Dmel\PBac{RB}veloe01260 Insertion
| General Information | |||
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| Symbol | Dmel\PBac{RB}veloe01260 | Species | D. melanogaster |
| Name | FlyBase ID | FBti0046975 | |
| Feature type | transposable_element_insertion_site | ||
| Description | |||
| Inserted element | PBac{RB} | Expression data | |
| Affected gene(s) | velo | Viability / fertility | |
| Causes allele(s) | veloe01260 | Stock availability | 1 publicly available |
| LINE ID | e01260 | ||
| Genomic Location | |||
| Chromosomal location | 3L ( 65C3 ) | Sequence location | 3L:6,740,123..6,740,123 [+] |
Map (
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| Member of Large Scale Dataset(s) | |||
| Dataset |
A set of transgenic insertion stocks derived by TE mobilization using the Tni\piggyBac-based construct PBac{RB}. The PBac{RB} construct carries the w[+mC] mini-white marker, a single long (199-bp) Scer\FRT site, and a "splice trap," a splice acceptor site derived from a D. melanogaster gene. The FRT site allows Scer\FLP-mediated recombination between other FRT-containing elements, and thus can be used to generate molecularly defined deletions.
PBac{RB} insertion lines from Exelixis were remapped 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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| Description |
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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) |
3L
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| Sequence Location |
3L:6,740,123..6,740,123 [+]
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| Orientation |
+
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Cytological location
(computed by FlyBase) |
65C3 ( inferred by FlyBase from sequence location )
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Cytological location
(reported) |
65C3 (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 | PBac{RB} | ||
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Location-dependent
role |
deletion generation component
carries FRT site(s)
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| Size | 5.971Kb | ||
| 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
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Sterility
References
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Phenotype Manifest In
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adult antennal lobe projection neuron DL1 adPN | somatic clone
antennal lobe glomerulus DL1 | somatic clone
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Detailed Description
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Statement
Reference
velo[e01260] mutants display projection neuron dendrite targeting defects.
velo[e01260] mutant neuroblast clones exhibit several defects. First, the number of neurons is reduced from an average of 35 ad projection
neurons in wild-type to 5 neurons in velo[e01260] mutant clones. Second, the overall dendritic mass is reduced and disorganised Third, dendrites aberrantly innervate the wrong
glomeruli within the antennal lobe, or ectopically project outside the antennal lobe.
velo[e01260] mutant DL1 projection neurons exhibit defects in axon morphology. Axons extend as wild-type and always reach the end of the
lateral horn, but only form 0-2 collaterals in the mushroom body calyx, and often have a missing or shorter dorsal branch
in the lateral horn. These axonal phenotypes are independent of the phenotypic class of dendrite mistargeting.
In velo[e01260] mutant neuroblast clones projection neuron cell numbers are drastically reduced from ~35 neurons in wild-type to an average
of 5.5 neurons.
Expression of CG12717[Scer\UAS.T:Ivir\HA1] under the control of Scer\GAL4[GH146] suppresses the DL1 projection neuron mistargeting phenotype found in velo[e01260] mutants. However, velo[e01260] mutant axon phenotypes cannot be reverted by CG12717[Scer\UAS.T:Ivir\HA1] expression.
Expression of Ulp1[Scer\UAS.T:Ivir\HA1] under the control of Scer\GAL4[GH146] suppresses the DL1 projection neuron mistargeting phenotype found in velo[e01260] mutants. However, velo[e01260] mutant axon phenotypes cannot be reverted by CG12717[Scer\UAS.T:Ivir\HA1] expression.
The number of velo[e01260] mutant neuroblast clone projection neuron cells is increased upon Ulp1[Scer\UAS.T:Ivir\HA1] or CG12717[Scer\UAS.T:Ivir\HA1] expression (under the control of Scer\GAL4[GH146]). However, the overall number is still lower than in wild-type.
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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 | |||
| 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
( 1 )
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| Harvard | |||
Linkouts
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Comments
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Location 3L:6720969-6720970 refined by FlyBase alignment of dbGSS accession CZ479066 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 |
e01260
PBac{RB}CG10107e01260
PBac{RB}e01260
PBac{RB}veloe01260
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| Secondary FlyBase IDs | |||
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References
( 10 )
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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