Application of TALEs, CRISPR/Cas and sRNAs as trans-acting regulators in prokaryotes

被引:27
作者
Copeland, Matthew F. [1 ]
Politz, Mark C. [1 ]
Pfleger, Brian F. [1 ]
机构
[1] Univ Wisconsin, Dept Chem & Biol Engn, Madison, WI 53706 USA
基金
美国国家科学基金会;
关键词
SEQUENCE-SPECIFIC CONTROL; DNA-BINDING SPECIFICITY; ARTIFICIAL SMALL RNAS; ESCHERICHIA-COLI; GENE-EXPRESSION; EFFECTORS; RECOGNITION; ACTIVATION; BACTERIA; SYSTEMS;
D O I
10.1016/j.copbio.2014.02.010
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The last several years have witnessed an explosion in the understanding and use of novel, versatile trans-acting elements. TALEs, CRISPR/Cas, and sRNAs can be easily fashioned to bind any specific sequence of DNA (TALEs, CRISPR/Cas) or RNA (sRNAs) because of the simple rules governing their interactions with nucleic acids. This unique property enables these tools to repress the expression of genes at the transcriptional or post-transcriptional levels, respectively, without prior manipulation of cis-acting and/or chromosomal target DNA sequences. These tools are now being harnessed by synthetic biologists, particularly those in the eukaryotic community, for genome-wide regulation, editing, or epigenetic studies. Here we discuss the exciting opportunities for using TALEs, CRISPR/Cas, and sRNAs as synthetic trans-acting regulators in prokaryotes.
引用
收藏
页码:46 / 54
页数:9
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