MicroRNA-1 and MicroRNA-133 in Spontaneous Myocardial Differentiation of Mouse Embryonic Stem Cells

被引:103
作者
Takaya, Tomohide [2 ]
Ono, Koh [2 ]
Kawamura, Teruhisa
Takanabe, Rieko
Kaichi, Shinji [3 ]
Morimoto, Tatsuya
Wada, Hiromichi
Kita, Toru [2 ]
Shimatsu, Akira
Hasegawa, Koji [1 ]
机构
[1] Natl Hosp Org, Kyoto Med Ctr, Clin Res Inst, Div Translat Res,Fushimi Ku, Kyoto 6128555, Japan
[2] Kyoto Univ, Grad Sch Med, Dept Cardiovasc Med, Kyoto, Japan
[3] Kyoto Univ, Grad Sch Med, Dept Pediat, Kyoto, Japan
关键词
Embryonic stem cells; MicroRNA; Myocardial differentiation; CYCLIN-DEPENDENT KINASE-9; CARDIAC-HYPERTROPHY; ES CELLS; IDENTIFICATION; MYOCYTES; P300; RNAS;
D O I
10.1253/circj.CJ-08-1032
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: MicroRNAs (miRNAs) regulate various biological processes through inhibiting the translation of RNA transcripts. Although miRNA-1 (miR-1) and miRNA-133 (miR-133) are abundantly expressed in the adult heart and involved in cardiac hypertrophy, the roles of these miRNAs in spontaneous myocardial differentiation are unknown. Methods and Results: The levels of miR-1 and miR-133 in mouse embryonic stem (ES) cells were increased during spontaneous differentiation by 2-dimensional culture, but reduced during forced myocardial differentiation by a histone deacetylase inhibitor, trichostatin A. The overexpression of miR-1 or miR-133 by lentiviral infection reduced the expression of a cardiac-specific gene, Nkx2.5, during differentiation of ES cells. In addition, miR-1 also inhibited a-myosin heavy chain expression. The results of luciferase assays revealed that miR-1 recognizes and targets the 3' untranslated region of cyclin-dependent kinase-9 (Cdk9) in ES cells. Overexpression of miR-1 decreased the protein amounts of Cdk9 without affecting the mRNA levels, indicating that miR-1 post-transcriptionally inhibits Cdk9 translation. Conclusions: miR-1 and miR-133 may play significant roles in the myocardial differentiation of mouse ES cells, and Cdk9 may be involved in this process as a target of miR-1. (Circ J 2009; 73: 1492-1497)
引用
收藏
页码:1492 / 1497
页数:6
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