Document Type
Article - post-print
Publication Date
2009
Abstract
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 real-time and lineage-traced expression patterns on a genomic scale.
Original Publication Citation
Evans, C., Olson, J., Ngo, K. et al. G-TRACE: rapid Gal4-based cell lineage analysis in Drosophila. Nat Methods 6, 603–605 (2009). https://doi.org/10.1038/nmeth.1356
Digital Commons @ LMU & LLS Citation
Evans, Cory J.; Olson, John M.; Ngo, Kathy T.; Kim, Eunha; Lee, Noemi E.; Kuoy, Edward; Patananan, Alexander N.; Sitz, Daniel; Tran, Phuong Thao; Do, Minh Tu; Yackle, Kevin; Cespedes, Albert; Hartenstein, Volker; Call, Gerald B.; Banerjee, Utpal; Beyder, Miriam; Bhatt, Kush V.; Bhoot, Chinmay; Bradshaw, Aaron W.; Brannigan, Tierney G.; Cao, Boyu; Cashell, Yancey Y.; Chai, Timothy; Chan, Alex W.; Chan, Carissa; Chang, Inho; Chang, Jonathan; Chang, Michael T.; Chang, Patrick W.; Chang, Stephen; and Chari, Neel, "G-TRACE: rapid Gal4-based cell lineage analysis in Drosophila" (2009). Biology Faculty Works. 81.
https://digitalcommons.lmu.edu/bio_fac/81