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ZFIN ID: ZDB-PUB-140317-25
An optogenetic gene expression system with rapid activation and deactivation kinetics
Motta-Mena, L.B., Reade, A., Mallory, M.J., Glantz, S., Weiner, O.D., Lynch, K.W., and Gardner, K.H.
Date: 2014
Source: Nature Chemical Biology   10(3): 196-202 (Journal)
Registered Authors: Reade, Anna
Keywords: none
MeSH Terms:
  • Activating Transcription Factors/radiation effects*
  • Animals
  • Bacterial Proteins/genetics*
  • Cell Line
  • Gene Expression/genetics*
  • Kinetics
  • Light*
  • Models, Biological
  • Optogenetics*
  • Promoter Regions, Genetic
  • RNA-Binding Proteins/metabolism
  • T-Lymphocytes/metabolism
  • Zebrafish/genetics
PubMed: 24413462 Full text @ Nat. Chem. Biol.

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.