A Database of Drosophila Genes & Genomes

FB2013_03, released May 7th, 2013
 

Dmel\P{EP}bchsEP2299 Insertion

General Information
Symbol Dmel\P{EP}bchsEP2299 Species D. melanogaster
Name FlyBase ID FBti0115740
Feature type transposable_element_insertion_site
Description
Inserted element P{EP} Expression data
Affected gene(s) bchs Viability / fertility
Causes allele(s) bchs12, bchs17, bchs58, bchsEP2299 Stock availability 2 publicly available
LINE ID EP(2)2299
Genomic Location
Chromosomal location 2L ( 26A1 ) Sequence location 2L:5,907,523..5,907,523 [+]
Map ( GBrowse ) GBrowse View Help detailed view FBti0057575 FBti0027137 FBti0103527 FBti0111543 FBti0103206 FBti0103200 FBti0024960 FBti0026383 FBti0030142 FBti0113121 FBti0115740 FBti0072236 FBti0047209 FBti0041435 FBti0124589
Member of Large Scale Dataset(s)
Dataset

A set of transgenic insertion stocks derived by TE mobilization using the P-element construct P{EP}. The P{EP} construct construct carries a w[+mC] mini-white visible marker, Scer\UAS binding sites for the Scer\GAL4 transcriptional regulator, and bacterial sequences that allow plasmid rescue. The GAL4-UAS system allows regulated expression of genes proximate to the site of the insertion: genes properly oriented with respect to the Scer\UAS sequences can be conditionally expressed via transgene-derived Scer\GAL4 activity.
Insertion lines from this collection were mapped and assessed for inclusion in the Gene Disruption Project collection; flanking sequence data were submitted to GenBank.
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Description
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FB2013_03
FB2013_02
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hide Detailed Mapping Data
Chromosome (arm)
Sequence Location
2L:5,907,523..5,907,523 [+]
Orientation
Cytological location
(computed by FlyBase)
26A1 ( inferred by FlyBase from sequence location )
Cytological location
(reported)
26A1-26A2 (in situ hybridization reported)
26A6-26A6 (reported as inferred from sequence location)
Comments concerning
location
hide Sequence Data
Flanking sequence
hide Inserted Element
Construct P{EP}
Location-dependent
role
mobile activating element (UASG)
Size 7.987Kb
Associated alleles
Molecular map
hide Affected Gene(s)
Insertion may
affect gene
hide Alleles and Phenotypes
Causes alleles
Lethality
References
Sterility
References
female fertile
male fertile
hide Phenotype Manifest In
adult abdomen & microchaeta
adult central nervous system
anterior fascicle & synapse
dorsocentral bristle
embryonic/larval brain | third instar larval stage
growth cone & eye photoreceptor cell
intersegmental nerve
neuron & eye photoreceptor cell
ommatidium
scutellar bristle
hide Detailed Description
Statement
Reference
Overexpression of bchs[EP2299] in the eye under the control of Scer\GAL4[GMR.PF] results in a rough eye phenotype and age related neuronal degeneration.
The bchs[EP2299]-overexpression phenotype in the eye is enhanced when Gga[dsRNA.Scer\UAS.1] is co-expressed under the control of Scer\GAL4[GMR.PF] resulting in a reduction in eye size and a marked bleaching in the middle of the eye.
Expression of bchs[EP2299] in the developing nervous system, driven by Scer\GAL4[elav-C155] results in a 14.6% increase in brain volume when compared to controls.
bchs[58]/Df(2L)cl7 and bchs[58] homozygous mutants display a 15 and 17% reduction in the brain volumes of third instar larvae, respectively.
Flies expressing bchsEP2299 under the control of Scer\GAL4GMR.PF have a roughened eye surface and a slight decrease in overall eye size compared to controls. Animals expressing bchsEP2299 under the control of Scer\GAL4GMR.PF show alterations in the neural projection patterns of photoreceptor cells compared to wild-type in mid-pupae; the number and basic array of R7 and R8 axonal projections remain relatively normal, but there is a loss of growth cone morphology, premature termination of developing synapses and axonal swellings or varicosities are seen.
rb1 is a complex modifier of the eye phenotype caused by expression of bchsEP2299 under the control of Scer\GAL4GMR.PF. g1 is a complex modifier of the eye phenotype caused by expression of bchsEP2299 under the control of Scer\GAL4GMR.PF. cm1 is a complex modifier of the eye phenotype caused by expression of bchsEP2299 under the control of Scer\GAL4GMR.PF.
