FB2025_01 , released February 20, 2025
Allele: Dmel\Lkb14B1-11
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General Information
Symbol
Dmel\Lkb14B1-11
Species
D. melanogaster
Name
FlyBase ID
FBal0141053
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Key Links
Genomic Maps

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

Amino acid replacement: Q98term.

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

C13677407T

Amino acid change:

Q100term | Lkb1-PA; Q100term | Lkb1-PB; Q100term | Lkb1-PC; Q100term | Lkb1-PD; Q100term | Lkb1-PE; Q100term | Lkb1-PF; Q100term | Lkb1-PH; Q100term | Lkb1-PI; Q100term | Lkb1-PJ

Reported amino acid change:

Q98term

Comment:

Site of nucleotide substitution in mutant inferred by FlyBase based on reported amino acid change. Position of mutation on reference sequence inferred by FlyBase curator.

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

Lkb14B1-11 mutant class IV dendritic arborizing neuron MARCM clones display mild pruning defects at 18 h after pupariation.

Mutant third instar larvae show normal clearance of dyed food from the gut.

Heterozygous females have a mild border follicle cell migration defect.

lkb14B1-11 germ line clones cause loss of anterior-posterior polarisation of the oocyte. bcd and osk mRNA localisation fails. Mutant oocytes show loss of anterior-posterior microtubule gradient, with a high density of microtubules round the cortex and the lowest concentration in the centre. The progeny of these females are developmentally arrested before cellularization. A proportion of the mutant oocytes exit meiosis and adopt a nurse cell fate. The penetrance of this phenotype increases with age. This may be due to perdurance of the lkb1 gene product in germ-line clones.

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

lkb14B1-11 heterozygous animals expressing Hsap\HTTQ138.Scer\UAS.T:Disc\RFP-mRFP pan-neuronally (under the control of Scer\GAL4elav-C155) exhibit an adult escaper frequency of 1.8% and 3.7% respectively. These animals are viable and have a relatively normal walking ability, although they do not inflate their wings.

lkb14B1-11/+ significantly enhances the border follicle cell migration defects caused by expression of par-1Scer\UAS.C*.T:Avic\GFP under the control of Scer\GAL4slbo.2.6.

The maternal effect embryonic phenotype of par-1k06821b/par-1W3 is enhanced by heterozygosity for lkb14B1-11.

Xenogenetic Interactions
Statement
Reference
Complementation and Rescue Data
Images (0)
Mutant
Wild-type
Stocks (1)
Notes on Origin
Discoverer

lkb14B1-11 was identified in a genetic screen for germ-line clone mutants that disrupt the localization of the product of the transgene stauαTub67C.T:Avic\GFP-m6 in the oocyte.

Selected as: a mutant that results in defective localisation of an Avic\GFP-stau marker in living oocytes in females containing homozygous germ-line clones.

External Crossreferences and Linkouts ( 0 )
Synonyms and Secondary IDs (2)
Reported As
Name Synonyms
Secondary FlyBase IDs
    References (8)