Isolation and characterization of Df(2L)BSC302
Stacey Christensen and Kevin Cook
Bloomington Stock Center
Indiana University
Df(2L)BSC302 was isolated as a FLP recombinase-induced recombination event involving P{XP}CG9265d00690 and PBac{WH}CG9249f00835. The deletion was isolated as a chromosome lacking miniwhite markers in progeny of P{hsFLP}1, y1 w1118; P{XP}CG9265d00690/PBac{WH}CG9249f00835 males crossed to w1118; P{hs-hid}2, wgSp-1/CyO females. These males were heat shocked as larvae as described in Parks et al., Nature Genetics 36: 288-292, 2004 (FBrf0175003). This cross and crosses in preceding and succeeding generations maintained the original genetic background of the Exelixis insertion stocks (Thibault et al., Nature Genetics 36: 283-287, 2004; FBrf0175002). The recombination event generated the genetic element P+PBac{XP5.WH5}BSC302 from the segment of P{XP}CG9265d00690 to the left of its FRT site and the segment of PBac{WH}CG9249f00835 to the right of its FRT site. Its presence was verified using the PCR methods and primers described in Parks et al. The cytological breakpoints of Df(2L)BSC302 predicted from the Release 5 genomic coordinates of the transposable element insertions sites are 39A1;39A6. It failed to complement Mppsk16403 and Df(2L)Exel7080.