FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
Allele: Dmel\tumDH15
Open Close
General Information
Symbol
Dmel\tumDH15
Species
D. melanogaster
Name
FlyBase ID
FBal0176032
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: ??term.

Amino acid replacement: R195term.

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

C13857840T

Amino acid change:

R195term | tum-PA

Reported amino acid change:

R195term

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

In tumDH15/tumDH15 embryos, VL1, DT1, LO1 and VT1 muscles are missing, or show attachment or elongation defects.

Homozygous embryos show defects in muscle morphology and muscle attachment site selection. These defects are not limited to a specific subset of muscles. Muscles are often curved compared to wild type, and myotubes with ectopic extensions that often attach to the wrong tendon cell or fail to extend towards their normal attachment site are seen. Tendon cells are present, differentiated and in their proper locations in the mutant embryos and mutant muscles do form stable attachments with the tendon cells, as occurs in wild type. Muscle specification and myoblast fusion are not impaired in the mutant embryos. Actin accumulates normally at the sites of muscle attachment in mutant embryos, even when attachments are formed at incorrect locations. The mutant muscles no longer show uniform microtubule polarity at stages 14/15 and 16, in contrast to wild type.

Homozygous embryos have an excess of naked cuticle at the expense of denticles. Most denticles in the mutant belts are similar in size to the smaller denticles normally found in rows 1-4 of the wild-type belt pattern.

Binucleate cells are found in the embryonic epithelium of homozygous tumDH15 and trans-heterozygous tumDH15/Df(2R)Exel7128 embryos from stage 11 (extended germ band) onward.

The prominent feature of tumDH15 mutant embryos is a failure of cell division. A transient loss of tissue integrity during germ band retraction can is noted in some embryos. Late-stage tumDH15 mutant embryos show defects in nervous system and muscle organisation.

Mitosis in homozygous tumDH15 embryos is indistinguishable from heterozygous sibling embryos up to until mid-to-late stage 11 (extended germ band), when aberrant telophase figures and a few binucleate cells are observed in the dividing epithelial cells of some of the embryos. Older embryos (stage 12) have binucleate cells and aberrant telophase figures in the epithelium. In many cases, some cells sow no evidence of furrowing at a time in late anaphase when wild-type cells are constricting. However, some cells progress further in cytokinesis than others. The many examples of aberrant microtubule organisation seen in anaphase and telophase cells indicate that cell division is failing after chromosome separation. These tumDH15 mutant cells have variable microtubule morphologies, ranging from relatively few detectable microtubules with no apparent central spindle, to multiple microtubule bundles.

External Data
Interactions
Show genetic interaction network for Enhancers & Suppressors
Phenotypic Class
Suppressor of
Statement
Reference
Other
Statement
Reference
Phenotype Manifest In
NOT Enhanced by
Suppressor of
Statement
Reference
Additional Comments
Genetic Interactions
Statement
Reference

A tumDH15 heterozygous mutant background suppresses the actin remodelling and subsequent basolateral invasion of epithelial cells seen in flies expressing CskGD9345 in a stripe of cells at the anterior/posterior boundary of the larval wing disc under the control of Scer\GAL4ptc-559.1.

RacGAP50CDH15 reduces the severity of the mutant phenotype seen in wgl-12 embryos at the restrictive temperature; the double mutant embryos are larger than single mutant wgl-12 embryos, and there is an increase in spacing between denticles in the double mutant embryos. The ability of wgl-17/+ to suppress the excess naked cuticle phenotype of nkd2 embryos is suppressed by RacGAP50CDH15; the triple mutant embryos secrete uniform cuticle with no denticle belts.

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

Expression of tumScer\UAS.Z.T:Hsap\MYC under the control of Scer\GAL4prd.RG1 rescues the epidermal cytokinesis defects of tumDH15 embryos, but does not rescue the muscle patterning defects.

Expression of tumScer\UAS.Z.T:Hsap\MYC under the control of Scer\GAL469B fails to rescue the muscle patterning defects of tumDH15 embryos.

Expression of tumScer\UAS.Z.T:Hsap\MYC under the control of Scer\GAL4G14 significantly improves muscle morphology and patterning defects in tumDH15 embryos.

Expression of tumScer\UAS.T:Hsap\MYC.cZa in tumDH15 mutant embryos driven by Scer\GAL4prd.RG1 rescues the binucleate phenotype. Stripes of binucleate cells alternate with rescued mononucleate cells.

Expression of tumΔPav.Scer\UAS driven by Scer\GAL4prd.RG1 fails to rescue cytokinesis in tumDH15 mutant embryos.

Expression of tumΔPbl.Scer\UAS driven by Scer\GAL4prd.RG1 fails to rescue cytokinesis in tumDH15 mutant embryos.

Expression of tumΔEIE.Scer\UAS driven by Scer\GAL4prd.RG1 fails to rescue cytokinesis in tumDH15 mutant embryos.

Expression of tumΔYRL.Scer\UAS driven by Scer\GAL4prd.RG1 fails to rescue cytokinesis in tumDH15 mutant embryos.

Images (0)
Mutant
Wild-type
Stocks (1)
Notes on Origin
Discoverer

Induced on: a wgl-12 chromosome. Selected as: a modifier of the wgl-12 mutant phenotype.

External Crossreferences and Linkouts ( 0 )
Synonyms and Secondary IDs (5)
Reported As
Name Synonyms
Secondary FlyBase IDs
    References (9)