Systematic elimination or silencing of groups of neurons will produce a map of brain regions and neurons critical for different behaviors that will pave the way for understanding how specific neurons encode and transform information. One way to assess how a neuron or a group of neurons participate in a behavior or guidance decision is to eliminate their function and assay the phenotypic consequences. For example, GAL4 lines have been used to target expression of toxins or genes that initiate programmed cell death to particular cell populations in the embryonic nervous system to show that these cells serve

as guideposts for axon guidance decisions of other neurons (Hidalgo et al., 1995, Lin et al., 1995 and Hidalgo and Brand, 1997). Expression of bacterial toxins LY294002 chemical structure from Diphtheria and Ricin kills cells by disrupting protein synthesis (Kunes and Steller, 1991, Bellen et al., 1992 and Moffat et al., 1992). Transgenes expressing the most potent forms can be lethal, but attenuated and inducible versions exist (Bellen et al., 1992, Lin et al., 1995, Smith et al., 1996, Hidalgo and Brand, 1997, Han et al., 2000 and Allen et al.,

2002). Expression of the proapoptotic genes grim, reaper, or hid can trigger programmed cell death ( Zhou et al., 1997); simultaneous expression of several apoptotic genes may be even more effective ( Wing et al., 1998). Proapoptotic gene expression was used to determine the behavioral role of the cells releasing eclosion hormone ( McNabb et al., 1997). The efficacy of the cell killers varies in different Montelukast Sodium neuronal types Akt molecular weight and developmental

stages. Coexpression of a visible reporter such as UAS-GFP is prudent to confirm that the targeted cells have been destroyed. GAL4 lines often express throughout development and the UAS-toxin constructs described are constitutively active, meaning that they begin to kill cells as soon as they are expressed. If the GAL4 expression begins at the same time as the process under study, this is not a problem, but delaying the time of cell death may be desirable if an adult phenotype is under investigation. There are several options for adding temporal control to GAL4 expression that have already been discussed. In addition, a cold-sensitive version of the ricin protein makes cell death dependent on the temperature of the flies (Moffat et al., 1992). Killing a cell is an extreme manipulation that may have undesirable collateral consequences. Silencing a neuron, either by preventing the release of neurotransmitter or by blocking changes in membrane potential (see below) is a more precise way to determine its function. Drosophila neurons release neurotransmitters such as glutamate, GABA, and acetylcholine from synaptic vesicles in response to localized calcium influx through voltage-activated calcium channels.