FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
Allele: Dmel\NmnatΔ4790-2
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General Information
Symbol
Dmel\NmnatΔ4790-2
Species
D. melanogaster
Name
FlyBase ID
FBal0198135
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Also Known As
NmnatΔ4792
Key Links
Nature of the Allele
Progenitor genotype
Cytology
Description

Imprecise excision of the P{EPgy2} element, resulting in deletion of the first three exons of the Nmnat gene.

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

At 24-28hrs after egg laying, dendrites of the dorsal class IV neuron (ddaC) in homozygous NmnatΔ4790-2 mutants do not show any patterning defects and are largely indistinguishable from those of wild-type controls. Although heterozygosity for NmnatΔ4790-2 has no effect on dendritic outgrowth or branching of ddaC at 48 hours after egg laying, there is a significant reduction in the total number of terminal dendritic branches and total dendrite length at 120 hours after egg laying. At 72 hours after egg laying, NmnatΔ4790-2 heterozygotes tend to have fewer terminal dendrites, although the average number of terminal dendritic branches is not significantly different from wild-type controls until after 72 hours after egg laying.

The axons of class IV neurons in NmnatΔ4790-2 heterozygotes are largely intact at 120 hours after egg laying. Axons enter the CNS appropriately and their projection patterns in the ventral nerve cord (VNC) are morphologically indistinguishable from wild-type controls.

Whereas wild-type ddaC clones elaborate highly branched dendrites, NmnatΔ4790-2 clones show a significant reduction in the total number of terminal dendritic branches, effectively reducing dendritic field coverage. There is no evidence of severed or degenerated dendrites in NmnatΔ4790-2 clones as dendritic trunks and branches are largely intact.

Class III neurons, that normally elaborate actin-rich protrusions along their dendrites, are largely devoid of terminal branches in NmnatΔ4790-2 clones. Class I neurons, which normally elaborate few terminal branches that cover a small receptive field, exhibit a minor, but statistically significant decrease in the total number of dendritic branches in NmnatΔ4790-2 clones.

Although class IV neurons do not exhibit an axon degeneration phenotype in NmnatΔ4790-2 heterozygotes, approximately 96% of homozygous NmnatΔ4790-2 sensory neuron clones show extensive fragmentation of axons and a near complete loss of axon terminals in the ventral nerve cord.

Different subtypes of motor neurons display both terminal and dendritic branching defects and extensive beading and fragmentation at 120 hours after egg laying in NmnatΔ4790-2 MARCM clones. The axon terminals of NmnatΔ4790-2 motor neuron clones are absent in the majority of neurons. Phenotypes are progressive, getting worse with age, as axons and dendrites of NmnatΔ4790-2 motor neuron clones are largely intact at 72 hours after egg laying.

Flies with eyes that contain NmnatΔ4790-2 clones show reduced depolarization and on/off responses in electroretinogram (ERG) recordings and show photoreceptor synaptic defects.

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

A transheterozygous combination of NmnatΔ4790-2 and wtsx1 does not show any synthetic phenotypes in affecting axon or dendrite development of class IV neurons.

Xenogenetic Interactions
Statement
Reference
Complementation and Rescue Data
Comments

Post-synaptic expression of the enzymatically-inactive NmnatWR.Scer\UAS transgene, under the control of Scer\GAL421-7 is sufficient to rescue the dendritic phenotypes observed in NmnatΔ4790-2 ddaC clones, demonstrating a cell-autonomous function for Nmnat in the proper maintenance of class IV dendrites.

Post-synaptic expression of NmnatScer\UAS.cZa under the control of Scer\GAL421-7 is sufficient to rescue the dendritic phenotypes observed in NmnatΔ4790-2 ddaC clones, demonstrating a cell-autonomous function for Nmnat in the proper maintenance of class IV dendrites.

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Mutant
Wild-type
Stocks (0)
Notes on Origin
Discoverer
External Crossreferences and Linkouts ( 0 )
Synonyms and Secondary IDs (4)
Reported As
Symbol Synonym
NmnatΔ4790-2
NmnatΔ4792
nmnatΔ4792
Name Synonyms
Secondary FlyBase IDs
    References (3)