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
相关论文
共 48 条
[21]   Conserved seed pairing, often flanked by adenosines, indicates that thousands of human genes are microRNA targets [J].
Lewis, BP ;
Burge, CB ;
Bartel, DP .
CELL, 2005, 120 (01) :15-20
[22]   Connecting microRNA genes to the core transcriptional regulatory circuitry of embryonic stem cells [J].
Marson, Alexander ;
Levine, Stuart S. ;
Cole, Megan F. ;
Frampton, Garrett M. ;
Brambrink, Tobias ;
Johnstone, Sarah ;
Guenther, Matthew G. ;
Johnston, Wendy K. ;
Wernig, Marius ;
Newman, Jamie ;
Calabrese, J. Mauro ;
Dennis, Lucas M. ;
Volkert, Thomas L. ;
Gupta, Sumeet ;
Love, Jennifer ;
Hannett, Nancy ;
Sharp, Phillip A. ;
Bartel, David P. ;
Jaenisch, Rudolf ;
Young, Richard A. .
CELL, 2008, 134 (03) :521-533
[23]  
Michael MZ, 2003, MOL CANCER RES, V1, P882
[24]   The expression profile of microRNAs in mouse embryos [J].
Mineno, J ;
Okamoto, S ;
Ando, T ;
Sato, M ;
Chono, H ;
Izu, H ;
Takayama, M ;
Asada, K ;
Mirochnitchenko, O ;
Inouye, M ;
Kato, I .
NUCLEIC ACIDS RESEARCH, 2006, 34 (06) :1765-1771
[25]   Application of massively parallel sequencing to microRNA profiling and discovery in human embryonic stem cells [J].
Morin, Ryan D. ;
O'Connor, Michael D. ;
Griffith, Malachi ;
Kuchenbauer, Florian ;
Delaney, Allen ;
Prabhu, Anna-Liisa ;
Zhao, Yongjun ;
McDonald, Helen ;
Zeng, Thomas ;
Hirst, Martin ;
Eaves, Connie J. ;
Marra, Marco A. .
GENOME RESEARCH, 2008, 18 (04) :610-621
[26]   Characterization of Dicer-deficient murine embryonic stem cells [J].
Murchison, EP ;
Partridge, JF ;
Tam, OH ;
Cheloufi, S ;
Hannon, GJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2005, 102 (34) :12135-12140
[27]   Generation of induced pluripotent stem cells without Myc from mouse and human fibroblasts [J].
Nakagawa, Masato ;
Koyanagi, Michiyo ;
Tanabe, Koji ;
Takahashi, Kazutoshi ;
Ichisaka, Tomoko ;
Aoi, Takashi ;
Okita, Keisuke ;
Mochiduki, Yuji ;
Takizawa, Nanako ;
Yamanaka, Shinya .
NATURE BIOTECHNOLOGY, 2008, 26 (01) :101-106
[28]   Klf4 cooperates with Oct3/4 and Sox2 to activate the Lefty1 core promoter in embryonic stem cells [J].
Nakatake, Yuhki ;
Fukui, Nobutaka ;
Iwamatsu, Yuko ;
Masui, Shinji ;
Takahashi, Kadue ;
Yagi, Rika ;
Yagi, Kiyohito ;
Miyazaki, Jun-ichi ;
Matoba, Ryo ;
Ko, Minoru S. H. ;
Niwa, Hitoshi .
MOLECULAR AND CELLULAR BIOLOGY, 2006, 26 (20) :7772-7782
[29]   Quantitative expression of Oct-3/4 defines differentiation, dedifferentiation or self-renewal of ES cells [J].
Niwa, H ;
Miyazaki, J ;
Smith, AG .
NATURE GENETICS, 2000, 24 (04) :372-376
[30]  
Park IH, 2008, NATURE, V451, P141, DOI [10.1038/nature06534, 10.1038/natureO6534]