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General Information
Symbol
Dmel\Vhl1
Species
D. melanogaster
Name
FlyBase ID
FBal0246016
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Also Known As
dVHL1
Key Links
Nature of the Allele
Mutations Mapped to the Genome
 
Type
Location
Additional Notes
References
Comment:

A deletion which removes the first 81 codons of Vhl. It was reported as removing the first two in-frame ATG codons but there is an intervening in-frame ATG in the sequenced strain at codon 50.

Associated Sequence Data
DNA sequence
Protein sequence
 
 
Progenitor genotype
Cytology
Nature of the lesion
Statement
Reference

Deletion that removes 81 codons, including the first two in-frame start codons.

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 ( 1 )
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

Homozygous mutants are sluggish after hatching and die at the end of the first instar larval stage.

Homozygous follicle cell clones do not affect cell proliferation or viability.

Homozygous follicle cell clones show prominent epithelial defects, including stacking of follicle cells and a multilayering phenotype of more than three layers of cells (38% of clones) and flattening or stretching of the follicular epithelium (42% of clones). The remaining 20% of clones show swelling.

Homozygous follicle cell clones already show disorganisation or loss of microtubules in pre-stage 6 egg chambers. Loss of microtubules along the lateral cortex becomes more obvious in later egg chambers containing homozygous clones.

Vhl1 homozygous females which have been rescued to adulthood by expression of VhlScer\UAS.T:Ivir\HA1 under the control of Scer\GAL4btl.PS are sterile, with 70% of the ovarioles containing only degenerated egg chambers. The remaining ovarioles have very severe epithelial defects in their egg chambers, including prominent expansion of the epithelium into the germ cell proper. In other cases, the entire follicle cell epithelium becomes multilayered and the nurse cell complex is collapsed. Microtubules are barely detectable in the mutant egg chambers.

Embryos derived from females carrying homozygous germline clones mated to heterozygous males do not hatch and show a complete failure of tracheal formation.

Homozygotes are sluggish after hatching but can feed and survive until the end of the first larval instar. No homozygotes survive past the second instar stage.

Mutant embryos show two distinct classes of mutant tracheal phenotypes; the first involves abnormal tubule migration and the second involves enlarged tracheal lumens and tortuous tracheal tubes. Embryos having both classes of phenotype are seen.

The abnormal tracheal tubule migration phenotype includes misdirected tubules and ectopic branching in addition to disruption of the dorsal trunk. This phenotype is seen in heterozygous embryos (56% of heterozygotes show moderate defects, 6% show severe defects) as well as in homozygous embryos, where the phenotype is more severe (65% of homozygotes show moderate defects, 35% show severe defects). In some mutant embryos an entire section of the dorsal trunk migrates dorsally or ventrally. Abnormal sprouting of filopodium-like projections can be seen in isolated cells. In very severe cases, the entire tracheal system is disrupted, with an abundance of ectopic branching and rounded tracheal cells detached from the epithelium.

The enlarged tracheal lumen phenotype includes tracheal tubules with tortuous paths and dilated dorsal trunks. The phenotype is seen in both heterozygous (63% of cases) and homozygous embryos. Stage 14 mutant embryos show appearance of luminal chitin (as occurs in wild type), but stage 15 mutant embryos show a defect in the clearance of luminal chitin that normally occurs at this stage (chitin remains abundant in the mature dorsal trunk and is filled up to the apical surface of the tracheal cells in the mutant embryos).

External Data
Interactions
Show genetic interaction network for Enhancers & Suppressors
Phenotypic Class
Phenotype Manifest In
Other
Statement
Reference
Additional Comments
Genetic Interactions
Statement
Reference

Vhl1/+ ; awdj2A4/+ double heterozygous embryos have a severely disrupted tracheal tree with ectopic filopodia and isolated, round cells.

The penetrance of the tracheal lumen defect seen in Vhl1/+ embryos is not modified by btlH82Δ3/+ or by pntΔ88/+.

Xenogenetic Interactions
Statement
Reference
Complementation and Rescue Data
Rescued by
Partially rescued by
Comments

The lethality of Vhl1 mutants is rescued by Vhlhs.PD or by expression of VhlScer\UAS.T:Ivir\HA1 under the control of Scer\GAL4btl.PS.

Expression of Vhlhs.PD using heat shock of 37[o]C for 30 minutes twice daily rescues the lethality of Vhl1 homozygotes, and the rescued adults show no external morphological defects.

The ectopic branching phenotype seen in the tracheal system of Vhl1 homozygous embryos is partially rescued by expression of VhlScer\UAS.cHa under the control of Scer\GAL4btl.PS.

Images (0)
Mutant
Wild-type
Stocks (0)
Notes on Origin
Discoverer
External Crossreferences and Linkouts ( 0 )
Synonyms and Secondary IDs (3)
Reported As
Name Synonyms
Secondary FlyBase IDs
    References (4)