FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
Allele: Dmel\trio6A
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General Information
Symbol
Dmel\trio6A
Species
D. melanogaster
Name
FlyBase ID
FBal0117304
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Key Links
Nature of the Allele
Progenitor genotype
Cytology
Description
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
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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

trio1/trio6A third instar larvae show a reduction in the number of boutons per muscle surface area (MSA). The number of boutons per MSA at muscle 4 is approximately 35% less than in controls.

trioS137203/trio6A third instar larvae show a reduction in the number of boutons per muscle surface area (MSA). The number of boutons per MSA at muscle 4 is approximately 35% less than in controls. The sizes of evoked excitatory junctional potentials (EJPs), miniature excitatory junctional potentials and the quantal content do not differ significantly from controls.

trio6A homozygous stage 17 embryos exhibit interrupted axon tracts.

Heterozygotes with Df(3L)Ar12-1 rarely survive to pupal stages. Mutants show a short stop phenotype, with defects in the ability of nerve branches to reach target muscles. ISNb (where the effect is most pronounced) and SNa are most sensitive to the loss of trio activity. In addition, there are occasional defects in epidermal muscle attachment sites. The CNS also shows pathfinding errors resulting in breaks in the longitudinal connectives. The axons often fail to traverse the segment boundary.

External Data
Interactions
Show genetic interaction network for Enhancers & Suppressors
Phenotypic Class
Phenotype Manifest In
Additional Comments
Genetic Interactions
Statement
Reference

trioS137203/trio6A does not suppress the larval neuromuscular junction overgrowth and increase in bouton number seen when Rac1V12.Scer\UAS is expressed in motor neurons under the control of Scer\GAL4BG380.

trioS137203/trio6A suppresses the increase in evoked excitatory junctional potential (EJPs) and quantal content seen when Rac1Scer\UAS.cLa is expressed in neurons under the control of Scer\GAL4OK6.

trioS137203/trio6A suppresses the increase in evoked excitatory junctional potential (EJPs) and quantal content seen when saxA.Scer\UAS.cBa and tkvQ199D.Scer\UAS.T:Ivir\HA1 are expressed in motor neurons under the control of Scer\GAL4BG380.

A large proportion of vav2 trio6A double mutant embryos exhibit gross patterning defects that make examination of axogenesis defects difficult. However in double mutant embryos that display less severe morphological defects the midline crossing phenotypes are enhanced compared to single mutants.

Stage 15 transheterozygous Df(2R)en-SFX31/trio6A embryos exhibit defects in central nervous system scaffolding with gaps in longitudinal tracts, loss of posterior commissures, or fusion of commissures in about 64% of the segments.

Stage 15 transheterozygous enE/trio6A embryos exhibit defects in central nervous system scaffolding with gaps in longitudinal tracts, loss of posterior commissures, or fusion of commissures in about 12% of the segments.

Xenogenetic Interactions
Statement
Reference
Complementation and Rescue Data
Partially rescued by
Not rescued by
Comments

Expression of trioScer\UAS.cBa in neurons under the control of Scer\GAL4OK6 rescues the reduction in synaptic bouton phenotype seen in trioS137203/trio6A third instar larvae. Expression of trioScer\UAS.cBa in muscles using Scer\GAL4G14 is unable to rescue the phenotype.

Expression of trioScer\UAS.cBa only in the larval stages using the neuronal driver Scer\GAL4elav.Switch.PO rescues the reduction in synaptic bouton phenotype seen in trioS137203/trio6A third instar larvae.

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Mutant
Wild-type
Stocks (1)
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Synonyms and Secondary IDs (3)
Reported As
Name Synonyms
Secondary FlyBase IDs
    References (8)