FB2024_03 , released June 25, 2024
Allele: Dmel\mir-14Δ1
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General Information
Symbol
Dmel\mir-14Δ1
Species
D. melanogaster
Name
FlyBase ID
FBal0150343
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Key Links
Mutagen
    Nature of the Allele
    Mutagen
    Progenitor genotype
    Cytology
    Description

    Imprecise excision of the mir-14k10213 insertion produces a 533bp deletion of the entire mir-14 gene.

    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

    mir-14Δ1/mir-14Δ1 flies show significant increases in posterior (P) wing compartment size and posterior / anterior (A) wing size ratio compared to controls. mir-14Δ1/mir-14Δ1 mutant wings are significantly larger than wild type wings.

    In wild type third instar larvae, two dorsal tracheal branches fuse to give rise to two terminal cells with multiple branches; a significantly increased percentage of mir-14Δ1/mir-14Δ1 mutant terminal branches have excess (>2) terminal cells.

    Salivary gland cell size is normal in homozygous wandering third instar larvae.

    Salivary gland fragments persist 24 hours after puparium in homozygous animals (no residual salivary gland material is present in wild-type animals at this stage).

    Homozygotes show a reduction in autophagy in the salivary glands, but not in the fat body, 14 hours after pupariation.

    Mutant adults have an elevated total body fat to total body protein ratio compared to controls.

    Mutant adults are more sensitive to starvation compared to controls.

    Mutants show no defects in targeting of the DL1 glomerulus in the antennal lobe.

    Mutants show significantly reduced survival to adulthood and also have a reduced adult life span compared to wild-type flies.

    Mutant animals show defects in anterior spiracle eversion at the larval-pupal transition; 52% of mutants show a failure to evert one or both spiracles.

    Homozygotes hatch at normal frequency, larvae survive to pupal stages at a rate similar to that of wild-type. Most mutant animals die during pupal development. Those that survive exhibit delayed eclosion and have a decreased mean and maximal lifespan. This decrease is particularly marked in females. Homozygotes are also much more susceptible than wild-type to being killed by salt stress. Homozygous adults have enlarged adipocytes. Animals have increased levels of Triacylglycerol and Diacylglycerol.

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

    mir-14Δ1/mir-14Δ1 is an enhancer of visible | dominant phenotype of hhMrt

    NOT Enhancer of
    Statement
    Reference

    mir-14[+]/mir-14Δ1 is a non-enhancer of visible | dominant phenotype of Bx1

    Suppressor of
    Statement
    Reference
    NOT Suppressor of
    Statement
    Reference

    mir-14[+]/mir-14Δ1 is a non-suppressor of visible | dominant phenotype of Bx1

    Phenotype Manifest In
    NOT Enhanced by
    Statement
    Reference
    Suppressed by
    NOT suppressed by
    Statement
    Reference
    Enhancer of
    Statement
    Reference

    mir-14Δ1/mir-14Δ1 is an enhancer of wing blade phenotype of hhMrt

    mir-14Δ1/mir-14Δ1 is an enhancer of wing vein L2 phenotype of hhMrt

    mir-14Δ1/mir-14Δ1 is an enhancer of wing vein L3 phenotype of hhMrt

    mir-14Δ1 is an enhancer of eye phenotype of rprGMR.PH

    NOT Enhancer of
    Statement
    Reference

    mir-14[+]/mir-14Δ1 is a non-enhancer of wing margin phenotype of Bx1

    Suppressor of
    NOT Suppressor of
    Statement
    Reference

    mir-14[+]/mir-14Δ1 is a non-suppressor of wing margin phenotype of Bx1

    Additional Comments
    Genetic Interactions
    Statement
    Reference

    mir-14Δ1/mir-14Δ1 significantly suppresses the wing curvature and decreases in posterior wing compartment size seen in Scer\GAL4hh-Gal4>hhHMS00492 flies; these flies actually show a significant increase in posterior wing compartment size (and P/A wing size ratio) compared to controls. Expression of hhHMS00492 driven by Scer\GAL4hh-Gal4 significantly (partially) suppresses the increases in wing size seen in mir-14Δ1/mir-14Δ1 mutants.

    mir-14Δ1/mir-14Δ1 significantly enhances wing phenotypes in hhMrt/+ flies, with 55% showing class I phenotypes, 31% showing class II phenotypes and 14% showing class III phenotypes.

    hhAC/+ or expression of hhHMS00492 driven by Scer\GAL4hh-Gal4 significantly suppresses the increased percentage of mir-14Δ1/mir-14Δ1 mutant dorsal tracheal branches that have excess (>2) terminal cells.

    Expression of Atg6GD11647 under the control of Scer\GAL4fkh.PU does not significantly alter the persistent salivary gland phenotype seen in mir-14Δ1 homozygotes 24 hours after pupariation.

    The reduction in salivary gland autophagy and persistent salivary gland phenotype which is seen in mir-14Δ1 homozygous pupae is suppressed in IP3K2Δ1/Y ; mir-14Δ1/mir-14Δ1 double mutant pupae.

    Expression of Ilp3Scer\UAS.cIa under the control of Scer\GAL4Ilp2.215-3 rescues the elevated total body fat to total body protein ratio seen in mir-14Δ1 adults.

    Expression of sugGD11090 under the control of Scer\GAL4Ilp2.215-3 partially rescues the elevated total body fat to total body protein ratio seen in mir-14Δ1 adults.

    The increased sensitivity of mir-14Δ1 adults to starvation can be partially suppressed by expression of sugGD11090 under the control of Scer\GAL4Ilp2.215-3.

    The reduced survival to adulthood and shorter than normal life span of mir-14Δ1 flies is suppressed by one copy of EcRV559fs. The defects in anterior spiracle eversion seen in mir-14Δ1 pupae are almost completely suppressed by one copy of EcRV559fs.

    Xenogenetic Interactions
    Statement
    Reference
    Complementation and Rescue Data
    Comments

    Expression of mir-14Scer\UAS.cLa.T:Disc\RFP driven by Scer\GAL4btl.PU rescues the excess tracheal terminal cell phenotype seen in mir-14Δ1/mir-14Δ1 third instar larvae.

    Expression of mir-14Scer\UAS.T:Ppyr\LUC under the control of Scer\GAL4fkh.PU rescues the persistent salivary gland phenotype seen in mir-14Δ1 homozygotes 24 hours after pupariation.

    Expression of mir-14Scer\UAS.T:Disc\RFP under the control of Scer\GAL4Lsp2.PH does not rescue the elevated total body fat to total body protein ratio seen in mir-14Δ1 adults.

    Expression of mir-14Scer\UAS.T:Disc\RFP under the control of either Scer\GAL4Ilp2.215-3 or Scer\GAL4arm.PS rescues the elevated total body fat to total body protein ratio seen in mir-14Δ1 adults.

    Images (0)
    Mutant
    Wild-type
    Stocks (2)
    Notes on Origin
    Discoverer
    External Crossreferences and Linkouts ( 0 )
    Synonyms and Secondary IDs (8)
    Reported As
    Name Synonyms
    Secondary FlyBase IDs
      References (13)