FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
Allele: Dmel\elav5
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General Information
Symbol
Dmel\elav5
Species
D. melanogaster
Name
FlyBase ID
FBal0003634
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Also Known As
elave5
Key Links
Mutagen
Nature of the Allele
Mutagen
Progenitor genotype
Cytology
Description

Interstitial deletion within elav.

Deletion of the entire protein coding region.

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

The neuromuscular junctions of elav5/elavts1 mutant third instar larvae (raised at the permissive temperature during embryonic development) show a strong reduction in the number of synaptic connections compared with controls.

elav5/elavts1 adult flies do not exhibit any fusion of the mushroom body beta lobes.

elav5 mutant flies exhibit loss of photoreceptors and central brain neurons.

elav5/elavts1 are short lived, show reduced locomotion and are ataxic.

elav5 mutant eyes (generated by expressing elavelav.PZ and excising the FRT cassette in the eye primordium) are small compared with controls.

elavts1/elav5 animals show a significant reduction in the number of type 1b boutons at the neuromuscular junction of muscle 13 when they are reared at the restrictive temperature during larval life.

elav5 mutants affect commissure formation in all neuromeres and lead to a reduction in the number of commissural fibers crossing the CNS midline. The commissural fibers are thinner than in wild-type in 95% of the neuromeres. The posterior commissure is missing entirely in 25% of the neuromeres and both commissures are absent in 5% of the neuromeres. A greater distance between the longitudinal tracts is observed in more than 80% of the neuromeres.

In elav5 mutant embryos, EW commissural axons frequently fail to cross the midline and instead grow ipsilaterally (80% of the neuromeres). Similarly, but to a lesser extent, EG commissural axons frequently do not cross the midline, preferentially extending on their own side (>50% of the neuromeres). Contralateral projections were found impaired in 30% of the neuromeres for the SP neurons and no contralateral projections are seen for the RP3 neurons.

Midline glial cells are specified normally and are present in normal numbers and have normal position and morphology in elav5 mutant embryos.

elav5 elavedr flies have rough eyes and a disorganised, vacuolar retina.

elav5 flies carrying one copy of elavRBD have reduced viability and abnormalities in the eye and optic lobes.

External Data
Interactions
Show genetic interaction network for Enhancers & Suppressors
Phenotypic Class
Enhanced by
Statement
Reference

elav5 has abnormal neuroanatomy phenotype, enhanceable by comm5/comm[+]

elav5 has abnormal neuroanatomy phenotype, enhanceable by sli2/sli[+]

NOT Enhanced by
Suppressed by
Statement
Reference

elav5/elavts1 has lethal | heat sensitive phenotype, suppressible by ewgSC3ORF.elav

elav5/elavts1 has abnormal neuroanatomy | heat sensitive phenotype, suppressible by ewgSC3ORF.elav

elav5 has abnormal neuroanatomy phenotype, suppressible by robo[+]/robo11

elav5 has lethal phenotype, suppressible by elav::Rbp9ER3

elav5 has lethal phenotype, suppressible by elav::SxlES1.2

elav5 has lethal phenotype, suppressible by elav::SxlES2

elav5 has lethal phenotype, suppressible by elav::Rbp9ER1

elav5 has lethal phenotype, suppressible by elav::Hsap\ELAVL4EH3

NOT suppressed by
Statement
Reference

elav5 has lethal phenotype, non-suppressible by elav::Rbp9ER12

elav5 has lethal phenotype, non-suppressible by elav::SxlES12

elav5 has lethal phenotype, non-suppressible by elav::SxlES1

Enhancer of
Statement
Reference
Suppressor of
Statement
Reference

elav5 is a suppressor of abnormal neuroanatomy phenotype of robo11

elav5 is a suppressor of abnormal neuroanatomy phenotype of sli2

Other
Phenotype Manifest In
Enhanced by
Statement
Reference

elav5 has symmetrical commissure phenotype, enhanceable by comm5/comm[+]

elav5 has connective phenotype, enhanceable by comm5/comm[+]

elav5 has symmetrical commissure phenotype, enhanceable by sli2/sli[+]

NOT Enhanced by
Suppressed by
Statement
Reference

elav5/elavts1 has NMJ bouton | heat sensitive phenotype, suppressible by ewgSC3ORF.elav

elav5/elavts1 has neuromuscular junction | heat sensitive phenotype, suppressible by ewgSC3ORF.elav

elav5 has symmetrical commissure phenotype, suppressible by robo[+]/robo11

elav5 has phenotype, suppressible by elav::Dvir\elavDvORF

NOT suppressed by
Statement
Reference
Enhancer of
Statement
Reference
Additional Comments
Genetic Interactions
Statement
Reference

The axon wiring defects seen in elav5 mutant embryos is not enhanced by Df(1)fneΔ or Rbp9P2690, or both.

Df(1)fneΔ does not enhance the neuromuscular junction phenotypes seen in elav5/elavts1 mutant third instar larvae.

Rbp9P2690/Df(2L)ED206 does not enhance the neuromuscular junction phenotypes seen in elav5/elavts1 mutant third instar larvae.

Expression of fneScer\UAS.T:Ivir\HA1 under the control of Scer\GAL4elav.PZ rescues the small eye phenotype seen in elav5 mutant eyes (generated by expressing elavelav.PZ and excising the FRT cassette in the eye primordium).

