The attP cassette in the Mi{MIC}ChATMI04508 insertion (which is in a coding intron common to all splice forms of ChAT) has been replaced with a Trojan GAL4 cassette that contains a splice acceptor site followed by the T2A peptide, the Scer\GAL4 coding sequence and an Hsp70 transcription termination signal. The insertion is in the correct orientation to gene trap ChAT. The splice acceptor ensures that the T2A-Scer\GAL4 open reading frame is incorporated into the ChAT mRNA, while the T2A sequence is expected to truncate the native ChAT gene product and promotes the separate translation of the Scer\GAL4 open reading frame. Thus Scer\GAL4 expression is driven by the native ChAT regulatory sequences.
ScerGAL4ChAT-MI04508-TG4.0 drives expression in neurons in the adult thoracico-abdominal ganglion that express ChAT; it also drives expression in neurons labeled by GABA or VGlut1 antibodies.
ScerGAL4ChAT-MI04508-TG4.0 drives expression in neurons that use acetylcholine as a neurotransmitter, and replicates the ChAT immunoreactivity pattern. Expression is observed in most neurons of the larval CNS, and in sensory neurons of the larval PNS.