Dmel\P{EP}JIL-1EP3657 Insertion
| General Information | |||
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| Symbol | Dmel\P{EP}JIL-1EP3657 | Species | D. melanogaster |
| Name | FlyBase ID | FBti0011744 | |
| Feature type | transposable_element_insertion_site | ||
| Description | |||
| Inserted element | P{EP} | Expression data | |
| Affected gene(s) | JIL-1 | Viability / fertility | |
| Causes allele(s) | JIL-1EP3657 | Stock availability | none publicly available |
| LINE ID | EP(3)3657 | ||
| Genomic Location | |||
| Chromosomal location | 3L ( 68A5 ) | Sequence location | 3L:11,085,410..11,085,410 [-] |
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:11,085,410..11,085,410 [-]
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| Orientation | |||
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Cytological location
(computed by FlyBase) |
68A5 ( inferred by FlyBase from sequence location )
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Cytological location
(reported) |
68A3-68A3 (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 | embryonic stage | maternal effect
lethal | partially | recessive
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Sterility
References
fertile
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Phenotype Manifest In
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abdominal sternite 5 | ectopic | male
abdominal sternite 6 | male
intersegmental nerve
ovary
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Detailed Description
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Statement
Reference
The hatch rate of homozygous embryos produced by homozygous parents is as low as 4-7%.
About 80% of homozygous animals derived from heterozygous parents eclose, although subsequent generations show further decreased
viability, probably due to decreased levels of maternal JIL-1 product. Only 8% of embryos derived from JIL-1z2/JIL-1EP3657 females mated to wild-type males hatch, of those larvae that hatch, 58% survive to pupation, and of those that survive to
pupation 95% eclose. 94% of embryos derived from wild-type females mated to JIL-1z2/JIL-1EP3657 males hatch, and of those larvae that hatch, 95% survive to pupation. 87% of embryos derived from JIL-1z2/+ females mated to JIL-1z2/JIL-1EP3657 males hatch, suggesting that some embryos with the JIL-1z2/JIL-1z2 or JIL-1z2/JIL-1EP3657 genotype can survive embryogenesis if provided with normal maternal JIL-1 product. No JIL-1z2/JIL-1z2 progeny survive to eclosion and the number of surviving JIL-1z2/JIL-1EP3657 adults is about half that of comparable sibling classes. Homozygous ovaries are moderately decreased in size compared to
wild-type ovaries. In 88% of homozygous males, the A6 sternite is covered by one or more large bristles, indicating a transformation
of A6 to the more anterior A5 segment. 93% of JIL-1z2/JIL-1EP3657 males have ventral sternite bristles on the A6 sternite, indicating a transformation of A6 to the more anterior A5 segment.
Mutant larvae expressing JIL-1EP3657 under the control of Scer\GAL4elav-C155 have ISN neuron pathfinding defects.
Homozygous larvae (derived from heterozygous females) have an eclosion rate of 81%. The number of males eclosing is 73% that
of females. Eclosed adults are fertile and able to produce offspring. The hatch rate of embryos derived from homozygous parents
is only 4%. The number of males eclosing is 48% that of females. Embryos derived from homozygous parents show a range of phenotypes
from embryos appearing wild type with regularly spaced nuclei to embryos where chromatin structure is completely disintegrated.
In intermediate phenotypes, nuclei in various stages of fragmentation are discernible. Centrosomes are often seen to be separated
from the nuclear remnants and in other cases aberrant and misaligned tubulin spindles are seen. The polytene chromosome banding
pattern is relatively normal in homozygous third instar larvae. Perturbation of the male X chromosome is relatively more severe
than that of the autosomes which are only subtly affected.
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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)3657
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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:11066257-11066258 confirmed by FlyBase alignment of dbGSS accession AQ073095 to D. melanogaster arm Release_4
and heterochromatin Release_3.2b. Insertion orientation confirmed.
insertion of mobile activating element
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Synonyms & Secondary IDs
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| Reported As | |||
| Symbol Synonym |
EP(3) 3657
P{EP}EP3657
P{EP}JIL-1EP3657
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| Secondary FlyBase IDs | |||
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References
( 13 )
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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