FB2026_02 , released June 18, 2026
Allele: Dmel\nero1
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General Information
Symbol
Dmel\nero1
Species
D. melanogaster
Name
FlyBase ID
FBal0240589
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Key Links
Allele class
Nature of the Allele
Allele class
Progenitor genotype
Cytology
Description

Imprecise excision of P{lacW}neros1921 generates a small deletion that removes 189bp of the nero open-reading frame.

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

nero1 mutants die as second instar (L2) larvae, whether they are homozygous or in heteroallelic combinations ((with Df(3R)04661).

nero1 mutants cause both mild bristle loss and a severe reduction in bristle size. nero1 mutant socket cells are specified but fail to reach their mature size. Cells adjacent to nero1 exhibit mutant bristles that are smaller in size as indicated by trichome size and spacing. Ectodermal cells that lack nero in the developing thoraxes 47APF are significantly smaller than adjacent wild-type cells.

Rhabdomere size in nero1 mutant eye clones are also reduced when compared with adjacent wild-type cells, suggesting a defect in photoreceptor size.

nero1 mutant clones generated using the Scer\FLP1ey.PN technique are generally irrecoverable. However, nero1 mutant clones are easily obtained using Scer\FLP1ey.PN when cell competition is ameliorated through the use of an FRT chromosome bearing a cell lethal mutation that effectively removes the mitotic wild-type, sister twin cells. Indeed, nero1 mutant clones generated using this technique completely overtake the eye, leading to eyes and heads that are much smaller than wild-type heads.

nero1 mutant clones generated in the wing imaginal disc are smaller and contain fewer cells than their associated wild-type twin spots. The differences in cell number between nero1 clones and their wild-type twin spots are less obvious in small clones and clearly increase as clones get larger. This is likely caused by differences in nero protein perdurance in small clones. nero mutant cells are most likely eliminated because of an inability to compete with wild-type cells.

nero1 mutant larval fat bodies prominently display enlarged, acidified structures, even when the animals are fed an amino acid source, suggesting that nero1 mutant larvae undergo a constitutive starvation response in the presence of an amino acid source.

nero1 mutant clones show a decreased level of BrdU incorporation, indicating a delay in cell cycle progression.

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

nero1 is an enhancer of decreased cell size phenotype of eEF501296

Suppressor of
Statement
Reference
Phenotype Manifest In
Suppressed by
Statement
Reference
NOT suppressed by
Additional Comments
Genetic Interactions
Statement
Reference

eIF-5A01296; nero1 double mutant larvae display a slightly more severe larval growth defect than eIF-5A01296 mutants alone.

Unlike either nero1 or Tsc1Q87X mutant clones, Tsc1Q87X nero1 double mutant clones cannot be recovered. Tsc1Q87Xfully suppresses the autophagic defect seen in nero1 mutant animals. However, this epistatic relationship is reveresed in other contexts such as larval growth and developmental timing. Tsc1Q87X mutant larvae appear to undergo precocious development. However, this precocious development is suppressed in Tsc1Q87X nero1 double mutant larvae.

Overexpression of eIF-5AScer\UAS.cPa (under the control of Scer\GAL4tub) is not sufficient to rescue bristle size defects associated with nero1 mutant clones.

Xenogenetic Interactions
Statement
Reference

Overexpression of Hsap\DOHHScer\UAS.cPa fully complements defects in bristle size associated with nero1 mutant clones on the thorax and does not cause any other obvious phenotype.

Overexpression of Hsap\DOHHH56A.Scer\UAS fails to suppress the defects in bristle size associated with nero1 mutant clones on the thorax and does not cause any other obvious phenotype.

Overexpression of Hsap\DOHHH89A.Scer\UAS fails to suppress the defects in bristle size associated with nero1 mutant clones on the thorax and does not cause any other obvious phenotype.

Overexpression of Hsap\DOHHH208A.Scer\UAS fails to suppress the defects in bristle size associated with nero1 mutant clones on the thorax and does not cause any other obvious phenotype.

Overexpression of Hsap\DOHHH240A.Scer\UAS fails to suppress the defects in bristle size associated with nero1 mutant clones on the thorax and does not cause any other obvious phenotype.

Complementation and Rescue Data
Comments

Overexpression of eIF-5AScer\UAS.cPa (under the control of Scer\GAL4tub) is not sufficient to rescue bristle size defects associated with nero1 mutant clones.

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Stocks (1)
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External Crossreferences and Linkouts ( 0 )
Synonyms and Secondary IDs (1)
Reported As
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Name Synonyms
Secondary FlyBase IDs
    References (1)