From: Kevin Cook <kcook@XXXX> To: flybase-updates@XXXX Cc: Stacey Christensen <sjchristXXXX>, Kim Cook <ruacookXXXX>, kaufman@XXXX Subject: Isolation and characterization of Df(1)BSC530 Date: Wed, 11 Jun 2008 14:29:55 -0400 ( 19:29 BST) Isolation and characterization of Df(1)BSC530 Stacey Christensen, Kim Cook and Kevin Cook Bloomington Stock Center Indiana University Df(1)BSC530 was isolated as a FLP recombinase-induced recombination event involving PBac{WH}f03741 and P{XP}CG13369[d06819]. The deletion was isolated as a chromosome lacking miniwhite markers in progeny of PBac{WH}f03741/P{XP}CG13369[d06819]; MKRS, P{hsFLP}86E/+ females crossed to Binsinscy/Y males. These females 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}BSC530 from the segment of PBac{WH}f03741 to the left of its FRT site and the segment of P{XP}CG13369[d06819] 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(1)BSC530 predicted from the Release 5 genomic coordinates of the transposable element insertions sites are 1A5;1B12. It failed to complement ac[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