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核仁蛋白核干细胞因子的缺失通过p53途径导致G1期细胞周期停滞。

Depletion of the nucleolar protein nucleostemin causes G1 cell cycle arrest via the p53 pathway.

作者信息

Ma Hanhui, Pederson Thoru

机构信息

Program in Cell Dynamics, Department of Biochemistry and Molecular Pharmacology, University of Massachusetts Medical School, Worcester, MA 01605, USA.

出版信息

Mol Biol Cell. 2007 Jul;18(7):2630-5. doi: 10.1091/mbc.e07-03-0244. Epub 2007 May 9.

Abstract

Nucleostemin (NS) is a nucleolar protein expressed in adult and embryo-derived stem cells, transformed cell lines, and tumors. NS decreases when proliferating cells exit the cell cycle, but it is unknown how NS is controlled, and how it participates in cell growth regulation. Here, we show that NS is down-regulated by the tumor suppressor p14(ARF) and that NS knockdown elevates the level of tumor suppressor p53. NS knockdown led to G1 cell cycle arrest in p53-positive cells but not in cells in which p53 was genetically deficient or depleted by small interfering RNA knockdown. These results demonstrate that, in the cells investigated, the level of NS is regulated by p14(ARF) and the control of the G1/S transition by NS operates in a p53-dependent manner.

摘要

核干细胞因子(NS)是一种在成体和胚胎来源的干细胞、转化细胞系及肿瘤中表达的核仁蛋白。当增殖细胞退出细胞周期时,NS水平下降,但NS如何被调控以及它如何参与细胞生长调节尚不清楚。在此,我们表明NS受肿瘤抑制因子p14(ARF)下调,且敲低NS可提高肿瘤抑制因子p53的水平。敲低NS导致p53阳性细胞出现G1期细胞周期阻滞,但在p53基因缺陷或通过小干扰RNA敲低而缺失的细胞中未出现这种情况。这些结果表明,在所研究的细胞中,NS水平受p14(ARF)调控,且NS对G1/S期转换的控制以p53依赖的方式进行。

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