| 论文题目: | Engineering Translational Activators with CRISPR-Cas System |
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| 作者: | Du Pei, Miao Chensi, Lou Qiuli, Wang Zefeng, and Lou Chunbo*. |
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| 刊物名称: | ACS Synth Biol |
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| 年份: | 2015 |
| 影响因子: | 5.037 |
| 论文下载: | 下载地址 |
| 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 exchangeable RNA modules. Csy4, a 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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