Zic3 is required for maintenance of pluripotency in embryonic stem cells

被引:110
作者
Lim, Linda Shushan
Loh, Yuin-Han
Zhang, Weiwei
Li, Yixun
Chen, Xi
Wang, Yinan
Bakre, Manjiri
Ng, Huck-Hui
Stanton, Lawrence W. [1 ]
机构
[1] Genome Inst Singapore, Stem Cell & Dev Biol Grp, Singapore 138672, Singapore
[2] Genome Inst Singapore, Gene Regulat Lab, Singapore 138672, Singapore
[3] Genome Inst Singapore, Informat & Math Sci Grp, Singapore 138672, Singapore
[4] Natl Univ Singapore, Dept Biol Sci, Singapore 117543, Singapore
关键词
D O I
10.1091/mbc.E06-07-0624
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Embryonic stem (ES) cell pluripotency is dependent upon sustained expression of the key transcriptional regulators Oct4, Nanog, and Sox2. Dissection of the regulatory networks downstream of these transcription factors has provided critical insight into the molecular mechanisms that regulate ES cell pluripotency and early differentiation. Here we describe a role for Zic3, a member of the Gli family of zinc finger transcription factors, in the maintenance of pluripotency in ES cells. We show that Zic3 is expressed in ES cells and that this expression is repressed upon differentiation. The expression of Zic3 in pluripotent ES cells is also directly regulated by Oct4, Sox2, and Nanog. Targeted repression of Zic3 in human and mouse ES cells by RNA interference-induced expression of several markers of the endodermal lineage. Notably, the expression of Nanog, a key pluripotency regulator and repressor of extraembryonic endoderm specification in ES cells, was significantly reduced in Zic3 knockdown cells. This suggests that Zic3 may prevent endodermal marker expression through Nanog-regulated pathways. Thus our results extend the ES cell transcriptional network beyond Oct4, Nanog, and Sox2, and further establish that Zic3 plays an important role in the maintenance of pluripotency by preventing endodermal lineage specification in embryonic stem cells.
引用
收藏
页码:1348 / 1358
页数:11
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