Literature DB >> 24213537

TALEN-based knockout library for human microRNAs.

Young-Kook Kim1, Gabbine Wee, Joha Park, Jongkyu Kim, Daehyun Baek, Jin-Soo Kim, V Narry Kim.   

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.

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Year:  2013        PMID: 24213537     DOI: 10.1038/nsmb.2701

Source DB:  PubMed          Journal:  Nat Struct Mol Biol        ISSN: 1545-9985            Impact factor:   15.369


  42 in total

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2.  Targeted genome engineering in human cells with the Cas9 RNA-guided endonuclease.

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4.  miR-200bc/429 cluster targets PLCgamma1 and differentially regulates proliferation and EGF-driven invasion than miR-200a/141 in breast cancer.

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5.  Conserved MicroRNA miR-8/miR-200 and its target USH/FOG2 control growth by regulating PI3K.

Authors:  Seogang Hyun; Jung Hyun Lee; Hua Jin; JinWu Nam; Bumjin Namkoong; Gina Lee; Jongkyeong Chung; V Narry Kim
Journal:  Cell       Date:  2009-12-11       Impact factor: 41.582

6.  Targeted genome editing in human cells with zinc finger nucleases constructed via modular assembly.

Authors:  Hye Joo Kim; Hyung Joo Lee; Hyojin Kim; Seung Woo Cho; Jin-Soo Kim
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7.  Targeting human microRNA genes using engineered Tal-effector nucleases (TALENs).

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8.  Magnetic separation and antibiotics selection enable enrichment of cells with ZFN/TALEN-induced mutations.

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9.  A reciprocal repression between ZEB1 and members of the miR-200 family promotes EMT and invasion in cancer cells.

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10.  TopHat2: accurate alignment of transcriptomes in the presence of insertions, deletions and gene fusions.

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  38 in total

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3.  3' Uridylation Confers miRNAs with Non-canonical Target Repertoires.

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Review 5.  In silico structure-based approaches to discover protein-protein interaction-targeting drugs.

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6.  Knockout of miR-221 and miR-222 reveals common and specific targets for paralogous miRNAs.

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7.  TargetLink, a new method for identifying the endogenous target set of a specific microRNA in intact living cells.

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Review 8.  Genome-Editing Technologies: Principles and Applications.

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Review 10.  A guide to genome engineering with programmable nucleases.

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Journal:  Nat Rev Genet       Date:  2014-04-02       Impact factor: 53.242

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