An optogenetic gene expression system with rapid activation and deactivation kinetics

• Published in: Nature chemical biology Vol. 10; no. 3; pp. 196 - 202
• Main Authors: Motta-Mena, Laura B, Reade, Anna, Mallory, Michael J, Glantz, Spencer, Weiner, Orion D, Lynch, Kristen W, Gardner, Kevin H
• Format: Journal Article
• Language: English
• Published: New York Nature Publishing Group US 01.03.2014; Nature Publishing Group
• Subjects: 13; 13/95; 631/1647/245; 631/337/572; 631/92/552; 631/92/96; 82; 96; 96/44; Activating Transcription Factors - radiation effects; Animals; Bacterial Proteins - genetics; Biochemical Engineering; Biochemistry; Bioorganic Chemistry; Cell Biology; Cell Line; Cellular biology; Chemistry; Chemistry/Food Science; Danio rerio; Deoxyribonucleic acid; DNA; Embryos; Gene expression; Gene Expression - genetics; Kinetics; Light; Mammals; Models, Biological; Optogenetics; Promoter Regions, Genetic; Proteins; RNA-Binding Proteins - metabolism; T-Lymphocytes - metabolism; Toxicity; Zebrafish - genetics
• ISSN: 1552-4450; 1552-4469
• DOI: 10.1038/nchembio.1430

Optogenetic systems permit the temporal and spatial control of gene expression using light. A variant of the LOV domain–containing EL222 protein displays responsive blue light–gated transcriptional control of genes in zebrafish and in mammalian cell lines. Optogenetic gene expression systems can control transcription with spatial and temporal detail unequaled with traditional inducible promoter systems. However, current eukaryotic light-gated transcription systems are limited by toxicity, dynamic range or slow activation and deactivation. Here we present an optogenetic gene expression system that addresses these shortcomings and demonstrate its broad utility. Our approach uses an engineered version of EL222, a bacterial light-oxygen-voltage protein that binds DNA when illuminated with blue light. The system has a large (>100-fold) dynamic range of protein expression, rapid activation (<10 s) and deactivation kinetics (<50 s) and a highly linear response to light. With this system, we achieve light-gated transcription in several mammalian cell lines and intact zebrafish embryos with minimal basal gene activation and toxicity. Our approach provides a powerful new tool for optogenetic control of gene expression in space and time.