Dynamic MicroRNA Expression Programs During Cardiac Differentiation of Human Embryonic Stem Cells Role for miR-499

被引:159
作者
Wilson, Kitchener D. [1 ,2 ]
Hu, Shijun [1 ]
Venkatasubrahmanyam, Shivkumar [4 ]
Fu, Ji-Dong [6 ]
Sun, Ning [1 ]
Abilez, Oscar J. [2 ,5 ]
Baugh, Joshua J. A. [5 ]
Jia, Fangjun [1 ]
Ghosh, Zhumur [1 ]
Li, Ronald A. [6 ,7 ]
Butte, Atul J. [4 ]
Wu, Joseph C. [1 ,3 ]
机构
[1] Stanford Univ, Sch Med, Dept Med Cardiol, Stanford, CA 94305 USA
[2] Stanford Univ, Sch Med, Dept Bioengn, Stanford, CA 94305 USA
[3] Stanford Univ, Sch Med, Inst Stem Cell Biol & Regenerat Med, Stanford, CA 94305 USA
[4] Stanford Univ, Sch Med, Dept Med Biomed Informat, Stanford, CA 94305 USA
[5] Stanford Univ, Sch Med, Dept Surg, Stanford, CA 94305 USA
[6] Mt Sinai Sch Med, Cardiovasc Res Ctr, New York, NY USA
[7] Univ Hong Kong, Stem Cell & Regenerat Med Program, Res Ctr Heart Brain Hormone & Healthy Aging, Hong Kong, Hong Kong, Peoples R China
基金
美国国家卫生研究院;
关键词
microRNA; microarrays; human embryonic stem cells; differentiation; cardiomyocyte; heart; GENES; HEART; MOUSE; CARDIOMYOCYTES; HYPERTROPHY; IDENTIFICATION; PROLIFERATION; MORPHOGENESIS; COEXPRESSION; CONDUCTION;
D O I
10.1161/CIRCGENETICS.109.934281
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background-MicroRNAs (miRNAs) are a newly discovered endogenous class of small, noncoding RNAs that play important posttranscriptional regulatory roles by targeting messenger RNAs for cleavage or translational repression. Human embryonic stem cells are known to express miRNAs that are often undetectable in adult organs, and a growing body of evidence has implicated miRNAs as important arbiters of heart development and disease. Methods and Results-To better understand the transition between the human embryonic and cardiac "miRNA-omes," we report here the first miRNA profiling study of cardiomyocytes derived from human embryonic stem cells. Analyzing 711 unique miRNAs, we have identified several interesting miRNAs, including miR-1, -133, and -208, that have been previously reported to be involved in cardiac development and disease and that show surprising patterns of expression across our samples. We also identified novel miRNAs, such as miR-499, that are strongly associated with cardiac differentiation and that share many predicted targets with miR-208. Overexpression of miR-499 and -1 resulted in upregulation of important cardiac myosin heavy-chain genes in embryoid bodies; miR-499 overexpression also caused upregulation of the cardiac transcription factor MEF2C. Conclusions-Taken together, our data give significant insight into the regulatory networks that govern human embryonic stem cell differentiation and highlight the ability of miRNAs to perturb, and even control, the genes that are involved in cardiac specification of human embryonic stem cells. (Circ Cardiovasc Genet. 2010;3:426-435.)
引用
收藏
页码:426 / U97
页数:44
相关论文
共 35 条
[1]  
*APPL BIOS, 2007, END CONTR REAL TIM Q
[2]   MicroRNAs: Genomics, biogenesis, mechanism, and function (Reprinted from Cell, vol 116, pg 281-297, 2004) [J].
Bartel, David P. .
CELL, 2007, 131 (04) :11-29
[3]   Microarray profiling of microRNAs reveals frequent coexpression with neighboring miRNAs and host genes [J].
Baskerville, S ;
Bartel, DP .
RNA, 2005, 11 (03) :241-247
[4]   A comparison of normalization methods for high density oligonucleotide array data based on variance and bias [J].
Bolstad, BM ;
Irizarry, RA ;
Åstrand, M ;
Speed, TP .
BIOINFORMATICS, 2003, 19 (02) :185-193
[5]   MicroRNA-208a is a regulator of cardiac hypertrophy and conduction in mice [J].
Callis, Thomas E. ;
Pandya, Kumar ;
Seok, Hee Young ;
Tang, Ru-Hang ;
Tatsuguchi, Mariko ;
Huang, Zhan-Peng ;
Chen, Jian-Fu ;
Deng, Zhongliang ;
Gunn, Bronwyn ;
Shumate, Janelle ;
Willis, Monte S. ;
Selzman, Craig H. ;
Wang, Da-Zhi .
JOURNAL OF CLINICAL INVESTIGATION, 2009, 119 (09) :2772-2786
[6]   Transcriptional and Functional Profiling of Human Embryonic Stem Cell-Derived Cardiomyocytes [J].
Cao, Feng ;
Wagner, Roger A. ;
Wilson, Kitchener D. ;
Xie, Xiaoyan ;
Fu, Ji-Dong ;
Drukker, Micha ;
Lee, Andrew ;
Li, Ronald A. ;
Gambhir, Sanjiv S. ;
Weissman, Irving L. ;
Robbins, Robert C. ;
Wu, Joseph C. .
PLOS ONE, 2008, 3 (10)
[7]   MicroRNA-133 controls cardiac hypertrophy [J].
Care, Alessandra ;
Catalucci, Daniele ;
Felicetti, Federica ;
Bonci, Desiree ;
Addario, Antonio ;
Gallo, Paolo ;
Bang, Marie-Louise ;
Segnalini, Patrizia ;
Gu, Yusu ;
Dalton, Nancy D. ;
Elia, Leonardo ;
Latronico, Michael V. G. ;
Hoydal, Morten ;
Autore, Camillo ;
Russo, Matteo A. ;
Dorn, Gerald W., II ;
Ellingsen, Oyvind ;
Ruiz-Lozano, Pilar ;
Peterson, Kirk L. ;
Croce, Carlo M. ;
Peschle, Cesare ;
Condorelli, Gianluigi .
NATURE MEDICINE, 2007, 13 (05) :613-618
[8]   MicroRNAs in Cardiovascular Biology and Heart Disease [J].
Catalucci, Daniele ;
Gallo, Paolo ;
Condorelli, Gianluigi .
CIRCULATION-CARDIOVASCULAR GENETICS, 2009, 2 (04) :402-408
[9]   The role of microRNA-1 and microRNA-133 in skeletal muscle proliferation and differentiation [J].
Chen, JF ;
Mandel, EM ;
Thomson, JM ;
Wu, QL ;
Callis, TE ;
Hammond, SM ;
Conlon, FL ;
Wang, DZ .
NATURE GENETICS, 2006, 38 (02) :228-233
[10]   Mouse ES cell-derived cardiac precursor cells are multipotent and facilitate identification of novel cardiac genes [J].
Christoforou, Nicolas ;
Miller, Ronald A. ;
Hill, Christine M. ;
Jie, Chunfa C. ;
McCallion, Andrew S. ;
Gearhart, John D. .
JOURNAL OF CLINICAL INVESTIGATION, 2008, 118 (03) :894-903