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Lin28a通过不同机制与RNA结合,对微小RNA(miRNA)水平产生正向和负向影响。

Lin28a uses distinct mechanisms of binding to RNA and affects miRNA levels positively and negatively.

作者信息

Nowak Jakub Stanislaw, Hobor Fruzsina, Downie Ruiz Velasco Angela, Choudhury Nila Roy, Heikel Gregory, Kerr Alastair, Ramos Andres, Michlewski Gracjan

机构信息

Wellcome Trust Centre for Cell Biology, University of Edinburgh, Edinburgh, EH9 3BF, United Kingdom.

Institute of Structural and Molecular Biology, University College London, London, WC1E 6XA, United Kingdom.

出版信息

RNA. 2017 Mar;23(3):317-332. doi: 10.1261/rna.059196.116. Epub 2016 Nov 23.

Abstract

Lin28a inhibits the biogenesis of let-7 miRNAs by triggering the polyuridylation and degradation of their precursors by terminal uridylyltransferases TUT4/7 and 3'-5' exoribonuclease Dis3l2, respectively. Previously, we showed that Lin28a also controls the production of neuro-specific miRNA-9 via a polyuridylation-independent mechanism. Here we reveal that the sequences and structural characteristics of pre-let-7 and pre-miRNA-9 are eliciting two distinct modes of binding to Lin28a. We present evidence that Dis3l2 controls miRNA-9 production. Finally, we show that the constitutive expression of untagged Lin28a during neuronal differentiation in vitro positively and negatively affects numerous other miRNAs. Our findings shed light on the role of Lin28a in differentiating cells and on the ways in which one RNA-binding protein can perform multiple roles in the regulation of RNA processing.

摘要

Lin28a分别通过末端尿苷酰转移酶TUT4/7引发let-7 miRNA前体的多聚尿苷酸化以及3'-5'外切核糖核酸酶Dis3l2导致其降解,从而抑制let-7 miRNA的生物合成。此前,我们发现Lin28a还通过一种不依赖多聚尿苷酸化的机制控制神经特异性miRNA-9的产生。在此我们揭示,pre-let-7和pre-miRNA-9的序列及结构特征引发了与Lin28a结合的两种不同模式。我们提供证据表明Dis3l2控制miRNA-9的产生。最后,我们表明在体外神经元分化过程中无标签Lin28a的组成型表达对许多其他miRNA产生正负两方面的影响。我们的研究结果揭示了Lin28a在分化细胞中的作用,以及一种RNA结合蛋白在RNA加工调控中发挥多种作用的方式。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4eca/5311490/6fc697076395/317f01.jpg

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