FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
Allele: Dmel\TlkΔ14
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General Information
Symbol
Dmel\TlkΔ14
Species
D. melanogaster
Name
FlyBase ID
FBal0151382
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Key Links
Allele class
Nature of the Allele
Allele class
Progenitor genotype
Cytology
Description

Imprecise excision of the P{lacW}tlkG0054 insertion has created a 2357bp deletion of most of the first intron and a portion of exon 2.

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

Females heterozygous for tlkΔ14 exhibit normal mitotic spindle morphology.

At 25oC females with mutant germ-line clones are sterile, layoing a small number of eggs that collapse shortly after deposition. At 18oC these females lay eggs that look normal, but a substantial portion of them appear to be shorter than wild type. Mutant embryos fail to hatch, and about two-thirds die during the first nine nuclear divisions. These embryos are usually devoid of DNA - those that do appear to be undergoing apoptosis. The other embryos form a syncitial blastoderm and only 12.5% of total embryos initiate gastrulation. these embryos harbour a number of distinct defects: The early nuclear divisions are asynchronous, as revealed by the appearance of both interphase and anaphase nuclei that is rarely observed in wild-type embryos. Furthermore, nuclei are connected by elongated DNA bridges indicating incomplete chromosomal segregation. Moreover, nuclei are heterogeneous in size and the DNA of the enlarged nuclei have a uniform cloudy appearance with some strongly stained DNA spots. When clones of tlkΔ14 cells are made in the imaginal disc, they are able to form clones of up to eight cells, and then dissappear from the growing tissue.

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

TlkΔ14 has abnormal mitotic cell cycle | temperature conditional phenotype, enhanceable by marsEP2477

Enhancer of
Statement
Reference

tlk[+]/TlkΔ14 is an enhancer of abnormal mitotic cell cycle | temperature conditional phenotype of marsEP2477

Phenotype Manifest In
Additional Comments
Genetic Interactions
Statement
Reference

The frequency of non-disjunction in male progenies from tlkΔ14/+; marsEP2477 females at 28.5[o]C is 4.4%, much higher than those from marsEP2477 (1.1%) or tlkΔ14/+ females (0.4%). This increase in frequency of non-disjunction is also temperature dependent, since there is no substantial increases in progeny from tlkΔ14/+; marsEP2477 females at 24[o]C when compared to marsEP2477 or tlkΔ14/+ females.

All tlkΔ14/+; marsEP2477 embryos at either metaphase or anaphase exhibit asynchrony so severe that it is impossible to distinguish what phase an embryo belongs to. Asynchronous chromosome segregation is observed in embryos where most of the nuclei are likely to be at anaphase. Despite this severe asynchrony during chromosome congression or segregation, the morphology of the mitotic spindles in tlkΔ14/+; marsEP2477 embryos is not significantly different from that in marsEP2477 embryos.

Xenogenetic Interactions
Statement
Reference
Complementation and Rescue Data
Comments
Images (0)
Mutant
Wild-type
Stocks (0)
Notes on Origin
Discoverer
External Crossreferences and Linkouts ( 0 )
Synonyms and Secondary IDs (2)
Reported As
Symbol Synonym
Name Synonyms
Secondary FlyBase IDs
    References (3)