核糖核酸
信号转导
细胞生物学
化学
合成生物学
纳米技术
计算生物学
生物
生物化学
材料科学
基因
作者
Chaoqun Wu,Ruo‐Yue Wu,Qiulong Zhang,Liangliang Wang,Yang Wang,Chu Dai,Chenxi Zhang,Liang Xu
标识
DOI:10.1002/ange.202319309
摘要
Abstract Engineering of genetic networks with a rtificial s ignaling p athways (ASPs) can reprogram cellular responses and phenotypes under different circumstances for a variety of diagnostic and therapeutic purposes. However, construction of ASPs between originally independent endogenous genes in mammalian cells is highly challenging. Here we report an amplifiable RNA circuit that can theoretically build regulatory connections between any endogenous genes in mammalian cells. We harness the system of catalytic hairpin assembly with combination of controllable CRISPR‐Cas9 function to transduce the signals from distinct messenger RNA expression of trigger genes into manipulation of target genes. Through introduction of these RNA‐based genetic circuits, mammalian cells are endowed with autonomous capabilities to sense the changes of RNA expression either induced by ligand stimuli or from various cell types and control the cellular responses and fates via apoptosis‐related ASPs. Our design provides a generalized platform for construction of ASPs inside the genetic networks of mammalian cells based on differentiated RNA expression.
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