Udvardy A
Institute of Biochemistry, Hungarian Academy of Sciences, Szeged, Hungary.
Eur J Biochem. 1996 Sep 1;240(2):307-13. doi: 10.1111/j.1432-1033.1996.0307h.x.
Cyclins and cyclin-dependent kinases are key regulators of the cell cycle. The binding of different cyclins, required to activate the catalytically inactive cyclin-dependent kinases, determines the substrate specificity of the enzymes. Cyclin-dependent-kinase inhibitors have an adverse effect, blocking the catalytic activity of cyclin-activated cyclin-dependent kinases. The cell cycle is a cyclic process of successive transient activation or inactivation of cyclin-dependent kinases by association with different cyclin regulatory subunits or cyclin-dependent kinase inhibitors. As the concentration of cyclin-dependent kinases is fairly constant during the cell cycle and exceeds the total amount of cyclins present in the cell, the exchange of regulatory subunits is determined by the availability of the different cyclins. Transcriptional control of cyclin gene expression is the most decisive factor determining the total amount of different cyclins synthesized. The actual concentration of a cyclin, however, is always the result of an equilibrium between the rates of its synthesis and degradation. While cyclin gene expression has long been known to be cell-cycle controlled, the idea of the rapid destruction of cyclins or cyclin-dependent-kinase inhibitors as an equally important factor contributing to the progress of the cell cycle is more recent. The role of controlled proteolysis in the regulation of cell cycle is discussed in this review. Two general features of this regulation are worth mentioning: cyclin-dependent kinases activated by different cyclin regulatory subunits have a central role both in the transcriptional regulation of their own genes and in the regulated, selective destruction of cyclins or cyclin-dependent kinase inhibitors; transcriptional regulation of cyclin gene expression ensures fine-tuned, continuous changes, and controlled proteolysis generates abrupt, irreversible transitions. The progress of the cell cycle is based on a delicate balance of the these mutual, but opposite regulations.
细胞周期蛋白和细胞周期蛋白依赖性激酶是细胞周期的关键调节因子。不同细胞周期蛋白的结合是激活无催化活性的细胞周期蛋白依赖性激酶所必需的,它决定了这些酶的底物特异性。细胞周期蛋白依赖性激酶抑制剂具有不利作用,会阻断细胞周期蛋白激活的细胞周期蛋白依赖性激酶的催化活性。细胞周期是一个循环过程,通过与不同的细胞周期蛋白调节亚基或细胞周期蛋白依赖性激酶抑制剂结合,使细胞周期蛋白依赖性激酶相继短暂激活或失活。由于细胞周期蛋白依赖性激酶的浓度在细胞周期中相当恒定,且超过细胞中存在的细胞周期蛋白总量,调节亚基的交换取决于不同细胞周期蛋白的可利用性。细胞周期蛋白基因表达的转录控制是决定合成的不同细胞周期蛋白总量的最决定性因素。然而,细胞周期蛋白的实际浓度始终是其合成速率和降解速率之间平衡的结果。虽然长期以来人们已知细胞周期蛋白基因表达受细胞周期控制,但细胞周期蛋白或细胞周期蛋白依赖性激酶抑制剂的快速降解作为促进细胞周期进程的同等重要因素的观点却是最近才出现的。本综述讨论了受控蛋白水解在细胞周期调控中的作用。这种调控的两个一般特征值得一提:由不同细胞周期蛋白调节亚基激活的细胞周期蛋白依赖性激酶在其自身基因的转录调控以及细胞周期蛋白或细胞周期蛋白依赖性激酶抑制剂的受控、选择性降解中都起着核心作用;细胞周期蛋白基因表达的转录调控确保了微调、持续的变化,而受控蛋白水解则产生突然、不可逆的转变。细胞周期的进程基于这些相互但相反的调控之间的微妙平衡。