A Database of Drosophila Genes & Genomes

FB2012_01, released January 20th, 2012
 

Dmel\P{EP}Cnx99AEP3522 Insertion

General Information
Symbol Dmel\P{EP}Cnx99AEP3522 Species D. melanogaster
Name FlyBase ID FBti0011634
Feature type transposable_element_insertion_site
Description
Inserted element P{EP} Expression data
Affected gene(s) Cnx99A Viability / fertility
Causes allele(s) Cnx99AEP3522 Stock availability 1 publicly available
LINE ID EP(3)3522
Genomic Location
Chromosomal location 3R ( 99A7 ) Sequence location 3R:25,145,356..25,145,356 [+]
Map ( GBrowse ) detailed view FBti0019453 FBti0049498 FBti0145316 FBti0066507 FBti0011634 FBti0049622
hide Recent Updates
Description
What does this section display?
This section contains items that were added to this record for each release. It currently only tracks new links between this FlyBase report and other FlyBase data classes (e.g. genes, references, stocks) or controlled vocabulary terms (e.g. GO, anatomy terms).
What does this section not display?
This section does not currently display links that were removed or gene model changes.
Update Feed
Click the icon below to subscribe to this FlyBase record and receive updates automatically through your feed reader.
FB2012_01
FB2011_10
All updates Click here to see a list of all updates to this record from FB2010_08 and on.
hide Detailed Mapping Data
Chromosome (arm)
Sequence Location
3R:25,145,356..25,145,356 [+]
Orientation
Cytological location
(computed by FlyBase)
99A7 ( inferred by FlyBase from sequence location )
Cytological location
(reported)
99A7-99A7 (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
hide Phenotype Manifest In
intermediate longitudinal fascicle
medial longitudinal fascicle
ventral nerve cord
ventral nerve cord commissure
hide Detailed Description
Statement
Reference
Expression of Cnx99A[EP3522] enhances the small eye phenotype associated with kay[Fbz.Scer\UAS], when both are expressed under the control of Scer\GAL4[ey.3.5.Exel]. Co-expression of Cnx99A[EP3522] with kay[Fbz.Scer\UAS] in differentiated post-mitotic neurons under the control of Scer\GAL4[elav-C155] partially suppresses the small synapse phenotype found in kay[Fbz.Scer\UAS] mutants.
Ventral nerve cord commissures in stage 17 Cnx99AEP3522; Scer\GAL4sca-4512 embryos are fused and/or \'fuzzy\'.The two most medial 1D4 longitudinal fascicles cross and recross the midline. Marker assays suggest some cell fate changes among ventral nerve cord cells. Similar defects in ventral nerve cord commissures and ventral nerve cord cell fate are seen in Cnx99AEP3522; Scer\GAL4sim.PS embryos, but only the most medial 1D4 longitudinal fascicle crosses the midline.
hide Expression Data
Reporter Expression
Additional Information
Statement
Reference
Marker for
Reflects
expression of
hide External Images
FlyView (LinkOut)
hide Data on Genetic Line
Line ID
Origin as a multiple insertion line
hide Progenitor(s) within the Genome
hide Related Aberration or Balancer
Aberration
Balancer
hide Stocks ( 1 )
Bloomington
hide Linkouts
hide Comments
Location 3R:25145355-25145356 determined by FlyBase alignment of dbGSS accession AQ072988 to D. melanogaster arm Release_4 and heterochromatin Release_3.2b. Insertion orientation revised.
insertion of mobile activating element
hide Synonyms & Secondary IDs
Reported As
Symbol Synonym
EP(3)3522
EP(3)3552
P{EP}Cnx99AEP3522
P{EP}EP3522
Secondary FlyBase IDs
hide References ( 10 )
Research paper
Franciscovich et al., 2008, Genetics 180(4): 2057--2071
Overexpression screen in Drosophila identifies neuronal roles of GSK-3 beta/shaggy as a regulator of AP-1-dependent developmental plasticity. [FBrf0207092]
Bellen et al., 2004, Genetics 167(2): 761--781
The BDGP gene disruption project: single transposon insertions associated with 40% of Drosophila genes. [FBrf0179132]
McGovern et al., 2003, Mech. Dev. 120(10): 1193--1207
A targeted gain of function screen in the embryonic CNS of Drosophila. [FBrf0167840]
Spradling et al., 1999, Genetics 153(1): 135--177
The Berkeley Drosophila genome project gene disruption project. Single P-element insertions mutating 25% of vital Drosophila genes. [FBrf0111489]
Rorth, 1996, Proc. Natl. Acad. Sci. USA 93(22): 12418--12422
A modular misexpression screen in Drosophila detecting tissue-specific phenotypes. [FBrf0090768]
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, 2001-, [title not yet available]
[title not yet available] [FBrf0132177]
BDGP Project Members, 2000-, Berkeley Drosophila Genome Project.
Berkeley Drosophila Genome Project. [FBrf0125078]
BDGP Project Members, 1994-1999, Berkeley Drosophila Genome Project.
Berkeley Drosophila Genome Project. [FBrf0067338]