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• W4220794922 abstract "A key challenge in designing intelligent artificial gene circuits is generating flexible connections between arbitrary components and directly coupling them with endogenous signaling pathways. The CRISPR signal conductor based on conditionally inducible artificial transcriptional regulators can link classic cellular protein signals with targeted gene expression, but there are still problems with multiple signal processing and gene delivery. With the discovery and characterization of new Cas systems and long noncoding RNA (lncRNA) functional motifs, and because of the compatibility of guide RNA with noncoding RNA elements at multiple sites, it is increasingly possible to solve these problems. In this study, we developed CRISPR signal conductor version 2.0 by integrating various lncRNA functional motifs into different parts of the crRNA in the CRISPR-dCasΦ system. This system can directly regulate the expression of target genes by recruiting cellular endogenous transcription factors and efficiently sense a variety of protein signals that are not detected by a classical synthetic system. The new system solved the problems of background leakage and insensitive signaling responses and enabled the construction of logic gates with as many as six input signals, which can be used to specifically target cancer cells. By rewiring endogenous signaling networks, we further demonstrated the effectiveness and biosafety of this system for in vivo cancer gene therapy." @default.
• W4220794922 created "2022-04-03" @default.
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• W4220794922 date "2022-03-15" @default.
• W4220794922 modified "2023-10-10" @default.
• W4220794922 title "CRISPR signal conductor 2.0 for redirecting cellular information flow" @default.
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• W4220794922 doi "https://doi.org/10.1038/s41421-021-00371-1" @default.
• W4220794922 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/35288535" @default.
• W4220794922 hasPublicationYear "2022" @default.
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