Experimental evidences for hsa-miR-497-5p as a negative regulator of SMAD3 gene expression

被引:22
|
作者
Jafarzadeh, Meisam [1 ]
Soltani, Bahram M. [1 ]
Dokanehiifard, Sadat [1 ]
Kay, Maryam [1 ]
Aghdami, Nasser [2 ]
Hosseinkhani, Saman [3 ]
机构
[1] Tarbiat Modares Univ, Fac Biol Sci, Dept Mol Genet, Tehran, Iran
[2] Royan Inst, Dept Regenerat Med, Tehran, Iran
[3] Tarbiat Modares Univ, Fac Biol Sci, Dept Biochem, Tehran, Iran
关键词
Hsa-miR-497-5p; SMAD3; TGF beta signaling pathway; MICRORNA; APOPTOSIS; PROLIFERATION;
D O I
10.1016/j.gene.2016.04.003
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The SMAD family comprises of transcription factors that function as signal transducers of transforming growth factor (TOM) superfamily members. MiRNAs are a class of small noncoding RNAs that may play a major role in post transcriptional regulation of SMAD genes. Here, we intended to investigate if hsa-miR-497-5p is capable of regulating SMAD3 gene expression. Hsa-miR-497-5p was bioinformatically predicted as a candidate regulator of SMAD3 gene expression and then, hsa-miR-497-5p expression status was analyzed in different cell lines using RT-qPCR. Overexpression of hsa-miR-497-5p in HEK293t cells resulted in downregulation of SMAD3 which was detected by RT-qPCR and western analysis. Further, dual luciferase assay results supported direct interaction of hsa-miR-497-5p with 3'-UTR sequences of SMAD3 transcript. Overexpression of hsa-miR-497-5p in HEK293t cells resulted in cell cycle arrest in G0/G1 phase, detected by flow cytometry. Overall, accumulative results indicated that hsa-miR-497-5p by targeting SMAD3 is potentially one of the regulators of the Tap signaling pathway. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:216 / 221
页数:6
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