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RNA结合蛋白Dnd1抑制微小RNA接近靶mRNA。

RNA-binding protein Dnd1 inhibits microRNA access to target mRNA.

作者信息

Kedde Martijn, Strasser Markus J, Boldajipour Bijan, Oude Vrielink Joachim A F, Slanchev Krasimir, le Sage Carlos, Nagel Remco, Voorhoeve P Mathijs, van Duijse Josyanne, Ørom Ulf Andersson, Lund Anders H, Perrakis Anastassis, Raz Erez, Agami Reuven

机构信息

The Netherlands Cancer Institute, Division of Tumor Biology, Plesmanlaan 121, 1066CX, Amsterdam, The Netherlands.

出版信息

Cell. 2007 Dec 28;131(7):1273-86. doi: 10.1016/j.cell.2007.11.034.

Abstract

MicroRNAs (miRNAs) are inhibitors of gene expression capable of controlling processes in normal development and cancer. In mammals, miRNAs use a seed sequence of 6-8 nucleotides (nt) to associate with 3' untranslated regions (3'UTRs) of mRNAs and inhibit their expression. Intriguingly, occasionally not only the miRNA-targeting site but also sequences in its vicinity are highly conserved throughout evolution. We therefore hypothesized that conserved regions in mRNAs may serve as docking platforms for modulators of miRNA activity. Here we demonstrate that the expression of dead end 1 (Dnd1), an evolutionary conserved RNA-binding protein (RBP), counteracts the function of several miRNAs in human cells and in primordial germ cells of zebrafish by binding mRNAs and prohibiting miRNAs from associating with their target sites. These effects of Dnd1 are mediated through uridine-rich regions present in the miRNA-targeted mRNAs. Thus, our data unravel a novel role of Dnd1 in protecting certain mRNAs from miRNA-mediated repression.

摘要

微小RNA(miRNA)是基因表达的抑制剂,能够控制正常发育和癌症中的各种过程。在哺乳动物中,miRNA利用6-8个核苷酸(nt)的种子序列与mRNA的3'非翻译区(3'UTR)结合并抑制其表达。有趣的是,偶尔不仅miRNA靶向位点,其附近的序列在整个进化过程中也高度保守。因此,我们推测mRNA中的保守区域可能作为miRNA活性调节剂的对接平台。在这里,我们证明了死端1(Dnd1)的表达,一种进化上保守的RNA结合蛋白(RBP),通过结合mRNA并阻止miRNA与其靶位点结合,抵消了人类细胞和斑马鱼原始生殖细胞中几种miRNA的功能。Dnd1的这些作用是通过miRNA靶向的mRNA中存在的富含尿苷的区域介导的。因此,我们的数据揭示了Dnd1在保护某些mRNA免受miRNA介导的抑制方面的新作用。

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