A Database of Drosophila Genes & Genomes

FB2012_01, released January 20th, 2012
 

Dmel\PBac{RB}WRNexoe04496 Insertion

General Information
Symbol Dmel\PBac{RB}WRNexoe04496 Species D. melanogaster
Name FlyBase ID FBti0041827
Feature type transposable_element_insertion_site
Description
Inserted element PBac{RB} Expression data
Affected gene(s) WRNexo Viability / fertility
Causes allele(s) WRNexoe04496 Stock availability 2 publicly available
LINE ID e04496
Genomic Location
Chromosomal location 3R ( 91A3 ) Sequence location 3R:14,191,845..14,191,845 [-]
Map ( GBrowse ) detailed view FBti0113579 FBti0145317 FBti0041827 FBti0128463 FBti0037672 FBti0052263 FBti0002898
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Description
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FB2012_01
FB2011_10
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Chromosome (arm)
Sequence Location
3R:14,191,845..14,191,845 [-]
Orientation
Cytological location
(computed by FlyBase)
91A3 ( inferred by FlyBase from sequence location )
Cytological location
(reported)
91A3 (reported as inferred from sequence location)
Comments concerning
location
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Flanking sequence
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Construct PBac{RB}
Location-dependent
role
deletion generation component
carries FRT site(s)
Size 5.971Kb
Associated alleles
Molecular map
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Insertion may
affect gene
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Causes alleles
Lethality
References
Sterility
References
female sterile
male fertile
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Statement
Reference
Homozygotes have no gross morphological abnormality. Eggs derived from homozygous females do not hatch. Homozygous larvae are very sensitive to camptothecin (CPT) compared to controls. Surviving adults have roughened eyes and many die as pharate adults. Clones are recovered in the wing at a very high frequency in homozygous flies compared to control heterozygotes. In addition, some clones in the homozygous wing blades are very large, while the rate clones seen in heterozygous flies are all single cells. The majority of the clones recovered in the homozygous flies appear to be the result of mitotic DNA recombination events.
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Reporter Expression
Additional Information
Statement
Reference
Marker for
Reflects
expression of
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FlyView (LinkOut)
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Line ID
Origin as a multiple insertion line
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Aberration
Balancer
hide Stocks ( 2 )
Bloomington
Harvard
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Location 3R:14191845-14191846 confirmed by FlyBase alignment of dbGSS accession CZ482261 to D. melanogaster arm Release_4 and heterochromatin Release_3.2b. Insertion orientation confirmed.
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Reported As
Symbol Synonym
PBac{RB}CG7670e04496
PBac{RB}WRNexoe04496
Secondary FlyBase IDs
hide References ( 12 )
Research paper
Saunders et al., 2008, Aging Cell 7(3): 418--425
Identification and characterization of a Drosophila ortholog of WRN exonuclease that is required to maintain genome integrity. [FBrf0205216]
Page et al., 2007, Fly 1(3): 172--181
A germline clone screen for meiotic mutants in Drosophila melanogaster. [FBrf0206085]
Bellen et al., 2004, Genetics 167(2): 761--781
The BDGP gene disruption project: single transposon insertions associated with 40% of Drosophila genes. [FBrf0179132]
Thibault et al., 2004, Nature Genetics 36(3): 283--287
A complementary transposon tool kit for Drosophila melanogaster using P and piggyBac. [FBrf0175002]
Supplementary material
Thibault, 2004, Nature Genetics 36(3):
Supplementary Table 2. [FBrf0174227]
Thibault, 2004, Nature Genetics 36(3):
Supplementary Table 3. [FBrf0174228]
Personal communication to FlyBase
Christensen et al., 2008.4.15, Isolation and characterization of Df(3R)BSC509.
Isolation and characterization of Df(3R)BSC509. [FBrf0204569]
Bloomington Drosophila Stock Center, 2004.11.6, Exelixis insertion alleles that are not in FlyBase.
Exelixis insertion alleles that are not in FlyBase. [FBrf0179797]
FlyBase analysis
FlyBase, 2005, Assessment of transgenic construct insertion sites.
Assessment of transgenic construct insertion sites. [FBrf0184339]
FlyBase, 1992-, FlyBase curation
FlyBase curation. [FBrf0105495]
Computer file
Gene Disruption Project members and Exelixis, 2005, Genomic mapping of Exelixis insertion collection.
Genomic mapping of Exelixis insertion collection. [FBrf0184340]
Gene Disruption Project members, 2001-, [title not yet available]
[title not yet available] [FBrf0132177]