Reference Report
| Reference | |||
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| Citation | Cook, K., Cook, K. (2010.5.7). Isolation and characterization of Df(2R)BSC879. (Export to RIS) | ||
| FlyBase ID | FBrf0210859 | ||
| Publication Type | Personal communication to FlyBase | ||
| PubMed ID | |||
| PubMed Abstract | |||
| Text of Personal Communication |
Df(2R)BSC879 was isolated as a FLP recombinase-induced recombination event involving P{XP}Ef1alpha48Dd10427 and PBac{RB}CG8378e02998. The deletion was isolated as a chromosome lacking miniwhite markers in progeny of P{hsFLP}1, y1 w1118; P{XP}Ef1alpha48Dd10427/PBac{RB}CG8378e02998 males crossed to w1118; P{hs-hid}2, wgSp-1/SM6a 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.RB3}BSC879 from the segment of P{XP}Ef1alpha48Dd10427 to the left of its FRT site and the segment of PBac{RB}CG8378e02998 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’-GCTTCTAAACGCTTACGCATAAACGATG-3’ for the RB3’ plus or RB3’ minus primer in the Hybrid PCR
protocol in the Supplementary Methods. The breakpoints of Df(2R)BSC879 predicted from the Release 5 genomic coordinates of
the transposable element insertion sites are 2R:7779605;8029867 and the cytological breakpoints predicted from these coordinates
are 48C5;48E2. Df(2R)BSC879 failed to complement jebk05644.
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| Language of Publication | English | ||
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Data from Reference
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Aberrations (2)
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Alleles (1)
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Constructs (1)
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Genes (1)
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Insertions (3)
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