FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
Allele: Dmel\Mdh21
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General Information
Symbol
Dmel\Mdh21
Species
D. melanogaster
Name
FlyBase ID
FBal0246393
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Key Links
Genomic Maps

Nature of the Allele
Progenitor genotype
Cytology
Description

236bp deletion that shifts the reading frame after codon 242, changing amino acid residues 243-253 from GAGSATLSMAY to EGQEEHPEGHX.

Mutations Mapped to the Genome
Curation Data
Type
Location
Additional Notes
References
Comment:

Approximate boundaries of a 236 bp deletion that shift the reading frame after residue 242 leading to early translation termination afte 10 novel amino acids.

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

Most of the mid-third instar (wandering behaviour) and late larval (everting anterior spiracles, barrel shape) ecdysone-triggered responses are normal in Mdh21/Df(3R)Exel6178 animals. However, defects in midgut programmed cell death are seen. The prepupal ecdysone-triggered responses (head eversion, wing and leg inflation and leg extension) also occur normally. In the salivary gland, mid-third instar glue synthesis is normal, late larval glue secretion is normal, but prepupal salivary gland programmed cell death is defective.

46% of Mdh21/Mdh22 pupae at 24 hr APF show persistent larval salivary glands and none eclose.

Mdh21/Df(3R)Exel6178 pupae appear virtually identical to controls at 12 hr APF, with no apparent defects in adult head eversion or leg eversion, and no delay between puparium formation and head eversion. However, whereas control salivary glands rupture and degrade soon after head eversion, mutant glands remain intact and maintain their morphological integrity. At 24 hr APF, 40-42% of Mdh21/Df(3R)Exel6178 pupae show persistent larval salivary glands and none eclose.

Mdh21/Df(3R)Exel6178 salivary glands do not exhibit caspase-driven programmed cell death at 14 hr or 20 hr APF, in contrast to salivary glands from controls. However, salivary gland autophagy is induced normally.

Mutants show defects in destruction of the larval salivary glands, having persistant larval salivary glands at the pupal stage.

External Data
Interactions
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Phenotypic Class
Phenotype Manifest In
Additional Comments
Genetic Interactions
Statement
Reference
Xenogenetic Interactions
Statement
Reference
Complementation and Rescue Data
Comments

One copy of Mdh2T:Hsap\MYC restores normal salivary gland cell death and efficiently rescues pupal lethality in Mdh21/Mdh22 animals.

Scer\GAL4Act5C.PU-mediated expression of Mdh2Scer\UAS.cWa restores normal salivary gland cell death and efficiently rescues pupal lethality in Mdh21/Df(3R)Exel6178 animals.

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Mutant
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Notes on Origin
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External Crossreferences and Linkouts ( 0 )
Synonyms and Secondary IDs (7)
Reported As
Name Synonyms
Secondary FlyBase IDs
    References (3)