Insertion lines from this collection were assessed for inclusion in the Gene Disruption Project collection; some lines were mapped by the GDP.
A set of transgenic insertion stocks derived by TE mobilization using the "piggyBac mutator" construct PBac{GAL4D,EYFP}. The dataset consists primarily of insertions on the third chromosomes that also carry proximal Scer\FRT sites, to allow generation of germ-line clones. The PBac{GAL4D,EYFP} construct carries the yellow fluorescent marker Avic\GFPEYFP.3xP3 (which can be distinguished from other GFP-based markers) and a modified Scer\GAL4 driver/reporter gene.
Reporter expression is observed in embryos in the salivary gland, amnioserosa, and gut, recapitulating aspects of the endogenous in situ pattern of GlcAT-P. In larvae, expression is observed in the tracheal system, in a subset of neurons and glia in the larval brain and ventral nerve cord, as well as in Kenyon cells. Expression is observed two ventral nerve cord neurons per neuromere that were identified as VUM motorneurons.
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