FB2024_03 , released June 25, 2024
Allele: Dmel\cpbM143
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General Information
Symbol
Dmel\cpbM143
Species
D. melanogaster
Name
FlyBase ID
FBal0103870
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: ?148term.

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

G1705839A

Amino acid change:

W148term | cpb-PA; W148term | cpb-PB

Reported amino acid change:

?148term

Comment:

G to A nucleotide change at the second or third position of the wild type Trp codon leads to a nonsense mutation (exact site of mutation unspecified). The mutation was annotated at the second base of the codon.

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

cpbM143 mutants exhibit accumulate of F-actin inside border cell clusters and exhibit delayed border cell migration at stages 9 and 10. Around 10% of cpbM143 mutant clusters disintegrate.

Homozygous clones in the wing disc have abnormally straight boundaries and the clones are rounder than their wild-type twin spots, suggesting that the clones minimise contacts with wild-type neighbours. The mutant clone tissue is folded, but maintains the columnar shape of a polarised epithelium.

Somatic mosaic cpbM143 eyes exhibit a rough phenotype, with ommatidia displaying a reduced number of photoreceptor cells. In addition, many cells have widened or split rhabdomeres.

cpbM143 mutant clones induced at the first or second larval instar could not be recovered in the wing blade primordium, although mutant clones could develop in the remainder of the wing disc.

The nuclei and surrounding cytoplasm of late third instar retinal photoreceptors in cpbM143 homozygous somatic clones often leave the retina and travel through the optic stalk into the brain.

cpbM143 mutants survive embryogenesis.

External Data
Interactions
Show genetic interaction network for Enhancers & Suppressors
Phenotypic Class
Phenotype Manifest In
Enhancer of
Statement
Reference

cpbM143/cpb[+] is an enhancer of wing disc phenotype of CskGD9345, Scer\GAL4ptc-559.1

Suppressor of
Statement
Reference

cpbM143/cpb[+] is a suppressor | partially of egg | germline clone phenotype of Pkn1T

cpbM143/cpb[+] is a suppressor | partially of nurse cell | germline clone phenotype of Pkn1T

cpbM143/cpb[+] is a suppressor | partially of egg | germline clone phenotype of Pkn2T

cpbM143/cpb[+] is a suppressor | partially of nurse cell | germline clone phenotype of Pkn2T

Additional Comments
Genetic Interactions
Statement
Reference

Presence of cpbM143/+ partially suppresses the shorter egg length and nurse cell F-actin accumulation seen in Pkn1T/Pkn1T or Pkn2T/Pkn2T germline clone egg chambers.

A cpbM143 heterozygous mutant background enhances 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.

Homozygous Abl4, heterozygous cpbM143 double mutants lay few eggs. The crossing of cpbM143/+ ; Abl4/+ mothers and fathers results in 20% of the progeny dying during embryogenesis. 15% of the progeny have minor defects in central nervous system (CNS) architecture, whereas 21% exhibit more severe CNS defects. As cpbM143 Abl4 double mutants are only 6.25% of the progeny, the frequency of lethality and CNS phenotypes suggest that the mutations may dominantly enhance one another.

Xenogenetic Interactions
Statement
Reference
Complementation and Rescue Data
Images (0)
Mutant
Wild-type
Stocks (2)
Notes on Origin
Discoverer

M. Postner

External Crossreferences and Linkouts ( 0 )
Synonyms and Secondary IDs (2)
References (14)