FB2024_03 , released June 25, 2024
Allele: Dmel\MED241
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General Information
Symbol
Dmel\MED241
Species
D. melanogaster
Name
FlyBase ID
FBal0246389
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Key Links
Genomic Maps

Nature of the Allele
Progenitor genotype
Cytology
Description

Amino acid replacement: Q212term.

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

C8193860T

Amino acid change:

Q212term | MED24-PA

Reported amino acid change:

Q212term

Comment:

Site of nucleotide substitution in mutant inferred by FlyBase based on reported amino acid change.

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

MED241/Df(3L)Exel6112 animals show normal mid-third instar (wandering behaviour) and late larval (everting anterior spiracles, barrel shape, midgut programmed cell death) ecdysone-triggered responses. 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.

The formation of the large acidic structures which normally occurs in salivary gland cells approximately 1.5 hours after head eversion is blocked in MED241/Df(3L)Exel6112 animals. Caspase activation at 2 hours after head eversion is also blocked. This results in a persistant salivary gland phenotype at 24 hours after puparium formation.

42-46% of MED241 pupae at 24 hr APF show persistent larval salivary glands and none or very few eclose. MED241/Df(3L)Exel6112 hemizygotes show similar phenotypes.

MED241/Df(3L)Exel6112 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.

MED241/Df(3L)Exel6112 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
Show genetic interaction network for Enhancers & Suppressors
Phenotypic Class
NOT suppressed by
Statement
Reference
Phenotype Manifest In
NOT suppressed by
Statement
Reference
Additional Comments
Genetic Interactions
Statement
Reference

Scer\GAL4Act5C.PU-mediated expression of Mdh2Scer\UAS.cWa fails to restore normal salivary gland cell death or rescue pupal lethality of MED241 animals.

Xenogenetic Interactions
Statement
Reference
Complementation and Rescue Data
Rescued by
Comments

Scer\GAL4Act5C.PU-mediated expression of MED24Scer\UAS.cWa restores normal salivary gland cell death and efficiently rescues pupal lethality in MED241 animals.

Images (0)
Mutant
Wild-type
Stocks (1)
Notes on Origin
Discoverer
External Crossreferences and Linkouts ( 0 )
Synonyms and Secondary IDs (8)
Reported As
Name Synonyms
Secondary FlyBase IDs
    References (3)