Life Science Division, Lawrence Berkeley National Laboratory, Berkeley, California, USA

摘要

We combined Gal4-UAS and the FLP recombinase–FRT and fluorescent reporters to generate cell clones that provide spatial, temporal and genetic information about the origins of individual cells in Drosophila melanogaster. We named this combination the Gal4 technique for real-time and clonal expression (G-TRACE). The approach should allow for screening and the identification of realtime and lineage-traced expression patterns on a genomic scale.