FB2024_03 , released June 25, 2024
Allele: Dmel\NimC4KO
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General Information
Symbol
Dmel\NimC4KO
Species
D. melanogaster
Name
FlyBase ID
FBal0218199
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

Both in-frame ATG codons of the NimC4 open reading frame have been replaced by stop codons.

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

NimC4KO mutant pupae exhibit do not exhibit defects in phagocytic clearance of ddaC neuron dendrite debris following pupal stage dendritic pruning. As in controls, debris from injured larval dendrites (severed with an infrared laser) is completely cleared.

The CNS of NimC4KO mutant stage 16 embryos exhibits defects in the engulfment of apoptotic neurons. There is an increase in the volume of unengulfed apoptotic particles compared to controls.

Homozygotes have no gross morphological abnormalities.

The number, position and overall morphology of central nervous system glia (including the highly phagocygotic cell body glia) appear normal in homozygous embryos. However, the clearance of apoptotic cells in these embryos is markedly impaired. The number and total volume of apoptotic particles in the central nervous system (CNS) is increased about 2-fold compared to wild type, and the apoptotic particles are much less likely to be engulfed, with the fraction of particles that are completely untouched being increased 3-fold compared to wild type. The number, migration pattern and morphology of the macrophages appear normal. However, the number and volume of apoptotic particles outside of the CNS is strongly increased compared to wild type and many particles remain unengulfed, often forming large clusters near the macrophages.

Search behaviour and motility of phagocytes are normal in homozygous embryos, but many apoptotic particles remain completely untouched for extended periods of time or are briefly touched without being tethered. Many apoptotic particles attach to the mutant phagocyte cell surface without being engulfed Occasionally, incomplete phagocytic cups are seen.

External Data
Interactions
Show genetic interaction network for Enhancers & Suppressors
Phenotypic Class
Enhancer of
NOT Enhancer of
NOT Suppressor of
Statement
Reference
Phenotype Manifest In
Enhancer of
NOT Enhancer of
Statement
Reference
NOT Suppressor of
Statement
Reference
Additional Comments
Genetic Interactions
Statement
Reference
Xenogenetic Interactions
Statement
Reference
Complementation and Rescue Data
Comments

Expression of NimC4ΔEMI-NIM2.Scer\UAS.T:Avic\GFP under the control of Scer\GAL4repo does not rescue the defects in the engulfment of apoptotic neurons seen in the CNS of NimC4KO mutant embryos.

Expression of NimC4ΔEMI-NIM2.Scer\UAS.T:Avic\GFP under the control of Scer\GAL4repo rescues the defects in the engulfment of apoptotic neurons seen in the CNS of NimC4KO mutant embryos.

Expression of NimC4ΔEMI.Scer\UAS.T:Avic\GFP under the control of Scer\GAL4repo does not rescue the defects in the engulfment of apoptotic neurons seen in the CNS of NimC4KO mutant embryos.

Expression of NimC4ΔNIM1.Scer\UAS.T:Avic\GFP under the control of Scer\GAL4repo does not rescue the defects in the engulfment of apoptotic neurons seen in the CNS of NimC4KO mutant embryos.

Expression of NimC4ΔNIM2.Scer\UAS.T:Avic\GFP under the control of Scer\GAL4repo does not rescue the defects in the engulfment of apoptotic neurons seen in the CNS of NimC4KO mutant embryos.

Expression of NimC4ΔNIM3-4.Scer\UAS.T:Avic\GFP under the control of Scer\GAL4repo does not rescue the defects in the engulfment of apoptotic neurons seen in the CNS of NimC4KO mutant embryos. The glial membranes appear normal in these flies.

Expression of NimC4ΔNIM3-4ΔTM.Scer\UAS.T:Avic\GFP under the control of Scer\GAL4repo does not rescue the defects in the engulfment of apoptotic neurons seen in the CNS of NimC4KO mutant embryos.

Expression of NimC4ΔNIM3ΔTM.Scer\UAS.T:Avic\GFP under the control of Scer\GAL4repo does not rescue the defects in the engulfment of apoptotic neurons seen in the CNS of NimC4KO mutant embryos.

Expression of NimC4ΔNIM4ΔTM.Scer\UAS.T:Avic\GFP under the control of Scer\GAL4repo does not rescue the defects in the engulfment of apoptotic neurons seen in the CNS of NimC4KO mutant embryos.

Expression of NimC4ΔTM.Scer\UAS.T:Avic\GFP under the control of Scer\GAL4repo rescues the defects in the engulfment of apoptotic neurons seen in the CNS of NimC4KO mutant embryos.

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Mutant
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Stocks (0)
Notes on Origin
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External Crossreferences and Linkouts ( 0 )
Synonyms and Secondary IDs (4)
Reported As
Symbol Synonym
Name Synonyms
Secondary FlyBase IDs
    References (8)