FB2024_03 , released June 25, 2024
Allele: Dmel\Tbcb1
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General Information
Symbol
Dmel\Tbcb1
Species
D. melanogaster
Name
FlyBase ID
FBal0277883
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: L87Q.

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

T19486404A

Amino acid change:

L87Q | TBCB-PA

Reported amino acid change:

L87Q

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

TBCB1 mutant DL1 olfactory projection neuron clones exhibit ectopic dendrite arborization. Loss of dorsal branches in axons is seen at low penetrance.

Significantly fewer microtubules are seen in TBCB1 mutant oocytes and nurse cell clones throughout oogenesis compared to controls, although a few microtubules remain. The interphasic microtubule network in the epithelial follicle cells is also strongly depleted. Actin cytoskeleton is unaffected.

Clonal TBCB1 mutant cystoblasts always divide correctly into 16 cell germline cysts, although microtubule defects are detected, including in the germarium. No proliferation defects are observed in follicle cell clones.

In third instar larval TBCB1 homozygous mutant brains the mitotic index is similar to control brains.

In third instar larval TBCB1/Df(2R)ED3728 mutant brains the mitotic index is similar to control brains.

Homozygous TBCB1 mutant neuroblasts cultured from larvae are able to form mitotic spindles and are able to divide. However cell cycle progression is delayed compared to heterozygous control cells; 65% of cells are delayed in interphase as well as mitosis. The remaining cells are either arrested in metaphase or anaphase.

The antero-dorsal positioning of the nucleus is impaired in the TBCB1 mutant stage 9-10 oocyte clones. However at stage 4 the process of oocyte differentiation appears to be unaffected. Large TBCB1 mutant follicle cell clones form a disorganised multistratified epithelium, consistent with cell-polarity defects.

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

Very few single-cell clones are obtained when TBCDmiRNA.Scer\UAS is expressed in TBCB1 mutant DL1 olfactory projection neuron clones under the control of Scer\GAL4GH146.

Flies double heterozygous for αTub84B5 and TBCB1 are viable, but display strongly reduced fertility and follicle cell polarity defects.

par-1W3 complements TBCB1.

Xenogenetic Interactions
Statement
Reference
Complementation and Rescue Data
Rescued by
Comments

Expression of TBCB+tBa rescues the lethality seen in TBCB1 mutant larvae.

Expression of TBCBUbi.T:Avic\GFP-EGFP rescues the lethality seen in TBCB1 mutant larvae. The microtubule and cell polarity defects seen in TBCB1 mutant clones are also rescued.

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Mutant
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External Crossreferences and Linkouts ( 0 )
Synonyms and Secondary IDs (4)
Reported As
Symbol Synonym
Name Synonyms
Secondary FlyBase IDs
    References (2)