4.5 Article

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

期刊

BIOCHEMICAL JOURNAL
卷 426, 期 -, 页码 171-181

出版社

PORTLAND PRESS LTD
DOI: 10.1042/BJ20091439

关键词

cell-cycle control; differentiation; enbryonic stem cell; G(1) cell-cycle arrest; Oct-4; p21; self-renewal

资金

  1. Ministry of Education. Science, and Technology, Republic of Korea [SC-2211]
  2. BioGreen21 Program, Rural Development Administration, Republic of Korea [20070501034009]
  3. Ministry of Education, Science, and Technology [2009-0093822]
  4. Ministry of Education and Human Resources Development [BK21]
  5. Sogang University [200811026.1]
  6. National Research Foundation of Korea [12-2008-11-001-00, 2009-0093822] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)
  7. Rural Development Administration (RDA), Republic of Korea [20070501034009, PJ00705420101136300] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

向作者/读者索取更多资源

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.

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