A 3852 base pair fragment from the flanking non-coding or intronic region of dnc is fused upstream of a Drosophila core synthetic promoter (DSCP) followed by sequence encoding a lexA::p65 driver. The driver sequence has been optimized for Drosophila codon usage. An Hsp70 transcriptional terminator is present.
Drives expression in Kenyon cells.
Expression driven by EcollexAGMR13F02 overlaps with that driven by the split-GAL4 combinations HsapRELAAD.R52G04 and ScerGAL4DBD.R49F03 that drive expression in the medulla columnar neuron VPN-MB2, and ScerGAL4DBD.R10E05 and HsapRELAAD.R28F07 that drive expression in medulla columnar neuron MC63.
Ecol\lexAGMR13F02, SLC22AlexAop.cGa has abnormal memory | adult stage phenotype, suppressible by AceKK101926/Scer\GAL4GH146
Gthe\ACR1lexAop.d.EYFP/Ecol\lexAGMR13F02 is a suppressor | conditional | partially of abnormal locomotor behavior | adult stage | conditional phenotype of Cnoc\ChR1::Csub\ChRCsChrimson.IVS.20xUAS.Venus, Scer\GAL40273-G4
Gthe\ACR1lexAop.d.EYFP/Ecol\lexAGMR13F02 is a suppressor | conditional | partially of abnormal locomotor behavior | adult stage | conditional phenotype of Cnoc\ChR1::Csub\ChRCsChrimson.IVS.20xUAS.Venus, Scer\GAL40273-G4, norpAP24
SLC22AlexAop.cGa/Ecol\lexAGMR13F02 is a suppressor of abnormal memory | adult stage phenotype of AceKK101926, Scer\GAL4GH146
Although alleles from the Janelia Farm lexA driver collection incorporate the same enhancer fragments used to create the Janelia Farm GAL4 driver alleles (GMR_Brain_exp_1), significant differences are frequently observed in the expression pattern of a given enhancer fragment inserted in the P{CaryP}attP40 or other docking site compared to the same fragment inserted in the P{CaryP}attP2 docking site. Generally the Ecol\lexA patterns are subsets of the Scer\GAL4 patterns.