Understanding functional miRNA-target interactions in vivo by site-specific genome engineering

被引:63
作者
Bassett, Andrew R. [1 ]
Azzam, Ghows [2 ]
Wheatley, Lucy [2 ]
Tibbit, Charlotte [1 ]
Rajakumar, Timothy [2 ]
McGowan, Simon [3 ]
Stanger, Nathan [2 ]
Ewels, Philip Andrew [4 ]
Taylor, Stephen [3 ]
Ponting, Chris P.
Liu, Ji-Long [1 ]
Sauka-Spengler, Tatjana [2 ]
Fulga, Tudor A. [2 ]
机构
[1] Univ Oxford, MRC, Funct Genom Unit, Dept Physiol Anat & Genet, Oxford OX1 3PT, England
[2] Univ Oxford, Weatherall Inst Mol Med, Radcliffe Dept Med, Oxford OX3 9DS, England
[3] Univ Oxford, Weatherall Inst Mol Med, Radcliffe Dept Med, Computat Biol Res Grp, Oxford OX3 9DS, England
[4] Stockholm Univ, Dept Biochem & Biophys, Sci Life Lab, S-10691 Stockholm, Sweden
来源
NATURE COMMUNICATIONS | 2014年 / 5卷
基金
英国医学研究理事会; 欧洲研究理事会;
关键词
CRISPR-CAS9; SYSTEM; HUMAN-CELLS; EFFICIENT; DROSOPHILA; IDENTIFICATION; EXPRESSION; REPRESSION; BINDING; PROTEIN; DESIGN;
D O I
10.1038/ncomms5640
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
MicroRNA (miRNA) target recognition is largely dictated by short 'seed' sequences, and single miRNAs therefore have the potential to regulate a large number of genes. Understanding the contribution of specific miRNA-target interactions to the regulation of biological processes in vivo remains challenging. Here we use transcription activator-like effector nuclease (TALEN) and clustered regularly interspaced short palindromic repeat (CRISPR)/Cas9 technologies to interrogate the functional relevance of predicted miRNA response elements (MREs) to post-transcriptional silencing in zebrafish and Drosophila. We also demonstrate an effective strategy that uses CRISPR-mediated homology-directed repair with short oligonucleotide donors for the assessment of MRE activity in human cells. These methods facilitate analysis of the direct phenotypic consequences resulting from blocking specific miRNA-MRE interactions at any point during development.
引用
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页数:11
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