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Section on Neural Function


Fluorescent images of larval brains showing neurons genetically targeted by the Split Gal4 technique. The brain in red, shows a cell group of interest that is parsed into the subsets shown in green using Split Gal4 hemidrivers. One hemidriver expresses in the pattern shown for the red brain, while the others express in random patterns such as the one shown in blue, which intersects the red pattern only in select neurons.We are actively engaged in generating tools for the identification and analysis of neuronal circuits in the fly. We have developed techniques for the constitutive suppression (White et. al., 2001) and enhancement of neuronal excitability (Luan, Lemon et al., 2006; Nitabach et al. 2006), as well as a tool for acutely activating neurons in response to small temperature shifts (Peabody et al., 2009).

We have also developed general methods for targeting genetic manipulations to cell types of interest. These include the intersectional Split Gal4 system (Luan et al., 2006), which permits refined targeting of transgenes to small subsets of neurons and has been augmented by our recently introduced suppressor of Split Gal4 activity, the Killer Zipper (Dolan, Luan et al., 2017).

We have also developed tools for targeting neurons that express a given gene of interest. The first of these was the T2A-Gal4 In-Frame-Fusion method (“T2A-GIFF;” Diao and White, 2012), which was followed by the more versatile and modular technology of “Trojan exons” (Diao et al., 2015). Trojan exons are interchangeable synthetic exons that are preceded by a universal splice acceptor and which can be inserted in-frame into a coding intron in any gene of interest. Cells expressing a gene can thus be targeted with high fidelity.

All of our published plasmids and fly lines are publicly available, most of them from public repositories (see below). Our published constructs for the Split Gal4 system, Trojan exons, Killer Zipper, and various effectors, such as EKO and NaChBac are available through both Addgene and the Drosophila Genomic Resources Center. If you are unable to find what you want, please contact us.

The figure shows schematically how synthetic exons, such as the T-GEM Trojan Exon depicted, can be inserted into an intron of a gene of interest (Gene; coding regions are shown in black) to force expression of the transcription factor Gal4 in the same pattern as the gene. Many of our published fly lines (particularly those that represent commonly used genetic tools) have been deposited at the Bloomington Drosophila Stock Center where they are publicly available. Other lines created by the lab are available upon request.