Dmel\P{lacW}Arkk11502 Insertion
| General Information | |||
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| Symbol | Dmel\P{lacW}Arkk11502 | Species | D. melanogaster |
| Name | FlyBase ID | FBti0006473 | |
| Feature type | transposable_element_insertion_site | ||
| Description | |||
| Inserted element | P{lacW} | Expression data | lacZ reporter |
| Affected gene(s) | Ark, Ecol\lacZ | Viability / fertility | viable |
| Causes allele(s) | Arkk11502, Ecol\lacZArk-k11502 | Stock availability | 3 publicly available |
| LINE ID | l(2)k11502 | ||
| Genomic Location | |||
| Chromosomal location | 2R ( 53E4 ) | Sequence location | 2R:12,907,578..12,907,578 [+] |
Map (
GBrowse
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| Member of Large Scale Dataset(s) | |||
| Dataset |
A set of mutant stocks derived by insertional mutagenesis using the P-element construct P{lacW}; most lines have a lethal or sterile phenotype. The P{lacW} construct carries a w[+mC] mini-white visible marker, Ecol\lacZ enhancer trap sequences, and bacterial sequences that allow plasmid rescue (FBrf0049800).
Insertion lines from this collection were assessed for inclusion in the Gene Disruption Project collection.
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Recent Updates
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| Description |
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FlyBase data classes (e.g. genes, references, stocks) or controlled
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| FB2013_03 | |||
| FB2013_02 | |||
| All updates | Click here to see a list of all updates to this record from FB2010_08 and on. | ||
Detailed Mapping Data
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| Chromosome (arm) | |||
| Sequence Location |
2R:12,907,578..12,907,578 [+]
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| Orientation | |||
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Cytological location
(computed by FlyBase) |
53E4 ( inferred by FlyBase from sequence location )
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Cytological location
(reported) |
53F1-53F2 (in situ hybridization reported)
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Comments concerning
location |
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Sequence Data
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| Flanking sequence | |||
Inserted Element
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| Construct | P{lacW} | ||
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Location-dependent
role |
lacZ enhancer trap
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| Size | 10.691Kb | ||
| Associated alleles | |||
| Molecular map |
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Affected Gene(s)
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Insertion may
affect gene |
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Alleles and Phenotypes
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| Causes alleles |
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Lethality
References
lethal | embryonic stage | recessive
partially lethal - majority die | pupal stage | recessive
viable
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Sterility
References
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Phenotype Manifest In
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dorsal closure embryo
embryonic/larval brain
embryonic/larval digestive system
embryonic/larval salivary gland
embryonic brain
embryonic head
eo neuron | supernumerary
eye photoreceptor cell
macrochaeta
macrochaeta | supernumerary
melanotic mass
ommatidium
pigment cell
scutellar bristle | ectopic
sensory mother cell | supernumerary
thecogen cell | supernumerary
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Detailed Description
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Statement
Reference
Arkk11502/Df(2R)BSC49 and Arkk11502/ArkP803-Δ15 third instar larvae show gut melanisation not accompanied by tissue overgrowth or hemocyte encapsulation.
Homozygous third instar larvae develop multiple black spots along the gut and sometimes in the salivary glands.
48% of Arkk11502 mutant flies exhibit extra macrochaetae on the scutellum. Arkk11502 mutants have one extra SOP cell in the scutellum region of the third instar wing disc. Analysis of the scutellum region of
the pupal notum (24-30 h after pupal formation (APF)) shows that there is an extra neuron and thecogen present, which are
derived from the extra SOP cell.
Unlike wild-type embyros UV irradition of Arkk11502 homozygous pre-gastrula embryos at 50 mJ/cm2 does not induce cell death.
Mutants show only slight cell death defects in the embryo and barely detectable defects in adults.
The outer morphology of homozygous larvae and flies appears normal, except for adult dorsal bristles; extra bristles are often
seen on the scutellum. Abnormal ommatidia with one extra photoreceptor cell are often seen. The morphology of the pigment
cell layer is disorganised compared to the regular pattern seen in wild-type flies. A significant decrease in apoptotic cells
is seen in stage 11-12 homozygous embryos compared to wild type. The brain hemispheres of third instar larvae are larger than
normal and contain a markedly decreased number of apoptotic cells.
Homozygous stage 12/1 embryos contain fewer apoptotic cells in the head region that wild-type embryos. The phenotype is highly
penetrant but some variation is seen. Embryos often show defects in head involution and the brain appears larger than normal.
Suppresses the eye phenotype caused by Dcp-1GMR.PS or Dcp-1N.GMR. A strong synergism in cell ablation is seen when Dcp-1GMR.PS and rprGMR.PW are coexpressed in the eye. This phenotype is not modified by Arkk11502.
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Expression Data
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| Reporter Expression | |||
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distribution deduced from reporter
Stage
Tissue/Position (including subcellular localization)
Reference
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| Additional Information | |||
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Statement
Reference
A basal level of expression is observed all over the embryo. Elevated levels are observed in the procephalic region. Later
expression is observed in a segmentally repeated pattern and in macrophages.
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| Marker for | |||
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Reflects
expression of |
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Reporter construct
used in assay |
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External Images
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| FlyView (LinkOut) | |||
Data on Genetic Line
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| Line ID |
l(2)k11502
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| Origin as a multiple insertion line | |||
Progenitor(s) within the Genome
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Related Aberration or Balancer
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| Aberration | |||
| Balancer | |||
Stocks
( 3 )
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| Bloomington | |||
| Kyoto | |||
Linkouts
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Comments
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Location 2R:12534936-12534937 confirmed by FlyBase alignment of dbGSS accession AQ025966 to D. melanogaster arm Release_4
and heterochromatin Release_3.2b. Insertion orientation confirmed.
Insertion separable from lethal phenotype induced on same chromosome.
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Synonyms & Secondary IDs
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| Reported As | |||
| Symbol Synonym |
P{lacW}Arkk11502
P{lacW}k11502
P{lacW}l(2)k11502k11502
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| Secondary FlyBase IDs | |||
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References
( 18 )
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| Research paper |
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| Supplementary material |
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| Personal communication to FlyBase |
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| FlyBase analysis |
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Recent Updates
