4.7 Article

Zfp143 Regulates Nanog Through Modulation of Oct4 Binding

期刊

STEM CELLS
卷 26, 期 11, 页码 2759-2767

出版社

WILEY
DOI: 10.1634/stemcells.2008-0398

关键词

Zfp143; Oct4; Nanog; Embryonic stem cell

资金

  1. Agency for Science, Technology and Research (A*STAR) of Singapore
  2. Singapore Stem Cell Consortium
  3. Singapore Millennium Foundation
  4. National University of Singapore
  5. Singapore-MIT alliance

向作者/读者索取更多资源

Identification of regulators governing the maintenance of embryonic stem (ES) cells is crucial to the understanding of ES cell biology. We identified a zinc finger protein, Zfp143, as a novel regulator for self-renewal. Depletion of Zfp143 by RNA interference causes loss of self-renewal of ES cells. Chromatin immunoprecipitation and electrophoretic mobility shift assays show the direct binding of Zfp143 to the Nanog proximal promoter. Knockdown of Zfp143 or mutation of the Zfp143 binding motif significantly downregulates Nanog proximal promoter activity. Importantly, enforced expression of Nanog is able to rescue the Zfp143 knockdown phenotype, indicating that Nanog is one of the key downstream effectors of Zfp143. More interestingly, we further show that Zfp143 regulates Nanog expression through modulation of Oct4 binding. Coimmunoprecipitation experiments revealed that Zfp143 and Oct4 physically interact with each other. This interaction is important because Oct4 binding to the Nanog promoter is promoted by Zfp143. Our study reveals a novel regulator functionally important for the self-renewal of ES cells and provides new insights into the expanded regulatory circuitry that maintains ES cell pluripotency. STEM CELLS 2008;26:2759-2767

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.7
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据