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细胞周期蛋白依赖性蛋白激酶:真核细胞周期的关键调节因子。

Cyclin-dependent protein kinases: key regulators of the eukaryotic cell cycle.

作者信息

Nigg E A

机构信息

Swiss Institute for Experimental Cancer Research (ISREC), Epalinges.

出版信息

Bioessays. 1995 Jun;17(6):471-80. doi: 10.1002/bies.950170603.

Abstract

Passage through the cell cycle requires the successive activation of different cyclin-dependent protein kinases (CDKs). These enzymes are controlled by transient associations with cyclin regulatory subunits, binding of inhibitory polypeptides and reversible phosphorylation reactions. To promote progression towards DNA replication, CDK/cyclin complexes phosphorylate proteins required for the activation of genes involved in DNA synthesis, as well as components of the DNA replication machinery. Subsequently, a different set of CDK/cyclin complexes triggers the phosphorylation of numerous proteins to promote the profound structural reorganizations that accompany the entry of cells into mitosis. At present, much research is focused on elucidating the links between CDK/cyclin complexes and signal transduction pathways controlling cell growth, differentiation and death. In future, a better understanding of the cell cycle machinery and its deregulation during oncogenesis may provide novel opportunities for the diagnostic and therapeutic management of cancer and other proliferation-related diseases.

摘要

细胞周期的进程需要不同的细胞周期蛋白依赖性蛋白激酶(CDK)相继激活。这些酶受与细胞周期蛋白调节亚基的瞬时结合、抑制性多肽的结合以及可逆磷酸化反应的控制。为促进向DNA复制的进程,CDK/细胞周期蛋白复合物磷酸化激活参与DNA合成的基因所需的蛋白质以及DNA复制机制的组成部分。随后,另一组不同的CDK/细胞周期蛋白复合物触发众多蛋白质的磷酸化,以促进细胞进入有丝分裂时伴随的深刻结构重组。目前,许多研究集中于阐明CDK/细胞周期蛋白复合物与控制细胞生长、分化和死亡的信号转导途径之间的联系。未来,对细胞周期机制及其在肿瘤发生过程中的失调有更深入的了解,可能为癌症和其他增殖相关疾病的诊断和治疗管理提供新的机会。

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