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p27Kip1是一种细胞周期蛋白依赖性激酶抑制剂,它将转化生长因子-β和接触抑制与细胞周期停滞联系起来。

p27Kip1, a cyclin-Cdk inhibitor, links transforming growth factor-beta and contact inhibition to cell cycle arrest.

作者信息

Polyak K, Kato J Y, Solomon M J, Sherr C J, Massague J, Roberts J M, Koff A

机构信息

Cell Biology and Genetics Program, Memorial Sloan-Kettering Cancer Center, New York, New York 10021.

出版信息

Genes Dev. 1994 Jan;8(1):9-22. doi: 10.1101/gad.8.1.9.

Abstract

Cell-cell contact and TGF-beta can arrest the cell cycle in G1. Mv1Lu mink epithelial cells arrested by either mechanism are incapable of assembling active complexes containing the G1 cyclin, cyclin E, and its catalytic subunit, Cdk2. These growth inhibitory signals block Cdk2 activation by raising the threshold level of cyclin E necessary to activate Cdk2. In arrested cells the threshold is set higher than physiological cyclin E levels and is determined by an inhibitor that binds to cyclin E-Cdk2 complexes. A 27-kD protein that binds to and prevents the activation of cyclin E-Cdk2 complexes can be purified from arrested cells but not from proliferating cells, using cyclin E-Cdk2 affinity chromatography. p27 is present in proliferating cells, but it is sequestered and unavailable to interact with cyclin E-Cdk2 complexes. Cyclin D2-Cdk4 complexes bind competitively to and down-regulate the activity of p27 and may thereby act in a pathway that reverses Cdk2 inhibition and enables G1 progression.

摘要

细胞间接触和转化生长因子-β(TGF-β)可使细胞周期停滞在G1期。通过这两种机制之一停滞的Mv1Lu貂上皮细胞无法组装包含G1期细胞周期蛋白、细胞周期蛋白E及其催化亚基细胞周期蛋白依赖性激酶2(Cdk2)的活性复合物。这些生长抑制信号通过提高激活Cdk2所需的细胞周期蛋白E的阈值水平来阻断Cdk2的激活。在停滞的细胞中,阈值设定高于生理细胞周期蛋白E水平,并且由一种与细胞周期蛋白E-Cdk2复合物结合的抑制剂决定。使用细胞周期蛋白E-Cdk2亲和层析法,可从停滞的细胞而非增殖细胞中纯化出一种与细胞周期蛋白E-Cdk2复合物结合并阻止其激活的27-kD蛋白。p27存在于增殖细胞中,但它被隔离且无法与细胞周期蛋白E-Cdk2复合物相互作用。细胞周期蛋白D2-Cdk4复合物竞争性结合并下调p27的活性,从而可能在一条逆转Cdk2抑制并使G1期进程得以进行的途径中发挥作用。

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