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基于 TALEN 的人类 microRNAs 敲除文库。

TALEN-based knockout library for human microRNAs.

机构信息

1] Center for RNA Research, Institute for Basic Science, Seoul, Korea. [2] School of Biological Sciences, Seoul National University, Seoul, Korea. [3].

出版信息

Nat Struct Mol Biol. 2013 Dec;20(12):1458-64. doi: 10.1038/nsmb.2701. Epub 2013 Nov 10.

Abstract

Various technical tools have been developed to probe the functions of microRNAs (miRNAs), yet their application has been limited by low efficacy and specificity. To overcome the limitations, we used transcription activator-like effector nucleases (TALENs) to knock out human miRNA genes. We designed and produced a library of 540 pairs of TALENs for 274 miRNA loci, focusing on potentially important miRNAs. The knockout procedure takes only 2-4 weeks and can be applied to any cell type. As a case study, we generated knockout cells for two related miRNAs, miR-141 and miR-200c, which belong to the highly conserved miR-200 family. Interestingly, miR-141 and miR-200c, despite their overall similarity, suppress largely nonoverlapping groups of targets, thus suggesting that functional miRNA-target interaction requires strict seed-pairing. Our study illustrates the potency of TALEN technology and provides useful resources for miRNA research.

摘要

已经开发出各种技术工具来探测 microRNAs(miRNAs)的功能,但它们的应用受到低效和特异性的限制。为了克服这些限制,我们使用转录激活因子样效应物核酸酶(TALENs)敲除人类 miRNA 基因。我们设计并生成了一个包含 540 对 TALEN 的文库,针对 274 个 miRNA 基因座,重点是可能重要的 miRNAs。敲除过程仅需 2-4 周,可应用于任何细胞类型。作为一个案例研究,我们生成了两个相关 miRNA(miR-141 和 miR-200c)的敲除细胞,它们属于高度保守的 miR-200 家族。有趣的是,miR-141 和 miR-200c 尽管整体相似,但抑制的靶基因群却大不相同,这表明功能 miRNA-靶基因相互作用需要严格的种子配对。我们的研究说明了 TALEN 技术的威力,并为 miRNA 研究提供了有用的资源。

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