FB2024_03 , released June 25, 2024
Allele: Dmel\l(2)gd1d7
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General Information
Symbol
Dmel\l(2)gd1d7
Species
D. melanogaster
Name
FlyBase ID
FBal0043607
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Also Known As
lgdd7
Key Links
Genomic Maps

Allele class
Nature of the Allele
Allele class
Progenitor genotype
Cytology
Description

Carries a single nucleotide deletion that results in a new translational frame and a premature stop codon after the addition of 22 new amino acids.

A 2 bp deletion at amino acid position 215 which results in a frame shift and a translational stop 14 amino acids downstream, leading to a truncated protein containing only the first DM14 domain.

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

A two base pair deletion within amino acid 215 that results in a frameshift and translation termination 14aa downstream. The two deleted bases within the codon were not specified.

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

21% of homozygous egg chambers contain 32 cells. 69% of homozygous germaria contain 'stem cysts' in which the female germline stem cells are interconnected to daughter cells.

l(2)gd1d7 wing discs contain enlarged maturing endosomes compared to wild type.

l(2)gd1d7 mutants do not exhibit autophagy or eye disc differentiation defects.

Scer\GAL4hh-Gal4-mediated expression of l(2)gd1NIG.4713R (in the presence of Dcr-2Scer\UAS.cDa) in a l(2)gd1d7/+ background results in posterior compartment peripodial cells of the wing disc adopting a columnar shape and forming a continuation of the lateral part of the disc epithelium - i.e. a transformation of peripodial into disc cells. TEM analysis shows that posterior compartment cells contain a class of endosomes that are enlarged compared to normal cells, though normal sized multi-vesicular bodies are also present. Lysosomes are of normal size.

Oocyte follicle cells mutant for l(2)gd1d7 precociously go through the mitotic-to-endocycle switch, as evidenced by the increased size of their nuclei compared to controls. The stalk that connects the egg chambers is elongated compared to controls. Endosomes are enlarged.

l(2)gd1SH0495/l(2)gd1d7 pharates exhibit: loss of notal bristles, duplications/quadruplications of notal socket cells at the expense of other cell fates of this organ, foreshortening (vein 4) or loss (veins 2 and 5) of vein tissue, ectopic formation of leg joints and a reduction of the tarsal region.

Wing pouch clones show increased cell death.

Adult flies bearing l(2)gd1d7 clones sometimes show tumorous growths in nota.

Cells of l(2)gd1d7 wing disc clones form/accumulate late endosomes.

If l(2)gd1d7 somatic clones are made in the wing disc during the first instar stage, they are rarely found in wing pouches of late third instar larvae, occasionally leaving scars. However clones are frequently recovered outside the pouch. If induced later some mutant clones are found in the wing pouch though many more twin spot clones are seen than mutant ones. Mutant clones are rounded in shape. Wings that develop from these discs show wing vein disruption. In l(2)gd1 mutant discs, some proneural clusters are formed, but the sensory organ precursors do not form.

Overgrowing imaginal discs show pattern duplications. Phenotype is more severe than for l(2)gd11.

Homozygotes display imaginal disc overgrowth and frequent disc duplication.

External Data
Interactions
Show genetic interaction network for Enhancers & Suppressors
Phenotypic Class
Enhanced by
Statement
Reference
Suppressed by
NOT suppressed by
Statement
Reference
Enhancer of
Statement
Reference

l(2)gd1[+]/l(2)gd1d7 is an enhancer of abnormal cytokinesis | dominant phenotype of shrbG5

Other
Phenotype Manifest In
Enhanced by
Statement
Reference
NOT Enhanced by
Statement
Reference
Suppressed by
Statement
Reference

l(2)gd1d7 has phenotype, suppressible by HrsD28

l(2)gd1d7 has phenotype, suppressible by aph-1D35

l(2)gd1d7 has phenotype, suppressible by aph-1[+]/aph-1D35

l(2)gd1d7 has phenotype, suppressible by car1/car1

l(2)gd1d7 has wing disc phenotype, suppressible by PsnC1

NOT suppressed by
Statement
Reference

l(2)gd1d7 has phenotype, non-suppressible by Rab5Tub.CFP

l(2)gd1d7 has phenotype, non-suppressible by Rab7Tub.Venus

l(2)gd1d7 has phenotype, non-suppressible by kuzES24

Enhancer of
Statement
Reference

l(2)gd1[+]/l(2)gd1d7 is an enhancer of female germline stem cell phenotype of shrbG5

l(2)gd1d7 is an enhancer of wing disc phenotype of NAx-M1

NOT Enhancer of
Statement
Reference

l(2)gd1d7 is a non-enhancer of eye disc | increased number phenotype of PsnC1

l(2)gd1d7 is a non-enhancer of sensory mother cell | increased number phenotype of PsnC1