Expression of bchsEP2299 in third instar eye discs, under the control of Scer\GAL4GMR.PF, does not affect the patterning of the disc. Expression in the developing retina results in photoreceptor growth cones with an unusually bulbous central region that are less expanded than wild-type growth cones. However, Scer\GAL4GMR.PF>bchsEP2299 growth cones appear to grow normally towards their targets. At the adult stage, flies of this genotype have small, glazed eyes that lack distinct ommatidia compared to those of wild-type flies.
Flies that are mutant for Df(3R)e-R1 show a strong enhancement of the Scer\GAL4GMR.PF>bchsEP2299 overexpression phenotype. Rab11 heterozygotes act as dominant enhancers of the Scer\GAL4GMR.PF>bchsEP2299 eye phenotype, resulting in adults with severely reduced eyes. The following alleles cause this enhancement: Rab11j2D1, Rab1193Bi, Rab11ex1, Rab11ex2, Rab11ETo11, and Rab11ETo3.
bchs12 mutants show no defects in the larval visual system or embryonic central nervous system.
The viability of Rab11ex1/Rab1193Bi is increased when flies are also mutant for bchs17/bchs12. The microchaeta loss of Rab11ex1/Rab1193Bi flies is completely suppressed by bchs17/bchs12. Further, posterior scutellar bristle length of Rab11ex1/Rab1193Bi flies is restored significantly by bchs17/bchs12. The bouton density and branching defects of Rab11ex1/Rab1193Bi larval NMJs at muscle 6/7 are significantly suppressed in bchs17/bchs12; Rab11ex1/Rab1193Bi double mutants.
Expression of bchs58 under the control of Scer\GAL4GMR.PF does not cause the small eye or growth cone phenotypes seen when wild-type bchs is overexpressed. bchs58 mutants show no defects in the larval visual system or embryonic central nervous system.
The microchaeta loss of Rab1193Bi flies is significantly suppressed by bchs58/+ and is completely suppressed by bchs58/bchs58.
bchs17 mutants show no defects in the larval visual system or embryonic central nervous system.
The viability of Rab11ex1/Rab1193Bi is increased when flies are also mutant for either Df(2L)cl7/bchs17, bchs17/bchs12 or bchs17/+. The microchaeta loss of Rab11ex1/Rab1193Bi flies is significantly suppressed by bchs17/+ and is completely suppressed by Df(2L)cl7/bchs17 or bchs17/bchs12. Further, posterior scutellar bristle length of Rab11ex1/Rab1193Bi flies is restored partially by bchs17/+ and more fully by Df(2L)cl7/bchs17 or bchs17/bchs12. The bouton density and branching defects of Rab11ex1/Rab1193Bi larval NMJs at muscle 6/7 are significantly suppressed in bchs17/bchs12; Rab11ex1/Rab1193Bi double mutants.
Expression of bchsEP2299 under the control of Scer\GAL4GMR.PF results in smaller eyes than normal which have a glossy appearance.
Expression of bchs[EP2299] under the control of Scer\GAL4[GMR.PU] results in a rough eye phenotype.
bchsEP2299 homozygotes and bchsEP2299/Df(2L)cl7 flies have a reduced average lifespan compared to wild-type. These flies also have age-dependent ubiquitinated aggregates, that appear to be insoluble, throughout the CNS.
Mutant larvae expressing bchsEP2299 under the control of Scer\GAL4elav-C155 have altered ISN synapses with abnormal bulges at the junctions between the axons and the synaptic branches.
Mutant larvae expressing bchsEP2299 under the control of Scer\GAL4elav-C155 have reduced or abnormal synapses.
Expression of bchsEP2299 under the control of Scer\GAL4sca-537.4 results in severe loss of microchaetae on the abdomen and loss of scutellar and dorsocentral macrochaetae. Sensory organs with one socket, no shaft and one sheath cell are seen.
