Isolation and characterization of Df(2L)BSC102
Jennifer Deal and Kevin Cook
Bloomington Stock Center
Indiana University
Df(2L)BSC102 was isolated as a FLP recombinase-induced recombination event involving PBac{WH}f02710 and P{XP}d10944. The deletion was isolated as a chromosome lacking miniwhite markers in progeny of P{hsFLP}1, y1 w1118; PBac{WH}f02710/ P{XP}d10944 males crossed to w1118; P{w+mC=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}BSC102 from the segment of PBac{WH}f02710 to the left of its FRT site and the segment of P{XP}d10944 to the right of its FRT site. Its presence was verified using the PCR methods and primers described in Parks et al. Exelixis, Inc. determined the insertion site of PBac{WH}f02710 to be at Release 3 genomic coordinate 21590694 on chromosome arm 2L and the insertion site of P{XP}d10944 to be at Release 3 genomic coordinate 21662045 on arm 2L. The Gene Disruption project determined the insertion site of PBac{WH}f02710 to be at Release 3 genomic coordinate 21590693 on arm 2L and the insertion site of P{XP}d10944 to be at Release 3 genomic coordinate 21662045 on arm 2L. The cytological breakpoints of Df(2L)BSC102 predicted from these coordinates are 40A2;40A5. Df(2L)BSC102 failed to complement Df(2L)Exel6049.