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靶向保护因子揭示了miR-430对Nodal激动剂和拮抗剂的抑制及平衡作用。

Target protectors reveal dampening and balancing of Nodal agonist and antagonist by miR-430.

作者信息

Choi Wen-Yee, Giraldez Antonio J, Schier Alexander F

机构信息

Department of Molecular and Cellular Biology, Harvard University, 16 Divinity Avenue, Cambridge, MA 02138, USA.

出版信息

Science. 2007 Oct 12;318(5848):271-4. doi: 10.1126/science.1147535. Epub 2007 Aug 30.

Abstract

MicroRNAs (miRNAs) repress hundreds of target messenger RNAs (mRNAs), but the physiological roles of specific miRNA-mRNA interactions remain largely elusive. We report that zebrafish microRNA-430 (miR-430) dampens and balances the expression of the transforming growth factor-beta (TGF-beta) Nodal agonist squint and the TGF-beta Nodal antagonist lefty. To disrupt the interaction of specific miRNA-mRNA pairs, we developed target protector morpholinos complementary to miRNA binding sites in target mRNAs. Protection of squint or lefty mRNAs from miR-430 resulted in enhanced or reduced Nodal signaling, respectively. Simultaneous protection of squint and lefty or absence of miR-430 caused an imbalance and reduction in Nodal signaling. These findings establish an approach to analyze the in vivo roles of specific miRNA-mRNA pairs and reveal a requirement for miRNAs in dampening and balancing agonist/antagonist pairs.

摘要

微小RNA(miRNA)可抑制数百种靶信使核糖核酸(mRNA),但特定miRNA-mRNA相互作用的生理作用仍大多不为人知。我们报告称,斑马鱼微小RNA-430(miR-430)可抑制并平衡转化生长因子-β(TGF-β)信号通路激动剂squint和TGF-β信号通路拮抗剂lefty的表达。为破坏特定miRNA-mRNA对的相互作用,我们开发了与靶mRNA中miRNA结合位点互补的靶标保护吗啉代寡核苷酸。对squint或lefty mRNA进行保护使其免受miR-430的影响,分别导致Nodal信号增强或减弱。同时对squint和lefty进行保护或缺失miR-430会导致Nodal信号失衡并减弱。这些发现建立了一种分析特定miRNA-mRNA对体内作用的方法,并揭示了miRNA在抑制和平衡激动剂/拮抗剂对方面的必要性。

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