A Database of Drosophila Genes & Genomes

FB2013_03, released May 7th, 2013
 

Reference Report

Reference
Citation Christensen, S., Gresens, J., Cook, K., Cook, K. (2007.10.29). Isolation and characterization of Df(3R)BSC316.  (Export to RIS)
FlyBase ID FBrf0200247
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(3R)BSC316
Date: Mon, 29 Oct 2007 12:07:15 -0400
Isolation and characterization of Df(3R)BSC316
Stacey Christensen, Jill Gresens, Kimberley Cook and Kevin Cook
Bloomington Stock Center
Indiana University
Df(3R)BSC316 was isolated as a FLP recombinase-induced recombination
event involving PBac{RB}tub[e03259] and P{XP}d09816. The deletion was
isolated as a chromosome lacking miniwhite markers in progeny of
w[1118]; Dr[1]/TM6B females crossed to P{hsFLP}1, w[1118];
PBac{RB}tub[e03259]/P{XP}d09816 males. 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.RB3}BSC316 from the segment of
PBac{RB}tub[e03259] to the left of its FRT site and the segment of
P{XP}d09816 to the right of its FRT site. Its presence was verified
using the PCR methods and primers described in Parks et al. 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)BSC316
predicted from the Release 5 genomic coordinates of the transposable
element insertion sites are 82A5;82B3. Df(3R)FDD-0201678 is a synonym
for Df(3R)BSC316.
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