| 论文题目: | Engineering Translational Activators with CRISPR-Cas System |
|---|---|
| 作者: | Du Pei , Miao Chensi , Lou Qiuli , Wang Zefeng* , and Lou Chunbo*. |
| 联系作者: | |
| 刊物名称: | Acs Synthetic Biology |
| 期: | 1 |
| 卷: | 5 |
| 页: | 74-80 |
| 年份: | 2016 |
| 影响因子: | 5.037 |
| 论文下载: | http://pubs.acs.org/doi/abs/10.1021/acssynbio.5b00130 |
| 摘要: | RNA parts often serve as. critical components in genetic engineering. Here we report a design of translational activators which is composed of an RNA endoribonuclease (Csy4) and two exchaneable RNA modules. Csy4, member of Cas endoribonuclease, cleaves at a specific recognition site; this cleavage releases a cis-repressive RNA module (crRNA) from the masked ribosome binding site (RBS), which subsequently allows the downstream translation initiation. Unlike small RNA as a translational activator, the endoribonuclease-based activator is able, to efficiently unfold the perfect RBS-crRNA pairing. As an exchangeable module, the crRNA-RBS duplex was forwardly and reversely engineered to modulate the dynamic range of translational activity. We further showed that Csy4 and its recognition site, together as a module, can also be replaced by orthogonal endoribonuclease-recognition site homologues. These modularly structured, high-performance translational activators would endow the programming of gene expression in, the translation level with higher feasibility. |
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