FB2024_03 , released June 25, 2024
Allele: Dmel\tutlk14703
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General Information
Symbol
Dmel\tutlk14703
Species
D. melanogaster
Name
FlyBase ID
FBal0064789
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Also Known As
l(2)k14703
Key Links
Nature of the Allele
Progenitor genotype
Associated Insertion(s)
Cytology
Description

P{lacW} insertion in the region between the 3' border of exon 8 and the 5' border of exon 11.

Allele components
Component
Use(s)
Inserted element
Encoded product / tool
Mutations Mapped to the Genome
Curation Data
Type
Location
Additional Notes
References
Variant Molecular Consequences
Associated Sequence Data
DNA sequence
Protein sequence
 
Expression Data
Reporter Expression
Additional Information
Statement
Reference
 
Marker for
Reflects expression of
Reporter construct used in assay
Human Disease Associations
Disease Ontology (DO) Annotations
Models Based on Experimental Evidence ( 0 )
Disease
Evidence
References
Modifiers Based on Experimental Evidence ( 0 )
Disease
Interaction
References
Comments on Models/Modifiers Based on Experimental Evidence ( 0 )
 
Disease-implicated variant(s)
 
Phenotypic Data
Phenotypic Class
Phenotype Manifest In
Detailed Description
Statement
Reference

In tutlk14703 embryos, the ISNb motor axons succesfully reach the vicinity of their respective targets. However, once there, many fail to send one or more of the final axon branches to contact their muscle targets. Around a quarter of the hemisegments also lack ISNd nerves.

Approximately 20% of tutlk14703 homozygotes reach adulthood. They exhibit an optic chiasm that is disorganised and exhibits graps in the R7 termination line.

Flies with eyes composed of tutlk14703 mutant cells and brains expressing wild-type levels of tutl (generated using the EGUF technique) exhibit smaller eyes than wild-type, although the optic chiasma and R7 projections appear normal, indicating that the source of retinal axon defects in tutlk14703 mutants is reduced tutl levels in the optic lobe, rather than in the retinal axons.

tutlk14703/tutl23 mutants display a mild R7 tiling phenotype.

Homozygous tutlk14703 embryos show no gastrulation defects.

Most homozygotes are able to survive to adulthood if competition with heterozygous siblings is eliminated. However, competition from heterozygous siblings results in the death of homozygous animals (85-100% lethality) before adulthood. General morphology of the mutant larvae is normal. Homozygous larvae have a severely compromised ability to roll over from an inverted position; the time required to right themselves is significantly longer than control larvae. Homozygous adults cannot fly, although they walk normally and energetically on a level surface. The jump response is intact and robust, but attempts at flight result in the flies flipping themselves onto their backs, where continued efforts to fly are shown by the adults flapping their wings at high speeds (this only results in the flies spinning frantically in circles). Adults that become inverted are rarely able to right themselves, despite what appears to be an intense effort to roll over. Only 12-36% of adults are able to roll over after 60 seconds, in contrast to wild-type which roll over immediately, almost always in less than one second.

External Data
Interactions
Show genetic interaction network for Enhancers & Suppressors
Phenotypic Class
Suppressor of
Statement
Reference

tutlk14703/tutl[+] is a suppressor of visible | heat sensitive phenotype of peb1

tutlk14703/tutl[+] is a suppressor of lethal | recessive | partially | embryonic stage phenotype of peb308

Phenotype Manifest In
Enhancer of
Statement
Reference
Suppressor of
Statement
Reference

tutlk14703 is a suppressor of eye phenotype of HUAS.cMa, Scer\GAL4GMR.PF

tutlk14703/tutl[+] is a suppressor of eye | heat sensitive phenotype of peb1

Additional Comments
Genetic Interactions
Statement
Reference
Xenogenetic Interactions
Statement
Reference
Complementation and Rescue Data
Comments

Expression of either tutlGH15753.Scer\UAS or tutlAT02763.Scer\UAS driven by the pan-neuronal driver Scer\GAL4elav-C155 rescues most aspects of tutlk14703/tutlex383 mutant eye defects.

Expression of tutlScer\UAS.cFa under the control of Scer\GAL4GMR.long rescues the mild tiling phenotype found in tutlk14703/tutl23 R7 terminals.

Images (0)
Mutant
Wild-type
Stocks (2)
Notes on Origin
Discoverer
Comments
Comments

Precise excision of the P{lacW} element rescues the semi-lethality and all the behavioural phenotypes of tutlk14703.

External Crossreferences and Linkouts ( 0 )
Synonyms and Secondary IDs (5)
Reported As
Name Synonyms
Secondary FlyBase IDs
    References (13)