Suppressor of
Statement
Reference

l(2)gd1[+]/l(2)gd1d7 is a suppressor of egg chamber phenotype of shrbG5

l(2)gd1[+]/l(2)gd1d7 is a suppressor of female germline cell phenotype of shrbG5

l(2)gd1d7 is a suppressor of arista | increased number phenotype of obk1

l(2)gd1d7 is a suppressor of wing disc phenotype of SerCS94/SerRX106

NOT Suppressor of
Statement
Reference

l(2)gd1d7 is a non-suppressor of eye disc | increased number phenotype of PsnC1

l(2)gd1d7 is a non-suppressor of sensory mother cell | increased number phenotype of PsnC1

Additional Comments
Genetic Interactions
Statement
Reference

The fraction of egg chambers containing 32 cells is reduced in l(2)gd1d7/shrbG5 double heterozygotes compared to shrbG5 heterozygotes. The fraction of germaria containing 'stem cysts' in which the female germline stem cells are interconnected to daughter cells is increased in l(2)gd1d7/shrbG5 double heterozygotes compared to shrbG5 heterozygotes.

Rab5αTub84B.T:Avic\GFP-ECFP or Rab7αTub84B.T:Avic\GFP-EYFP do not rescue the ectopic N activation phenotype (ectopic expression of wg) in l(2)gd1d7 wing discs.

Scer\GAL4hh-Gal4-mediated expression of tkvScer\UAS.T:Avic\GFP, Nintra.Scer\UAS.T:Avic\GFP-EGFP,T:Mmus\Cd8a or T48Scer\UAS.T:Avic\GFP suppresses the ectopic N activation phenotype (ectopic expression of wg) in the posterior of l(2)gd1d7 wing discs. In contrast, expression of NScer\UAS.cUa enhances the phenotype, while Hsap\LAMP1Scer\UAS.T:Avic\GFP-EGFP has no effect.

The ectopic N activation phenotype (ectopic expression of Ecol\lacZDdc.be2.E(spl)m8-HLH) in l(2)gd1d7 wing disk clones is suppressed if cells are also mutant for HrsD28 or aph-1D35, but not for kuzES24.

Heterozygosity for aph-1D35suppresses the ectopic N activation phenotype (ectopic expression of wg) in l(2)gd1d7 wing discs.

Scer\GAL4hh-Gal4-mediated expression of Vha68-1GD7717 suppresses the ectopic N activation phenotype (ectopic expression of wg) in the posterior of l(2)gd1d7 wing discs.

Scer\GAL4hh-Gal4-mediated expression of NΔEGF1-36.Scer\UAS.T:Hsim\VP16,T:Ecol\lexA enhances while NBC.Scer\UAS.T:Ecol\lexA suppresses the ectopic N activation phenotype (ectopic expression of wg) in the posterior of l(2)gd1d7 wing discs.

Scer\GAL4hh-Gal4-mediated expression of Rab7GD11800 suppresses the ectopic N activation phenotype (ectopic expression of wg) in the posterior of l(2)gd1d7 wing discs.

Homozygosity of car1 suppresses the ectopic N activation phenotype (ectopic expression of wg) in l(2)gd1d7 wing discs.

Scer\GAL4hh-Gal4-mediated expression of Vps39GD12152 suppresses the ectopic N activation phenotype (ectopic expression of wg) in the posterior of l(2)gd1d7 wing discs.

The ectopic upregulation of N signaling seen in l(2)gd1d7 clones is suppressed when clones also carry the HrsD28 mutation.

Heterozygosity for PsnC1 weakens the l(2)gd1SH0495/l(2)gd1d7 leg phenotypes.

Wing pouch clones double mutant for l(2)gd1d7 and Su(H)8 show the same increase in cell death as observed in l(2)gd1d7 clones.

The proliferation defects seen in l(2)gd1d7 wing disc cells are suppressed by the addition of PsnC1. NAx-M1, l(2)gd1d7 mutant wing discs show an extreme phenotype where the disc loses all visible organisation and forms a rounded ball of cells. The neurogenic phenotype seen in PsnC1 is unaffected by the addition of l(2)gd1d7. The small eye disc phenotype also resembles that of PsnC1.

Xenogenetic Interactions
Statement
Reference

Scer\GAL4hh-Gal4-mediated expression of Hsap\LAMP1Scer\UAS.T:Avic\GFP-EGFP has no effect on the ectopic N activation phenotype (ectopic expression of wg) in the posterior of l(2)gd1d7 wing discs.

Complementation and Rescue Data
Images (0)
Mutant
Wild-type
Stocks (1)
Notes on Origin
Discoverer
Comments
Comments

l(2)gd11, l(2)gd14, l(2)gd1d7 and l(2)gd1d10 all harbor the same lesion.

External Crossreferences and Linkouts ( 0 )
Synonyms and Secondary IDs (3)
References (15)