Identification of Zfp-57 as a downstream molecule of STAT3 and Oct-3/4 in embryonic stem cells

被引:34
|
作者
Akagi, T
Usuda, M
Matsuda, T
Ko, MSH
Niwa, H
Asano, M
Koide, H
Yokota, T
机构
[1] Kanazawa Univ, Grad Sch Med Sci, Dept Stem Cell Biol, Kanazawa, Ishikawa 9208640, Japan
[2] Harvard Univ, Sch Med, Dept Genet, Boston, MA 02115 USA
[3] NIA, Genet Lab, NIH, Baltimore, MD 21224 USA
[4] RIKEN, Ctr Dev Biol, Lab Pluripotent Cell Studies, Kobe, Hyogo 6500047, Japan
[5] Kanazawa Univ, Adv Res Ctr, Inst Expt Anim, Kanazawa, Ishikawa 9208640, Japan
关键词
ES cells; STAT3; Oct-3/4; Zfp-57; self-renewal; targeted disruption; RNAi;
D O I
10.1016/j.bbrc.2005.03.118
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
Embryonic stem (ES) cells are pluripotent cells derived from the inner cell mass of blastocysts. Transcription factor STAT3 is essential for the self-renewal of ES cells. In this study, we searched for downstream molecules of STAT3 in ES cells. Using DNA chip analysis, we obtained zinc finger protein (Zfp)-57. The expression of Zfp-57 was restricted to undifferentiated ES cells and activation of STAT3 led to expression of Zfp-57. We also found that forced expression of a dominant-negative mutant of STAT3 or repression of Oct-3/4 expression led to down-regulation of Zfp-57. Targeted disruption of Zfp-57 resulted in no gross phenotypical defects, including expression of undifferentiated-state-specific genes. These data suggest that Zfp-57 is a downstream molecule of STAT3 and Oct-3/4 in ES cells, although dispensable for their self-renewal. (c) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:23 / 30
页数:8
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