[89A1-89A1];[89A5-89A5];
A set of ~800 largely isogenic deficiency stocks created by FLP-induced recombination between FRT-carrying transgenic insertions; molecularly defined deletion endpoints correspond to initial location of the progenitor insertions. Designed to fill gaps in deletion coverage and breakpoint placement; also used to replace older available deficiencies that have not been molecularly mapped.
89A1;89A5
Breakpoint from FlyBase's release 5 sequence location of progenitor insertion.
Inferred to overlap with: Df(3R)ED5705.
Inferred to overlap with: Df(3R)Exel8162.
The presence of P+PBac{XP5.RB3}BSC569 was verified using the PCR methods and primers described in FBrf0175003, with the substitution of the primer 5'-CCAATGCGTTTATTTCAGGTCACG-3' for the RB3' plus or RB3' minus primer in the Hybrid PCR protocol in the Supplementary Methods.
The cytological breakpoints of Df(3R)BSC569 predicted from the Release 5 genomic coordinates of the progenitor P{XP}d03302 and PBac{RB}CG14876e02690 transposable element insertion sites are 89A1;89A5.