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Reporter Expression
Additional Information
Statement
Reference
Marker for
Reflects
expression of
Reporter construct
used in assay
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FlyView (LinkOut)
hide Data on Genetic Line
Line ID
Origin as a multiple insertion line
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hide Related Aberration or Balancer
Aberration
Balancer
hide Stocks ( 2 )
Bloomington
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hide Comments
Location 2L:5907523-5907524 confirmed by FlyBase alignment of dbGSS accession AQ254846 to D. melanogaster arm Release_4 and heterochromatin Release_3.2b. Insertion orientation confirmed.
insertion of mobile activating element
hide Synonyms & Secondary IDs
Reported As
Symbol Synonym
P{EP}bchsEP2299
P{EP}Beach1EP2299
P{EP}EP2299
P{EP}EP2299EP2299
Secondary FlyBase IDs
  • FBti0011017
  • FBti0076726
  • FBti0076727
  • FBti0076728
hide References ( 20 )
Research paper
Luan et al., 2012, PLoS ONE 7(9): e45163
The Unique GGA Clathrin Adaptor of Drosophila melanogaster Is Not Essential. [FBrf0219559]
Eissenberg et al., 2011, Traffic 12(12): 1821--1838
Drosophila GGA Model: An Ultimate Gateway to GGA Analysis. [FBrf0216574]
Kriston-Vizi et al., 2011, BMC Bioinformatics 12: 232
Gebiss: an ImageJ plugin for the specification of ground truth and the performance evaluation of 3d segmentation algorithms. [FBrf0214312]
Simonsen et al., 2007, Genetics 176(2): 1283--1297
Genetic modifiers of the Drosophila blue cheese gene link defects in lysosomal transport with decreased life span and altered ubiquitinated-protein profiles. [FBrf0201586]
Khodosh et al., 2006, Development 133(23): 4655--4665
Bchs, a BEACH domain protein, antagonizes Rab11 in synapse morphogenesis and other developmental events. [FBrf0195140]
Mueller et al., 2005, Genetics 171(3): 1137--1152
Genetic modifier screens on hairless gain-of function phenotypes reveal genes involved in cell differentiation, cell growth and apoptosis in Drosophila melanogaster. [FBrf0190751]
Bellen et al., 2004, Genetics 167(2): 761--781
The BDGP gene disruption project: single transposon insertions associated with 40% of Drosophila genes. [FBrf0179132]
Raymond et al., 2004, J. Cell Sci. 117(13): 2777--2789
A screen for modifiers of RacGAP(84C) gain-of-function in the Drosophila eye revealed the LIM kinase Cdi/TESK1 as a downstream effector of Rac1 during spermatogenesis. [FBrf0179402]
Finley et al., 2003, J. Neurosci. 23(4): 1254--1264
blue cheese mutations define a novel, conserved gene involved in progressive neural degeneration. [FBrf0159061]
Horn et al., 2003, Genetics 163(2): 647--661
piggyBac-based insertional mutagenesis and enhancer detection as a tool for functional insect genomics. [FBrf0158985]
Kraut et al., 2001, Curr. Biol. 11(6): 417--430
A gain-of-function screen for genes controlling motor axon guidance and synaptogenesis in Drosophila. [FBrf0135708]
Abdelilah-Seyfried et al., 2000, Genetics 155(2): 733--752
A gain-of-function screen for genes that affect the development of the Drosophila adult external sensory organ. [FBrf0128367]
Rorth, 1996, Proc. Natl. Acad. Sci. U.S.A. 93(22): 12418--12422
A modular misexpression screen in Drosophila detecting tissue-specific phenotypes. [FBrf0090768]
Supplementary material
Kraut et al., 2001, Curr. Biol. 11(6):
A gain-of-function screen for genes controlling motor axon guidance and synaptogenesis in Drosophila. [FBrf0135968]
Personal communication to FlyBase
Gene Disruption Project members, 2001-, (Computer file)
(Computer file) [FBrf0132177]
BDGP Project Members, 2000-, Berkeley Drosophila Genome Project. (Computer file)
Berkeley Drosophila Genome Project. (Computer file) [FBrf0125078]
BDGP Project Members, 1994-1999, BDGP Project Members, 1994-1999, Berkeley Drosophila Genome Project. (Computer file)
BDGP Project Members, 1994-1999, Berkeley Drosophila Genome Project. (Computer file) [FBrf0067338]
FlyBase analysis
FlyBase Curators, 2013, Members of TE insertion collections.
Members of TE insertion collections. [FBrf0220668]
FlyBase, 2005, Assessment of transgenic construct insertion sites.
Assessment of transgenic construct insertion sites. [FBrf0184339]
FlyBase, 1992-, FlyBase curation.
FlyBase curation. [FBrf0105495]