@article {68117,
	title = {An essential experimental control for functional connectivity mapping with optogenetics.},
	journal = {bioRxiv},
	year = {2022},
	month = {2022 May 28},
	abstract = {<p>To establish functional connectivity between two candidate neurons that might form a circuit element, a common approach is to activate an optogenetic tool such as Chrimson in the candidate pre-synaptic neuron and monitor fluorescence of the calcium-sensitive indicator GCaMP in a candidate post-synaptic neuron. While performing such experiments, we found that low levels of leaky Chrimson expression can lead to strong artifactual GCaMP signals in presumptive postsynaptic neurons even when Chrimson is not intentionally expressed in any particular neurons. Withholding all-<em>trans</em>\&nbsp;retinal, the chromophore required as a co-factor for Chrimson response to light, eliminates GCaMP signal but does not provide an experimental control for leaky Chrimson expression. Leaky Chrimson expression appears to be an inherent feature of current Chrimson transgenes, since artifactual connectivity was detected with Chrimson transgenes integrated into three different genomic locations (two insertions tested in larvae; a third insertion tested in the adult fly). These false-positive signals may complicate the interpretation of functional connectivity experiments. We illustrate how a no-Gal4 negative control improves interpretability of functional connectivity assays. We also propose a simple but effective procedure to identify experimental conditions that minimize potentially incorrect interpretations caused by leaky Chrimson expression.</p>
},
	doi = {10.1101/2022.05.26.493610},
	url = {https://doi.org/10.1101/2022.05.26.493610},
	author = {David Tadres and Hiroshi M. Shiozaki and Ibrahim Tastekin and David L. Stern and Matthieu Louis}
}
