HMGA1 is a new target of miR-195 involving isoprenaline-induced cardiomyocyte hypertrophy

被引:38
|
作者
You, Xiang Yu [1 ]
Huang, Jiong Hua [1 ]
Liu, Bin [1 ]
Liu, Shao Jun [1 ]
Zhong, Yun [1 ]
Liu, Shi Ming [1 ]
机构
[1] Guangzhou Med Univ, Hosp 2, Cardiovasc Dept, Guangzhou Inst Cardiovasc Dis, Guangzhou 510260, Guangdong, Peoples R China
关键词
microRNA-195; cardiomyocyte hypertrophy; microRNA target; HMGA1; CARDIAC-HYPERTROPHY; SUPPRESSES TUMORIGENICITY; CELLS; TRANSCRIPTION; APOPTOSIS; CANCER;
D O I
10.1134/S0006297914060078
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
Emerging data have shown that microRNAs (miRNAs) have important functions in the processes of cardiac hypertrophy and heart failure that occur during the postnatal period. Cardiac overexpression of miR-195 results in pathological cardiac growth and heart failure in transgenic mice. In the present study, we analyzed the roles of miR-195 in cardiomyocyte hypertrophy and found that miR-195 was greatly upregulated during isoprenaline-induced cardiomyocyte hypertrophy. By using mRNA microarray and molecular approach, we identified a novel putative target of miR-195 called high-mobility group A1 (HMGA1). Total mRNA microarray showed that HMGA1 was downregulated in primary cardiomyocytes that overexpressed miR-195. Using luciferase activity assay, we demonstrated that miR-195 interacts with the 3'-untranslated region of HMGA1 mRNA. Moreover, we showed that miR-195 in primary cardiomyocytes downregulates the expression of HMGA1 at the protein level. Taken together, our data demonstrated that miR-195 can negatively regulate a new target, HMGA1, which is involved in cardiomyocyte hypertrophy.
引用
收藏
页码:538 / 544
页数:7
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