Cas9
清脆的
亚基因组mRNA
RNA结合蛋白
计算生物学
核糖核酸
生物
合成生物学
翻译(生物学)
引导RNA
质粒
基因
信使核糖核酸
细胞生物学
遗传学
作者
Moe Hirosawa,Hirohide Saito
标识
DOI:10.1007/978-1-0716-3718-0_12
摘要
Expanding the number of available RNA-binding proteins (RBPs) is vital to establishing posttranscriptional circuits in mammalian cells. We focused on CRISPR-Cas systems and exploited Cas proteins for their versatility as RBPs. The translation of genes encoded in an mRNA becomes regulatable by a Cas protein by inserting a crRNA/sgRNA sequence recognizable by the specific Cas protein into its 5′UTR. These Cas protein-responsive switches vastly expand the available tools in synthetic biology because of the wide range of Cas protein orthologs that can be used as trigger proteins. Here, we describe the design principle of Cas protein-responsive switches, both plasmid and RNA versions, using Streptococcus pyogenes Cas9 (SpCas9) as an example and show an example of its use in mammalian cells, HEK293FT cells.
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