“…As in mammalian epilepsy, in which a large number of genes and neuronal mechanisms have been associated with seizure disorders (McNamara, 1994; Shoffner et al, 1990; Noebels, 2003; Klassen et al, 2011), several studies on Drosophila bang-sensitive mutants have documented a number of genes encoding proteins of different functional categories, including ion channels (Parker et al, 2011), mitochondrial proteins (Roydon et al, 1987; Fergestad et al, 2006) and lipid metabolism (Pavlidis & Tanouye, 1995; Pavlidis et al, 1994). The resultant cellular phenotypes induced in these mutants span from altered synaptic transmission and nerve excitability (Ganetzky & Wu, 1982; Jan & Jan, 1978; Engel & Wu, 1994; Marley & Baines, 2011), to spike frequency coding (Engel, 1995), as well as general seizure-like nerve and muscle spike discharge and neural pathway failure (Pavlidis & Tanouye, 1995; Kuebler & Tanouye, 2000; 2001; Lee & Wu, 2002; 2006). Therefore, the Drosophila bang-sensitive mutants may provide a rich source for mutational and cellular analysis to identify interacting molecular and cellular networks that are responsible for seizure phenotypes.…”