FB2024_03 , released June 25, 2024
Allele: Dmel\midGA174
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General Information
Symbol
Dmel\midGA174
Species
D. melanogaster
Name
FlyBase ID
FBal0178888
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Key Links
Nature of the Allele
Progenitor genotype
Cytology
Description

Nucleotide substitution: C680T. (Nucleotide numbering is according to cDNA clone RE27439).

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
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Comments on Models/Modifiers Based on Experimental Evidence ( 0 )
 
Disease-implicated variant(s)
 
Phenotypic Data
Phenotypic Class
Phenotype Manifest In
Detailed Description
Statement
Reference

Some cells of the central nervous system of homozygous midGA174 embryos exhibit abnormal neuronal cell fate specification.

midGA174 and midGA174/Df(2L)x528 mutant embryos show a significant loss of NB1-1 in the odd-numbered abdominal segments (68.7 % and 70.8% loss, respectively) while the loss of NB1-1 in the even-numbered abdominal segments is minimal (5 and 9.7%). Likewise, loss of NB2-5 and NB2-4 neuroblasts is higher in odd-numbered than in even-numbered abdominal segments, although the loss is less extreme than for NB1-1 neuroblasts (NB2-5 odd loss: 32% in midGA174 embryos and 29% in midGA174/Df(2L)x528 embryos; even loss is 7% and 8.3%; NB2-4 loss is 19% for midGA174 embryos and 17.8% for midGA174/Df(2L)x528 embryos; even loss is 3.6% and 4.1%). There is no evidence that row 1/2 neuroblasts adopt row 3/4 identities in these embryos. In contrast, formation of early row 7 neuroblasts is unaffected in midGA174 embryos. Similarly to the situation with neuroblasts, GMC7-1a forms correctly in these embryos but GMC1-1a is frequently absent in odd-numbered segments.

Stage 16 midGA174 embryos show no ectopic EL neuron clusters, suggesting that NB3-3 identity is correctly specified.

In 46% of hemisegments, midGA174 embryos show a one eve-positive extra neuron per hemisegment at a position similar to the RP2 neuron. This extra neuron projects its axon toward the ventral midline, indicating that it is not, in fact, an RP2 neuron. The ectopic neuron occurs in similar amounts in odd-numbered and even-numbered segments.

The mature ventral nerve cord of midGA174 embryos shows a frequent loss of the lateral-most en-positive cell clusters. The medio-lateral cluster contains 3-4 instead of 5-6 cells and these cells are spatially disarranged. At the ventral midline, the number of midGA174 cells is reduced to 4-5 in most segments and midGA174 cells are completely absent in 12% of segments.

Mutant larvae show loss of denticles in the ventral most part of the abdominal denticle belts.

External Data
Interactions
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Phenotypic Class
Phenotype Manifest In
Enhanced by
Additional Comments
Genetic Interactions
Statement
Reference

Embryos doubly mutant for midGA174 and exexKK30 do not show enhancement of the respective single mutant central nervous system phenotypes.

Embryos doubly mutant for midGA174 and HGTXD25 exhibit gross defects in the architecture of the central nervous system.

Xenogenetic Interactions
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Reference
Complementation and Rescue Data
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Mutant
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External Crossreferences and Linkouts ( 0 )
Synonyms and Secondary IDs (1)
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    References (3)