| Literature DB >> 36257931 |
William C W Chen1,2,3,4,5, Leonid Gaidukov6,7, Yong Lai6,8, Ming-Ru Wu6,9, Jicong Cao6, Michael J Gutbrod10,11, Gigi C G Choi6,12, Rachel P Utomo6,13, Ying-Chou Chen6,8,14, Liliana Wroblewska15, Manolis Kellis10,11, Lin Zhang16, Ron Weiss6,7, Timothy K Lu17,18,19.
Abstract
Precise, scalable, and sustainable control of genetic and cellular activities in mammalian cells is key to developing precision therapeutics and smart biomanufacturing. Here we create a highly tunable, modular, versatile CRISPR-based synthetic transcription system for the programmable control of gene expression and cellular phenotypes in mammalian cells. Genetic circuits consisting of well-characterized libraries of guide RNAs, binding motifs of synthetic operators, transcriptional activators, and additional genetic regulatory elements express mammalian genes in a highly predictable and tunable manner. We demonstrate the programmable control of reporter genes episomally and chromosomally, with up to 25-fold more activity than seen with the EF1α promoter, in multiple cell types. We use these circuits to program the secretion of human monoclonal antibodies and to control T-cell effector function marked by interferon-γ production. Antibody titers and interferon-γ concentrations significantly correlate with synthetic promoter strengths, providing a platform for programming gene expression and cellular function in diverse applications.Entities:
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Year: 2022 PMID: 36257931 PMCID: PMC9579178 DOI: 10.1038/s41467-022-33287-9
Source DB: PubMed Journal: Nat Commun ISSN: 2041-1723 Impact factor: 17.694