中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
MicroRNAs modulate the Wnt signaling pathway through targeting its inhibitors

文献类型:期刊论文

作者Liu, YG; Huang, TW; Zhao, XL; Cheng, LP
刊名BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
出版日期2011
卷号408期号:2页码:259-264
关键词MicroRNA Inhibitors Wnt/beta-catenin pathway Gsk3b Wnt1-cre Dicer (Dicer1) conditional knockout
通讯作者Cheng, LP (reprint author), Chinese Acad Sci, State Key Lab Neurosci, Inst Neurosci, Shanghai Inst Biol Sci, 320 Yue Yang Rd, Shanghai 200031, Peoples R China.,lpcheng@ion.ac.cn
英文摘要Increasing evidence indicates that microRNAs (miRNAs) play important roles in mouse brain development. We and several other reports recently have demonstrated that Wnt1-cre-mediated loss of Dicer, the key enzyme for miRNA biosynthesis, results in malformation of the midbrain and cerebellum and failure of neural crest and dopaminergic differentiation. The underlying mechanisms, however, remain poorly understood. The resemblance of some of the phenotypes in the Wnt1-cre Dicer conditional knockout embryos and Wnt1(-/-),Wnt1(-/-);Wnt3(-/-) and Wnt1-cre;beta-cateninn(flox/flox) knockout embryos reminds us that loss of miRNA may disrupt the Wnt-beta-catenin signaling. Here we provide evidence that miRNAs modulate the Wnt signaling pathway through targeting its inhibitors. First, we predicted miRNA binding sites in the 3' UTRs of candidate inhibitors of the Wnt signaling pathway and luciferase assays revealed that several inhibitors of Wnt signaling pathway were targeted by miRNAs. Second, we demonstrated that several miRNAs could modulate the expression of Gsk3b. an inhibitor of Wnt signaling, post-transcriptional in 293T cells. Third, we found that several miRNAs were able to regulate the Wnt-beta-catenin signaling activity in 293T cells. More interestingly, the expression of beta-catenin protein was dramatically reduced in the Wnt1-cre-meidiated Dicer knockout brain tissue compared with control. Our studies therefore suggest that miRNAs might exert their functions, at least in part, by modulating the Wnt signaling pathway through targeting its inhibitors. (C) 2011 Elsevier Inc. All rights reserved.
学科主题Biochemistry & Molecular Biology; Biophysics
类目[WOS]Biochemistry & Molecular Biology ; Biophysics
关键词[WOS]NEURAL CREST ; BETA-CATENIN ; INT-1 PROTOONCOGENE ; MIDBRAIN ; MALFORMATION ; PROGENITORS ; FAILURE ; BRAIN ; DICER ; GENE
收录类别SCI
语种英语
WOS记录号WOS:000290606200012
版本出版稿
源URL[http://202.127.25.143/handle/331003/740]  
专题上海生化细胞研究所_上海生科院生化细胞研究所
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Liu, YG,Huang, TW,Zhao, XL,et al. MicroRNAs modulate the Wnt signaling pathway through targeting its inhibitors[J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS,2011,408(2):259-264.
APA Liu, YG,Huang, TW,Zhao, XL,&Cheng, LP.(2011).MicroRNAs modulate the Wnt signaling pathway through targeting its inhibitors.BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS,408(2),259-264.
MLA Liu, YG,et al."MicroRNAs modulate the Wnt signaling pathway through targeting its inhibitors".BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS 408.2(2011):259-264.

入库方式: OAI收割

来源:上海生物化学与细胞生物学研究所

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