Oct-4 controls cell-cycle progression of embryonic stem cells

被引:87
作者
Lee, Jungwoon [1 ]
Go, Yeorim [1 ]
Kang, Inyoung [1 ]
Han, Yong-Mahn [2 ]
Kim, Jungho [1 ]
机构
[1] Sogang Univ, Mol & Cellular Biol Lab, Dept Life Sci, Seoul 121742, South Korea
[2] Korea Adv Inst Sci & Technol, Dept Biol Sci, Taejon 305701, South Korea
关键词
cell-cycle control; differentiation; enbryonic stem cell; G(1) cell-cycle arrest; Oct-4; p21; self-renewal; TRANSCRIPTION FACTOR OCT-4; POU-DOMAIN; SELF-RENEWAL; GERM-LINE; EXTRAEMBRYONIC MEMBRANES; MAMMALIAN EMBRYO; ES CELLS; EXPRESSION; GENE; BINDING;
D O I
10.1042/BJ20091439
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Mouse and human ES (embryonic stem) cells display unusual proliferative properties and can produce pluripotent stem cells indefinitely. Both processes might be important for maintaining the 'stemness' of ES cells; however, little is known about how the cell-cycle fate is regulated in ES cells. Oct-4, a master switch of pluripotency, plays an important role in maintaining the phuripotent state of ES cells and may prevent the expression of genes activated during differentiation. Using ZHBTc4 ES cells, we have investigated the effect of Oct-4 oil ES cell-cycle control, and we found that Oct-4 down-regulation in ES cells inhibits proliferation by blocking cell-cycle progression in G(0)/G(1). Deletion analysis of the functional domains of Oct-4 indicates that the overall integrity of the Oct-4 functional domains is important for the stimulation of S-phase entry. We also show in the present study that the p21 gene is a target for Oct-4 repression. Furthermore, p21 protein levels were repressed by Oct-4 and were induced by the down-regulation of Oct-4 in ZHBTc4 ES cells. Therefore the down-regulation of p21 by Oct-4 may contribute to the maintenance of ES cell proliferation.
引用
收藏
页码:171 / 181
页数:11
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