From: kcook@XXXX
Subject: Isolation and characterization of Df(3L)BSC675
Date: December 28, 2008 1:15:50 PM GMT- 05:00
Isolation and characterization of Df(3L)BSC675
Stacey Christensen, Kim Cook and Kevin Cook
Bloomington Stock Center
Indiana University
Df(3L)BSC675 was isolated as a FLP recombinase-induced recombination event involving P{XP}chrbd03716 and PBac{WH}CG14133f05716. The deletion was isolated as a chromosome carrying two copies of the miniwhite marker in progeny of w1118; P{hs-hid}3, Dr1/TM6C, Sb1 cu1 females crossed to P{hsFLP}1, y1 w1118; P{XP}chrbd03716/PBac{WH}CG14133f05716 males. The 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{XP3.WH3}BSC675 from the segment of P{XP}chrbd03716 to the left of its FRT site and the segment of PBac{WH}CG14133f05716 to the right of its FRT site. The cytological breakpoints of Df(3L)BSC675 predicted from the Release 5 genomic coordinates of the transposable element insertions sites are 68C10;68D2. Df(3L)BSC675 failed to complement rtP and rt2.
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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 