Expression of Rbp9Scer\UAS.T:Ivir\HA1 under the control of Scer\GAL4elav.PZ rescues the small eye phenotype seen in elav5 mutant eyes (generated by expressing elavelav.PZ and excising the FRT cassette in the eye primordium).

Expression of Rbp9Scer\UAS.T:Ivir\HA1 under the control of Scer\GAL4elav.PZ rescues the small eye phenotype seen in elav5 mutant eyes (generated by expressing elavelav.PZ and excising the FRT cassette in the eye primordium).

Expression of SxlScer\UAS.cHa under the control of Scer\GAL4elav.PZ does not rescue the small eye phenotype seen in elav5 mutant eyes (generated by expressing elavelav.PZ and excising the FRT cassette in the eye primordium).

Expression of fneelav.T:Ivir\HA1 rescues the reduction in bouton number seen in elavts1/elav5 mutant larvae (raised at the permissive temperature during embryonic development).

Expression of Rbp9elav.T:Ivir\HA1 rescues the reduction in bouton number seen in elavts1/elav5 mutant larvae (raised at the permissive temperature during embryonic development).

Expression of Rbp9elav.T:Ivir\HA1 does not rescue the viability of elav5.

Expression of Rbp9elav.T:Uuuu\nls-Unk.T:Ivir\HA1 does not rescue the viability of elav5.

elavts1/elav5 animals eclose as adults when they are rescued by ewgelav.NS (providing that embryogenesis occurs at the permissive temperature for the elavts1 allele). However, the rescued adults show motor defects and are flightless.

The reduction in bouton number at the neuromuscular junction which is seen in elavts1/elav5 animals reared at the restrictive temperature during larval life is rescued by ewgelav.NS.

elav5 mutants that are heterozygous for comm5 exhibit a comm-like phenotype, whereas comm5/+ embryos display no abnormalities. In elav5; comm5/+ embryos commissures are missing entirely in more than 80% of the neuromeres, indicating that most commissural axons fail to cross the midline in these embryos. The longitudinal tracts frequently adopt a more lateral position (i.e. higher distance from the midline) relative to elav5 embryos.

Reduction of robo in a robo1 heterozygous background partially suppresses the elav5 mutant commissural phenotype. Thicker commissural tracts (relative to elav5 embryos) are made in more than 50% of the neuromeres.

Reduction of sli in a sli2 heterozygous background leads to a fused commissures phenotype in elav5 mutant embryos.

Expression of commScer\UAS.cWa under the control of Scer\GAL4eg-Mz360 in elav5 mutant EW and EG neurons suppresses the elav5 phenotype, with these neurons once again crossing the midline to generate commissures.

Expression of fraScer\UAS.cKa in elav5 mutant EW and EG neurons (under the control of Scer\GAL4eg-Mz360) does not modify the proportion of contralateral projection defects in elav5 mutant embryos. For example, EW axons fail to cross the midline in 755 of the neuromeres in such embryos.

Two transgenic lines of elav::Rbp9ER1 and one of elav::SxlES2 show slight rescue of elav5 (4, 6 and 5% rescue respectively).

Xenogenetic Interactions
Statement
Reference

Expression of Hsap\ELAVL1Scer\UAS.T:Ivir\HA1 under the control of Scer\GAL4elav.PZ rescues the small eye phenotype seen in elav5 mutant eyes (generated by expressing elavelav.PZ and excising the FRT cassette in the eye primordium).

Expression of Hsap\ELAVL1elav.T:Ivir\HA1 slightly rescues the viability of elav5.

Expression of Hsap\ELAVL1elav.T:Ivir\HA1 rescues the reduction in bouton number seen in elavts1/elav5 mutant larvae (raised at the permissive temperature during embryonic development).

Complementation and Rescue Data
Partially rescued by

elav5 is partially rescued by elavΔOh

elav5 is partially rescued by elavDmORF

elav5 is partially rescued by elavΔCh

elav5 is partially rescued by elav20.t15.5

elav5 is partially rescued by elavRBD

Not rescued by
Comments

Expression of elavScer\UAS.T:Ivir\HA1.cZa under the control of Scer\GAL4elav.PZ rescues the small eye phenotype seen in elav5 mutant eyes (generated by expressing elavelav.PZ and excising the FRT cassette in the eye primordium).

Expression of elavT:Ivir\HA1 rescues the reduction in bouton number seen in elavts1/elav5 mutant flies (raised at the permissive temperature during embryonic development).

elavts1/elav5 animals eclose as adults when they are rescued by elavDmORF (providing that embryogenesis occurs at the permissive temperature for the elavts1 allele).

The reduction in bouton number at the neuromuscular junction which is seen in elavts1/elav5 animals reared at the restrictive temperature during larval life is rescued by elavDmORF.

Expression of elavScer\UAS.cKa in en-expressing neurons (under the control of Scer\GAL4e13C) in elav5 mutant embryos restores formation of en-expressing posterior commissures (as in wild-type).

Images (0)
Mutant
Wild-type
Stocks (1)
Notes on Origin
Discoverer

Lefevre.

External Crossreferences and Linkouts ( 0 )
Synonyms and Secondary IDs (3)
References (21)