Abstract
AbstractPrecise control of gene expression is critical for biological research and biotechnology. However, transient plasmid transfections in mammalian cells produce a wide distribution of copy numbers per cell, and consequently, high expression heterogeneity. Here, we report plasmid-based synthetic circuits – Equalizers – that buffer copy-number variation at the single-cell level. Equalizers couple a transcriptional negative feedback loop with post-transcriptional incoherent feedforward control. Computational modeling suggests that the combination of these two topologies enables Equalizers to operate over a wide range of plasmid copy numbers. We demonstrate experimentally that Equalizers outperform other gene dosage compensation topologies and produce as low cell-to-cell variation as chromosomally integrated genes. We also show that episome-encoded Equalizers enable the rapid generation of extrachromosomal cell lines with stable and uniform expression. Overall, Equalizers are simple and versatile devices for homogeneous gene expression and can facilitate the engineering of synthetic circuits that function reliably in every cell.
Publisher
Springer Science and Business Media LLC
Subject
General Physics and Astronomy,General Biochemistry, Genetics and Molecular Biology,General Chemistry
Reference67 articles.
1. Rice, A. M. & McLysaght, A. Dosage sensitivity is a major determinant of human copy number variant pathogenicity. Nat. Commun. 8, 14366 (2017).
2. Kfir, S. et al. Pathway- and expression level-dependent effects of oncogenic n-ras: p27(kip1) mislocalization by the ral-GEF pathway and erk-mediated interference with smad signaling. Mol. Cell Biol. 25, 8239–8250 (2005).
3. Liu, Y. & Lehmann, M. A genomic response to the yeast transcription factor GAL4 in drosophila. Fly 2, 92–98 (2008).
4. Wang, X. & Li, S. Protein mislocalization: mechanisms, functions and clinical applications in cancer. Biochim. Biophys. Acta 1846, 13–25 (2014).
5. Moriya, H. Quantitative nature of overexpression experiments. Mol. Biol. Cell 26, 3932–3939 (2015).
Cited by
13 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献