Date: Thu, 22 Mar 2007 14:52:06 -0400 From: Kevin Cook <kcook@XXXX> Subject: Isolation and characterization of Df(2L)BSC252 Cc: Stacey Christensen <sjchristXXXX>, mdealXXXX, kaufman@XXXX Isolation and characterization of Df(2L)BSC252 Stacey Christensen and Kevin Cook Bloomington Stock Center Indiana University Df(2L)BSC252 was isolated as a FLP recombinase-induced recombination event involving PBac{WH}Sos[f05577] and P{XP}d02133. The deletion was isolated as a chromosome lacking miniwhite markers in progeny of P{hsFLP}1, y[1] w[1118]; PBac{WH}Sos[f05577]/P{XP}d02133 males crossed to w[1118]; P{hs-hid}2, wg[Sp-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}BSC252 from the segment of PBac{WH}Sos[f05577] to the left of its FRT site and the segment of P{XP}d02133 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)BSC252 predicted from the Release 4 genomic coordinates of the transposable element insertions sites are 34D1;34F1. It failed to complement tam[3], Ance[34Eb-2] and rk[4]. __________________________________________________________ Kevin Cook, Ph.D. Bloomington Drosophila Stock Center Department of Biology http://flystocks.bio.indiana.edu Jordan Hall 142 Indiana University 812-856-1213 1001 E. Third St. 812-855-2577 (fax) Bloomington, IN 47405-7005 kcook@XXXX