FB2026_02 , released June 18, 2026
Allele: Dmel\nudE39A
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General Information
Symbol
Dmel\nudE39A
Species
D. melanogaster
Name
FlyBase ID
FBal0221533
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Key Links
Nature of the Allele
Cytology
Description

Imprecise excision of the progenitor insertion, resulting in a deletion that removes the first three exons and part of the fourth exon of nudE. This deletion removes the first 37 codons of nudE, including the initiation codon.

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

nudE39A/nudE39A or nudE39A/Df(3L)BSC673 third instar larval class IV da neurons show significant decreases in dendrite length and branch number compared to controls; mutant neurons also display a severe axon splitting phenotype (multiple fine branches form a short distance from the soma, rather than extending as a single process). The number of Golgi complexes mislocalizing to axons significantly increases in nudE39A/nudE39A larvae. nudE39A/nudE39A regulates microtubule growth and dynamics in both axons and dendrites (significant increase in Eb1 comets), as well as orientation of axonal microtubules (rather than wild type purely anterograde movement, mutant microtubules show anterograde and retrograde movement).

Homozygous germline clones result in a failure to specify the oocyte.

Spermatids from mutant third instar larvae testes do not show cytokinesis defects.

The mitotic progression of many cells in homozygous and nudE39A/Df(3L)AC1 larval brains is arrested at prometaphase or metaphase, with very few cells continuing to anaphase. The mitotic index is substantially elevated compared to that of wild type. 89.4% of homozygous mitotic cells and 96.9% of nudE39A/Df(3L)AC1 mitotic cells have overcondensed chromosomes.

Only a small minority of mitotic cells have normal (bipolar, straight) spindles in homozygous larval brains, with the most frequent defects being broad, unfocused spindle poles and the failure of centrosomes to remain attached to the spindles. Other defects include curved spindles, the presence of two centrosomes at one pole but none at the other pole, and supernumerary centrosomes.

The chromosomes fail to form a tight metaphase plate in most mitotic figures of homozygous larval brains. 61% of mutant cells have uncongressed chromosomes compared to only 42% in control cells.

The centrosomes fail to move from the cortex to the nuclear envelope just before the first meiotic division in homozygous spermatocytes, in contrast to wild type. 88% of cells at meiosis metaphase I in homozygous testes show spindle-detachment defects. The mutant metaphase I spermatocytes often have spindle-like bipolar arrays of microtubules which are assembled around the chromosomes but not connected to the membrane-bound asters.

The proportions of cells in meiotic anaphase or telophase are normal in mutant testes, and there is no failure in cytokinesis. However, chromosome segregation is often aberrant at late anaphase and telophase, with DNA apportioned unequally to the two daughter cells or with DNA remaining in the middle of the spindle. As a result, mutant onion stage spermatids have nuclei of different sizes. In addition, the sizes of the Nebenkern is uneven.

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

nudE39A/nudE39A enhances dendrite morphology defects in class IV da neurons of third instar larvae with expression of DlicdsRNA.Scer\UAS.cUa (along with UAS-dcr2) driven by Scer\GAL4ppk.PU.

γTub23CA15-2/γTub23CA14-9 does not affect the amount of axonal microtubule retrograde transport seen in nudE39A/nudE39A class IV da neurons in third instar larvae.

Expression of Lis-1Scer\UAS.cLa driven by Scer\GAL4ppk.PU significantly suppresses decreases in dendrite length, branch number and distribution seen in nudE39A/nudE39A third instar larval ddaC neurons.

The mitotic index and the proportion of mitotic figures in anaphase relative to those in prometaphase or metaphase is nearly normal in the brains of nudE39A zwilch1229 double homozygous larvae.

Xenogenetic Interactions
Statement
Reference
Complementation and Rescue Data
Partially rescued by
Comments

nudE+tAa rescues nudE39A/Df(3L)BSC673 lethality, with morphologically normal adults apart from slightly disordered wing margin bristles; decreases in dendrite length and branch number and the splitting axon phenotype in third instar larval class IV da neurons are rescued. Expression of nudEScer\UAS.A driven by Scer\GAL4ppk.PU partially rescues the decreases in dendrite length and branch number and the axon splitting phenotype (but not lethality) in nudE39A/nudE39A third instar larval class IV da neurons. Expression of nudEΔC.Scer\UAS driven by Scer\GAL4ppk.PU fully rescues decreases in dendrite length and branch number in nudE39A/nudE39A third instar larval class IV da neurons (significantly better rescue compared to nudEScer\UAS.A). nudEΔC fully rescues decreases in dendrite length and branch number in nudE39A/nudE39A third instar larval class IV da neurons. nudEE113A.R124A partially rescues decreases in dendrite length and branch number in nudE39A/Df(3L)BSC673 third instar larval ddaC neurons.

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Synonyms and Secondary IDs (3)
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Name Synonyms
Secondary FlyBase IDs
    References (4)