contexts.
真核细胞周期的进展以特定的转变为特征,细胞不可逆地从周期的 i-1 期进入 i 期。这些不可逆的细胞周期转变由潜在的双稳态开关调节,这些开关具有一些共同的特征。一种抑制蛋白使进展停滞,而一种激活蛋白促进进展。抑制剂和激活剂被锁定在双负反馈回路中,形成一个单向的拨动开关,保证不可逆地向前推进细胞周期,并反对从 i 期向后退回到 i-1 期。在许多情况下,激活剂是一种酶,可以通过多个步骤修饰抑制剂,而低修饰的抑制剂与激活剂结合紧密,抵抗其酶活性。这些相互作用是反应基序的基础,为细胞周期转变的许多特征性质提供了简单而通用的解释。为了证明这一说法,我们详细地将该基序应用于芽殖酵母的 G1/S 转变和哺乳动物细胞的有丝分裂检查点。该基序的变体可能支持其他情况下不可逆的细胞决策。