静息细胞中一条控制p27Kip1稳定性、亚细胞定位及肿瘤抑制作用的信号通路。

A pathway in quiescent cells that controls p27Kip1 stability, subcellular localization, and tumor suppression.

作者信息

Besson Arnaud, Gurian-West Mark, Chen Xueyan, Kelly-Spratt Karen S, Kemp Christopher J, Roberts James M

机构信息

Howard Hughes Medical Institute, Division of Basic Sciences, Seattle, Washington 98109, USA.

出版信息

Genes Dev. 2006 Jan 1;20(1):47-64. doi: 10.1101/gad.1384406.

Abstract

We have created two knock-in mouse models to study the mechanisms that regulate p27 in normal cells and cause misregulation of p27 in tumors: p27(S10A), in which Ser10 is mutated to Ala; and p27(CK-), in which point mutations abrogate the ability of p27 to bind cyclins and CDKs. These two mutant alleles identify steps in a pathway that controls the proteasomal degradation of p27 uniquely in quiescent cells: Dephosphorylation of p27 on Ser10 inhibits p27 nuclear export and promotes its assembly into cyclin-CDK complexes, which is, in turn, necessary for p27 turnover. We further show that Ras-dependent lung tumorigenesis is associated with increased phosphorylation on Ser10 and cytoplasmic mislocalization of p27. Indeed, we find that p27(S10A) is refractory to Ras-induced cytoplasmic translocation and that p27(S10A) mice are tumor resistant. Thus, phosphorylation of p27 on Ser10 is an important event in the regulation of the tumor suppressor function of p27.

摘要

我们构建了两种基因敲入小鼠模型,以研究在正常细胞中调节p27以及在肿瘤中导致p27调控异常的机制:p27(S10A),其中Ser10突变为Ala;以及p27(CK-),其中点突变消除了p27结合细胞周期蛋白和细胞周期蛋白依赖性激酶(CDK)的能力。这两个突变等位基因确定了一条在静止细胞中独特地控制p27蛋白酶体降解的途径中的步骤:p27在Ser10上的去磷酸化抑制p27的核输出并促进其组装成细胞周期蛋白-CDK复合物,这反过来又是p27周转所必需的。我们进一步表明,Ras依赖性肺癌发生与Ser10上磷酸化增加以及p27的细胞质错误定位有关。事实上,我们发现p27(S10A)对Ras诱导的细胞质易位具有抗性,并且p27(S10A)小鼠具有肿瘤抗性。因此,p27在Ser10上的磷酸化是调节p27肿瘤抑制功能的一个重要事件。

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