Abstract
Identifying the neuronal ensembles that respond to specific stimuli and mapping their projection patterns in living animals are fundamental challenges in neuroscience. To this end, we engineered a synthetic promoter, the enhanced synaptic activity-responsive element (E-SARE), that drives neuronal activity-dependent gene expression more potently than other existing immediate-early gene promoters. Expression of a drug-inducible Cre recombinase downstream of E-SARE enabled imaging of neuronal populations that respond to monocular visual stimulation and tracking of their long-distance thalamocortical projections in living mice. Targeted cell-attached recordings and calcium imaging of neurons in sensory cortices revealed that E-SARE reporter expression correlates with sensory-evoked neuronal activity at the single-cell level and is highly specific to the type of stimuli presented to the animals. This activity-dependent promoter can expand the repertoire of genetic approaches for high-resolution anatomical and functional analysis of neural circuits.
| Original language | English |
|---|---|
| Pages (from-to) | 889-895 |
| Number of pages | 7 |
| Journal | Nature Methods |
| Volume | 10 |
| Issue number | 9 |
| DOIs | |
| Publication status | Published - Sept 2013 |
Keywords / Materials (for Non-textual outputs)
- Molecular neuroscience
- Genetic mapping
- DNA probes
- Somatosensory system