miR-200b mediates post-transcriptional repression of ZFHX1B

被引:145
作者
Christoffersen, Nanna Ronbjerg
Silahtaroglu, Asli
Orom, Ulf Andersson
Kauppinen, Sakari
Lund, Anders H.
机构
[1] Biotech Res & Innovat Ctr, DK-2200 Copenhagen, Denmark
[2] Univ Copenhagen, Wilhelm Johannsen Ctr Funct Genome Res, Dept Cellular & Mol Med, DK-2200 Copenhagen, Denmark
[3] Univ Copenhagen, Fac Hlth Sci, Copenhagen, Denmark
关键词
microRNA; translational repression; E-cadherin; miR-200b; ZFHX1B;
D O I
10.1261/rna.586807
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
MicroRNAs have important functions during animal development and homeostasis through post-transcriptional regulation of their cognate mRNA targets. ZFHX1B is a transcriptional repressor involved in the TGF beta signaling pathway and in processes of epithelial to mesenchymal transition via regulation of E-cadherin. We show that Zfhx1b and miR-200b are regionally coexpressed in the adult mouse brain and that miR-200b represses the expression of Zfhx1b via multiple sequence elements present in the 3'- untranslated region. Overexpression of miR-200b leads to repression of endogenous ZFHX1B, and inhibition of miR-200b relieves the repression of ZFHX1B. In accordance with these findings, miR-200b regulates the activity of the E-cadherin promoter.
引用
收藏
页码:1172 / 1178
页数:7
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