A Database of Drosophila Genes & Genomes

FB2013_03, released May 7th, 2013
 

Reference Report

Reference
Citation Christensen, S., Cook, K., Cook, K. (2007.10.29). Isolation and characterization of Df(3L)BSC401.  (Export to RIS)
FlyBase ID FBrf0200257
Publication Type Personal communication to FlyBase
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PubMed Abstract
Text of Personal Communication
To: flybase-updatesXXXXXXXXXXXXXXX, Stacey Christensen <sjchristXXXXXXXXXXXXXXX>
From: Kevin Cook <kcook@XXXXXXXXXXXXXXX>
Subject: Isolation and characterization of Df(2R)BSC401
Date: Mon, 29 Oct 2007 12:08:33 -0400
Isolation and characterization of Df(2R)BSC401
Stacey Christensen, Kimberley Cook and Kevin Cook
Bloomington Stock Center
Indiana University
Df(2R)BSC401 was isolated as a FLP recombinase-induced recombination
event involving PBac{WH}CG18327[f01465] and P{XP}d01851. The deletion
was isolated as a chromosome lacking miniwhite markers in progeny of
P{hsFLP}1, y[1] w[1118]; PBac{WH}CG18327[f01465]/P{XP}d01851 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}BSC401 from the segment
of PBac{WH}CG18327[f01465] to the left of its FRT site and the
segment of P{XP}d01851 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(2R)BSC401 predicted from the
Release 5 genomic coordinates of the transposable element insertions
sites are 50E1;50E4. It failed to complement Sox15[KG09145].
Df(2R)FDD-0270175 is a synonym for Df(2R)BSC401.
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