Depletion of the nucleolar protein nucleostemin causes g1 cell cycle arrest via the p53 pathway

被引:93
作者
Ma, Hanhui [1 ]
Pederson, Thoru
机构
[1] Univ Massachusetts, Sch Med, Program Cell Dynam, Worcester, MA 01605 USA
[2] Univ Massachusetts, Sch Med, Dept Mol Pharmacol & Biochem, Worcester, MA 01605 USA
关键词
D O I
10.1091/mbc.E07-03-0244
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
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.
引用
收藏
页码:2630 / 2635
页数:6
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