MicroRNA-145 Regulates OCT4, SOX2, and KLF4 and Represses Pluripotency in Human Embryonic Stem Cells

被引:908
作者
Xu, Na [1 ]
Papagiannakopoulos, Thales [1 ]
Pan, Guangjin [2 ]
Thomson, James A. [2 ]
Kosik, Kenneth S. [1 ]
机构
[1] Univ Calif Santa Barbara, Dept Mol Cellular & Dev Biol, Neurosci Res Inst, Santa Barbara, CA 93106 USA
[2] Univ Wisconsin, Genome Ctr Wisconsin, Madison, WI 53706 USA
关键词
SELF-RENEWAL; MOUSE; DIFFERENTIATION; CIRCUITRY; EXPRESSION; GENES; NANOG; FIBROBLASTS; BIOGENESIS; LINEAGES;
D O I
10.1016/j.cell.2009.02.038
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
MicroRNAs (miRNAs) are posttranscriptional modulators of gene expression and play an important role in many developmental processes. We report here that expression of microRNA-145 (miR-145) is low in self-renewing human embryonic stem cells (hESCs) but highly upregulated during differentiation. We identify the pluripotency factors OCT4, SOX2, and KLF4 as direct targets of miR-145 and show that endogenous miR-145 represses the 3' untranslated regions of OCT4, SOX2, and KLF4. Increased miR-145 expression inhibits hESC self-renewal, represses expression of pluripotency genes, and induces lineage-restricted differentiation. Loss of miR-145 impairs differentiation and elevates OCT4, SOX2, and KLF4. Furthermore, we find that the miR-145 promoter is bound and repressed by OCT4 in hESCs. This work reveals a direct link between the core reprogramming factors and miR-145 and uncovers a double-negative feedback loop involving OCT4, SOX2, KLF4, and miR-145.
引用
收藏
页码:647 / 658
页数:12
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