Dmel\P{EP}Pdk1EP837 Insertion
| General Information | |||
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| Symbol | Dmel\P{EP}Pdk1EP837 | Species | D. melanogaster |
| Name | FlyBase ID | FBti0016500 | |
| Feature type | transposable_element_insertion_site | ||
| Description | |||
| Inserted element | P{EP} | Expression data | |
| Affected gene(s) | Pdk1 | Viability / fertility | |
| Causes allele(s) | Pdk13, Pdk14, Pdk15, Pdk1EP837 | Stock availability | none publicly available |
| LINE ID | EP(3)0837 | ||
| Genomic Location | |||
| Chromosomal location | 3L ( 61B1 ) | Sequence location | 3L:131,762..131,762 [+] |
Map (
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| 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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Recent Updates
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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 |
3L:131,762..131,762 [+]
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| Orientation | |||
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Cytological location
(computed by FlyBase) |
61B1 ( inferred by FlyBase from sequence location )
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Cytological location
(reported) |
61A4-61A4 (reported as inferred from sequence location)
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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{EP} | ||
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Location-dependent
role |
mobile activating element (UASG)
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| Size | 7.987Kb | ||
| Associated alleles | |||
| Molecular map | |||
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
lethal | recessive
viable
viable | somatic clone
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Sterility
References
male sterile
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Phenotype Manifest In
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adult head
ommatidium
wing
wing disc | somatic clone
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Detailed Description
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Statement
Reference
Neuronal expression of Pdk1[EP837] under the control of Scer\GAL4[elav-C155] increases sensitivity to ethanol sedation.
Age-related locomotor impairment is significantly delayed in mutant males compared to controls.
Mutant males show increased resistance to paraquat compared to controls.
Homozygous clones in the wing disc are reduced in size by 78% compared to their wild-type twin spot clones.
Animals expressing both Akt1Scer\UAS.cRa and Pk61CEP837 under the control of Scer\GAL4GMR.PF have a large-eye phenotype. Expression of Lk6EP30.18 in this background strongly suppresses this phenotype.
Flies co-expressing Akt1Scer\UAS.cRa and Pk61CEP837 under the control of Scer\GAL4GMR.PF have a large eye phenotype. The large eye phenotype caused by co-expression of Akt1Scer\UAS.cRa and Pk61CEP837 under the control of Scer\GAL4GMR.PF is suppressed by co-expression of scylEP22.1. The large eye phenotype caused by co-expression of Akt1Scer\UAS.cRa and Pk61CEP837 under the control of Scer\GAL4GMR.PF is suppressed by co-expression of chrbEP1035. The large eye phenotype caused by co-expression of Akt1Scer\UAS.cRa and Pk61CEP837 under the control of Scer\GAL4GMR.PF is suppressed nearly to wild type by simultaneous co-expression of both scylEP22.1 and chrbEP1035.
Co-expression of Pk61CEP837 enhances the bent wing phenotype caused by expression of S6kScer\UAS.cMa under the control of Scer\GAL4ap-md544.
Expression of Pk61CEP837 under the control of Scer\GAL4ap-md544 has no effect on the wing.
When Pk61CEP837 and Akt1Scer\UAS.T:Ivir\HA1 are coexpressed under the control of Scer\GAL4GMR.PF, the eyes display a severely crumpled morphology. The eye bristles are enlarged even more severely, and the boundaries of
all ommatidia and photoreceptor cells disappear. The addition of Pka-R1BDK.Scer\UAS to Pk61CEP837, Akt1Scer\UAS.T:Ivir\HA1 flies has no effect on the eye phenotype.
Expression of Pk61CEP837 when driven by Scer\GAL4GMR.PF causes an increase in ommatidial size (about 1.33 fold bigger than wild-type). When driven by Scer\GAL4ap-md544 the wing is convex towards the dorsal side.
Coexpression of Akt1Scer\UAS.cRa and Pk61CEP837 under the control of Scer\GAL4GMR.PF causes a substantial increase in eye size. Coexpression of Akt1Scer\UAS.cRa and Pk61CEP837 under the control of Scer\GAL4GMR.PB in clones of cells in the eye results in a cell autonomous increase in cell size.
Expression of Pk61CEP837 under the control of Scer\GAL4GMR.PF results in a slight but significant increase in eye size. Expression of Pk61CEP837 under the control of Scer\GAL4GMR.PB in clones of cells in the eye does not increase cell size.
The heads of mosaic flies with homozygous heads (generated using the "ey-FLP" system) are reduced in size.
Homozygous Pk61C5 larvae and transheterozygous Pk61C5/Pk61CEP3091 larvae die during the second instar. Pk61C5/Pk61C4 flies are delayed in development for one day, smaller than normal and have an 18% reduction in body weight. This reduction
in size and weight is primarily due to a decrease in cell size. Pk61C5/Pk61C4 male flies are almost completely sterile, although they show no obvious defect in sperm morphology or in mating behaviour.
Photoreceptor cells within homozygous clones in the eye are about 30% smaller than heterozygous cells outside the clone. This
phenotype is cell autonomous. The heads of mosaic flies with homozygous heads (generated using the "ey-FLP" system) are reduced
in size.
Pk61C5/Pk61C4 flies are delayed in development for one day, smaller than normal and have an 18% reduction in body weight. This reduction
in size and weight is primarily due to a decrease in cell size. Pk61C5/Pk61C4 male flies are almost completely sterile, although they show no obvious defect in sperm morphology or in mating behaviour.
The heads of mosaic flies with homozygous heads (generated using the "ey-FLP" system) are reduced in size.
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Expression Data
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| Reporter Expression | |||
| Additional Information | |||
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Statement
Reference
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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 |
EP(3)0837
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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
( 0 )
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Linkouts
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Comments
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Location 3L:115294-115295 confirmed by FlyBase alignment of dbGSS accession AQ254649 to D. melanogaster arm Release_4 and
heterochromatin Release_3.2b. Insertion orientation confirmed.
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Synonyms & Secondary IDs
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| Reported As | |||
| Symbol Synonym |
EP837PDK1
EP(3)387
EP(3)0837
EPPDK1
P{EP}EP0837
P{EP}Pdk1EP837
P{EP}Pk61CEP0837
P{EP}Pk61CEP837
UAS-dPDK1
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| Secondary FlyBase IDs | |||
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References
( 17 )
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| Research paper |
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| Personal communication to FlyBase |
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| FlyBase analysis |
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