| Literature DB >> 27271196 |
Garrett G Gross1, Christoph Straub2, Jimena Perez-Sanchez3,4, William P Dempsey1, Jason A Junge1, Richard W Roberts5, Le A Trinh1, Scott E Fraser1, Yves De Koninck3,4, Paul De Koninck3,4, Bernardo L Sabatini2, Don B Arnold1.
Abstract
Although neuronal activity can be modulated using a variety of techniques, there are currently few methods for controlling neuronal connectivity. We introduce a tool (GFE3) that mediates the fast, specific and reversible elimination of inhibitory synaptic inputs onto genetically determined neurons. GFE3 is a fusion between an E3 ligase, which mediates the ubiquitination and rapid degradation of proteins, and a recombinant, antibody-like protein (FingR) that binds to gephyrin. Expression of GFE3 leads to a strong and specific reduction of gephyrin in culture or in vivo and to a substantial decrease in phasic inhibition onto cells that express GFE3. By temporarily expressing GFE3 we showed that inhibitory synapses regrow following ablation. Thus, we have created a simple, reversible method for modulating inhibitory synaptic input onto genetically determined cells.Entities:
Mesh:
Substances:
Year: 2016 PMID: 27271196 PMCID: PMC5312699 DOI: 10.1038/nmeth.3894
Source DB: PubMed Journal: Nat Methods ISSN: 1548-7091 Impact factor: 28.547